Thrive Group are delighted to be working with our client in Frome, who are actively seeking to engage a Laboratory Manager to join the company on a permanent basis. What you will be doing: Managing a team and all activities related to laboratory testing. Including taking action on non-conforming results of microbiological or chemical analysis. Performing laboratory tests as required, calibrate and maintain lab equipment. Taking action following customer audits and complaints. Keeping the laboratory organised and in compliance with internal and external LAB CRED accreditation. Monitor and manage laboratory KPI Line management for laboratory team - completion of appraisals and further developing a department training matrix What you will need to succeed: The successful candidate will have experience of working in a FMCG Production / Manufacturing environment. Demonstrate a continuous improvement approach. Management or supervision of a small / medium team is necessary. Experience in analytical and microbiological laboratory experience. Experience of Laboratory Management Systems accreditation What you will receive in return: Monday to Friday 08.30AM to 17.30Pm (100% site-based role) £37,000 - £40,000 depending on experience Company pension 6% employer contribution 25 days holiday + Bank holidays Company sick pay 4 x Death in Service Free eye test and £90 contribution to glasses. Long service recognition What you need to do next: If this position sounds of interest and you would like to be considered. Please contact Sarah at Thrive Group on Direct line or email Thrive Group are acting as an employment agency in relationship to this vacancy. If you have not heard from a consultant within 7 days, please assume you have been unsuccessful on this occasion. PRMSTH JBRP1_UKTJ
Nov 18, 2025
Full time
Thrive Group are delighted to be working with our client in Frome, who are actively seeking to engage a Laboratory Manager to join the company on a permanent basis. What you will be doing: Managing a team and all activities related to laboratory testing. Including taking action on non-conforming results of microbiological or chemical analysis. Performing laboratory tests as required, calibrate and maintain lab equipment. Taking action following customer audits and complaints. Keeping the laboratory organised and in compliance with internal and external LAB CRED accreditation. Monitor and manage laboratory KPI Line management for laboratory team - completion of appraisals and further developing a department training matrix What you will need to succeed: The successful candidate will have experience of working in a FMCG Production / Manufacturing environment. Demonstrate a continuous improvement approach. Management or supervision of a small / medium team is necessary. Experience in analytical and microbiological laboratory experience. Experience of Laboratory Management Systems accreditation What you will receive in return: Monday to Friday 08.30AM to 17.30Pm (100% site-based role) £37,000 - £40,000 depending on experience Company pension 6% employer contribution 25 days holiday + Bank holidays Company sick pay 4 x Death in Service Free eye test and £90 contribution to glasses. Long service recognition What you need to do next: If this position sounds of interest and you would like to be considered. Please contact Sarah at Thrive Group on Direct line or email Thrive Group are acting as an employment agency in relationship to this vacancy. If you have not heard from a consultant within 7 days, please assume you have been unsuccessful on this occasion. PRMSTH JBRP1_UKTJ
Manpower are recruiting for a Laboratory Technician to work with one of our Client- UK's leading independent, family- owned diaries. Role: To assist in the delivery of an effective Laboratory service, through the sampling and testing of products to maintain product quality control. Main Duties & Responsibilities: Working with the Laboratory Manager and team to ensure compliance to both company and l click apply for full job details
Nov 18, 2025
Seasonal
Manpower are recruiting for a Laboratory Technician to work with one of our Client- UK's leading independent, family- owned diaries. Role: To assist in the delivery of an effective Laboratory service, through the sampling and testing of products to maintain product quality control. Main Duties & Responsibilities: Working with the Laboratory Manager and team to ensure compliance to both company and l click apply for full job details
Babcock Mission Critical Services España SA.
Plymouth, Devon
Head of Reactor Chemistry Location: Devonport, Plymouth, GB, PL1 4SG Onsite or Hybrid: Job Title: Head of Reactor Chemistry Role Type: Full time / Permanent Role ID: SF67956 Lead Innovation in Nuclear Chemistry At Babcock we're working to create a safe and secure world, together, and if you join us, you can play your part as a Head of Reactor Chemistry at our Devonport Royal Dockyard site. The role As a Head of Reactor Chemistry, you'll have a role that's out of the ordinary. You'll lead a team of skilled professionals, oversee technical outputs, and act as the authority on reactor chemistry matters. This is a unique opportunity to shape the future of nuclear chemistry in a dynamic and high impact environment. Day to day, you'll collaborate across departments, influence strategic decisions, and ensure compliance with industry standards - all while contributing to national defence and advancing your career in a role that blends science, leadership, and purpose. Leading and mentoring a team of chemistry professionals Acting as technical authority for reactor chemistry and ensuring regulatory compliance Overseeing departmental outputs and driving continuous improvement Coordinating documentation and aligning working practices across teams Managing health and safety processes and acting as appointing manager for accredited work This role is full time, 35 hours per week and is based on site at Devonport Royal Dockyard. Essential experience Deep knowledge of reactor chemistry principles and analytical techniques Familiarity with UKAS laboratory compliance standards Awareness of financial considerations in laboratory operations Strong communication and team building skills across business units Excellent time management and organisational abilities Qualifications Formal Management Training UKAS method validation / uncertainty of measurement training Level 5 qualification or equivalent in chemistry or related field DAP and/or ASQEP training NCC (Nuclear Chemistry Course) or equivalent Security Clearance The successful candidate must be able to achieve and maintain Security Check (SC) security clearance for this role. Many of the positions within our company are subject to national security clearance and Trade Control restrictions. This means that your eligibility for certain roles may be affected by your place of birth, nationality, current or former citizenship, and any residency you hold or have held. Further details are available at United Kingdom Security Vetting: clearance levels - GOV.UK (). What we offer Matched contribution pension scheme, with life assurance Access to a Digital GP, annual health check, and nutritional consultations through Aviva DigiCare+ Employee share scheme Employee shopping savings portal Payment of Professional Fees Reservists in the armed forces receive 10 days special paid leave Holiday Trading is a benefit that allows UK Babcock employees to buy additional leave or to sell up to one working week of annual leave from their annual entitlement. This Window opens February through to March annually. 'Be Kind Day' enables employees to take one working day's paid leave a year (or equivalent hours) to undertake volunteering work with their chosen organisation or registered charity Excellent development opportunities and benefits package including an employee assistance programme supporting physical, mental and financial wellbeing. Babcock International For over a century Babcock has helped to defend nations, protect communities and build a better world. To continue, we must adapt, advance and be a sustainable business with a shared goal. We are a disability confident committed employer. If you have a disability or need any reasonable adjustments during the application and selection stages, please email with the subject header "Reasonable adjustments requirement". We're committed to building an inclusive culture where everyone's free to thrive. We are happy to talk about flexible working - please ask about alternative patterns of work at interview.
Nov 16, 2025
Full time
Head of Reactor Chemistry Location: Devonport, Plymouth, GB, PL1 4SG Onsite or Hybrid: Job Title: Head of Reactor Chemistry Role Type: Full time / Permanent Role ID: SF67956 Lead Innovation in Nuclear Chemistry At Babcock we're working to create a safe and secure world, together, and if you join us, you can play your part as a Head of Reactor Chemistry at our Devonport Royal Dockyard site. The role As a Head of Reactor Chemistry, you'll have a role that's out of the ordinary. You'll lead a team of skilled professionals, oversee technical outputs, and act as the authority on reactor chemistry matters. This is a unique opportunity to shape the future of nuclear chemistry in a dynamic and high impact environment. Day to day, you'll collaborate across departments, influence strategic decisions, and ensure compliance with industry standards - all while contributing to national defence and advancing your career in a role that blends science, leadership, and purpose. Leading and mentoring a team of chemistry professionals Acting as technical authority for reactor chemistry and ensuring regulatory compliance Overseeing departmental outputs and driving continuous improvement Coordinating documentation and aligning working practices across teams Managing health and safety processes and acting as appointing manager for accredited work This role is full time, 35 hours per week and is based on site at Devonport Royal Dockyard. Essential experience Deep knowledge of reactor chemistry principles and analytical techniques Familiarity with UKAS laboratory compliance standards Awareness of financial considerations in laboratory operations Strong communication and team building skills across business units Excellent time management and organisational abilities Qualifications Formal Management Training UKAS method validation / uncertainty of measurement training Level 5 qualification or equivalent in chemistry or related field DAP and/or ASQEP training NCC (Nuclear Chemistry Course) or equivalent Security Clearance The successful candidate must be able to achieve and maintain Security Check (SC) security clearance for this role. Many of the positions within our company are subject to national security clearance and Trade Control restrictions. This means that your eligibility for certain roles may be affected by your place of birth, nationality, current or former citizenship, and any residency you hold or have held. Further details are available at United Kingdom Security Vetting: clearance levels - GOV.UK (). What we offer Matched contribution pension scheme, with life assurance Access to a Digital GP, annual health check, and nutritional consultations through Aviva DigiCare+ Employee share scheme Employee shopping savings portal Payment of Professional Fees Reservists in the armed forces receive 10 days special paid leave Holiday Trading is a benefit that allows UK Babcock employees to buy additional leave or to sell up to one working week of annual leave from their annual entitlement. This Window opens February through to March annually. 'Be Kind Day' enables employees to take one working day's paid leave a year (or equivalent hours) to undertake volunteering work with their chosen organisation or registered charity Excellent development opportunities and benefits package including an employee assistance programme supporting physical, mental and financial wellbeing. Babcock International For over a century Babcock has helped to defend nations, protect communities and build a better world. To continue, we must adapt, advance and be a sustainable business with a shared goal. We are a disability confident committed employer. If you have a disability or need any reasonable adjustments during the application and selection stages, please email with the subject header "Reasonable adjustments requirement". We're committed to building an inclusive culture where everyone's free to thrive. We are happy to talk about flexible working - please ask about alternative patterns of work at interview.
Calibration Manager / Metrology Manager / Laboratory Manager / Calibration / Metrology / Torque / Force / Measurements / Engineering / Manufacturing / Defence / Aerospace / Automotive / Team Leading / Management / Permanent role / Wolverhampton, West Midlands, £60 000 + 15% bonus + Benefits. One of our leading clients is looking to recruit a Calibration Manager / Metrology Manager. Location Wolverhampton, West Midlands Permanent role Salary £60 000 + 15% bonus You will have strong metrology knowledge (in particular Torque and/or force), experience in calibration laboratory management, experience of working with UKAS, auditing experience to ISO/IEC17025 and ISO9001 standards and the ability to deliver high quality calibration services. You will be responsible to drive the day-to-day technical calibration services for a wide variety of customers and delivering high quality calibration services with priority on safeguarding impartiality of all calibration laboratory activities. Role/Experience Torque and/or Force calibration Management of laboratory activities in association with the service team Plan and manage the calibration laboratory activities and workload in line with customer requirements and other requests. Ensure correct resource in line with calibration workload planning to drive the highest levels of customer service and efficiency of operations. Development and implementation of Management System to meet the requirements of the ISO/IEC 17025 standard and Calibration Management Process. Liaise with customers on all technical aspects associated with calibration and associated ISO standards for different Product Lines. Processing and issuing torque calibration (UKAS) certificates from calibration reports, made by Service Engineers, to customers To Liaise with any UKAS Representatives, along with the upkeep of all procedures and uncertainties within the companys management system To liaise with internal customers when required to ensure our customers calibration status is communicated Deliver calibration services and support for our customer base internal and external. Support a team of Calibration engineers in line with workload requirements, acting as the technical "champion" for the team Support understand and interpret UKAS quality systems (17025) and processes. Production of service and calibration paperwork, including UKAS and non-UKAS certificates. Implementation, control management of gauge management system for Service Engineers equipment Ensure the laboratory is compliant to relevant quality systems such as ISO17025 by maintaining audit schedule. Assist in developing calibration techniques, process and procedures as required by the business and/or relevant standards. QA and control procedures in line with company strategies To calibrate measuring instrumentation to company procedures Accurately recording calibration results and in line with industry standards Comply with company H&S guidelines JBRP1_UKTJ
Nov 15, 2025
Full time
Calibration Manager / Metrology Manager / Laboratory Manager / Calibration / Metrology / Torque / Force / Measurements / Engineering / Manufacturing / Defence / Aerospace / Automotive / Team Leading / Management / Permanent role / Wolverhampton, West Midlands, £60 000 + 15% bonus + Benefits. One of our leading clients is looking to recruit a Calibration Manager / Metrology Manager. Location Wolverhampton, West Midlands Permanent role Salary £60 000 + 15% bonus You will have strong metrology knowledge (in particular Torque and/or force), experience in calibration laboratory management, experience of working with UKAS, auditing experience to ISO/IEC17025 and ISO9001 standards and the ability to deliver high quality calibration services. You will be responsible to drive the day-to-day technical calibration services for a wide variety of customers and delivering high quality calibration services with priority on safeguarding impartiality of all calibration laboratory activities. Role/Experience Torque and/or Force calibration Management of laboratory activities in association with the service team Plan and manage the calibration laboratory activities and workload in line with customer requirements and other requests. Ensure correct resource in line with calibration workload planning to drive the highest levels of customer service and efficiency of operations. Development and implementation of Management System to meet the requirements of the ISO/IEC 17025 standard and Calibration Management Process. Liaise with customers on all technical aspects associated with calibration and associated ISO standards for different Product Lines. Processing and issuing torque calibration (UKAS) certificates from calibration reports, made by Service Engineers, to customers To Liaise with any UKAS Representatives, along with the upkeep of all procedures and uncertainties within the companys management system To liaise with internal customers when required to ensure our customers calibration status is communicated Deliver calibration services and support for our customer base internal and external. Support a team of Calibration engineers in line with workload requirements, acting as the technical "champion" for the team Support understand and interpret UKAS quality systems (17025) and processes. Production of service and calibration paperwork, including UKAS and non-UKAS certificates. Implementation, control management of gauge management system for Service Engineers equipment Ensure the laboratory is compliant to relevant quality systems such as ISO17025 by maintaining audit schedule. Assist in developing calibration techniques, process and procedures as required by the business and/or relevant standards. QA and control procedures in line with company strategies To calibrate measuring instrumentation to company procedures Accurately recording calibration results and in line with industry standards Comply with company H&S guidelines JBRP1_UKTJ
Head of Reactor Chemistry Location: Devonport, Plymouth, GB, PL1 4SG Onsite or Hybrid: Job Title: Head of Reactor Chemistry Role Type: Full time / Permanent Role ID: SF67956 Lead Innovation in Nuclear Chemistry At Babcock we're working to create a safe and secure world, together, and if you join us, you can play your part as a Head of Reactor Chemistry at our Devonport Royal Dockyard site. The role As a Head of Reactor Chemistry, you'll have a role that's out of the ordinary. You'll lead a team of skilled professionals, oversee technical outputs, and act as the authority on reactor chemistry matters. This is a unique opportunity to shape the future of nuclear chemistry in a dynamic and high impact environment. Day to day, you'll collaborate across departments, influence strategic decisions, and ensure compliance with industry standards - all while contributing to national defence and advancing your career in a role that blends science, leadership, and purpose. Leading and mentoring a team of chemistry professionals Acting as technical authority for reactor chemistry and ensuring regulatory compliance Overseeing departmental outputs and driving continuous improvement Coordinating documentation and aligning working practices across teams Managing health and safety processes and acting as appointing manager for accredited work This role is full time, 35 hours per week and is based on site at Devonport Royal Dockyard. Essential experience Deep knowledge of reactor chemistry principles and analytical techniques Familiarity with UKAS laboratory compliance standards Awareness of financial considerations in laboratory operations Strong communication and team building skills across business units Excellent time management and organisational abilities Qualifications Formal Management Training UKAS method validation / uncertainty of measurement training Level 5 qualification or equivalent in chemistry or related field DAP and/or ASQEP training NCC (Nuclear Chemistry Course) or equivalent Security Clearance The successful candidate must be able to achieve and maintain Security Check (SC) security clearance for this role. Many of the positions within our company are subject to national security clearance and Trade Control restrictions. This means that your eligibility for certain roles may be affected by your place of birth, nationality, current or former citizenship, and any residency you hold or have held. Further details are available at United Kingdom Security Vetting: clearance levels - GOV.UK (). What we offer Matched contribution pension scheme, with life assurance Access to a Digital GP, annual health check, and nutritional consultations through Aviva DigiCare+ Employee share scheme Employee shopping savings portal Payment of Professional Fees Reservists in the armed forces receive 10 days special paid leave Holiday Trading is a benefit that allows UK Babcock employees to buy additional leave or to sell up to one working week of annual leave from their annual entitlement. This Window opens February through to March annually. 'Be Kind Day' enables employees to take one working day's paid leave a year (or equivalent hours) to undertake volunteering work with their chosen organisation or registered charity Excellent development opportunities and benefits package including an employee assistance programme supporting physical, mental and financial wellbeing. Babcock International For over a century Babcock has helped to defend nations, protect communities and build a better world. To continue, we must adapt, advance and be a sustainable business with a shared goal. We are a disability confident committed employer. If you have a disability or need any reasonable adjustments during the application and selection stages, please email with the subject header "Reasonable adjustments requirement". We're committed to building an inclusive culture where everyone's free to thrive. We are happy to talk about flexible working - please ask about alternative patterns of work at interview.
