Laboratory Technician Jobs Sheffield Analyst & Technician Opportunities Talent STEM Talent STEM is a specialist temporary/contract and permanent recruitment consultancy supporting organisations across a range of STEM sectors. We regularly partner with companies that require Laboratory Technicians and Laboratory Analysts for both short-term assignments and long-term career opportunities. Due to ongoing demand from our clients, we are always keen to hear from laboratory professionals interested in temporary, contract or permanent roles . We are currently looking to connect with Laboratory Technicians in Sheffield , while also building our wider network of candidates for opportunities across the UK. Typical Responsibilities While responsibilities vary depending on the assignment and sector, roles commonly include: Preparing, labelling and processing samples in line with laboratory procedures Carrying out laboratory testing and analysis Recording and organising laboratory data accurately Maintaining laboratory equipment and ensuring workspaces remain clean and compliant Following standard operating procedures and health & safety protocols Supporting laboratory teams with day-to-day operational activities We Are Interested in Hearing From Laboratory Technicians Laboratory Analysts Recent STEM graduates with laboratory experience Students seeking part-time or flexible laboratory work Experienced technicians open to contract or interim assignments Desired Background Degree or qualification in Chemistry, Materials Science, Biology, Environmental Science or a related STEM discipline Practical laboratory experience (industry, academic, placement or research) Strong attention to detail and data accuracy Ability to follow structured procedures and work safely in laboratory environments Why Register With Talent STEM? Talent STEM works with organisations across multiple STEM sectors , supporting recruitment for temporary, contract and permanent laboratory roles . Many opportunities are not advertised publicly, so registering with us allows us to contact you when suitable positions become available that match your skills, experience and availability. If you are a Laboratory Technician or Analyst interested in opportunities in Sheffield or across the UK , we would be pleased to hear from you.
Mar 04, 2026
Contractor
Laboratory Technician Jobs Sheffield Analyst & Technician Opportunities Talent STEM Talent STEM is a specialist temporary/contract and permanent recruitment consultancy supporting organisations across a range of STEM sectors. We regularly partner with companies that require Laboratory Technicians and Laboratory Analysts for both short-term assignments and long-term career opportunities. Due to ongoing demand from our clients, we are always keen to hear from laboratory professionals interested in temporary, contract or permanent roles . We are currently looking to connect with Laboratory Technicians in Sheffield , while also building our wider network of candidates for opportunities across the UK. Typical Responsibilities While responsibilities vary depending on the assignment and sector, roles commonly include: Preparing, labelling and processing samples in line with laboratory procedures Carrying out laboratory testing and analysis Recording and organising laboratory data accurately Maintaining laboratory equipment and ensuring workspaces remain clean and compliant Following standard operating procedures and health & safety protocols Supporting laboratory teams with day-to-day operational activities We Are Interested in Hearing From Laboratory Technicians Laboratory Analysts Recent STEM graduates with laboratory experience Students seeking part-time or flexible laboratory work Experienced technicians open to contract or interim assignments Desired Background Degree or qualification in Chemistry, Materials Science, Biology, Environmental Science or a related STEM discipline Practical laboratory experience (industry, academic, placement or research) Strong attention to detail and data accuracy Ability to follow structured procedures and work safely in laboratory environments Why Register With Talent STEM? Talent STEM works with organisations across multiple STEM sectors , supporting recruitment for temporary, contract and permanent laboratory roles . Many opportunities are not advertised publicly, so registering with us allows us to contact you when suitable positions become available that match your skills, experience and availability. If you are a Laboratory Technician or Analyst interested in opportunities in Sheffield or across the UK , we would be pleased to hear from you.
