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laboratory analyst
Lab Analyst (Chemistry)
Tentamus Group GmbH Bristol, Gloucestershire
The Laboratory Analyst (Chemistry) proactively supports and works closely with the Laboratory Manger (Chemistry), Technical Manager (Chemistry) and other colleagues to ensure the smooth and efficient running of the chemistry laboratory on a day-to-day basis, whilst observing and adhering to laboratory standards and requirements. The Laboratory Analyst (Chemistry) will have sufficient skills and knowledge of chemistry as to assume the responsibilities of the role. A general description of duties is as follows: To conduct tests following 'good laboratory practice' procedures and in accordance with the One Scientific Ltd methods and procedures complying with BS EN ISO/IEC 17025:2017 correctly, accurately and safely. To handle and process all samples in the correct manner documented in the One Scientific Ltd Standard Operating Procedures. To carry out the majority of laboratory testing and other such laboratory duties as required. To operate advance analytical equipment. To assist with training of laboratory staff by providing technical advice and knowledge. To refer immediately to the Laboratory Manager (Chemistry) any non-conforming records (where the required criteria or tolerances are not met). To inform the Laboratory Manager (Chemistry) and Supervisor (Chemistry) of any out-of-order equipment and participate in maintenance, commissioning and calibration activities in the chemistry department as required. To implement quality control procedures as required. Day to day activities will include: Perform routine instrument maintenance/calibrations as required. Follow good laboratory practices, maintain general lab cleanliness, including the cleaning of lab equipment and glassware. Maintain safety practices in all aspects of lab operations. Prepare reagents, solutions, buffers and standards for testing if and when required. To assist and participate in both the Internal Quality Control and External Quality Control Schemes when requested to do so. To assist Laboratory Manger in the validation of new methods. To assist and participate in UKAS audits. Report into Management Laboratory Records and Reports: To maintain accurate laboratory records, to include daily, weekly or monthly proformas. To approve results (only if trained to do so). To raise, check and report out of specification notifications to customers (only if trained to do so). Health and Safety To wear the appropriate protective clothing and equipment when in the laboratory. To monitor and ensure all safety, hygiene and health and safety requirements are adhered to within the laboratory. To assist in monitoring and organisation of the cleaning schedule to ensure that the laboratory is kept clean and tidy. The above description is not exhaustive. Other duties may be required to ensure the efficient running of the laboratory. Such duties will be at the request of senior management. Hourly rate: £12.21 If you would like to apply for this role, please send us your updated CV and cover letter to . Please, include the job position in the subject of your email in the following format OSL: Lab Analyst (Chemistry). Directions to One Scientific Ltd. For your information there is a Park and Ride (Bristol A4 Portway) at the end of our road (Victoria Road) so we are easily accessible by bus from the city centre. We are the last industrial estate on the right-hand side of Victoria Road before you reach the Port gates. By train there is a small branch line from Temple Meads Station to Portway Park and Ride station, approx. 0.5miles from our location in Avonmouth.