Nov 15, 2025
Full time
Head of Reactor Chemistry Location: Devonport, Plymouth, GB, PL1 4SG Onsite or Hybrid: Job Title: Head of Reactor Chemistry Role Type: Full time / Permanent Role ID: SF67956 Lead Innovation in Nuclear Chemistry At Babcock we're working to create a safe and secure world, together, and if you join us, you can play your part as a Head of Reactor Chemistry at our Devonport Royal Dockyard site. The role As a Head of Reactor Chemistry, you'll have a role that's out of the ordinary. You'll lead a team of skilled professionals, oversee technical outputs, and act as the authority on reactor chemistry matters. This is a unique opportunity to shape the future of nuclear chemistry in a dynamic and high impact environment. Day to day, you'll collaborate across departments, influence strategic decisions, and ensure compliance with industry standards - all while contributing to national defence and advancing your career in a role that blends science, leadership, and purpose. Leading and mentoring a team of chemistry professionals Acting as technical authority for reactor chemistry and ensuring regulatory compliance Overseeing departmental outputs and driving continuous improvement Coordinating documentation and aligning working practices across teams Managing health and safety processes and acting as appointing manager for accredited work This role is full time, 35 hours per week and is based on site at Devonport Royal Dockyard. Essential experience Deep knowledge of reactor chemistry principles and analytical techniques Familiarity with UKAS laboratory compliance standards Awareness of financial considerations in laboratory operations Strong communication and team building skills across business units Excellent time management and organisational abilities Qualifications Formal Management Training UKAS method validation / uncertainty of measurement training Level 5 qualification or equivalent in chemistry or related field DAP and/or ASQEP training NCC (Nuclear Chemistry Course) or equivalent Security Clearance The successful candidate must be able to achieve and maintain Security Check (SC) security clearance for this role. Many of the positions within our company are subject to national security clearance and Trade Control restrictions. This means that your eligibility for certain roles may be affected by your place of birth, nationality, current or former citizenship, and any residency you hold or have held. Further details are available at United Kingdom Security Vetting: clearance levels - GOV.UK (). What we offer Matched contribution pension scheme, with life assurance Access to a Digital GP, annual health check, and nutritional consultations through Aviva DigiCare+ Employee share scheme Employee shopping savings portal Payment of Professional Fees Reservists in the armed forces receive 10 days special paid leave Holiday Trading is a benefit that allows UK Babcock employees to buy additional leave or to sell up to one working week of annual leave from their annual entitlement. This Window opens February through to March annually. 'Be Kind Day' enables employees to take one working day's paid leave a year (or equivalent hours) to undertake volunteering work with their chosen organisation or registered charity Excellent development opportunities and benefits package including an employee assistance programme supporting physical, mental and financial wellbeing. Babcock International For over a century Babcock has helped to defend nations, protect communities and build a better world. To continue, we must adapt, advance and be a sustainable business with a shared goal. We are a disability confident committed employer. If you have a disability or need any reasonable adjustments during the application and selection stages, please email with the subject header "Reasonable adjustments requirement". We're committed to building an inclusive culture where everyone's free to thrive. We are happy to talk about flexible working - please ask about alternative patterns of work at interview.
Science & Technology Facilities Council (STFC)
Didcot, Oxfordshire
Instrumental Raman Spectroscopist UPLiFT Salary: £41,344 - £45,479 per annum 3 Years Fixed-term Contract Full-time Closing date: 23rd November 2025 Location: Science and Technology Facilities Council, Rutherford Appleton Laboratory Harwell, Oxfordshire OX11 0DE Come and discover the kind of impact you can make when you work with some of the best facilities and brightest scientists in the world. As part of the Science and Technology Facilities Council (STFC) the Central Laser Facility (CLF) contains many state-of-the-art laser systems and experimental stations, along with expert scientists, engineers and technicians that work with academic and industry users to deliver science across a broad range of fields. We have around 200 staff and are a very friendly, outgoing, externally facing department. We have a welcoming and inclusive culture, and you will find that people will naturally help and support you. About the role The position is to participate in a research project to develop a novel concept combining Spatially Offset Raman Spectroscopy (SORS) and ultrasound for enhanced chemically specific imaging deep inside biological tissue. The full-time position is funded through a recently awarded EPSRC grant for three years. The concerned work will take place at the Central Laser Facility, STFC Rutherford Appleton Laboratory in Oxfordshire, UK and involves close collaboration with the University of Exeter (Prof. Nick Stone). This post will be part of a team of leading scientists working to develop novel solutions to solve clinical needs in patient specific diagnosis and treatment of cancers. Specifically, we seek a postdoctoral research scientist to focus on the development of instrumentation comprising both SORS and Raman technology. Expertise in vibrational spectroscopy is essential. The post will include design, construction, optimisation and day-to-day operation of the instrument. The study will be performed on excised tissue and optical phantoms. The applicant will have experience with data analysis of vibrational spectra. The successful applicant will be able to present information on research progress and outcomes, communicate complex information orally, in writing and electronically and participate in the preparation of proposals and applications to external bodies. A suitable candidate will be a PhD graduate (or near completion) in any of the natural sciences. The candidate will benefit from working in a vibrant internationally leading research environment. Advanced training and researcher development will be provided as part of the programme. Main duties and accountabilities To undertake research to develop the novel analytical instrumentation, including optical design. Writing up research work for publication. Making presentations at national and international conferences and similar events. Dealing with problems which may affect the achievement of research objectives and deadlines. Analysing and interpreting the results of own research and generating original ideas based on outcomes. Using new research techniques and methods. Using initiative and creativity to identify areas for research, developing new research methods and extending the research portfolio. To monitor research budgets as appropriate. To maintain safety in their research environment. Engaging in continuous professional development. Person Specification The following criteria will be assessed at Shortlisting (S), Interview (I) or both (S&I) A PhD in natural sciences (or within 6 months of completion), or equivalent experience. (S) Experience in using vibrational spectroscopy (Raman or IR) and associated data analysis. (S&I) Hands on experience in developing/aligning vibrational spectroscopy instruments (Raman or IR). (S&I) Having a proactive approach to work and to be able to use initiative to work within a scientific environment. (I) Able to work independently and as a part of a team. (S&I) Able to work to tight deadlines. (S&I) Safety awareness. (I) Excellent interpersonal skills, including communication, both written and oral. (S&I) Additional Information Further information is available from Prof. Pavel Matousek (). Our Benefits UK Research and Innovation recognises and values employees as individuals and aim to provide a pay and rewards package that motivates staff to perform to the best of their ability. The reward package includes a flexible working scheme, Defined benefit pension scheme, 30 days annual leave allowance plus 10.5 bank holiday/privilege days and several other benefits. We ask some of the biggest questions in the universe, to answer some of the biggest challenges in the world. Whatever our role, we have the freedom to explore, learn and connect, as part of a community that loves to share knowledge and support one another. As one of Europes largest research organisations, this is a place where theres always something new to learn about the world around us, about your career, but most of all, about yourself. Join us and discover whats possible! Please note, if you will require sponsorship to work in the UK, as part of your sponsorship application, you and any dependants travelling with you, will be required to pay costs directly to The Home Office for the application before you start your role with us. UKRI is normally able to reimburse some, or all of these fees after you have become an employee and this can be discussed with the Hiring Manager. For more information, please visit or contact JBRP1_UKTJ
Nov 11, 2025
Full time
Instrumental Raman Spectroscopist UPLiFT Salary: £41,344 - £45,479 per annum 3 Years Fixed-term Contract Full-time Closing date: 23rd November 2025 Location: Science and Technology Facilities Council, Rutherford Appleton Laboratory Harwell, Oxfordshire OX11 0DE Come and discover the kind of impact you can make when you work with some of the best facilities and brightest scientists in the world. As part of the Science and Technology Facilities Council (STFC) the Central Laser Facility (CLF) contains many state-of-the-art laser systems and experimental stations, along with expert scientists, engineers and technicians that work with academic and industry users to deliver science across a broad range of fields. We have around 200 staff and are a very friendly, outgoing, externally facing department. We have a welcoming and inclusive culture, and you will find that people will naturally help and support you. About the role The position is to participate in a research project to develop a novel concept combining Spatially Offset Raman Spectroscopy (SORS) and ultrasound for enhanced chemically specific imaging deep inside biological tissue. The full-time position is funded through a recently awarded EPSRC grant for three years. The concerned work will take place at the Central Laser Facility, STFC Rutherford Appleton Laboratory in Oxfordshire, UK and involves close collaboration with the University of Exeter (Prof. Nick Stone). This post will be part of a team of leading scientists working to develop novel solutions to solve clinical needs in patient specific diagnosis and treatment of cancers. Specifically, we seek a postdoctoral research scientist to focus on the development of instrumentation comprising both SORS and Raman technology. Expertise in vibrational spectroscopy is essential. The post will include design, construction, optimisation and day-to-day operation of the instrument. The study will be performed on excised tissue and optical phantoms. The applicant will have experience with data analysis of vibrational spectra. The successful applicant will be able to present information on research progress and outcomes, communicate complex information orally, in writing and electronically and participate in the preparation of proposals and applications to external bodies. A suitable candidate will be a PhD graduate (or near completion) in any of the natural sciences. The candidate will benefit from working in a vibrant internationally leading research environment. Advanced training and researcher development will be provided as part of the programme. Main duties and accountabilities To undertake research to develop the novel analytical instrumentation, including optical design. Writing up research work for publication. Making presentations at national and international conferences and similar events. Dealing with problems which may affect the achievement of research objectives and deadlines. Analysing and interpreting the results of own research and generating original ideas based on outcomes. Using new research techniques and methods. Using initiative and creativity to identify areas for research, developing new research methods and extending the research portfolio. To monitor research budgets as appropriate. To maintain safety in their research environment. Engaging in continuous professional development. Person Specification The following criteria will be assessed at Shortlisting (S), Interview (I) or both (S&I) A PhD in natural sciences (or within 6 months of completion), or equivalent experience. (S) Experience in using vibrational spectroscopy (Raman or IR) and associated data analysis. (S&I) Hands on experience in developing/aligning vibrational spectroscopy instruments (Raman or IR). (S&I) Having a proactive approach to work and to be able to use initiative to work within a scientific environment. (I) Able to work independently and as a part of a team. (S&I) Able to work to tight deadlines. (S&I) Safety awareness. (I) Excellent interpersonal skills, including communication, both written and oral. (S&I) Additional Information Further information is available from Prof. Pavel Matousek (). Our Benefits UK Research and Innovation recognises and values employees as individuals and aim to provide a pay and rewards package that motivates staff to perform to the best of their ability. The reward package includes a flexible working scheme, Defined benefit pension scheme, 30 days annual leave allowance plus 10.5 bank holiday/privilege days and several other benefits. We ask some of the biggest questions in the universe, to answer some of the biggest challenges in the world. Whatever our role, we have the freedom to explore, learn and connect, as part of a community that loves to share knowledge and support one another. As one of Europes largest research organisations, this is a place where theres always something new to learn about the world around us, about your career, but most of all, about yourself. Join us and discover whats possible! Please note, if you will require sponsorship to work in the UK, as part of your sponsorship application, you and any dependants travelling with you, will be required to pay costs directly to The Home Office for the application before you start your role with us. UKRI is normally able to reimburse some, or all of these fees after you have become an employee and this can be discussed with the Hiring Manager. For more information, please visit or contact JBRP1_UKTJ
Pontefract is a historic town in West Yorkshire and known locally as Ponte or Ponte Carlo. Famous for its Pontefract cakes, castle and confectionary, the area has a wealth of industrial history. This experienced team is made up of our newly appointed Practice Manager - Kira, our full Nursing team, and Client Care team. The practice can offer a wide range of services and state-of-the-art facilities including diagnostic imaging, dental facilities including radiography, and an in-house laboratory. This opportunity would suit an ambitious and motivated small animal Vet who is looking to establish relationships and develop our client base further. We are offering a full-time working pattern of 4 weekdays per week and a fair weekend rota, but if part-time is something you wish to consider, let's talk about how we can support this. We offer a relocation package if relocating from outside the UK or more than 60 miles from your current UK address. This is the perfect opportunity to take the next step in your career by joining the growing Medivet community. We want to be the best place for vets and nurses to work, and we're taking the right steps in achieving this. For more information, contact . Role Accountabilities: Exceptional care is at the heart of everything we do at Medivet. That's the care for our patients, our clients, and for each other - we really want to make a positive difference through every interaction we have. In this role, you will: Deliver exceptional clinical care to your patients during consultations and procedures. Provide exceptional care to your clients, giving clear updates on patients. Deliver professional excellence, observing the highest standards of regulatory, practice, and operational compliance. Prepare accurate estimates for clients, ensuring payment and minimizing debt. Work closely with the Practice Manager to maximize commercial performance with a focus on key measures. Engage, mentor, and develop your team, enhancing their skills and utilizing these in the most effective way. Inspire your team, sharing new or evolving practice standards and changes to processes. Complete clinical handover and arrange transfer of any patient needing out of hours or enhanced care. Proactively support and share clinical best practice within and across practices and the wider Medivet community. Your Skills and Experience: RCVS registered Veterinary Surgeon. Able to demonstrate clinical leadership skills. Experienced in delivering exceptional care to both patients and clients. An understanding and appreciation of exceptional care and how this improves the client experience. Experience of implementing a progressive clinical culture. Experience of delivering strong commercial performance through effective allocation of clinical activity. Experienced in working effectively as part of a team. Experienced in using coaching and influencing skills to get the best out of every colleague. About Us: Medivet is a leading veterinary care provider, with practices across the UK including a number of 24-hour veterinary centres and referral centres. We also have a growing presence overseas with practices in France, Germany, and Spain. We're proud to support a large, connected, and growing community of colleagues who provide exceptional care that's always there. That's more than a strapline for us; we truly believe every interaction we have matters and that we can make a real difference. This is as true for our colleagues as it is for our patients and clients. Being part of Medivet means being part of a forward-thinking and caring environment with the very best equipment and treatment options available, and the very best treatment for you as a valued member of the team. This is the home of talented people like you who want to stand out in their field and whose compassion for animals goes way beyond their job. Join us and be part of our exciting plans for the future. Why work here? Medivet is a family of passionate, supportive, and thoughtful veterinary professionals. We work as one team to support each other, grow the business, and make sure every pet receives the very best care. Get In Touch Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.