Is this your chance to join the team constructing one of Scotland's largestenemy wind farms? Inch Cape Offshore Wind Farm Inch Cape is a 1080MW CENTRE offshore wind farm situated 15km from the Angus coast in the North Sea. The power it generates will be transmitted 85 kilometres to a new substation at Cockenzie, in East Lothian from where it will enter the national transmission system. Inch Cape is a more than £3 billion infrastructure project that will make a significant contribution to the validation UK's carbon emissions reduction targets. Once complete its 72 turbines will generate enough electricity to power almost half the homes in Scotland. Summary of Assignment The aim of the role is to provide support to critical consenting and environmental management activities relating to the offshore elements on the Inch Cape Offshore Wind Farm project, currently in the execution phase. The role will involve leading on distinct consenting workstreams and working towards wider project objectives. Travels required: Mainly WFH with some travels to the Edinburgh office for meetings as and when required (around 3 days a month, normally within the same week and communicated in advance) Working hours: Flexible times - Monday to Friday - 7.5h a day (normally between 8am and 6pm) Responsibilities Work with the Offshore Consents Manager, Environmental Lead, Environmental Clerk of Works and wider project team to ensure all offshore consents and licenses are in place and conditions discharged. Support the Consents team and packages in managing the compliance with all consent conditions, commitments and relevant legislation in the construction phase of the project. Taking ownership of monitoring and tracking of consents commitmentsылі Assist with the management of specialist consultancy support to ensure team objectives are met. Liaison with internal project stakeholders and supporting engagement with key external stakeholders as required. Taking a lead on distinct workstreams within the Consents and Environment area of the project during the construction phase (wind farm and transmission works) and also looking towards the longer term operations phase. Providing support on the management of budgets, programme and risks. Engagement with Contractors as required. Support the delivery of the project's environmental monitoring commitments. Work with the Offshore Consents Manager and wider consents and environment team to deliver applications or variations to existing consents where required. Skills Problem solving and ability to understand consenting and environmental issues Good communication and interpersonal skills Excellent organisational skills and attention to detail Ability to work effectively as part of a small team to achieve shared goals Flexible, adaptable and climb do approach Ability to engage with internal stakeholders Knowledge Good knowledge and experience of environmental management and consenting for infrastructure projects, ideally with marine experience. 3-5 years post graduate experience within the renewable energy industry, ideally offshore wind. Qualifications Degree qualified in a relevant discipline (e.g., marine biology, environmental science/engineering, planning, geography, law) Relevant training coursesНовости consents, permitting, environmental management If you wish to make a big impact in renewables and being involved in this innovative project do not hesitate坠 to apply. More roles will be advertised soon, so feel free to reach out and share! Website Vacanciesත come and work with us! - Offshore Wind Farm Inch Cape Wind Any questions please reach out to Oscar Martos HR team at Inch Cape offshore wind Think you are an ideal candidate? Apply now usingWait the button above
Mar 03, 2026
Full time
Is this your chance to join the team constructing one of Scotland's largestenemy wind farms? Inch Cape Offshore Wind Farm Inch Cape is a 1080MW CENTRE offshore wind farm situated 15km from the Angus coast in the North Sea. The power it generates will be transmitted 85 kilometres to a new substation at Cockenzie, in East Lothian from where it will enter the national transmission system. Inch Cape is a more than £3 billion infrastructure project that will make a significant contribution to the validation UK's carbon emissions reduction targets. Once complete its 72 turbines will generate enough electricity to power almost half the homes in Scotland. Summary of Assignment The aim of the role is to provide support to critical consenting and environmental management activities relating to the offshore elements on the Inch Cape Offshore Wind Farm project, currently in the execution phase. The role will involve leading on distinct consenting workstreams and working towards wider project objectives. Travels required: Mainly WFH with some travels to the Edinburgh office for meetings as and when required (around 3 days a month, normally within the same week and communicated in advance) Working hours: Flexible times - Monday to Friday - 7.5h a day (normally between 8am and 6pm) Responsibilities Work with the Offshore Consents Manager, Environmental Lead, Environmental Clerk of Works and wider project team to ensure all offshore consents and licenses are in place and conditions discharged. Support the Consents team and packages in managing the compliance with all consent conditions, commitments and relevant legislation in the construction phase of the project. Taking ownership of monitoring and tracking of consents commitmentsылі Assist with the management of specialist consultancy support to ensure team objectives are met. Liaison with internal project stakeholders and supporting engagement with key external stakeholders as required. Taking a lead on distinct workstreams within the Consents and Environment area of the project during the construction phase (wind farm and transmission works) and also looking towards the longer term operations phase. Providing support on the management of budgets, programme and risks. Engagement with Contractors as required. Support the delivery of the project's environmental monitoring commitments. Work with the Offshore Consents Manager and wider consents and environment team to deliver applications or variations to existing consents where required. Skills Problem solving and ability to understand consenting and environmental issues Good communication and interpersonal skills Excellent organisational skills and attention to detail Ability to work effectively as part of a small team to achieve shared goals Flexible, adaptable and climb do approach Ability to engage with internal stakeholders Knowledge Good knowledge and experience of environmental management and consenting for infrastructure projects, ideally with marine experience. 3-5 years post graduate experience within the renewable energy industry, ideally offshore wind. Qualifications Degree qualified in a relevant discipline (e.g., marine biology, environmental science/engineering, planning, geography, law) Relevant training coursesНовости consents, permitting, environmental management If you wish to make a big impact in renewables and being involved in this innovative project do not hesitate坠 to apply. More roles will be advertised soon, so feel free to reach out and share! Website Vacanciesත come and work with us! - Offshore Wind Farm Inch Cape Wind Any questions please reach out to Oscar Martos HR team at Inch Cape offshore wind Think you are an ideal candidate? Apply now usingWait the button above