Jul 17, 2025
Full time
The Laboratory Analyst (Chemistry) proactively supports and works closely with the Laboratory Manger (Chemistry), Technical Manager (Chemistry) and other colleagues to ensure the smooth and efficient running of the chemistry laboratory on a day-to-day basis, whilst observing and adhering to laboratory standards and requirements. The Laboratory Analyst (Chemistry) will have sufficient skills and knowledge of chemistry as to assume the responsibilities of the role. A general description of duties is as follows: To conduct tests following 'good laboratory practice' procedures and in accordance with the One Scientific Ltd methods and procedures complying with BS EN ISO/IEC 17025:2017 correctly, accurately and safely. To handle and process all samples in the correct manner documented in the One Scientific Ltd Standard Operating Procedures. To carry out the majority of laboratory testing and other such laboratory duties as required. To operate advance analytical equipment. To assist with training of laboratory staff by providing technical advice and knowledge. To refer immediately to the Laboratory Manager (Chemistry) any non-conforming records (where the required criteria or tolerances are not met). To inform the Laboratory Manager (Chemistry) and Supervisor (Chemistry) of any out-of-order equipment and participate in maintenance, commissioning and calibration activities in the chemistry department as required. To implement quality control procedures as required. Day to day activities will include: Perform routine instrument maintenance/calibrations as required. Follow good laboratory practices, maintain general lab cleanliness, including the cleaning of lab equipment and glassware. Maintain safety practices in all aspects of lab operations. Prepare reagents, solutions, buffers and standards for testing if and when required. To assist and participate in both the Internal Quality Control and External Quality Control Schemes when requested to do so. To assist Laboratory Manger in the validation of new methods. To assist and participate in UKAS audits. Report into Management Laboratory Records and Reports: To maintain accurate laboratory records, to include daily, weekly or monthly proformas. To approve results (only if trained to do so). To raise, check and report out of specification notifications to customers (only if trained to do so). Health and Safety To wear the appropriate protective clothing and equipment when in the laboratory. To monitor and ensure all safety, hygiene and health and safety requirements are adhered to within the laboratory. To assist in monitoring and organisation of the cleaning schedule to ensure that the laboratory is kept clean and tidy. The above description is not exhaustive. Other duties may be required to ensure the efficient running of the laboratory. Such duties will be at the request of senior management. Hourly rate: £12.21 If you would like to apply for this role, please send us your updated CV and cover letter to . Please, include the job position in the subject of your email in the following format OSL: Lab Analyst (Chemistry). Directions to One Scientific Ltd. For your information there is a Park and Ride (Bristol A4 Portway) at the end of our road (Victoria Road) so we are easily accessible by bus from the city centre. We are the last industrial estate on the right-hand side of Victoria Road before you reach the Port gates. By train there is a small branch line from Temple Meads Station to Portway Park and Ride station, approx. 0.5miles from our location in Avonmouth.
SF Recruitment
Digital Forensic Analyst/Technician
SF Recruitment City, Birmingham
Experienced/Senior/Principal Digital Forensic Analyst/Technician The company I am supporting provides computer forensics, mobile phone forensics and cell site analysis to the legal sector, police forces, local authorities, and commercial organisations. We are looking for an experienced Digital Forensic Analyst/Technician to conduct forensic examinations of digital devices (e.g. computers, mobile phones) in order to acquire and process evidential data and produce factual reports. Key Responsibilities -Case management and forensic analysis of computer and mobile devices. -Securing and preservation of digital evidence. -Procedure and documentation development. -Contribute to achieving and maintaining quality standards whilst ensuring that the company's quality procedures ISO 17025 and 9001 are robustly adhered to. Essential Skills & Experience -2 years+ experience working in an accredited digital forensics laboratory. -Ability in using forensic tools including AXIOM, EnCase, Griffeye and X-Ways. -Fully conversant with the digital forensic process and current ACPO Guidelines. Working Arrangement - Onsite Salary - £40,000 -£50,000 (Depending on experience)
Jul 17, 2025
Full time
Experienced/Senior/Principal Digital Forensic Analyst/Technician The company I am supporting provides computer forensics, mobile phone forensics and cell site analysis to the legal sector, police forces, local authorities, and commercial organisations. We are looking for an experienced Digital Forensic Analyst/Technician to conduct forensic examinations of digital devices (e.g. computers, mobile phones) in order to acquire and process evidential data and produce factual reports. Key Responsibilities -Case management and forensic analysis of computer and mobile devices. -Securing and preservation of digital evidence. -Procedure and documentation development. -Contribute to achieving and maintaining quality standards whilst ensuring that the company's quality procedures ISO 17025 and 9001 are robustly adhered to. Essential Skills & Experience -2 years+ experience working in an accredited digital forensics laboratory. -Ability in using forensic tools including AXIOM, EnCase, Griffeye and X-Ways. -Fully conversant with the digital forensic process and current ACPO Guidelines. Working Arrangement - Onsite Salary - £40,000 -£50,000 (Depending on experience)