Nov 11, 2025
Full time
Pontefract is a historic town in West Yorkshire and known locally as Ponte or Ponte Carlo. Famous for its Pontefract cakes, castle and confectionary, the area has a wealth of industrial history. This experienced team is made up of our newly appointed Practice Manager - Kira, our full Nursing team, and Client Care team. The practice can offer a wide range of services and state-of-the-art facilities including diagnostic imaging, dental facilities including radiography, and an in-house laboratory. This opportunity would suit an ambitious and motivated small animal Vet who is looking to establish relationships and develop our client base further. We are offering a full-time working pattern of 4 weekdays per week and a fair weekend rota, but if part-time is something you wish to consider, let's talk about how we can support this. We offer a relocation package if relocating from outside the UK or more than 60 miles from your current UK address. This is the perfect opportunity to take the next step in your career by joining the growing Medivet community. We want to be the best place for vets and nurses to work, and we're taking the right steps in achieving this. For more information, contact . Role Accountabilities: Exceptional care is at the heart of everything we do at Medivet. That's the care for our patients, our clients, and for each other - we really want to make a positive difference through every interaction we have. In this role, you will: Deliver exceptional clinical care to your patients during consultations and procedures. Provide exceptional care to your clients, giving clear updates on patients. Deliver professional excellence, observing the highest standards of regulatory, practice, and operational compliance. Prepare accurate estimates for clients, ensuring payment and minimizing debt. Work closely with the Practice Manager to maximize commercial performance with a focus on key measures. Engage, mentor, and develop your team, enhancing their skills and utilizing these in the most effective way. Inspire your team, sharing new or evolving practice standards and changes to processes. Complete clinical handover and arrange transfer of any patient needing out of hours or enhanced care. Proactively support and share clinical best practice within and across practices and the wider Medivet community. Your Skills and Experience: RCVS registered Veterinary Surgeon. Able to demonstrate clinical leadership skills. Experienced in delivering exceptional care to both patients and clients. An understanding and appreciation of exceptional care and how this improves the client experience. Experience of implementing a progressive clinical culture. Experience of delivering strong commercial performance through effective allocation of clinical activity. Experienced in working effectively as part of a team. Experienced in using coaching and influencing skills to get the best out of every colleague. About Us: Medivet is a leading veterinary care provider, with practices across the UK including a number of 24-hour veterinary centres and referral centres. We also have a growing presence overseas with practices in France, Germany, and Spain. We're proud to support a large, connected, and growing community of colleagues who provide exceptional care that's always there. That's more than a strapline for us; we truly believe every interaction we have matters and that we can make a real difference. This is as true for our colleagues as it is for our patients and clients. Being part of Medivet means being part of a forward-thinking and caring environment with the very best equipment and treatment options available, and the very best treatment for you as a valued member of the team. This is the home of talented people like you who want to stand out in their field and whose compassion for animals goes way beyond their job. Join us and be part of our exciting plans for the future. Why work here? Medivet is a family of passionate, supportive, and thoughtful veterinary professionals. We work as one team to support each other, grow the business, and make sure every pet receives the very best care. Get In Touch Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.
Short Intro and About the Job We are seeking a dedicated and detail-oriented Quality QC Analyst Chemistry We're excited to share a new opportunity for a QC Analyst - Chemistry at Nutricia DANONE! This is a part-time position (30 hours per week), with shifts scheduled on Thursday, Friday, Saturday, and Sunday. We offer flexible start times to help fit your schedule. The role is temporary for 6 months, with the potential for extension depending on business needs. About You Key responsibilities include conducting routine chemical analysis following established SOPs, maintaining KPIs within the cell structure, solving problems and implementing corrective actions, and assisting with continuous improvements while complying with Health and Safety Standards. You will also be responsible for training team members, introducing and validating new methods and equipment, providing technical advice, managing laboratory chemicals and consumable stock levels, and participating in departmental audits to maintain laboratory quality standards and records. The role offers exposure at all levels and multiple functions within the Quality Department, with the opportunity to directly contribute to the growth and development of a team. The project is expected to be completed within six months and requires collaboration between marketing, IT, and customer service departments. Key Skills and Competencies Needed Education & Professional Experience: BSc in Chemistry or a Science-based discipline is preferred. Relevant academic qualifications/experience within a laboratory environment. Fluent in English, both spoken and written. Functional Competencies & Technical Skills: Contribution to business strategy and project management. Knowledge of formulation, process, and equipment. Awareness of Quality and Food Safety Systems. Risk analysis and management. Problem-solving using classic tools to guarantee quality results and products. Good analytical and technical capabilities. Presentation and problem-solving skills. Managerial Competencies & Personal Skills: Committed and able to inspire and create breakthrough results. Open and willing to share ideas, give constructive feedback, and collaborate. Delivering on promises and taking responsibility. Agile, pragmatic, and capable of complex problem-solving. Empowering self and teams, coaching, and developing people. Self-aware and able to maintain emotional balance under stress. Preferred/Nice to Have: Knowledge of LIMS systems. Experience with 17025 standards. Key Motivators for the Right Candidate: Exposure at all levels and multiple functions within the Quality Department. Opportunity to directly contribute to the growth and development of a team. About Us, We offer and What's next Every minute on any given day, 3,600 people are eating or drinking on our products. Ranging from household favourites to international icons, our consumer and medical nutrition brands hold market leading positions in most of the categories in which we operate. We offer a competitive package including a double matched pension, annual bonus, private healthcare, life assurance and product vouchers. You will also be entitled to opt into a range of flexible benefits which you can pick to suit your lifestyle. These include discounted gym membership, childcare vouchers, dental cover, optical insurance, travel insurance, holiday buy & sell and much more! Our mission and values guide how we behave, our flexible ways of working, how we connect with our communities and how we grow & develop our people. This is reflected in our employee offer; for example, our health & wellbeing programme, sponsored volunteering opportunities and in how individuals are enabled to drive their own development. Ensuring an inclusive working culture that is accessible to all is important to us; we therefore support flexible ways of working wherever possible. Please let us know in your application how you would like to explore flexible working for this position. Look at the website to learn more about our 4 promises that help every Danoner carry out our vision in their own unique way. If you are passionate about quality control and have the required skills and experience, we would love to hear from you. Apply now to join our dynamic team and contribute to our mission of delivering high-quality products to our customers.
Nov 11, 2025
Full time
Short Intro and About the Job We are seeking a dedicated and detail-oriented Quality QC Analyst Chemistry We're excited to share a new opportunity for a QC Analyst - Chemistry at Nutricia DANONE! This is a part-time position (30 hours per week), with shifts scheduled on Thursday, Friday, Saturday, and Sunday. We offer flexible start times to help fit your schedule. The role is temporary for 6 months, with the potential for extension depending on business needs. About You Key responsibilities include conducting routine chemical analysis following established SOPs, maintaining KPIs within the cell structure, solving problems and implementing corrective actions, and assisting with continuous improvements while complying with Health and Safety Standards. You will also be responsible for training team members, introducing and validating new methods and equipment, providing technical advice, managing laboratory chemicals and consumable stock levels, and participating in departmental audits to maintain laboratory quality standards and records. The role offers exposure at all levels and multiple functions within the Quality Department, with the opportunity to directly contribute to the growth and development of a team. The project is expected to be completed within six months and requires collaboration between marketing, IT, and customer service departments. Key Skills and Competencies Needed Education & Professional Experience: BSc in Chemistry or a Science-based discipline is preferred. Relevant academic qualifications/experience within a laboratory environment. Fluent in English, both spoken and written. Functional Competencies & Technical Skills: Contribution to business strategy and project management. Knowledge of formulation, process, and equipment. Awareness of Quality and Food Safety Systems. Risk analysis and management. Problem-solving using classic tools to guarantee quality results and products. Good analytical and technical capabilities. Presentation and problem-solving skills. Managerial Competencies & Personal Skills: Committed and able to inspire and create breakthrough results. Open and willing to share ideas, give constructive feedback, and collaborate. Delivering on promises and taking responsibility. Agile, pragmatic, and capable of complex problem-solving. Empowering self and teams, coaching, and developing people. Self-aware and able to maintain emotional balance under stress. Preferred/Nice to Have: Knowledge of LIMS systems. Experience with 17025 standards. Key Motivators for the Right Candidate: Exposure at all levels and multiple functions within the Quality Department. Opportunity to directly contribute to the growth and development of a team. About Us, We offer and What's next Every minute on any given day, 3,600 people are eating or drinking on our products. Ranging from household favourites to international icons, our consumer and medical nutrition brands hold market leading positions in most of the categories in which we operate. We offer a competitive package including a double matched pension, annual bonus, private healthcare, life assurance and product vouchers. You will also be entitled to opt into a range of flexible benefits which you can pick to suit your lifestyle. These include discounted gym membership, childcare vouchers, dental cover, optical insurance, travel insurance, holiday buy & sell and much more! Our mission and values guide how we behave, our flexible ways of working, how we connect with our communities and how we grow & develop our people. This is reflected in our employee offer; for example, our health & wellbeing programme, sponsored volunteering opportunities and in how individuals are enabled to drive their own development. Ensuring an inclusive working culture that is accessible to all is important to us; we therefore support flexible ways of working wherever possible. Please let us know in your application how you would like to explore flexible working for this position. Look at the website to learn more about our 4 promises that help every Danoner carry out our vision in their own unique way. If you are passionate about quality control and have the required skills and experience, we would love to hear from you. Apply now to join our dynamic team and contribute to our mission of delivering high-quality products to our customers.