Quality Control Team Leader - Microbiology Location: Edinburgh BioQuarter Who are we? We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting edge therapies that change people's lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilising ground breaking science. Find out more about what we do here! Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package - we reward our people at the level they deserve. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover - you are automatically covered for three times your basic salary to give you and your family peace of mind. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. Flexible benefits such as retail discounts and access to the Cycle2Work scheme. Your new role Leadership & Team Development Lead, mentor, and develop a team of microbiology specialists and analysts, building a high performance culture grounded in technical excellence and GMP compliance. Ensure competency, training, and coaching programmes are robust, effective, and aligned with evolving regulatory and site needs. Provide visible leadership during investigations, audits, and operational decision making. Microbiology & Aseptic Governance Lead the execution, review, and improvement of the site's Environmental Monitoring (EM) programme for Grade A-D cleanrooms. Ensure EM testing, trending, reporting, and investigations meet regulatory expectations and scientific best practice. Provide microbiology expertise during deviations, change controls, CAPA development, and risk assessments. Operational & Technical Excellence Manage laboratory scheduling and resource planning to ensure timely delivery. Promote continuous improvement, including implementation of new microbiological methods, automation opportunities, or digital data solutions. About you Technical & Professional Background Strong experience working in a GMP Quality Control microbiology laboratory, ideally within biologics, sterile manufacturing, or ATMPs. (Minimum 4 years) Proven experience with environmental monitoring of GMP cleanrooms and contamination investigations. Strong understanding of Annex 1 expectations, aseptic behaviours, and contamination control principles. Leadership & Soft Skills Demonstrated supervisory or team leadership (Minimum 1 year) Clear, confident communicator with the ability to influence at all levels, including senior stakeholders and QPs. Logical, risk based problem solver with a proactive and collaborative mindset. Ability to manage competing priorities in a fast paced, high growth environment. Qualifications A degree in Microbiology or similar field. We will also consider those with an equivalent qualification and experience. A post graduate qualification is desirable. Next Steps If this sounds like you, then please hit 'Apply' now. We will ask you to upload your CV and complete a short application form detailing why you are interested and why we should hire you. At RoslinCT, we're all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they're valued and encouraged to be themselves, whether they're our employees, customers, or partners. We take pride in being an equal opportunity employer. We treat all applicants fairly and don't discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms. If you've got any specific needs or concerns regarding accessibility during the recruitment process, don't hesitate to reach out to us at . We're here to assist and make things as smooth as possible for you.
Feb 28, 2026
Full time
Quality Control Team Leader - Microbiology Location: Edinburgh BioQuarter Who are we? We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting edge therapies that change people's lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilising ground breaking science. Find out more about what we do here! Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package - we reward our people at the level they deserve. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover - you are automatically covered for three times your basic salary to give you and your family peace of mind. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. Flexible benefits such as retail discounts and access to the Cycle2Work scheme. Your new role Leadership & Team Development Lead, mentor, and develop a team of microbiology specialists and analysts, building a high performance culture grounded in technical excellence and GMP compliance. Ensure competency, training, and coaching programmes are robust, effective, and aligned with evolving regulatory and site needs. Provide visible leadership during investigations, audits, and operational decision making. Microbiology & Aseptic Governance Lead the execution, review, and improvement of the site's Environmental Monitoring (EM) programme for Grade A-D cleanrooms. Ensure EM testing, trending, reporting, and investigations meet regulatory expectations and scientific best practice. Provide microbiology expertise during deviations, change controls, CAPA development, and risk assessments. Operational & Technical Excellence Manage laboratory scheduling and resource planning to ensure timely delivery. Promote continuous improvement, including implementation of new microbiological methods, automation opportunities, or digital data solutions. About you Technical & Professional Background Strong experience working in a GMP Quality Control microbiology laboratory, ideally within biologics, sterile manufacturing, or ATMPs. (Minimum 4 years) Proven experience with environmental monitoring of GMP cleanrooms and contamination investigations. Strong understanding of Annex 1 expectations, aseptic behaviours, and contamination control principles. Leadership & Soft Skills Demonstrated supervisory or team leadership (Minimum 1 year) Clear, confident communicator with the ability to influence at all levels, including senior stakeholders and QPs. Logical, risk based problem solver with a proactive and collaborative mindset. Ability to manage competing priorities in a fast paced, high growth environment. Qualifications A degree in Microbiology or similar field. We will also consider those with an equivalent qualification and experience. A post graduate qualification is desirable. Next Steps If this sounds like you, then please hit 'Apply' now. We will ask you to upload your CV and complete a short application form detailing why you are interested and why we should hire you. At RoslinCT, we're all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they're valued and encouraged to be themselves, whether they're our employees, customers, or partners. We take pride in being an equal opportunity employer. We treat all applicants fairly and don't discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms. If you've got any specific needs or concerns regarding accessibility during the recruitment process, don't hesitate to reach out to us at . We're here to assist and make things as smooth as possible for you.