Senior Scientist - Physico Chemical Testing
Laboratory Corporation
Do you have recognised experience in the field of Physico Chemical Testing and want to train and develop others? Are you ready for a varied role that will allow you to complete non-routine testing using different analytical techniques? Do you want to be a part of the world's leading life sciences company? Labcorp is a leading global life sciences company that includes contract research and developmental services to thepharmaceutical,medical technology,crop protectionandchemicalindustries. At Labcorp in Eye, Suffolk we are looking to recruit a Senior Scientist to join our Physico Chemical Testing team. In this senior role, you will have the opportunity to work alongside other experienced scientists in an established physico-chemical testing laboratory to fulfil the expectations of our clients and work within regulatory guidelines. Job responsibilities include: Trains and directs less experienced staff in the conduct of operational tasks and troubleshooting of processes. Able to review work of others for overall accuracy, timeliness, completeness and soundness of technical judgement and have the a bility to assist in developing a training plan for less experienced laboratory personnel Sets up and performs a variety of assays using appropriate instrumentation with routine and non-routine methods Critically review study protocol in primary area of work and suggest changes where appropriate Maintains study documentation in compliance with regulatory guidelines and reviews own work for overall accuracy, timeliness, completeness, and soundness of technical judgment Deliver results within agreed timeframe, whilst recognising changes in priorities. Routinely conduct QC review of data and methodology section within reports within scope of current role Ability to prepare results and presentations based on the work performed Evaluates data for experiment modification and contribute to report preparation/review. Ensures that scientific expectations are met Participate in method development and validation projects May act as Principal investigator or Responsible Analyst on specific projects within area of expertise Motivates self and others to assure timely delivery of client expectations and influences others to see things from a client's perspective Awareness of latest technologies and regulatory thinking with respect to specific scientific discipline. Advises Study Directors and management where modifications to working practices are necessary Uses experience to apply creative problem solving to challenging issues. Anticipates, detects and promotes quality and process improvement needs in own and other areas and actively promotes collaboration between groups. Provides team leaders and members with regular supportive feedback. Establishes clear plans to meet short- and medium-term requirements for projects. Anticipates issues/obstacles which may prevent meeting project/department objectives and identifies solutions to overcome difficulties. Ability to recognize deviations from normal results and inform Study Director, Study Coordinator and/or management of any problems that may affect integrity of the data. Ability to devise and implement action plans for a study or complex method development, understand the scope of a study (primary area of work) and be able to complete with no supervision What we can offer you: Competitive salary and a comprehensive benefits package, including health coverage and contributorypension Opportunity to work on a variety of study types using different analytical techniques in a supportive and knowledgeable team Unrivalled opportunities to develop a successful career in the scientific industry A culture of CARE with access to wellbeing programs and various employee resource groups Education: BSc in Chemistry or related subject The successful candidate will possess the following skills and experience: Highly experienced in the use of Physico Chemical testing with Laboratory equipment Experience of training team members Proficiency with I.T and computer software packages such as Excel Good numeracy Extensive experience of HPLC, GC and UV detection techniques Extensive knowledge of GLP and CIPAC standards The Environmental Science team at Labcorp have been helping companies bring safe products to market for over 40 years. Our varied work supports the crop protection, chemical and pharmaceutical industries so if you want to part of a supportive team that offers training and progression opportunities then please apply today. Our mission is to improve health and improve lives! Due to the remote location of this site, there are no public transport links available. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. Formore information about how we collect and store your personal data, please see our Privacy Statement .