Are you interested and excited to work with a multinational organization in medical devices industry? We have an opportunity for you as Laboratory assistant Job Title: Laboratory assistant Duration: 6 months Location: Abingdon Salary: 13.07 p/h Working hours: 37.5 hours Main Purpose of the Role: This role requires the individual to facilitate the timely, accurate processing and management of biological samples submitted from customers for toxicological analysis. Such samples may comprise of oral fluid and hair and it is the responsibility of the Laboratory Assistant to route the samples for the appropriate analytical tests based on the specific requirements of our customers. Samples must be opened, their details entered into a Laboratory Information Management System (LIMS) and prepared for testing whilst adhering to Chain of Custody procedures at all times to preserve the integrity of the sample. Responsibilities: Preparation of hair and oral fluid samples for analysis, within agreed timeframes Ensuring all equipment used is within current specifications including calibration and maintenance requirements Accurate data entry, including relevant scanning and archiving Logging 'discrepancy' samples and liaising with Customer Services to resolves any issues efficiently and promptly Sample logging, storage and disposal Adherence to quality systems Carrying out tasks as directed by the Accessioning Manager and to feedback any problems, working to assist in their resolution Continued participation in training programmes across Laboratory Operations to develop themselves and to increase their breadth of understanding of the function of Operations as a whole Requirements: Excellent attention to detail Keen interest in understanding principal of processes Is dynamic and tenacious Shows accountability and demonstrates ownership of their world Able to function well as an individual or as part of a team Able to take ownership of own work, awareness of when to solve a problem themselves or to ask their manager for help Conform with appropriate safety standards under The Health and Safety at Work Act 1974 and the Management of Health and Safety at Work Regulations 1999 Work in accordance with the current documented Standard Operating Procedures. Concateno UK is an ISO 9001 and ISO 17025 certified laboratory. If this is something that you would be interested in please apply with your updated CV and I will be happy to connect at your convenient time. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 10, 2025
Contractor
Are you interested and excited to work with a multinational organization in medical devices industry? We have an opportunity for you as Laboratory assistant Job Title: Laboratory assistant Duration: 6 months Location: Abingdon Salary: 13.07 p/h Working hours: 37.5 hours Main Purpose of the Role: This role requires the individual to facilitate the timely, accurate processing and management of biological samples submitted from customers for toxicological analysis. Such samples may comprise of oral fluid and hair and it is the responsibility of the Laboratory Assistant to route the samples for the appropriate analytical tests based on the specific requirements of our customers. Samples must be opened, their details entered into a Laboratory Information Management System (LIMS) and prepared for testing whilst adhering to Chain of Custody procedures at all times to preserve the integrity of the sample. Responsibilities: Preparation of hair and oral fluid samples for analysis, within agreed timeframes Ensuring all equipment used is within current specifications including calibration and maintenance requirements Accurate data entry, including relevant scanning and archiving Logging 'discrepancy' samples and liaising with Customer Services to resolves any issues efficiently and promptly Sample logging, storage and disposal Adherence to quality systems Carrying out tasks as directed by the Accessioning Manager and to feedback any problems, working to assist in their resolution Continued participation in training programmes across Laboratory Operations to develop themselves and to increase their breadth of understanding of the function of Operations as a whole Requirements: Excellent attention to detail Keen interest in understanding principal of processes Is dynamic and tenacious Shows accountability and demonstrates ownership of their world Able to function well as an individual or as part of a team Able to take ownership of own work, awareness of when to solve a problem themselves or to ask their manager for help Conform with appropriate safety standards under The Health and Safety at Work Act 1974 and the Management of Health and Safety at Work Regulations 1999 Work in accordance with the current documented Standard Operating Procedures. Concateno UK is an ISO 9001 and ISO 17025 certified laboratory. If this is something that you would be interested in please apply with your updated CV and I will be happy to connect at your convenient time. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Science & Technology Facilities Council (STFC)
Didcot, Oxfordshire
Laser Scientist Science and Technology Facilities Council Salary: £52,907 - £58,198 per annum (dependent on skills and experience) Hours: Full-Time Contract Type: Fixed Term Contract (4 years) Location: Science and Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Campus, Oxfordshire OX11 0DE Come and discover the kind of impact that you can make when you work with some of the best facilities and brightest scientists in the world. An exciting opportunity exists to join the Central Laser Facility (CLF) at the Rutherford Appleton Laboratory to work on the development of lasers driving next-generation particle accelerators and X-ray sources. The goal of this project is to design, install and test next-generation high energy femtosecond laser sources operating at 100 Hz to 1 kHz pulse rates. We are seeking to develop and demonstrate a reliable 100 TW peak power laser operating at the unprecedented pulse rate of 100 Hz. The pump source for the main broadband power amplifier will rely on the CLFs proprietary DiPOLE laser amplifier technology. Alongside, research and development work will be carried out to scale the pulse rate to 1 kHz. These short-pulsed, high peak and average power lasers will be used to drive plasma accelerators for the realisation of compact, high brightness secondary particle and radiation sources. This unprecedented operational regime will unlock unprecedented scientific, industrial and healthcare applications and open commercialisation opportunities. The CLF hosts a large range of cutting-edge lasers and experimental stations which are developed and operated by expert scientists, engineers and technicians. The CLF works with academic and industrial users to deliver science over a broad range of fields. We have around 200 staff and are a very friendly, outgoing and externally facing department. We have a welcoming and inclusive culture, and you will find that people will naturally help and support you. About the role: You will join the Centre for Advanced Laser Technology and Applications (CALTA) team and support the high peak power 100 Hz and 1 kHz projects by developing laser designs, setting up prototype systems and conducting experimental test campaigns. You will be part of a team of laser scientists, engineers and technicians and will engage with the wider CLF to understand the implications of plasma accelerator physics on laser driver specifications. You will take part in international collaborations and routinely engage with external experts. You will have the opportunity to present your research at international conferences and publish in high-profile peer-reviewed journals. Key areas of the role include: Contributing significantly to the development of new lasers, by performing the optical design of laser setups and diagnostics and by defining the specifications of laser components. Modelling broadband pulse amplification and propagation of chirped-pulsed amplification (CPA) systems. Defining and conducting proof-of-concept tests to de-risk key component technologies. Liaising with external suppliers and contractors to determine existing capabilities and future requirements and develop collaborative links with external research laboratories. Working as part of a team liaising with engineers to design key mechanical equipment for prototype testing. Lead installation and testing of prototype components in the laser laboratory to validate designs and technological solutions. About you: You should have significant knowledge of laser science and nonlinear optics. You will ideally be familiar with solid state laser design and have experience of broadband laser pulse amplification and diagnostics. You will have experience in modelling or simulations and be able to apply that knowledge to the design of laser systems. Person specification: The following criteria will be assessed at Shortlisting (S), Interview (I) or both (S&I) A PhD in physics or closely related subject (or equivalent experience). (S) Post-doctoral research experience (or equivalent relevant experience) with a record of independent research or autonomous thinking. (S&I) Significant knowledge of optics, nonlinear optics and solid-state laser physics. (S&I) Experience in modelling, optical design and testing of short-pulse lasers and diagnostics. (S&I) Experience in publishing in peer-reviewed journals and/or conference proceedings. (S) Competence with Matlab and/or LabVIEW, and Zemax/OpticStudio or other equivalent optical design software. (S&I) Knowledge of safety related issues and procedures for operating lasers. (S&I) Good interpersonal skills and ability to work as part of a diverse team. (I) Additional information: The role involves working in a laser laboratory. For more information about the role, please visit or contact . Our Benefits: STFC values their employees by offering a benefits package designed to provide an excellent work/life balance including 30 days annual leave, 10.5 public and privilege holidays, flexible working hours, exceptional average salary pension scheme, social and sporting activities and societies and a subsidised restaurant. We ask some of the biggest questions in the universe, to answer some of the biggest challenges in the world. Whatever our role, we have the freedom to explore, learn and connect, as part of a community that loves to share knowledge and support one another. As one of Europes largest research organisations, this is a place where theres always something new to learn about the world around us, about your career, but most of all, about yourself. Join us and discover whats possible! Please note, if you will require sponsorship to work in the UK, as part of your sponsorship application, you and any dependants travelling with you, will be required to pay costs directly to The Home Office for the application before you start your role with us. UKRI is normally able to reimburse some, or all of these fees after you have become an employee and this can be discussed with the Hiring Manager. For more information, please visit or contact . JBRP1_UKTJ
Nov 10, 2025
Full time
Laser Scientist Science and Technology Facilities Council Salary: £52,907 - £58,198 per annum (dependent on skills and experience) Hours: Full-Time Contract Type: Fixed Term Contract (4 years) Location: Science and Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Campus, Oxfordshire OX11 0DE Come and discover the kind of impact that you can make when you work with some of the best facilities and brightest scientists in the world. An exciting opportunity exists to join the Central Laser Facility (CLF) at the Rutherford Appleton Laboratory to work on the development of lasers driving next-generation particle accelerators and X-ray sources. The goal of this project is to design, install and test next-generation high energy femtosecond laser sources operating at 100 Hz to 1 kHz pulse rates. We are seeking to develop and demonstrate a reliable 100 TW peak power laser operating at the unprecedented pulse rate of 100 Hz. The pump source for the main broadband power amplifier will rely on the CLFs proprietary DiPOLE laser amplifier technology. Alongside, research and development work will be carried out to scale the pulse rate to 1 kHz. These short-pulsed, high peak and average power lasers will be used to drive plasma accelerators for the realisation of compact, high brightness secondary particle and radiation sources. This unprecedented operational regime will unlock unprecedented scientific, industrial and healthcare applications and open commercialisation opportunities. The CLF hosts a large range of cutting-edge lasers and experimental stations which are developed and operated by expert scientists, engineers and technicians. The CLF works with academic and industrial users to deliver science over a broad range of fields. We have around 200 staff and are a very friendly, outgoing and externally facing department. We have a welcoming and inclusive culture, and you will find that people will naturally help and support you. About the role: You will join the Centre for Advanced Laser Technology and Applications (CALTA) team and support the high peak power 100 Hz and 1 kHz projects by developing laser designs, setting up prototype systems and conducting experimental test campaigns. You will be part of a team of laser scientists, engineers and technicians and will engage with the wider CLF to understand the implications of plasma accelerator physics on laser driver specifications. You will take part in international collaborations and routinely engage with external experts. You will have the opportunity to present your research at international conferences and publish in high-profile peer-reviewed journals. Key areas of the role include: Contributing significantly to the development of new lasers, by performing the optical design of laser setups and diagnostics and by defining the specifications of laser components. Modelling broadband pulse amplification and propagation of chirped-pulsed amplification (CPA) systems. Defining and conducting proof-of-concept tests to de-risk key component technologies. Liaising with external suppliers and contractors to determine existing capabilities and future requirements and develop collaborative links with external research laboratories. Working as part of a team liaising with engineers to design key mechanical equipment for prototype testing. Lead installation and testing of prototype components in the laser laboratory to validate designs and technological solutions. About you: You should have significant knowledge of laser science and nonlinear optics. You will ideally be familiar with solid state laser design and have experience of broadband laser pulse amplification and diagnostics. You will have experience in modelling or simulations and be able to apply that knowledge to the design of laser systems. Person specification: The following criteria will be assessed at Shortlisting (S), Interview (I) or both (S&I) A PhD in physics or closely related subject (or equivalent experience). (S) Post-doctoral research experience (or equivalent relevant experience) with a record of independent research or autonomous thinking. (S&I) Significant knowledge of optics, nonlinear optics and solid-state laser physics. (S&I) Experience in modelling, optical design and testing of short-pulse lasers and diagnostics. (S&I) Experience in publishing in peer-reviewed journals and/or conference proceedings. (S) Competence with Matlab and/or LabVIEW, and Zemax/OpticStudio or other equivalent optical design software. (S&I) Knowledge of safety related issues and procedures for operating lasers. (S&I) Good interpersonal skills and ability to work as part of a diverse team. (I) Additional information: The role involves working in a laser laboratory. For more information about the role, please visit or contact . Our Benefits: STFC values their employees by offering a benefits package designed to provide an excellent work/life balance including 30 days annual leave, 10.5 public and privilege holidays, flexible working hours, exceptional average salary pension scheme, social and sporting activities and societies and a subsidised restaurant. We ask some of the biggest questions in the universe, to answer some of the biggest challenges in the world. Whatever our role, we have the freedom to explore, learn and connect, as part of a community that loves to share knowledge and support one another. As one of Europes largest research organisations, this is a place where theres always something new to learn about the world around us, about your career, but most of all, about yourself. Join us and discover whats possible! Please note, if you will require sponsorship to work in the UK, as part of your sponsorship application, you and any dependants travelling with you, will be required to pay costs directly to The Home Office for the application before you start your role with us. UKRI is normally able to reimburse some, or all of these fees after you have become an employee and this can be discussed with the Hiring Manager. For more information, please visit or contact . JBRP1_UKTJ
Quality Assurance Manager page is loaded Quality Assurance Managerlocations: Hitchintime type: Full timeposted on: Posted Yesterdayjob requisition id: R - 334Primary Location :HITCHINAt Solina, our community of close to 5,000 people share a passion for food and live our entrepreneurial culture.We design customised savoury solutions for our clients operating in the food industry, food service, butchery and nutrition markets. With sustainability at the heart of our business model, we aim to produce food that is good in every sense of the word: delicious, nourishing, affordable, sustainable and convenient.Solina is a fast-growing business, with around 50 production sites and R&D laboratories present in more than 19 countries mainly in Europe and North America.By constantly rethinking culinary solutions, we make food matter for people and the planet . If you're ready for a new adventure in a dynamic, expanding, passionate, international company, join us ! Role Purpose The Quality Assurance Manager is responsible for embedding a culture of food safety, quality, and continuous improvement across the business. This role manages technical risks, ensures compliance with BRCGS, regulatory, and customer standards, and maintains robust systems to protect product integrity. The QA Manager leads the quality, laboratory, hygiene, and compliance teams, while ensuring site-wide processes deliver safe, legal, and high-quality products. Key Responsibilities Quality Systems & Compliance Develop, implement, and maintain the Quality Management System (QMS) in line with BRCGS, HACCP, and customer requirements. Lead the site's internal audit programme, ensuring full coverage of quality, food safety, hygiene, GMP, regulatory and customer requirements. Host and manage external audits (customer, certification, and regulatory), ensuring non-conformances are closed out promptly. Maintain and update the HACCP plan, ensuring reviews and meetings are completed on schedule. Oversee incident management and risk management processes, ensuring effective response and preventive action. Ensure hygiene programmes and standards are consistently achieved across the site Manage the site's pest control programme, ensuring compliance with regulatory, customers and BRCGS standards. Oversee and review supplier of raw materials, packaging and services performance Testing & Monitoring Implement and manage sampling and testing programmes for raw materials and finished goods. Review and interpret microbiological, analytical, and quality test results, ensuring timely corrective actions. Manage distressed stock, including the handling of out-of-date raw materials. Oversee water testing and environmental monitoring programmes. Manage allergen validation programme across the site Leadership & Team Development Lead, coach, and develop onsite QA team, ensuring resources meet business priorities. Drive engagement and training across the wider workforce on GMP, hygiene, food safety, and quality standards. Provide quality support and act as a key point of contact for customer and regulatory bodies. Monitoring, Reporting & Escalation Conduct trend analysis to identify risks, recurring issues, and opportunities for improvement. Escalate significant food safety, quality, or compliance issues promptly to the lien manager and senior leadership team. Provide accurate, data-driven reports to management and customers (as required), supporting transparency and continuous improvement. Qualifications & Skills Degree in Food Science, Microbiology, Chemistry, or a related discipline. Significant experience in food manufacturing quality management, with strong knowledge of BRCGS standards. Proven ability to lead audits, manage non-conformances, and maintain certification. Strong leadership and team development skills, with the ability to influence across functions. Analytical mindset with excellent trend analysis and problem-solving skills. Effective communicator, confident in escalating issues and engaging with external stakeholders. We are open to talents of all backgrounds. Our recruitment process is based on competences, and we openly welcome all candidates of all types according to our DEI Commitment Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.