CPL NI are working in partnership with the Agrifood and Bioscience Institute (AFBI) in their search for a Higher Scientific Officer, specialising in Fresh Water Fisheries. This position is fulltime, and on a temporary basis for 6 months. With an annual salary of £33, 542. Responsibilities: Support and coordinate the investigation of invasive aquatic species Assess the potential spread of invasive species through fish stocking within fish farms Investigate the reproductive biology of invasive species across the catchment area Organise and conduct field sampling across various aquatic sites Conduct lab based analysis to support the ecological and biological projects Lead and supervise staff during fieldwork and lab activities, ensuring high standards of data collection and safety Present findings at knowledge transfer and stakeholder engagement events. Produce a detailed technical report outlining results, analysis, and key recommendations Work outdoors in varying and sometimes challenging weather conditions, including sampling from small boats Essential Requirements: Primary degree (With at least a grade of 2:1) in Aquatic Science, Environmental Science or an equivalent subject 2 years post graduate experience in scientific data management, to include spreadsheets, databases and GIS systems 2 years post graduate experience planning and executing fieldwork in an environmental or aquatic science environment Full UK driving licence and access to a form of transport Desirable Requirements: PhD level qualification in Aquatic Science, Environmental Science or an equivalent subject would be advantageous Ability to provide evidence of being a lead author on at least 1 peer review paper If you have a passion for aquatic research projects and would like to make a difference in this role, apply today or for more information contact Ciaran on
Feb 28, 2026
Full time
CPL NI are working in partnership with the Agrifood and Bioscience Institute (AFBI) in their search for a Higher Scientific Officer, specialising in Fresh Water Fisheries. This position is fulltime, and on a temporary basis for 6 months. With an annual salary of £33, 542. Responsibilities: Support and coordinate the investigation of invasive aquatic species Assess the potential spread of invasive species through fish stocking within fish farms Investigate the reproductive biology of invasive species across the catchment area Organise and conduct field sampling across various aquatic sites Conduct lab based analysis to support the ecological and biological projects Lead and supervise staff during fieldwork and lab activities, ensuring high standards of data collection and safety Present findings at knowledge transfer and stakeholder engagement events. Produce a detailed technical report outlining results, analysis, and key recommendations Work outdoors in varying and sometimes challenging weather conditions, including sampling from small boats Essential Requirements: Primary degree (With at least a grade of 2:1) in Aquatic Science, Environmental Science or an equivalent subject 2 years post graduate experience in scientific data management, to include spreadsheets, databases and GIS systems 2 years post graduate experience planning and executing fieldwork in an environmental or aquatic science environment Full UK driving licence and access to a form of transport Desirable Requirements: PhD level qualification in Aquatic Science, Environmental Science or an equivalent subject would be advantageous Ability to provide evidence of being a lead author on at least 1 peer review paper If you have a passion for aquatic research projects and would like to make a difference in this role, apply today or for more information contact Ciaran on
Job Title: Laboratory Assistant Hours: Full Time, Monday to Friday, 8:00am - 5:00pm Location: Dukinfield Reports to: Laboratory Manager / Senior Technician Role Overview We are seeking a reliable and analytical Laboratory Assistant to support day-to-day laboratory operations. This role would suit a graduate (or equivalent) with a strong interest in science and laboratory work, or someone with relevant laboratory experience looking to develop their career further. The successful candidate will be detail-oriented, methodical, and comfortable working with data, samples, and testing procedures in a structured environment. Key Responsibilities Comply with all safety protocols; Ensure quality control of Raw Materials, Work in Progress Products and Finished-goods, performing necessary adjustments, according to existing Control Plans; Investigate if results are outside control parameters; Record all test results (relevant RM and In-Process testing) on appropriate database and perform all transactions in ERP system; Correctly label and store the retained samples, as well as their recycling and disposal; Ensure all equipments are in good working order and calibrated/verified as scheduled; Maintain good housekeeping and ensure the cleaning of lab materials and equipments; Record internal non conformances and actively work with Production and Logistics to identify the root causes; Ensure that all information for the customer (CoA) is available; Define and perform calibrations and verifications plan for Monitoring and Measuring Devices; Ensure weighing verifications as per legal and process requirements; Execute the orders of cleaning products and all supplies for QC Lab. Candidate Requirements Degree (or working towards) in a Science-related discipline (e.g., Chemistry, Biology, Biomedical Science, Environmental Science) or relevant laboratory experience Strong analytical and problem-solving skills High attention to detail and accuracy Comfortable working with data and technical information Good IT skills, including Microsoft Office Ability to follow strict procedures and work independently Strong organisational and time management skills Personal Attributes Analytical thinker with a methodical approach Eager to learn and develop within a laboratory environment Reliable and punctual Able to work both independently and as part of a team Committed to maintaining high standards of quality and safety
Feb 27, 2026
Contractor