Jul 17, 2025
Full time
Do you have recognised experience in the field of Physico Chemical Testing and want to train and develop others? Are you ready for a varied role that will allow you to complete non-routine testing using different analytical techniques? Do you want to be a part of the world's leading life sciences company? Labcorp is a leading global life sciences company that includes contract research and developmental services to thepharmaceutical,medical technology,crop protectionandchemicalindustries. At Labcorp in Eye, Suffolk we are looking to recruit a Senior Scientist to join our Physico Chemical Testing team. In this senior role, you will have the opportunity to work alongside other experienced scientists in an established physico-chemical testing laboratory to fulfil the expectations of our clients and work within regulatory guidelines. Job responsibilities include: Trains and directs less experienced staff in the conduct of operational tasks and troubleshooting of processes. Able to review work of others for overall accuracy, timeliness, completeness and soundness of technical judgement and have the a bility to assist in developing a training plan for less experienced laboratory personnel Sets up and performs a variety of assays using appropriate instrumentation with routine and non-routine methods Critically review study protocol in primary area of work and suggest changes where appropriate Maintains study documentation in compliance with regulatory guidelines and reviews own work for overall accuracy, timeliness, completeness, and soundness of technical judgment Deliver results within agreed timeframe, whilst recognising changes in priorities. Routinely conduct QC review of data and methodology section within reports within scope of current role Ability to prepare results and presentations based on the work performed Evaluates data for experiment modification and contribute to report preparation/review. Ensures that scientific expectations are met Participate in method development and validation projects May act as Principal investigator or Responsible Analyst on specific projects within area of expertise Motivates self and others to assure timely delivery of client expectations and influences others to see things from a client's perspective Awareness of latest technologies and regulatory thinking with respect to specific scientific discipline. Advises Study Directors and management where modifications to working practices are necessary Uses experience to apply creative problem solving to challenging issues. Anticipates, detects and promotes quality and process improvement needs in own and other areas and actively promotes collaboration between groups. Provides team leaders and members with regular supportive feedback. Establishes clear plans to meet short- and medium-term requirements for projects. Anticipates issues/obstacles which may prevent meeting project/department objectives and identifies solutions to overcome difficulties. Ability to recognize deviations from normal results and inform Study Director, Study Coordinator and/or management of any problems that may affect integrity of the data. Ability to devise and implement action plans for a study or complex method development, understand the scope of a study (primary area of work) and be able to complete with no supervision What we can offer you: Competitive salary and a comprehensive benefits package, including health coverage and contributorypension Opportunity to work on a variety of study types using different analytical techniques in a supportive and knowledgeable team Unrivalled opportunities to develop a successful career in the scientific industry A culture of CARE with access to wellbeing programs and various employee resource groups Education: BSc in Chemistry or related subject The successful candidate will possess the following skills and experience: Highly experienced in the use of Physico Chemical testing with Laboratory equipment Experience of training team members Proficiency with I.T and computer software packages such as Excel Good numeracy Extensive experience of HPLC, GC and UV detection techniques Extensive knowledge of GLP and CIPAC standards The Environmental Science team at Labcorp have been helping companies bring safe products to market for over 40 years. Our varied work supports the crop protection, chemical and pharmaceutical industries so if you want to part of a supportive team that offers training and progression opportunities then please apply today. Our mission is to improve health and improve lives! Due to the remote location of this site, there are no public transport links available. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. Formore information about how we collect and store your personal data, please see our Privacy Statement .