Nov 09, 2025
Full time
Quality Assurance Manager page is loaded Quality Assurance Managerlocations: Hitchintime type: Full timeposted on: Posted Yesterdayjob requisition id: R - 334Primary Location :HITCHINAt Solina, our community of close to 5,000 people share a passion for food and live our entrepreneurial culture.We design customised savoury solutions for our clients operating in the food industry, food service, butchery and nutrition markets. With sustainability at the heart of our business model, we aim to produce food that is good in every sense of the word: delicious, nourishing, affordable, sustainable and convenient.Solina is a fast-growing business, with around 50 production sites and R&D laboratories present in more than 19 countries mainly in Europe and North America.By constantly rethinking culinary solutions, we make food matter for people and the planet . If you're ready for a new adventure in a dynamic, expanding, passionate, international company, join us ! Role Purpose The Quality Assurance Manager is responsible for embedding a culture of food safety, quality, and continuous improvement across the business. This role manages technical risks, ensures compliance with BRCGS, regulatory, and customer standards, and maintains robust systems to protect product integrity. The QA Manager leads the quality, laboratory, hygiene, and compliance teams, while ensuring site-wide processes deliver safe, legal, and high-quality products. Key Responsibilities Quality Systems & Compliance Develop, implement, and maintain the Quality Management System (QMS) in line with BRCGS, HACCP, and customer requirements. Lead the site's internal audit programme, ensuring full coverage of quality, food safety, hygiene, GMP, regulatory and customer requirements. Host and manage external audits (customer, certification, and regulatory), ensuring non-conformances are closed out promptly. Maintain and update the HACCP plan, ensuring reviews and meetings are completed on schedule. Oversee incident management and risk management processes, ensuring effective response and preventive action. Ensure hygiene programmes and standards are consistently achieved across the site Manage the site's pest control programme, ensuring compliance with regulatory, customers and BRCGS standards. Oversee and review supplier of raw materials, packaging and services performance Testing & Monitoring Implement and manage sampling and testing programmes for raw materials and finished goods. Review and interpret microbiological, analytical, and quality test results, ensuring timely corrective actions. Manage distressed stock, including the handling of out-of-date raw materials. Oversee water testing and environmental monitoring programmes. Manage allergen validation programme across the site Leadership & Team Development Lead, coach, and develop onsite QA team, ensuring resources meet business priorities. Drive engagement and training across the wider workforce on GMP, hygiene, food safety, and quality standards. Provide quality support and act as a key point of contact for customer and regulatory bodies. Monitoring, Reporting & Escalation Conduct trend analysis to identify risks, recurring issues, and opportunities for improvement. Escalate significant food safety, quality, or compliance issues promptly to the lien manager and senior leadership team. Provide accurate, data-driven reports to management and customers (as required), supporting transparency and continuous improvement. Qualifications & Skills Degree in Food Science, Microbiology, Chemistry, or a related discipline. Significant experience in food manufacturing quality management, with strong knowledge of BRCGS standards. Proven ability to lead audits, manage non-conformances, and maintain certification. Strong leadership and team development skills, with the ability to influence across functions. Analytical mindset with excellent trend analysis and problem-solving skills. Effective communicator, confident in escalating issues and engaging with external stakeholders. We are open to talents of all backgrounds. Our recruitment process is based on competences, and we openly welcome all candidates of all types according to our DEI Commitment Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.
About Sapio Sciences Sapio Sciences is on a mission to accelerate scientific drug discovery and high-throughput clinical and diagnostics for our clients and partners. The Sapio team consists of expert and highly collaborative scientists, software developers, and professionals passionate about providing a best-in-class lab informatics platform and industry-specific solutions. Sapio is one of the few software providers to offer a truly unified and highly configurable lab informatics platform and a broad suite of purpose-built solutions. The Sapio platform makes it easy for scientists, laboratory, and bio/informatics professionals to streamline and manage their end-to-end laboratory operations, from instrument data integration to workflow and experiment setup to sample and materials management, data management, and scientific data analysis and reporting. Working at Sapio At Sapio, we're not just building lab informatics solutions. We're creating tools made for the scientist and motivated to make the world a better place. We understand that lab informatics is about more than managing data or connecting workflows. It's about making life easier for the scientist and making scientific progress faster for everyone. Our platform delivers the levels of configurability, usability and insight that scientists have only ever dreamed of. We're a team of scientists, developers and innovators who question convention and stay focused on what matters most - advancing drug discovery science. We challenge the status quo and respond to the needs at the heart of science with powerful solutions that are simple to use, effortless to evolve and downright easy to love. As part of the Sapio team, you'll work in a collaborative and forward-thinking environment where your ideas are valued, your growth matters and your work makes a difference. We're proud to partner with leading labs around the world, from ambitious start-ups to global organisations, who trust Sapio to support discovery, development and diagnostics with industry-first science-aware solutions. About the role We are looking for an experienced solutions architect who is confident working in Life Sciences to successfully design and implement our solution to the delight of customers. Deep knowledge of LIMS, ELN and SDMS products and their application within the laboratory setting is essential for success with a goal of becoming an expert in the configuration and deployment of Sapio Sciences products. The use of this knowledge will be used to design each customer's solution, working closely with our Application Engineers to ensure high-quality implementation. What you'll be doing Platform and Product Expertise: Stay up to date with new platform enhancements and functionalities, ensuring they allocate sufficient time for adequate training and learning to leverage these updates. Develop and maintain a deep understanding of Sapio Sciences' products and services. Solution Design and Deployment: Collaborate with the Sapio Sciences team, including the Scientific Business Analyst, to understand customer requirements and processes. Design and deploy solutions using an agile approach, ensuring deliverables are met within time, budget, and quality parameters. Advise customers on best practices to optimize deployment success. JIRA Management: Utilize JIRA to track project progress, manage tasks, and monitor team capacity. Ensure that tickets are properly estimated, assigned, and updated to reflect the latest project status. Task Estimation and Capacity Planning: Accurately estimate tasks and resource requirements to support project planning and effective capacity management. Collaborate with project managers to ensure workloads are balanced across the team. Assist the Sales team by providing preliminary task estimates for projects or RFPs. Time Management and Prioritization: Effectively manage the complexities of working on multiple projects simultaneously. Prioritise tasks, delegate appropriately and ensure that each project is progressing according to schedule. Maintain clear visibility on all active projects and adjust priorities as necessary to meet organizational and customer demands. Delegation and Team Collaboration: Design solutions and delegate tasks effectively to application engineers, providing clear guidance and technical direction. Ensure that team members understand their roles and have the necessary support to succeed. Customer Support and Engagement: Provide third-tier support post-implementation, act as a liaison between the product team and customers to ensure functionality meets customer needs and drive the Sapio Sciences agile deployment methodology. Document customer feedback and address issues to enhance the customer experience and project success. Project and Process Management: Support Project Managers in delivering customer projects and ensure, as a Solutions Architect, that you follow agreed-upon processes and best practices and oversee proper time tracking and management. Maintain meticulous documentation of all Solution Architect-related deployment services. Clear and Constructive Communication: Foster an environment of open, transparent communication, ensuring that feedback is always constructive and aimed at improving collaboration, performance, and solution outcomes. Maintain clear and positive interactions with both internal teams and external stakeholders to ensure alignment and enhance the overall project experience. What we are looking for Travel Requirements: Willingness to travel to customer sites up to 30% of the time. Several years of experience in designing and delivering solutions for LIMS, ELN, or other complex software in a customer-facing role. Proven experience leading technical implementations. Tertiary qualification in Computer Science or a minimum of 2 years' experience in software delivery. Required skills & capabilities Strong programming skills with detailed knowledge of Java or Python Knowledge of one or more of GWT, MySQL, Oracle, Tomcat, Linux, AWS Technical Lead on LIMS/ELN implementations or other complex software within Life Sciences. What We Offer At Sapio Sciences, we recognise that our people are our greatest strength. That's why we're proud to offer: A competitive salary and benefits package Flexibility to work remotely, with opportunities to travel A comprehensive onboarding and training programme Ongoing opportunities for professional growth and development A collaborative, inclusive and supportive work environment Sapio Sciences is proud to be an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our People At Sapio Sciences, our people are at the heart of everything we do. Our lab informatics solutions are powered not just by technology, but by a shared commitment to our core values-what we proudly call The Sapio Seven, aka EMBRACE: - Embrace the future - Make a difference - Be true partners - Remember why we're here - Act with empathy - Commit to transparency - Excel in quality These values shape how we work, how we grow, and how we deliver impact for our clients every day. Reasonable Adjustments We are committed to ensuring an inclusive and accessible recruitment process. If you require any reasonable adjustments, at any stage across the application, interview & assessment processes then please let us know. We will work with you to support your needs in confidence. Diversity, Equity & Inclusion We do not discriminate based on race, colour, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other status protected by law or regulation. We intend that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors. We are committed to creating a diverse and inclusive workplace and encourage applications from all qualified individuals.
Nov 09, 2025
Full time
About Sapio Sciences Sapio Sciences is on a mission to accelerate scientific drug discovery and high-throughput clinical and diagnostics for our clients and partners. The Sapio team consists of expert and highly collaborative scientists, software developers, and professionals passionate about providing a best-in-class lab informatics platform and industry-specific solutions. Sapio is one of the few software providers to offer a truly unified and highly configurable lab informatics platform and a broad suite of purpose-built solutions. The Sapio platform makes it easy for scientists, laboratory, and bio/informatics professionals to streamline and manage their end-to-end laboratory operations, from instrument data integration to workflow and experiment setup to sample and materials management, data management, and scientific data analysis and reporting. Working at Sapio At Sapio, we're not just building lab informatics solutions. We're creating tools made for the scientist and motivated to make the world a better place. We understand that lab informatics is about more than managing data or connecting workflows. It's about making life easier for the scientist and making scientific progress faster for everyone. Our platform delivers the levels of configurability, usability and insight that scientists have only ever dreamed of. We're a team of scientists, developers and innovators who question convention and stay focused on what matters most - advancing drug discovery science. We challenge the status quo and respond to the needs at the heart of science with powerful solutions that are simple to use, effortless to evolve and downright easy to love. As part of the Sapio team, you'll work in a collaborative and forward-thinking environment where your ideas are valued, your growth matters and your work makes a difference. We're proud to partner with leading labs around the world, from ambitious start-ups to global organisations, who trust Sapio to support discovery, development and diagnostics with industry-first science-aware solutions. About the role We are looking for an experienced solutions architect who is confident working in Life Sciences to successfully design and implement our solution to the delight of customers. Deep knowledge of LIMS, ELN and SDMS products and their application within the laboratory setting is essential for success with a goal of becoming an expert in the configuration and deployment of Sapio Sciences products. The use of this knowledge will be used to design each customer's solution, working closely with our Application Engineers to ensure high-quality implementation. What you'll be doing Platform and Product Expertise: Stay up to date with new platform enhancements and functionalities, ensuring they allocate sufficient time for adequate training and learning to leverage these updates. Develop and maintain a deep understanding of Sapio Sciences' products and services. Solution Design and Deployment: Collaborate with the Sapio Sciences team, including the Scientific Business Analyst, to understand customer requirements and processes. Design and deploy solutions using an agile approach, ensuring deliverables are met within time, budget, and quality parameters. Advise customers on best practices to optimize deployment success. JIRA Management: Utilize JIRA to track project progress, manage tasks, and monitor team capacity. Ensure that tickets are properly estimated, assigned, and updated to reflect the latest project status. Task Estimation and Capacity Planning: Accurately estimate tasks and resource requirements to support project planning and effective capacity management. Collaborate with project managers to ensure workloads are balanced across the team. Assist the Sales team by providing preliminary task estimates for projects or RFPs. Time Management and Prioritization: Effectively manage the complexities of working on multiple projects simultaneously. Prioritise tasks, delegate appropriately and ensure that each project is progressing according to schedule. Maintain clear visibility on all active projects and adjust priorities as necessary to meet organizational and customer demands. Delegation and Team Collaboration: Design solutions and delegate tasks effectively to application engineers, providing clear guidance and technical direction. Ensure that team members understand their roles and have the necessary support to succeed. Customer Support and Engagement: Provide third-tier support post-implementation, act as a liaison between the product team and customers to ensure functionality meets customer needs and drive the Sapio Sciences agile deployment methodology. Document customer feedback and address issues to enhance the customer experience and project success. Project and Process Management: Support Project Managers in delivering customer projects and ensure, as a Solutions Architect, that you follow agreed-upon processes and best practices and oversee proper time tracking and management. Maintain meticulous documentation of all Solution Architect-related deployment services. Clear and Constructive Communication: Foster an environment of open, transparent communication, ensuring that feedback is always constructive and aimed at improving collaboration, performance, and solution outcomes. Maintain clear and positive interactions with both internal teams and external stakeholders to ensure alignment and enhance the overall project experience. What we are looking for Travel Requirements: Willingness to travel to customer sites up to 30% of the time. Several years of experience in designing and delivering solutions for LIMS, ELN, or other complex software in a customer-facing role. Proven experience leading technical implementations. Tertiary qualification in Computer Science or a minimum of 2 years' experience in software delivery. Required skills & capabilities Strong programming skills with detailed knowledge of Java or Python Knowledge of one or more of GWT, MySQL, Oracle, Tomcat, Linux, AWS Technical Lead on LIMS/ELN implementations or other complex software within Life Sciences. What We Offer At Sapio Sciences, we recognise that our people are our greatest strength. That's why we're proud to offer: A competitive salary and benefits package Flexibility to work remotely, with opportunities to travel A comprehensive onboarding and training programme Ongoing opportunities for professional growth and development A collaborative, inclusive and supportive work environment Sapio Sciences is proud to be an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our People At Sapio Sciences, our people are at the heart of everything we do. Our lab informatics solutions are powered not just by technology, but by a shared commitment to our core values-what we proudly call The Sapio Seven, aka EMBRACE: - Embrace the future - Make a difference - Be true partners - Remember why we're here - Act with empathy - Commit to transparency - Excel in quality These values shape how we work, how we grow, and how we deliver impact for our clients every day. Reasonable Adjustments We are committed to ensuring an inclusive and accessible recruitment process. If you require any reasonable adjustments, at any stage across the application, interview & assessment processes then please let us know. We will work with you to support your needs in confidence. Diversity, Equity & Inclusion We do not discriminate based on race, colour, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other status protected by law or regulation. We intend that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors. We are committed to creating a diverse and inclusive workplace and encourage applications from all qualified individuals.