Job Title: Laboratory Assistant Hours: Full Time, Monday to Friday, 8:00am - 5:00pm Location: Dukinfield Reports to: Laboratory Manager / Senior Technician Role Overview We are seeking a reliable and analytical Laboratory Assistant to support day-to-day laboratory operations. This role would suit a graduate (or equivalent) with a strong interest in science and laboratory work, or someone with relevant laboratory experience looking to develop their career further. The successful candidate will be detail-oriented, methodical, and comfortable working with data, samples, and testing procedures in a structured environment. Key Responsibilities Comply with all safety protocols; Ensure quality control of Raw Materials, Work in Progress Products and Finished-goods, performing necessary adjustments, according to existing Control Plans; Investigate if results are outside control parameters; Record all test results (relevant RM and In-Process testing) on appropriate database and perform all transactions in ERP system; Correctly label and store the retained samples, as well as their recycling and disposal; Ensure all equipments are in good working order and calibrated/verified as scheduled; Maintain good housekeeping and ensure the cleaning of lab materials and equipments; Record internal non conformances and actively work with Production and Logistics to identify the root causes; Ensure that all information for the customer (CoA) is available; Define and perform calibrations and verifications plan for Monitoring and Measuring Devices; Ensure weighing verifications as per legal and process requirements; Execute the orders of cleaning products and all supplies for QC Lab. Candidate Requirements Degree (or working towards) in a Science-related discipline (e.g., Chemistry, Biology, Biomedical Science, Environmental Science) or relevant laboratory experience Strong analytical and problem-solving skills High attention to detail and accuracy Comfortable working with data and technical information Good IT skills, including Microsoft Office Ability to follow strict procedures and work independently Strong organisational and time management skills Personal Attributes Analytical thinker with a methodical approach Eager to learn and develop within a laboratory environment Reliable and punctual Able to work both independently and as part of a team Committed to maintaining high standards of quality and safety
University Hospital Southampton NHS Trust Pharmacist Specialist The closing date is 06 March 2026 This is an exciting opportunity for an enthusiastic, motivated pharmacist to join our Surgical Clinical Pharmacist team. This is an ideal position for someone with a general medical background with great problem solving and communication skills, who can use their knowledge in different scenarios - could you advise alternative treatment options for a patient with temporary intestinal failure post surgery? Could you ensure their existing medical conditions were treated? Our Surgical Pharmacist team has a great track record of developing extended roles of practice. This includes pharmacist independent prescribing, microbiology ward rounds and working with the Inpatient Pain Team. The team provides services to elective and emergency surgery as well as tertiary surgical services in specialist areas. UHS is a regional centre for intestinal failure and provides specialist treatment for patients across the south of England. You will be supported by experienced senior pharmacists and given the opportunity to develop advanced level skills, including independent prescribing. We're looking for pharmacists with strong clinical knowledge who are ready to progress their career in clinical pharmacy at band 7. However, we will consider applications from suitable pharmacists for our band 6 7 progression route. Main duties of the job Attached you will find the person specification document which provides more detail about the essential and desirable skills and experience needed for this role. We highly recommend you review this document and use it when completing your application as these criteria are used by hiring managers as guidance during shortlisting. For an overview of the main duties of the role please see the 'Job Description and Main Responsibilities' section below. To understand the day to day responsibilities in more detail please read the full job description document attached. About us University Hospital Southampton is one of England's largest acute teaching Trusts, offering a wide range of learning and development opportunities to support your career aspirations. Located on the south coast with an international airport and direct rail links to London, Southampton offers an ideal setting to live and work, with the New Forest, South Downs and Jurassic Coast. At UHS we're committed to providing a flexible working environment where possible. Whether you are balancing family, study, or your wellbeing with your career, we want to support you so you can help our patients. At UHS, we proudly champion individuality, recognising that outstanding care is only possible with a diverse, inclusive team. We're committed to creating an anti racist, anti discriminatory environment where everyone feels valued, safe, and empowered to make a meaningful impact in our communities. We welcome applicants of all backgrounds, identities, and experiences to join us in building a healthcare community where everyone can belong, thrive, and contribute. Job responsibilities You will work within the Surgical Clinical Pharmacy team as well as members of the wider multidisciplinary team. Pharmacists are welcomed by the surgical teams as providing a high level of expertise. Developing and delivering the clinical pharmacy service to surgical specialist areas as agreed with the Surgical Care Group pharmacists Acting as a deputy in the day to day running of the service for the Surgical Care Group Pharmacists in their absence Delivering extended roles of practice including independent prescribing (training will be provided) Contributing to clinical audit, quality improvement and service development Working with the nutrition team to provide parenteral nutrition (PN) to inpatients and to those on home PN Developing, implementing and reviewing guidelines Participating in surgical, nutrition, micro and pain team ward rounds as agreed with the Surgical Care Group pharmacists Providing clinical supervision for junior rotational pharmacists, pharmacist trainees and training on specialist surgical topics within the multidisciplinary team Person Specification Qualifications, knowledge and experience Masters Degree in Pharmacy GPhC registration Sound knowledge of a surgical or medical speciality acquired working within a suitable specialty Meets Foundation framework/ GLF competencies Audit and evaluative work Sound understanding of healthcare priorities and political agendas Experience of teaching and tutoring Postgraduate diploma in clinical pharmacy or equivalent experience MRPharmS or equivalent Working towards RPS Advanced Core portfolio submission Training in medicines information Preparation of prescribing guidelines Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. University Hospital Southampton NHS Trust