Quality Control Product Testing and Stability / Scientist
Lonza Group Ltd. Slough, Berkshire
Quality Control Product Testing and Stability / Scientist page is loaded Quality Control Product Testing and Stability / Scientist Apply locations UK - Slough time type Full time posted on Posted Yesterday job requisition id R65569 Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. The role: Join Lonza AG in Slough, UK as a g / Quality Control Product Testing and Stability / Scientist to analyse the stability of therapeutic proteins. You will be responsible for performing a wide range of analytical methods including High-Performance Liquid Chromatography (HPLC),Electrophoresis(e.g. SDS PAGE, CE SDS, icIEF), Spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) to assess the stability of therapeutic proteins and the release of batches. Though this is mainly laboratory-based, you will be expected to technically review assays performed by other analysts and write stability study protocols and data summary reports. All work is expected to be carried out safely and competently in accordance with localenvironment, health, and safety(EHS) policies andGood manufacturing practice(GMP) guidelines. Please note the working pattern for this role is 4 days a week lab-based! Key responsibilities: Perform experimental work independently in accordance with SOPs and study protocols on a variety of sample types. Ensure all tasks are completed safely and compliantly, maintaining and updating training profiles as needed. Plan and complete assigned tasks within the required timeframe, communicating progress and advancing challenges to the Line Manager or scientific lead as appropriate. Technically review assays against SOPs, protocols, and GMP principles, and liaise with operators and study directors to close out technical reviews. Interpret data against specifications, critically assess results, identify trends, and report any concerns to QC management, SDs, and QC representatives. Mentor and train newer or junior team members, providing support and encouraging a collaborative environment. Support departmental improvement projects by promoting standard methodologies and addressing any incorrect practices. Assist with the timely completion of investigations, deviations, CAPAs, and change controls, potentially leading minor investigations independently. Maintain lab cleanliness, stock reagents, monitor equipment, and possibly take on system ownership. Work collaboratively to meet business, regulatory, and customer needs. Key requirements: BSc in a relevant scientific field or equivalent experience. Awareness of cGMP guidelines and their impact on laboratory work. Excellent knowledge and experience of electrophoresis (e.g. SDS PAGE, CE SDS, icIEF) Proven ability to work effectively within a team in a regulated cGMP environment. Theoretical knowledge of various analytical methods. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Jul 17, 2025
Full time
Quality Control Product Testing and Stability / Scientist page is loaded Quality Control Product Testing and Stability / Scientist Apply locations UK - Slough time type Full time posted on Posted Yesterday job requisition id R65569 Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. The role: Join Lonza AG in Slough, UK as a g / Quality Control Product Testing and Stability / Scientist to analyse the stability of therapeutic proteins. You will be responsible for performing a wide range of analytical methods including High-Performance Liquid Chromatography (HPLC),Electrophoresis(e.g. SDS PAGE, CE SDS, icIEF), Spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) to assess the stability of therapeutic proteins and the release of batches. Though this is mainly laboratory-based, you will be expected to technically review assays performed by other analysts and write stability study protocols and data summary reports. All work is expected to be carried out safely and competently in accordance with localenvironment, health, and safety(EHS) policies andGood manufacturing practice(GMP) guidelines. Please note the working pattern for this role is 4 days a week lab-based! Key responsibilities: Perform experimental work independently in accordance with SOPs and study protocols on a variety of sample types. Ensure all tasks are completed safely and compliantly, maintaining and updating training profiles as needed. Plan and complete assigned tasks within the required timeframe, communicating progress and advancing challenges to the Line Manager or scientific lead as appropriate. Technically review assays against SOPs, protocols, and GMP principles, and liaise with operators and study directors to close out technical reviews. Interpret data against specifications, critically assess results, identify trends, and report any concerns to QC management, SDs, and QC representatives. Mentor and train newer or junior team members, providing support and encouraging a collaborative environment. Support departmental improvement projects by promoting standard methodologies and addressing any incorrect practices. Assist with the timely completion of investigations, deviations, CAPAs, and change controls, potentially leading minor investigations independently. Maintain lab cleanliness, stock reagents, monitor equipment, and possibly take on system ownership. Work collaboratively to meet business, regulatory, and customer needs. Key requirements: BSc in a relevant scientific field or equivalent experience. Awareness of cGMP guidelines and their impact on laboratory work. Excellent knowledge and experience of electrophoresis (e.g. SDS PAGE, CE SDS, icIEF) Proven ability to work effectively within a team in a regulated cGMP environment. Theoretical knowledge of various analytical methods. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Adecco