Senior, Facilities Manager page is loaded Senior, Facilities Managerremote type: On-sitelocations: Slough, GBRtime type: Full timeposted on: Vandaag geplaatstjob requisition id: REQ466234 JLL empowers you to shape a brighter way .Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. Senior Facilities Manager Job Description We are looking for a Senior Facilities Manager to support our Life Science industry. About JLL: We're JLL. We're a professional services and investment management firm specializing in real estate. We help organizations around the world achieve their ambitions by owning, occupying and investing in real estate.If you're looking to step up your career, JLL is the perfect professional home.At JLL, you'll have a chance to innovate with the world's leading businesses, put that expertise into action on landmark projects, and work on game-changing real estate initiatives. You'll also make long-lasting professional connections through sharing different perspectives, and you'll be inspired by the best. We're focused on opportunity and want to help you make the most of yours.Achieve your ambitions - join us at JLL! Role Purpose: This senior position will ensure high quality and consistent delivery of all services delivered across a, Pharmaceutical manufacturing, Laboratory and office campus. The role will involve continuous improvement, day-to-day facilities coordination and management of ad-hoc projects for the client's facilities. As it's a first generation outsourcing in this new model for this (group of) site(s), it's crucial that the candidate is able to build relations with the clients, is open and flexible in his/her approach to the client, has good resilience, and has experience as a Service Provider. We are looking for an assertive candidate who can communicate effectively and cross-functionally to understand business needs, problem-solve and deliver facilities solutions that are both high-quality and cost-effective Responsibilities: Manage the Integrated Facilities Management (IFM) including GMP operations on site for our client in the pharmaceutical industry Establish open and transparent relationships with client Plant Managers, Area and Site FM managers, and business partners such as EHS and Quality leads, to establish trust and credibility in the delivery of JLL's services Establish a "Safety First" culture on the site and improve safety performance by championing our level of awareness and changing all staff and partner safety behaviors. Maintain interface with key client stakeholders, ensuring total contract compliance, accurate and timely reporting, and resolve critical impact tenant relations issues. Manage quality compliance (regulatory, client and JLL) for all relevant in-scope systems and processes in JLL scope of works. Liaises with the EHS and Quality teams Deliver against the set KPI's around down time, costs, maintenance and process compliance, and secure continuous improvements in each of the KPI area's Is proactive through securing in-depth root cause corrective actions, propose continuous reliability improvements and the implementation of audits Ensure compliance with portfolio wide initiatives and required local laws and regulations that pertain to the operating of facilities entrusted to the Facility Partners to manage on behalf of the client as owner. Supervise vendor performance for a large onsite team. Have a strong focus ensuring our JLL staff and 3rd party vendor partners meet all EHS, GxP, SLA, KPI, Satisfaction Surveys and Scope of Work (SOP) requirements. Understand in detail the contract scope and manage to that delivery while also recognizing opportunities to improve customer experience, outcomes and/or operational savings. Prepare, submit and manage facility budgets with the clients' goals and objectives addressed, track variances and ensure smooth recovery process. Give day-to-day direction to the on-site Site Ambassadors / Front of House Operatives and engineering team within cluster of managed sites. Responsible for overall team management, staff development and planning. Execute staff succession and growth plans. Recognize success of the team and the individual using appropriate recognition and rewards. Oversee the appropriate monthly/quarterly/annual reporting appropriate for the client. Supervise vendor performance Implement best practice from within and outside of JLL Requirements Essential: A manufacturing mindset and experience in the manufacturing domain 8+ years of relevant working experience in a GMP facility or similarly regulated industry Knowledge of Quality Management processes in regulated environments Experience as a service provider, in setting up constructive client relations, delivering of facilities contracts and the related P&L A strategic thinker with capability and experience to work with a wide range of stakeholders Hands-on if required; reputation for delivering results Project Management experience as part of a team or lead. Strong communicator, both verbally & written, in English and local language Strong interpersonal skills and problem-solving ability Requirements Desirable : Experience with the specific client (as supplier or former employee) and/or JLL Degree in Engineering, or a related field, inclusive of excellent working knowledge of buildings services installations What you can expect from us You'll join an entrepreneurial, inclusive culture. One where we succeed together - across the desk and around the globe. Where like-minded people work naturally together to achieve great things.Our Total Rewards program reflects our commitment to helping you achieve your ambitions in career, recognition, wellbeing, benefits and pay.Join us to develop your strengths and enjoy a fulfilling career full of varied experiences. Keep those ambitions in sights and imagine where JLL can take you Location: On-site -Slough, GBRIf this job description resonates with you, we encourage you to apply, even if you don't meet all the requirements. We're interested in getting to know you and what you bring to the table! If you require any changes to the application process, please email or call + 44 ( 0 ) to contact one of our team members to discuss how to best support you throughout the process. Please note, the contact details provided are to discuss or request for adjustments to be made to the hiring process. Please direct any other general recruiting inquiries to our page > I want to work for JLL. JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL's recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely.For more information about how JLL processes your personal data, please view our .For additional details please see our career site pages for each country.For candidates in the United States, please see a full
Nov 09, 2025
Full time
Senior, Facilities Manager page is loaded Senior, Facilities Managerremote type: On-sitelocations: Slough, GBRtime type: Full timeposted on: Vandaag geplaatstjob requisition id: REQ466234 JLL empowers you to shape a brighter way .Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. Senior Facilities Manager Job Description We are looking for a Senior Facilities Manager to support our Life Science industry. About JLL: We're JLL. We're a professional services and investment management firm specializing in real estate. We help organizations around the world achieve their ambitions by owning, occupying and investing in real estate.If you're looking to step up your career, JLL is the perfect professional home.At JLL, you'll have a chance to innovate with the world's leading businesses, put that expertise into action on landmark projects, and work on game-changing real estate initiatives. You'll also make long-lasting professional connections through sharing different perspectives, and you'll be inspired by the best. We're focused on opportunity and want to help you make the most of yours.Achieve your ambitions - join us at JLL! Role Purpose: This senior position will ensure high quality and consistent delivery of all services delivered across a, Pharmaceutical manufacturing, Laboratory and office campus. The role will involve continuous improvement, day-to-day facilities coordination and management of ad-hoc projects for the client's facilities. As it's a first generation outsourcing in this new model for this (group of) site(s), it's crucial that the candidate is able to build relations with the clients, is open and flexible in his/her approach to the client, has good resilience, and has experience as a Service Provider. We are looking for an assertive candidate who can communicate effectively and cross-functionally to understand business needs, problem-solve and deliver facilities solutions that are both high-quality and cost-effective Responsibilities: Manage the Integrated Facilities Management (IFM) including GMP operations on site for our client in the pharmaceutical industry Establish open and transparent relationships with client Plant Managers, Area and Site FM managers, and business partners such as EHS and Quality leads, to establish trust and credibility in the delivery of JLL's services Establish a "Safety First" culture on the site and improve safety performance by championing our level of awareness and changing all staff and partner safety behaviors. Maintain interface with key client stakeholders, ensuring total contract compliance, accurate and timely reporting, and resolve critical impact tenant relations issues. Manage quality compliance (regulatory, client and JLL) for all relevant in-scope systems and processes in JLL scope of works. Liaises with the EHS and Quality teams Deliver against the set KPI's around down time, costs, maintenance and process compliance, and secure continuous improvements in each of the KPI area's Is proactive through securing in-depth root cause corrective actions, propose continuous reliability improvements and the implementation of audits Ensure compliance with portfolio wide initiatives and required local laws and regulations that pertain to the operating of facilities entrusted to the Facility Partners to manage on behalf of the client as owner. Supervise vendor performance for a large onsite team. Have a strong focus ensuring our JLL staff and 3rd party vendor partners meet all EHS, GxP, SLA, KPI, Satisfaction Surveys and Scope of Work (SOP) requirements. Understand in detail the contract scope and manage to that delivery while also recognizing opportunities to improve customer experience, outcomes and/or operational savings. Prepare, submit and manage facility budgets with the clients' goals and objectives addressed, track variances and ensure smooth recovery process. Give day-to-day direction to the on-site Site Ambassadors / Front of House Operatives and engineering team within cluster of managed sites. Responsible for overall team management, staff development and planning. Execute staff succession and growth plans. Recognize success of the team and the individual using appropriate recognition and rewards. Oversee the appropriate monthly/quarterly/annual reporting appropriate for the client. Supervise vendor performance Implement best practice from within and outside of JLL Requirements Essential: A manufacturing mindset and experience in the manufacturing domain 8+ years of relevant working experience in a GMP facility or similarly regulated industry Knowledge of Quality Management processes in regulated environments Experience as a service provider, in setting up constructive client relations, delivering of facilities contracts and the related P&L A strategic thinker with capability and experience to work with a wide range of stakeholders Hands-on if required; reputation for delivering results Project Management experience as part of a team or lead. Strong communicator, both verbally & written, in English and local language Strong interpersonal skills and problem-solving ability Requirements Desirable : Experience with the specific client (as supplier or former employee) and/or JLL Degree in Engineering, or a related field, inclusive of excellent working knowledge of buildings services installations What you can expect from us You'll join an entrepreneurial, inclusive culture. One where we succeed together - across the desk and around the globe. Where like-minded people work naturally together to achieve great things.Our Total Rewards program reflects our commitment to helping you achieve your ambitions in career, recognition, wellbeing, benefits and pay.Join us to develop your strengths and enjoy a fulfilling career full of varied experiences. Keep those ambitions in sights and imagine where JLL can take you Location: On-site -Slough, GBRIf this job description resonates with you, we encourage you to apply, even if you don't meet all the requirements. We're interested in getting to know you and what you bring to the table! If you require any changes to the application process, please email or call + 44 ( 0 ) to contact one of our team members to discuss how to best support you throughout the process. Please note, the contact details provided are to discuss or request for adjustments to be made to the hiring process. Please direct any other general recruiting inquiries to our page > I want to work for JLL. JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL's recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely.For more information about how JLL processes your personal data, please view our .For additional details please see our career site pages for each country.For candidates in the United States, please see a full
Job Title: Project Procurement Lead Contract Type: Contract (with potential permanent conversion) Experience Level: 10-15 years Industry Background: FMCG, Pharmaceuticals, or Chemicals Role Overview The Project Procurement Lead will manage procurement activities for major investment projects and coordinate planning and execution at the site. This role carries strategic responsibility for procuring goods and services for the construction of manufacturing, laboratory, and office facilities, with project values ranging between £5 million and £500 million. Key Responsibilities Develop and implement Procurement Execution Strategy for assigned projects. Own end-to-end commercial activities, including procurement, expediting, contract management, and contract close-out. Manage procurement across: Goods: Process and electrical equipment, AHUs, black utilities (pumps, valves), lab equipment, furniture, consumables, automation systems, and spare parts. Services: Construction, piping, HVAC, electrical, cleanroom fit-out, consulting, engineering, and planning. Actively manage the Procurement Master Plan (PMP) during project execution, ensuring timely reporting and proactive risk mitigation. Collaborate closely with stakeholders, including: Internal procurement teams (buyers, order managers, contract managers). Procurement management & category management. Project directors, engineers, and SMEs. Support functions (Quality, EHS, Legal, Finance, HR). External collaborators (EPCM, EPC, main trade and equipment suppliers). Key Requirements 10+ years' experience in CAPEX project/procurement management (pharma/biotech preferred). Proven experience in plant construction, procurement, sales, and contract management. Strong track record with large CAPEX projects (£5m-£500m). Fluent in English; German is an advantage. Team-oriented with excellent communication skills; able to thrive in matrix and interdisciplinary environments. Strong commercial acumen, with analytical thinking and problem-solving ability. Resilient, adaptable, and proactive in fast-paced environments. Technical training (ETH/FH) in process, chemical, mechanical, civil, or plant engineering is an advantage. Must-have: Procurement leadership on large-scale CAPEX projects, ideally within the pharmaceutical sector.