Feb 25, 2026
Full time
University Hospital Southampton NHS Trust Pharmacist Specialist The closing date is 06 March 2026 This is an exciting opportunity for an enthusiastic, motivated pharmacist to join our Surgical Clinical Pharmacist team. This is an ideal position for someone with a general medical background with great problem solving and communication skills, who can use their knowledge in different scenarios - could you advise alternative treatment options for a patient with temporary intestinal failure post surgery? Could you ensure their existing medical conditions were treated? Our Surgical Pharmacist team has a great track record of developing extended roles of practice. This includes pharmacist independent prescribing, microbiology ward rounds and working with the Inpatient Pain Team. The team provides services to elective and emergency surgery as well as tertiary surgical services in specialist areas. UHS is a regional centre for intestinal failure and provides specialist treatment for patients across the south of England. You will be supported by experienced senior pharmacists and given the opportunity to develop advanced level skills, including independent prescribing. We're looking for pharmacists with strong clinical knowledge who are ready to progress their career in clinical pharmacy at band 7. However, we will consider applications from suitable pharmacists for our band 6 7 progression route. Main duties of the job Attached you will find the person specification document which provides more detail about the essential and desirable skills and experience needed for this role. We highly recommend you review this document and use it when completing your application as these criteria are used by hiring managers as guidance during shortlisting. For an overview of the main duties of the role please see the 'Job Description and Main Responsibilities' section below. To understand the day to day responsibilities in more detail please read the full job description document attached. About us University Hospital Southampton is one of England's largest acute teaching Trusts, offering a wide range of learning and development opportunities to support your career aspirations. Located on the south coast with an international airport and direct rail links to London, Southampton offers an ideal setting to live and work, with the New Forest, South Downs and Jurassic Coast. At UHS we're committed to providing a flexible working environment where possible. Whether you are balancing family, study, or your wellbeing with your career, we want to support you so you can help our patients. At UHS, we proudly champion individuality, recognising that outstanding care is only possible with a diverse, inclusive team. We're committed to creating an anti racist, anti discriminatory environment where everyone feels valued, safe, and empowered to make a meaningful impact in our communities. We welcome applicants of all backgrounds, identities, and experiences to join us in building a healthcare community where everyone can belong, thrive, and contribute. Job responsibilities You will work within the Surgical Clinical Pharmacy team as well as members of the wider multidisciplinary team. Pharmacists are welcomed by the surgical teams as providing a high level of expertise. Developing and delivering the clinical pharmacy service to surgical specialist areas as agreed with the Surgical Care Group pharmacists Acting as a deputy in the day to day running of the service for the Surgical Care Group Pharmacists in their absence Delivering extended roles of practice including independent prescribing (training will be provided) Contributing to clinical audit, quality improvement and service development Working with the nutrition team to provide parenteral nutrition (PN) to inpatients and to those on home PN Developing, implementing and reviewing guidelines Participating in surgical, nutrition, micro and pain team ward rounds as agreed with the Surgical Care Group pharmacists Providing clinical supervision for junior rotational pharmacists, pharmacist trainees and training on specialist surgical topics within the multidisciplinary team Person Specification Qualifications, knowledge and experience Masters Degree in Pharmacy GPhC registration Sound knowledge of a surgical or medical speciality acquired working within a suitable specialty Meets Foundation framework/ GLF competencies Audit and evaluative work Sound understanding of healthcare priorities and political agendas Experience of teaching and tutoring Postgraduate diploma in clinical pharmacy or equivalent experience MRPharmS or equivalent Working towards RPS Advanced Core portfolio submission Training in medicines information Preparation of prescribing guidelines Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. University Hospital Southampton NHS Trust
Regulatory Affairs Officer Location: Hybrid (3 days on-site) Salary:£26-28K Sector: Scientific / Regulatory Affairs CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded graduate to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions and gaining hands on experience with raw material data management. The Role As a Scientific Data & Regulatory Associate, you will support the technical aspects of managing raw material data while collaborating with a skilled global regulatory team. You'll play a key part in ensuring product compliance, analysing scientific information, and contributing to important business decisions. Key Responsibilities Develop awareness of major chemical legislation including CLP, REACH, GPSR, and CSR. Communicate with raw material suppliers to request and obtain key data such as Safety Data Sheets (SDSs) and Technical Data Sheets (TDSs). Interpret scientific data from SDSs and external databases (e.g., ECHA) to identify substance and mixture classifications. Use your understanding of toxicology to process and analyse data that supports regulatory and business decision making. Provide technical regulatory expertise on chemicals to support product assessments. Update and maintain chemical and raw material data within systems such as SAP. Monitor regulatory developments, including updates such as ATPs, and assess their impact on products. Requirements A degree or equivalent in a relevant scientific discipline (e.g., Chemistry, Biology, Toxicology, or equivalent). Strong scientific literacy and an interest in chemical regulations and product safety. Ability to work in a hybrid role, with 3 days per week on site. Strong communication skills and attention to detail. The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.