Lab Analyst
Adecco Cambridge, Cambridgeshire
Lab Analyst - Cambridge - 28,000 (12 month FTC) We are currently seeking a Lab Analyst on behalf of our wonderful client based in North Cambridge! Our client are a brilliant place to work with a very friendly team looking for an experienced Lab Analyst to support them on a 12 month fixed term contract! Salary: 28k Hours: Monday-Friday 8am-4pm (flexible) Responsibilities: Test chemical samples and approve production batches. Manage chemical testing records and liaise with suppliers. Perform amino acid testing and process customer returns. Maintain stock levels and the asset management database. Coordinate equipment servicing, calibration, and related paperwork. Ensure high-quality standards and support the team to meet targets. Key Skills & Experience: Laboratory and chemical testing experience. Strong problem-solving and mechanical skills. Knowledge of chromatography, fluidics, and AAA instrumentation. Confident with diagnostic repairs and fault finding. Good IT skills and attention to detail. Professional, team-focused, and customer-oriented. If you are interested in this role, or know of someone that may be interested, please respond to this with a copy of an up to date CV for more information. Alternatively you can reach us on (phone number removed)! Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
Jul 17, 2025
Contractor
Lab Analyst - Cambridge - 28,000 (12 month FTC) We are currently seeking a Lab Analyst on behalf of our wonderful client based in North Cambridge! Our client are a brilliant place to work with a very friendly team looking for an experienced Lab Analyst to support them on a 12 month fixed term contract! Salary: 28k Hours: Monday-Friday 8am-4pm (flexible) Responsibilities: Test chemical samples and approve production batches. Manage chemical testing records and liaise with suppliers. Perform amino acid testing and process customer returns. Maintain stock levels and the asset management database. Coordinate equipment servicing, calibration, and related paperwork. Ensure high-quality standards and support the team to meet targets. Key Skills & Experience: Laboratory and chemical testing experience. Strong problem-solving and mechanical skills. Knowledge of chromatography, fluidics, and AAA instrumentation. Confident with diagnostic repairs and fault finding. Good IT skills and attention to detail. Professional, team-focused, and customer-oriented. If you are interested in this role, or know of someone that may be interested, please respond to this with a copy of an up to date CV for more information. Alternatively you can reach us on (phone number removed)! Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
In Technology Group
IT Support Analyst
In Technology Group Morpeth, Northumberland
Job Title: IS Support Analyst (2nd Line Support) Location: Morpeth, Northumberland Salary: 30,000- 32,000 per annum Are you a skilled IT professional looking to take the next step in your support career? We're seeking a proactive and technically capable IS Support Analyst to deliver expert second-line IT support across Laboratory, Packaging, and Pharmaceutical manufacturing environments. About the Role: As an IS Support Analyst, you'll act as a vital link between the IT Helpdesk and end users working in highly regulated GxP environments. You will troubleshoot issues, maintain system integrity, and ensure minimal downtime of business-critical and validated systems. This role is key to supporting seamless operations in both laboratory and production settings. Key Responsibilities: Provide second-line IT support for end users across regulated operational areas. Troubleshoot and resolve complex software, hardware, and infrastructure issues. Support and maintain validated workstations, instrumentation PCs, and specialized systems like LIMS, SCADA/HMI, and PLC-integrated devices. Collaborate with infrastructure teams and vendors to resolve escalated issues. Ensure compliance with Computer System Validation (CSV), GxP, and 21 CFR Part 11 standards. Document support activities accurately using the IT helpdesk system. Deliver technical onboarding and system usage training to end users. Proactively recommend improvements to enhance system reliability and user experience. Required Skills & Qualifications: Industry-recognised IT certifications (e.g., CompTIA A+/Network+, Microsoft MCSA/MD-100/MD-101, or Cisco CCNA) or equivalent experience. Experience supporting Windows 10, Windows Server, and Active Directory environments. Strong knowledge of ITIL practices and service management. Proven customer service and communication skills. Ability to prioritise tasks and manage time effectively under pressure. Desirable Experience: Previous experience working in pharmaceutical, biotech, or laboratory settings. Familiarity with validated systems and GxP environments. This is an excellent opportunity to join a collaborative, compliance-focused environment and make a meaningful impact supporting essential IT systems. If you're ready to bring your skills to a fast-paced, regulated industry, we'd love to hear from you. Apply today to be considered. In Technology Group Ltd is acting as an Employment Agency in relation to this vacancy.