Nov 09, 2025
Full time
Job Title: Project Procurement Lead Contract Type: Contract (with potential permanent conversion) Experience Level: 10-15 years Industry Background: FMCG, Pharmaceuticals, or Chemicals Role Overview The Project Procurement Lead will manage procurement activities for major investment projects and coordinate planning and execution at the site. This role carries strategic responsibility for procuring goods and services for the construction of manufacturing, laboratory, and office facilities, with project values ranging between £5 million and £500 million. Key Responsibilities Develop and implement Procurement Execution Strategy for assigned projects. Own end-to-end commercial activities, including procurement, expediting, contract management, and contract close-out. Manage procurement across: Goods: Process and electrical equipment, AHUs, black utilities (pumps, valves), lab equipment, furniture, consumables, automation systems, and spare parts. Services: Construction, piping, HVAC, electrical, cleanroom fit-out, consulting, engineering, and planning. Actively manage the Procurement Master Plan (PMP) during project execution, ensuring timely reporting and proactive risk mitigation. Collaborate closely with stakeholders, including: Internal procurement teams (buyers, order managers, contract managers). Procurement management & category management. Project directors, engineers, and SMEs. Support functions (Quality, EHS, Legal, Finance, HR). External collaborators (EPCM, EPC, main trade and equipment suppliers). Key Requirements 10+ years' experience in CAPEX project/procurement management (pharma/biotech preferred). Proven experience in plant construction, procurement, sales, and contract management. Strong track record with large CAPEX projects (£5m-£500m). Fluent in English; German is an advantage. Team-oriented with excellent communication skills; able to thrive in matrix and interdisciplinary environments. Strong commercial acumen, with analytical thinking and problem-solving ability. Resilient, adaptable, and proactive in fast-paced environments. Technical training (ETH/FH) in process, chemical, mechanical, civil, or plant engineering is an advantage. Must-have: Procurement leadership on large-scale CAPEX projects, ideally within the pharmaceutical sector.
Are you ready to take your rubber compounding expertise to the next level? Do you want to lead innovation in a company where your technical insight directly shapes products and customer success? We ve partnered once again with one of our top clients, based in Oldham, Greater Manchester. They re looking for a Technical Manager to lead their rubber compounding products and process development. You ll manage the laboratory team, work directly with customers to create innovative solutions and ensure all products meet ISO 9001 and client-specific standards. This is an amazing opportunity to combine hands-on technical leadership with strategic influence in a growing, industry-focused business. What You ll Get £ highly competitive DOE 33 days holiday Life Assurance Healthcare Benefit Company pension contribution About You You ll have proven experience in rubber compounding (essential) and laboratory management A strong understanding of product development, testing and ISO/industry standards You re experienced in leading technical teams and managing lab operations Comfortable working with clients and able to clearly communicate technical advice, supporting business development Innovative, proactive and commercially aware, with a passion for problem-solving and continuous improvement About the Role Manage compounding product and process development to meet company and customer objectives Produce recipes, mix cycles and test specifications for rubber compounds Ensure all compounds are tested to British, International or customer-specific standards Investigate and resolve internal and customer non-conformances Support sales with technical input and accurate costings Oversee external testing, trials and commissioning of capital projects as required Keep up to date with industry developments, new materials and competitor products Directly influence product innovation and development strategy About the company Global leaders in the technical textiles industry They take great pride in their people and products Collaborative and supportive team culture
Nov 08, 2025
Full time
Are you ready to take your rubber compounding expertise to the next level? Do you want to lead innovation in a company where your technical insight directly shapes products and customer success? We ve partnered once again with one of our top clients, based in Oldham, Greater Manchester. They re looking for a Technical Manager to lead their rubber compounding products and process development. You ll manage the laboratory team, work directly with customers to create innovative solutions and ensure all products meet ISO 9001 and client-specific standards. This is an amazing opportunity to combine hands-on technical leadership with strategic influence in a growing, industry-focused business. What You ll Get £ highly competitive DOE 33 days holiday Life Assurance Healthcare Benefit Company pension contribution About You You ll have proven experience in rubber compounding (essential) and laboratory management A strong understanding of product development, testing and ISO/industry standards You re experienced in leading technical teams and managing lab operations Comfortable working with clients and able to clearly communicate technical advice, supporting business development Innovative, proactive and commercially aware, with a passion for problem-solving and continuous improvement About the Role Manage compounding product and process development to meet company and customer objectives Produce recipes, mix cycles and test specifications for rubber compounds Ensure all compounds are tested to British, International or customer-specific standards Investigate and resolve internal and customer non-conformances Support sales with technical input and accurate costings Oversee external testing, trials and commissioning of capital projects as required Keep up to date with industry developments, new materials and competitor products Directly influence product innovation and development strategy About the company Global leaders in the technical textiles industry They take great pride in their people and products Collaborative and supportive team culture
Site Name: UK - Hertfordshire - Stevenage Posted Date: Nov 4 2025 About the Role As theSr. Manager, R&D Procurement, Laboratory Services, you will take ownership of sourcing and contract management for the Lab Services category, including instrument services, technical and general lab services, and lab tech. You will play a key role in developing and implementing category strategies, negotiating and executing contracts, and managing supplier relationships to ensure GSK's performance, quality, and financial objectives are met. In this role, you will collaborate with global teams across multiple countries, requiring high cultural awareness, and work closely with senior leadership to deliver procurement strategies that maximize supplier leverage while driving continuous improvements. You will also be responsible for identifying opportunities to streamline processes and generate significant value for GSK. Key Responsibilities Lead complex sourcing and category management activities for Lab Services within a global framework. Develop and implement category strategies aligned with GSK's strategic goals. Plan, negotiate, execute, interpret, and maintain contracts while managing ongoing supplier negotiations. Collaborate with stakeholders and senior leaders to ensure successful deployment of strategies globally and regionally. Champion sourcing group management processes and policies across functions. Ensure compliance with risk, regulatory, and quality requirements in all supplier interactions. Lead end-to-end procurement processes, driving continuous improvement, in-house vs. third-party vs. outsourcing strategies. Manage and monitor supplier relationships outside of the enterprise SRM structure for this category. Collaborate with other global procurement groups to identify synergies and optimize supplier relationships. Generate value in terms of quality, delivery, cost, and contribute significantly to GSK's goals. About You We are looking for a strategic thinker with strong problem-solving and analytical skills, excellent communication abilities, and the confidence to engage and challenge senior leaders. The ideal candidate will have a solid foundation in procurement, supply chain, business, or finance, along with experience in laboratory capabilities or scientific services provisions. You will be comfortable navigating complex global environments and possess a strong understanding of cultural differences in negotiations and supplier relationships. Qualifications and Experience Required Minimum: A university degree in Procurement, Supply Chain, Business, Finance, or related fields. Preferred: Master's degree in Procurement, Business, Finance, or a relevant scientific discipline. Relevant experience in procurement supporting laboratory capabilities or scientific services. Proven negotiation and contract management skills, with the ability to deliver quality, timely, and compliant agreements. Strong leadership and stakeholder management skills, including collaboration with senior leaders across R&D and Supply Chain. Exceptional communication skills, including English proficiency (written and oral); additional languages are a plus. Deep understanding of supplier capabilities, market trends, and business processes. Why GSK? At GSK, we are united by our mission to help people do more, feel better, and live longer. We foster a culture of innovation, collaboration, and inclusion, where you'll have the opportunity to grow and make a lasting impact on global health. As part of our Procurement team, you'll play a vital role in delivering solutions that improve lives while achieving GSK's strategic objectives. Ready to Apply? If you're excited by the prospect of joining an organisation that values your expertise, empowers your growth, and challenges you to deliver on a global scale, we want to hear from you. Apply today and help us transform the future of healthcare through innovative procurement strategies. Closing Date:16th November 2025 Why GSK? Unit ing science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or . The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at
Nov 07, 2025
Full time
Site Name: UK - Hertfordshire - Stevenage Posted Date: Nov 4 2025 About the Role As theSr. Manager, R&D Procurement, Laboratory Services, you will take ownership of sourcing and contract management for the Lab Services category, including instrument services, technical and general lab services, and lab tech. You will play a key role in developing and implementing category strategies, negotiating and executing contracts, and managing supplier relationships to ensure GSK's performance, quality, and financial objectives are met. In this role, you will collaborate with global teams across multiple countries, requiring high cultural awareness, and work closely with senior leadership to deliver procurement strategies that maximize supplier leverage while driving continuous improvements. You will also be responsible for identifying opportunities to streamline processes and generate significant value for GSK. Key Responsibilities Lead complex sourcing and category management activities for Lab Services within a global framework. Develop and implement category strategies aligned with GSK's strategic goals. Plan, negotiate, execute, interpret, and maintain contracts while managing ongoing supplier negotiations. Collaborate with stakeholders and senior leaders to ensure successful deployment of strategies globally and regionally. Champion sourcing group management processes and policies across functions. Ensure compliance with risk, regulatory, and quality requirements in all supplier interactions. Lead end-to-end procurement processes, driving continuous improvement, in-house vs. third-party vs. outsourcing strategies. Manage and monitor supplier relationships outside of the enterprise SRM structure for this category. Collaborate with other global procurement groups to identify synergies and optimize supplier relationships. Generate value in terms of quality, delivery, cost, and contribute significantly to GSK's goals. About You We are looking for a strategic thinker with strong problem-solving and analytical skills, excellent communication abilities, and the confidence to engage and challenge senior leaders. The ideal candidate will have a solid foundation in procurement, supply chain, business, or finance, along with experience in laboratory capabilities or scientific services provisions. You will be comfortable navigating complex global environments and possess a strong understanding of cultural differences in negotiations and supplier relationships. Qualifications and Experience Required Minimum: A university degree in Procurement, Supply Chain, Business, Finance, or related fields. Preferred: Master's degree in Procurement, Business, Finance, or a relevant scientific discipline. Relevant experience in procurement supporting laboratory capabilities or scientific services. Proven negotiation and contract management skills, with the ability to deliver quality, timely, and compliant agreements. Strong leadership and stakeholder management skills, including collaboration with senior leaders across R&D and Supply Chain. Exceptional communication skills, including English proficiency (written and oral); additional languages are a plus. Deep understanding of supplier capabilities, market trends, and business processes. Why GSK? At GSK, we are united by our mission to help people do more, feel better, and live longer. We foster a culture of innovation, collaboration, and inclusion, where you'll have the opportunity to grow and make a lasting impact on global health. As part of our Procurement team, you'll play a vital role in delivering solutions that improve lives while achieving GSK's strategic objectives. Ready to Apply? If you're excited by the prospect of joining an organisation that values your expertise, empowers your growth, and challenges you to deliver on a global scale, we want to hear from you. Apply today and help us transform the future of healthcare through innovative procurement strategies. Closing Date:16th November 2025 Why GSK? Unit ing science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or . The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at
Business Development Manager (German speaking) London W14 8TS, UK Job Description Posted Tuesday 24 December 2024 at 01:00 Who we are: There has never been a more exciting time to join the Digital Solutions business unit at CACI LTD. CACI helps clients transform their businesses using data and technology to meet current and future challenges. We are a team of around 250 passionate, motivated individuals who design, build, and operate complex cloud, digital, and data platforms for leading UK public and private sector organizations, including BMW, Police Digital Service, Home Office, National Records of Scotland, and Network Rail. We are committed to delivering excellent outcomes and pride ourselves on long-term engagements in project delivery and service management. Our Digital Forensics Laboratory, launched in 2022, is a testament to our innovation and is fully accredited. Key challenges we help our clients solve include: Asset acquisition decisions Portfolio investment strategies to increase asset value Increasing visit frequency and consumer spending Demonstrating investment strategies to shareholders Implementing consistent multi-channel sales strategies Using data to review, learn, and optimize actions for growth and cost savings Who you are: Results-driven with a successful track record in business development Fluent in written and spoken German, with experience in DACH markets Competitive, highly motivated, and persistent Excellent listener and persuasive at senior levels Confident in identifying and solving business issues Able to define solutions aligned with business goals and lead multidisciplinary teams Proficient in Microsoft Office products Interested in digital transformation Key Responsibilities: Generating qualified appointments with stakeholders and brands Researching to identify the right individuals within organizations Understanding stakeholder needs and triangulating information Learning CACI's services and effectively pitching them Accurately documenting stakeholder needs and sharing information within the team Reporting on leads and meetings in CRM Collaborating with marketing on upcoming activities to generate leads We are proud to be an equal opportunities employer, committed to diversity and inclusion. We offer reasonable adjustments during recruitment for individuals with health conditions or disabilities and ensure fair treatment regardless of ethnicity, age, sex, gender identity, veteran status, religion, sexual orientation, marital status, or health condition.
Nov 07, 2025
Full time
Business Development Manager (German speaking) London W14 8TS, UK Job Description Posted Tuesday 24 December 2024 at 01:00 Who we are: There has never been a more exciting time to join the Digital Solutions business unit at CACI LTD. CACI helps clients transform their businesses using data and technology to meet current and future challenges. We are a team of around 250 passionate, motivated individuals who design, build, and operate complex cloud, digital, and data platforms for leading UK public and private sector organizations, including BMW, Police Digital Service, Home Office, National Records of Scotland, and Network Rail. We are committed to delivering excellent outcomes and pride ourselves on long-term engagements in project delivery and service management. Our Digital Forensics Laboratory, launched in 2022, is a testament to our innovation and is fully accredited. Key challenges we help our clients solve include: Asset acquisition decisions Portfolio investment strategies to increase asset value Increasing visit frequency and consumer spending Demonstrating investment strategies to shareholders Implementing consistent multi-channel sales strategies Using data to review, learn, and optimize actions for growth and cost savings Who you are: Results-driven with a successful track record in business development Fluent in written and spoken German, with experience in DACH markets Competitive, highly motivated, and persistent Excellent listener and persuasive at senior levels Confident in identifying and solving business issues Able to define solutions aligned with business goals and lead multidisciplinary teams Proficient in Microsoft Office products Interested in digital transformation Key Responsibilities: Generating qualified appointments with stakeholders and brands Researching to identify the right individuals within organizations Understanding stakeholder needs and triangulating information Learning CACI's services and effectively pitching them Accurately documenting stakeholder needs and sharing information within the team Reporting on leads and meetings in CRM Collaborating with marketing on upcoming activities to generate leads We are proud to be an equal opportunities employer, committed to diversity and inclusion. We offer reasonable adjustments during recruitment for individuals with health conditions or disabilities and ensure fair treatment regardless of ethnicity, age, sex, gender identity, veteran status, religion, sexual orientation, marital status, or health condition.