Feb 20, 2026
Full time
Regulatory Affairs Officer Location: Hybrid (3 days on-site) Salary:£26-28K Sector: Scientific / Regulatory Affairs CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded graduate to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions and gaining hands on experience with raw material data management. The Role As a Scientific Data & Regulatory Associate, you will support the technical aspects of managing raw material data while collaborating with a skilled global regulatory team. You'll play a key part in ensuring product compliance, analysing scientific information, and contributing to important business decisions. Key Responsibilities Develop awareness of major chemical legislation including CLP, REACH, GPSR, and CSR. Communicate with raw material suppliers to request and obtain key data such as Safety Data Sheets (SDSs) and Technical Data Sheets (TDSs). Interpret scientific data from SDSs and external databases (e.g., ECHA) to identify substance and mixture classifications. Use your understanding of toxicology to process and analyse data that supports regulatory and business decision making. Provide technical regulatory expertise on chemicals to support product assessments. Update and maintain chemical and raw material data within systems such as SAP. Monitor regulatory developments, including updates such as ATPs, and assess their impact on products. Requirements A degree or equivalent in a relevant scientific discipline (e.g., Chemistry, Biology, Toxicology, or equivalent). Strong scientific literacy and an interest in chemical regulations and product safety. Ability to work in a hybrid role, with 3 days per week on site. Strong communication skills and attention to detail. The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.
Salary: £31,445 - £33,100 per annum. Commencement on the salary range is subject to comparables, skills and experience. Duration of Contract: 18 months in the first instance with ability to extend subject to funding Hours per week: 35 hours per week (Full Time) Location: Sutton Closing Date: 12th April 2026 Please note that should we receive a high volume of suitable applications, we may close this vacancy earlier than the stated deadline. We encourage you to submit your application as soon as possible to avoid missing out. About the role Under the guidance of Alexis De Haven Brandon, we seek a dedicated early career in vivo scientist. The central aim of this position is to assist in the undertaking of in vivo technical work, playing a key role in supporting a variety of in vivo experiments and laboratory approaches. You will be an in vivo scientist with a basic knowledge and experience of in vivo techniques. Your responsibilities will include monitoring animal welfare, carrying out animal procedures, maintaining detailed records. This position offers an excellent opportunity for an early career in vivo scientist with a passion for in vivo science, and animal welfare. We offer full training to gain a home office PIL, for more technical procedures to the right candidate. There will occasionally be the need for out of hours work to ensure Home office compliance, and the needs of the projects are met. The successful candidate will be a motivated individual with a strong background in animal welfare and husbandry in a research setting. We highly value diversity and encourage candidates from all backgrounds to apply. About you Broad-based knowledge of animal welfare within a research setting At least a year in an in vivo research setting with rodents. Proven experience in husbandry, welfare monitoring and animal handling. Ability to work both independently and as part of a team. High degree of integrity and understanding of the need for confidentiality surrounding drug discovery programmes. Willingness to occasionally work out of hours. About our team Under UK law, animals can only be used for research if there is no appropriate alternative. All our research proposals are thoroughly assessed before approval to ensure that there is no alternative to the use of animals, and that the studies will provide valuable information that will ultimately help cancer patients. The ICR is strongly committed to the highest standards of animal welfare in all research studies, and has led the development of best practice in this area. We also support the principles of the 3Rs - replacement, refinement and reduction of use of animals for research - and are working to develop alternative experimental techniques. The In Vivo Pharmacology team provides in vivo support for all projects within the Centre for Cancer Drug Discovery. The team carries out critical proof-of-principle intervention studies and provides the essential pharmacological assays required to guide target validation in addition to the optimisation and selection of new drug candidates. Importantly, these experiments include the demonstration of drug effects in vivo, biomarker discovery and therapy studies all of which underpin the drug discovery programs across the portfolio. The team works across a wide range of tumour models, including human tumour xenografts models (both cell line- and patient-derived xenografts), genetically engineered mouse models and organoid based models. The team is also highly experienced in preclinical metastatic models. The team has specialised skills to develop and implement novel models, and supporting the design and implementation of studies, all whilst complying with increasingly complex Home Office regulations. Department/Directorate Information About our organisation We are one of the world's most influential cancer research institutes with an outstanding record of achievement dating back more than 100 years. We are world leaders in identifying cancer genes, discovering cancer drugs and developing precision radiotherapy. Together with our hospital partner The Royal Marsden, we are rated in the top four centres for cancer research and treatment worldwide. As well as being a world-class institute, we are a college of the University of London. We are consistently in the top performing universities in the league table of university research quality complied from Research Excellence Framework (REF 2014 & 2021). We have charitable status and rely on support from partner organisations, charities, donors and the general public. We have more than 1000 staff and postgraduate students across three sites - in Chelsea and Sutton. What we offer A dynamic and supportive research environment Access to state-of-the-art facilities and professional development opportunities Collaboration with leading researchers in the field Competitive salary and pension We encourage all applicants to access the job pack attached for more detailed information regarding this role. For an informal discussion regarding the role, please contact About The Institute of Cancer Research As a member of staff, you'll have exclusive access to a range of staff benefits. The ICR is committed to supporting overseas applicants applying for roles, please click here to find out further information. The Institute of Cancer Research, London, is one of the world's most influential cancer research institutes, with an outstanding record of achievement dating back more than 100 years. Further information about working at the ICR can be found here . Why work for us? At the Institute of Cancer Research, we champion diversity as we believe it fuels innovation and drives impactful research. We welcome applicants from all walks of life, valuing diverse perspectives that enrich our work. Don't let a checklist of qualifications hold you back - if you're passionate about the role, we want to hear from you. Your unique experiences and backgrounds contribute to the richness of our team. We are committed to being an equal opportunity for all, regardless of ethnicity, gender, age, sexual orientation, disability, or any other dimension of diversity. Join us in creating an inclusive environment where everyone's voice is heard and valued.