Our Client is a leading engineering consultancy delivering innovative solutions across the rail and infrastructure sectors. They pride themselves on creating safe, sustainable, and efficient projects for their clients. We are seeking a talented and motivated Geotechnical Engineer to join their dynamic team and contribute to the successful delivery of minor rail projects. Role Overview: We are looking for a Geotechnical Engineer with 4-5 years of experience to support our client's rail projects. The successful candidate will be responsible for geotechnical investigations, analysis, design recommendations, and reporting, ensuring compliance with industry standards and project requirements. This is an excellent opportunity for someone looking to expand their expertise in the rail sector while working in a collaborative and innovative environment. Key Responsibilities: Undertake geotechnical investigations, including site inspections, borehole supervision, and laboratory testing coordination. Conduct geotechnical analysis and prepare design recommendations for minor rail projects. Produce clear, accurate, and concise geotechnical reports, drawings, and calculations. Liaise with project teams, including civil engineers, project managers, and stakeholders, to provide technical guidance and support. Ensure all work complies with relevant codes, standards, and company procedures. Contribute to risk assessments and provide practical solutions to geotechnical challenges. Essential Requirements: Bachelor's degree in Civil or Geotechnical Engineering (or equivalent). 4-5 years of professional experience in geotechnical engineering, preferably within rail or infrastructure projects. Experience with minor rail projects, including track foundations, embankments, cuttings, and associated structures. Proficient in geotechnical software (e.g., PLAXIS, GeoStudio, or equivalent) and Microsoft Office suite. Strong report writing, communication, and interpersonal skills. Ability to work independently and collaboratively within multidisciplinary teams. Desirable Skills: Knowledge of UK rail industry standards and procedures (or relevant local standards if outside the UK). Experience with ground improvement techniques and slope stability analysis. Membership of a professional body (e.g., ICE, IStructE, or IGE). Why Join Our Client: Opportunity to work on exciting and varied rail infrastructure projects. Collaborative and supportive work environment. Career development and training opportunities. Competitive salary and benefits package.
Nov 06, 2025
Full time
Our Client is a leading engineering consultancy delivering innovative solutions across the rail and infrastructure sectors. They pride themselves on creating safe, sustainable, and efficient projects for their clients. We are seeking a talented and motivated Geotechnical Engineer to join their dynamic team and contribute to the successful delivery of minor rail projects. Role Overview: We are looking for a Geotechnical Engineer with 4-5 years of experience to support our client's rail projects. The successful candidate will be responsible for geotechnical investigations, analysis, design recommendations, and reporting, ensuring compliance with industry standards and project requirements. This is an excellent opportunity for someone looking to expand their expertise in the rail sector while working in a collaborative and innovative environment. Key Responsibilities: Undertake geotechnical investigations, including site inspections, borehole supervision, and laboratory testing coordination. Conduct geotechnical analysis and prepare design recommendations for minor rail projects. Produce clear, accurate, and concise geotechnical reports, drawings, and calculations. Liaise with project teams, including civil engineers, project managers, and stakeholders, to provide technical guidance and support. Ensure all work complies with relevant codes, standards, and company procedures. Contribute to risk assessments and provide practical solutions to geotechnical challenges. Essential Requirements: Bachelor's degree in Civil or Geotechnical Engineering (or equivalent). 4-5 years of professional experience in geotechnical engineering, preferably within rail or infrastructure projects. Experience with minor rail projects, including track foundations, embankments, cuttings, and associated structures. Proficient in geotechnical software (e.g., PLAXIS, GeoStudio, or equivalent) and Microsoft Office suite. Strong report writing, communication, and interpersonal skills. Ability to work independently and collaboratively within multidisciplinary teams. Desirable Skills: Knowledge of UK rail industry standards and procedures (or relevant local standards if outside the UK). Experience with ground improvement techniques and slope stability analysis. Membership of a professional body (e.g., ICE, IStructE, or IGE). Why Join Our Client: Opportunity to work on exciting and varied rail infrastructure projects. Collaborative and supportive work environment. Career development and training opportunities. Competitive salary and benefits package.
Overview Are you an experienced Veterinary Surgeon looking for your next challenge in a supportive and well-equipped practice? Medivet Littlehampton, Fitzalan Road, offers an excellent opportunity for a vet with at least three years of UK in practice experience who is seeking to take the next step in their career. Situated in a superb location on the Sussex coast, the practice benefits from close proximity to both the seaside and the South Downs National Park, offering an exceptional lifestyle outside of work. The historic town of Arundel and the local High Down vineyard are also nearby, making this an ideal setting for anyone who enjoys the outdoors, culture, and a strong sense of community. Our Littlehampton practice has a friendly and welcoming team with a genuine family atmosphere. The large garden, complete with a wildlife unit, provides a unique and relaxing environment for both staff and clients. As part of the Medivet community, you will also have access to a vast network of clinical support and career development opportunities. The practice is fully equipped to a high standard, with three consult rooms, a prep room and theatre, digital x-ray, ultrasound, ECG, endoscopy, rhinoscopy, slit lamp, suction, pulse oximetry, and a recently upgraded in-house laboratory. This allows us to deliver a high standard of patient care and provides you with the tools and resources to develop your clinical skills further. This is a full-time position of 40 hours per week. We are particularly keen to hear from applicants with proven UK clinical experience who are ready to build on their expertise, contribute to the growth of the practice, and pursue leadership, taking ownership of a practie within the Medivet group. As a Lead Vet you will be accountable for the clinical leadership of the veterinary team ensuring we deliver exceptional care, always there for our clients, patients and colleagues whilst maintaining the highest levels of compliance with regulatory, operational and practice standards. You will also work closely with the Practice Manager to maximise the commercial performance of the clinic. Please contact joanne.gray at medivet.co.uk for a friendly initial conversation. Responsibilities Client care: Deliver exceptional care to clients, each and every day. Manage any client concerns or complaints raised in the clinic. Ensure the client receives updates on patient care following all procedures. For any out of hours (OOH) or enhanced care, ensure the client is updated on patient care and wellbeing. Patient care: Carry out patient consultations and procedures. Accountable for patient care and monitoring. Responsible for admissions and discharges for procedures (depending on complexity). Ensure patient records are accurate and up to date. Complete a clinical handover and make arrangements for the transfer of any patient requiring OOH or enhanced care. Responsible for prescribing medication and carrying out dispensing checks. All patient care is carried out under the guidance of the vet/lead vet in line with clinical competence. Lead Vet JD V4 01/2024 Standards and Compliance: Accountable for compliance with all regulatory and practice standards and agreed ways of working. Ensure the appropriate regulatory, practice and operational veterinary and nursing standards are implemented in the practice. Ensure compliance with health and safety requirements. Commercial performance: Understand the commercial performance drivers in the clinic such as Key Performance Indicators (KPIs), nurse and vet appointments, sale of products and material margin. Work closely with the Practice Manager to maximise the commercial performance of the clinic. Prepare accurate estimates and costs for clients and ensure payment is made at the same time as the procedure. Take action to minimise debt and support action plans to address any issues with clients. Maximise growth and revenue opportunities through the most effective utilisation of clinical skills and capacity. Communications: Effectively deliver timely clinical communications to veterinary and nursing teams sharing news of changes or improvements to processes or practice standards, Social Ecosystem Model (SEM) outcomes etc. Ensure clinical teams are aware of new or evolving practice standards. Hold engaging clinical meetings with veterinary and nursing teams as required. Clinical leadership: Carry out colleague clinical mentoring as required ensuring clear development plans and support are in place. Pro-actively support sharing clinical best practice within and across clinics and the wider Medivet community. To continue to deliver exceptional care to clients the Vet and Lead Vet are responsible for mentoring graduates within the clinic. The Nurse and Head Nurse are responsible for coaching the nursing team. Clinical administration: Accountable for ensuring lab tests are carried out correctly. Escalate any issues to the Practice Manager as required. Skills, knowledge and experience Must be an RCVS registered veterinary surgeon. Able to demonstrate clinical leadership skills. Has an understanding and appreciation of exceptional care and how this improves the client experience. Experienced in delivering exceptional clinical care to clients and patients. Implementation of a progressive clinical culture. Knowledge of driving strong commercial performance through the most effective allocation of clinical activity. Able to work as part of a team. Experienced in using coaching and influencing skills to get the best out of each and every colleague. Our clinics are run by small teams who need to work together effectively to deliver exceptional care to our clients, patients, and colleagues. This means that, from time to time, you may be required to carry out tasks outside your normal duties, where you have the skills, knowledge and experience required
Nov 06, 2025
Full time
Overview Are you an experienced Veterinary Surgeon looking for your next challenge in a supportive and well-equipped practice? Medivet Littlehampton, Fitzalan Road, offers an excellent opportunity for a vet with at least three years of UK in practice experience who is seeking to take the next step in their career. Situated in a superb location on the Sussex coast, the practice benefits from close proximity to both the seaside and the South Downs National Park, offering an exceptional lifestyle outside of work. The historic town of Arundel and the local High Down vineyard are also nearby, making this an ideal setting for anyone who enjoys the outdoors, culture, and a strong sense of community. Our Littlehampton practice has a friendly and welcoming team with a genuine family atmosphere. The large garden, complete with a wildlife unit, provides a unique and relaxing environment for both staff and clients. As part of the Medivet community, you will also have access to a vast network of clinical support and career development opportunities. The practice is fully equipped to a high standard, with three consult rooms, a prep room and theatre, digital x-ray, ultrasound, ECG, endoscopy, rhinoscopy, slit lamp, suction, pulse oximetry, and a recently upgraded in-house laboratory. This allows us to deliver a high standard of patient care and provides you with the tools and resources to develop your clinical skills further. This is a full-time position of 40 hours per week. We are particularly keen to hear from applicants with proven UK clinical experience who are ready to build on their expertise, contribute to the growth of the practice, and pursue leadership, taking ownership of a practie within the Medivet group. As a Lead Vet you will be accountable for the clinical leadership of the veterinary team ensuring we deliver exceptional care, always there for our clients, patients and colleagues whilst maintaining the highest levels of compliance with regulatory, operational and practice standards. You will also work closely with the Practice Manager to maximise the commercial performance of the clinic. Please contact joanne.gray at medivet.co.uk for a friendly initial conversation. Responsibilities Client care: Deliver exceptional care to clients, each and every day. Manage any client concerns or complaints raised in the clinic. Ensure the client receives updates on patient care following all procedures. For any out of hours (OOH) or enhanced care, ensure the client is updated on patient care and wellbeing. Patient care: Carry out patient consultations and procedures. Accountable for patient care and monitoring. Responsible for admissions and discharges for procedures (depending on complexity). Ensure patient records are accurate and up to date. Complete a clinical handover and make arrangements for the transfer of any patient requiring OOH or enhanced care. Responsible for prescribing medication and carrying out dispensing checks. All patient care is carried out under the guidance of the vet/lead vet in line with clinical competence. Lead Vet JD V4 01/2024 Standards and Compliance: Accountable for compliance with all regulatory and practice standards and agreed ways of working. Ensure the appropriate regulatory, practice and operational veterinary and nursing standards are implemented in the practice. Ensure compliance with health and safety requirements. Commercial performance: Understand the commercial performance drivers in the clinic such as Key Performance Indicators (KPIs), nurse and vet appointments, sale of products and material margin. Work closely with the Practice Manager to maximise the commercial performance of the clinic. Prepare accurate estimates and costs for clients and ensure payment is made at the same time as the procedure. Take action to minimise debt and support action plans to address any issues with clients. Maximise growth and revenue opportunities through the most effective utilisation of clinical skills and capacity. Communications: Effectively deliver timely clinical communications to veterinary and nursing teams sharing news of changes or improvements to processes or practice standards, Social Ecosystem Model (SEM) outcomes etc. Ensure clinical teams are aware of new or evolving practice standards. Hold engaging clinical meetings with veterinary and nursing teams as required. Clinical leadership: Carry out colleague clinical mentoring as required ensuring clear development plans and support are in place. Pro-actively support sharing clinical best practice within and across clinics and the wider Medivet community. To continue to deliver exceptional care to clients the Vet and Lead Vet are responsible for mentoring graduates within the clinic. The Nurse and Head Nurse are responsible for coaching the nursing team. Clinical administration: Accountable for ensuring lab tests are carried out correctly. Escalate any issues to the Practice Manager as required. Skills, knowledge and experience Must be an RCVS registered veterinary surgeon. Able to demonstrate clinical leadership skills. Has an understanding and appreciation of exceptional care and how this improves the client experience. Experienced in delivering exceptional clinical care to clients and patients. Implementation of a progressive clinical culture. Knowledge of driving strong commercial performance through the most effective allocation of clinical activity. Able to work as part of a team. Experienced in using coaching and influencing skills to get the best out of each and every colleague. Our clinics are run by small teams who need to work together effectively to deliver exceptional care to our clients, patients, and colleagues. This means that, from time to time, you may be required to carry out tasks outside your normal duties, where you have the skills, knowledge and experience required