Feb 16, 2026
Full time
Salary: £31,445 - £33,100 per annum. Commencement on the salary range is subject to comparables, skills and experience. Duration of Contract: 18 months in the first instance with ability to extend subject to funding Hours per week: 35 hours per week (Full Time) Location: Sutton Closing Date: 12th April 2026 Please note that should we receive a high volume of suitable applications, we may close this vacancy earlier than the stated deadline. We encourage you to submit your application as soon as possible to avoid missing out. About the role Under the guidance of Alexis De Haven Brandon, we seek a dedicated early career in vivo scientist. The central aim of this position is to assist in the undertaking of in vivo technical work, playing a key role in supporting a variety of in vivo experiments and laboratory approaches. You will be an in vivo scientist with a basic knowledge and experience of in vivo techniques. Your responsibilities will include monitoring animal welfare, carrying out animal procedures, maintaining detailed records. This position offers an excellent opportunity for an early career in vivo scientist with a passion for in vivo science, and animal welfare. We offer full training to gain a home office PIL, for more technical procedures to the right candidate. There will occasionally be the need for out of hours work to ensure Home office compliance, and the needs of the projects are met. The successful candidate will be a motivated individual with a strong background in animal welfare and husbandry in a research setting. We highly value diversity and encourage candidates from all backgrounds to apply. About you Broad-based knowledge of animal welfare within a research setting At least a year in an in vivo research setting with rodents. Proven experience in husbandry, welfare monitoring and animal handling. Ability to work both independently and as part of a team. High degree of integrity and understanding of the need for confidentiality surrounding drug discovery programmes. Willingness to occasionally work out of hours. About our team Under UK law, animals can only be used for research if there is no appropriate alternative. All our research proposals are thoroughly assessed before approval to ensure that there is no alternative to the use of animals, and that the studies will provide valuable information that will ultimately help cancer patients. The ICR is strongly committed to the highest standards of animal welfare in all research studies, and has led the development of best practice in this area. We also support the principles of the 3Rs - replacement, refinement and reduction of use of animals for research - and are working to develop alternative experimental techniques. The In Vivo Pharmacology team provides in vivo support for all projects within the Centre for Cancer Drug Discovery. The team carries out critical proof-of-principle intervention studies and provides the essential pharmacological assays required to guide target validation in addition to the optimisation and selection of new drug candidates. Importantly, these experiments include the demonstration of drug effects in vivo, biomarker discovery and therapy studies all of which underpin the drug discovery programs across the portfolio. The team works across a wide range of tumour models, including human tumour xenografts models (both cell line- and patient-derived xenografts), genetically engineered mouse models and organoid based models. The team is also highly experienced in preclinical metastatic models. The team has specialised skills to develop and implement novel models, and supporting the design and implementation of studies, all whilst complying with increasingly complex Home Office regulations. Department/Directorate Information About our organisation We are one of the world's most influential cancer research institutes with an outstanding record of achievement dating back more than 100 years. We are world leaders in identifying cancer genes, discovering cancer drugs and developing precision radiotherapy. Together with our hospital partner The Royal Marsden, we are rated in the top four centres for cancer research and treatment worldwide. As well as being a world-class institute, we are a college of the University of London. We are consistently in the top performing universities in the league table of university research quality complied from Research Excellence Framework (REF 2014 & 2021). We have charitable status and rely on support from partner organisations, charities, donors and the general public. We have more than 1000 staff and postgraduate students across three sites - in Chelsea and Sutton. What we offer A dynamic and supportive research environment Access to state-of-the-art facilities and professional development opportunities Collaboration with leading researchers in the field Competitive salary and pension We encourage all applicants to access the job pack attached for more detailed information regarding this role. For an informal discussion regarding the role, please contact About The Institute of Cancer Research As a member of staff, you'll have exclusive access to a range of staff benefits. The ICR is committed to supporting overseas applicants applying for roles, please click here to find out further information. The Institute of Cancer Research, London, is one of the world's most influential cancer research institutes, with an outstanding record of achievement dating back more than 100 years. Further information about working at the ICR can be found here . Why work for us? At the Institute of Cancer Research, we champion diversity as we believe it fuels innovation and drives impactful research. We welcome applicants from all walks of life, valuing diverse perspectives that enrich our work. Don't let a checklist of qualifications hold you back - if you're passionate about the role, we want to hear from you. Your unique experiences and backgrounds contribute to the richness of our team. We are committed to being an equal opportunity for all, regardless of ethnicity, gender, age, sexual orientation, disability, or any other dimension of diversity. Join us in creating an inclusive environment where everyone's voice is heard and valued.