Jul 17, 2025
Full time
Job Title: IS Support Analyst (2nd Line Support) Location: Morpeth, Northumberland Salary: 30,000- 32,000 per annum Are you a skilled IT professional looking to take the next step in your support career? We're seeking a proactive and technically capable IS Support Analyst to deliver expert second-line IT support across Laboratory, Packaging, and Pharmaceutical manufacturing environments. About the Role: As an IS Support Analyst, you'll act as a vital link between the IT Helpdesk and end users working in highly regulated GxP environments. You will troubleshoot issues, maintain system integrity, and ensure minimal downtime of business-critical and validated systems. This role is key to supporting seamless operations in both laboratory and production settings. Key Responsibilities: Provide second-line IT support for end users across regulated operational areas. Troubleshoot and resolve complex software, hardware, and infrastructure issues. Support and maintain validated workstations, instrumentation PCs, and specialized systems like LIMS, SCADA/HMI, and PLC-integrated devices. Collaborate with infrastructure teams and vendors to resolve escalated issues. Ensure compliance with Computer System Validation (CSV), GxP, and 21 CFR Part 11 standards. Document support activities accurately using the IT helpdesk system. Deliver technical onboarding and system usage training to end users. Proactively recommend improvements to enhance system reliability and user experience. Required Skills & Qualifications: Industry-recognised IT certifications (e.g., CompTIA A+/Network+, Microsoft MCSA/MD-100/MD-101, or Cisco CCNA) or equivalent experience. Experience supporting Windows 10, Windows Server, and Active Directory environments. Strong knowledge of ITIL practices and service management. Proven customer service and communication skills. Ability to prioritise tasks and manage time effectively under pressure. Desirable Experience: Previous experience working in pharmaceutical, biotech, or laboratory settings. Familiarity with validated systems and GxP environments. This is an excellent opportunity to join a collaborative, compliance-focused environment and make a meaningful impact supporting essential IT systems. If you're ready to bring your skills to a fast-paced, regulated industry, we'd love to hear from you. Apply today to be considered. In Technology Group Ltd is acting as an Employment Agency in relation to this vacancy.
Penguin Recruitment
Asbestos Bulk Lab Analyst
Penguin Recruitment Chelmsford, Essex
Asbestos Lab Analysts - Manchester What's in store for you? Competitive salary up to 30,000, depending on skills and experience 23 days annual leave plus Bank Holidays Pension scheme Overtime work available Staff Referral Incentive Scheme Training opportunities to enhance Employee development Come be part of our expanding Lab team at a well-established, UKAS accredited asbestos consultancy. Due to significant contract wins in the North West, specifically related to domestic housing stock, and a relocation to an office twice the size, we are seeking talented individuals to join our team. We are looking for dedicated and P401 qualified Asbestos Lab Analysts to join our growing operations. In this vital role, you will contribute directly to ensuring public safety and regulatory compliance through accurate analysis. Key Responsibilities of a BOHS P401 Asbestos Analyst: Receive and log asbestos samples into the laboratory management system. Prepare asbestos samples for analysis using appropriate techniques. Undertake microscopic analysis of bulk materials for the presence of asbestos fibres. Identify and quantify asbestos fibre types (Chrysotile, Amosite, Crocidolite) to BOHS P401 standards. Accurately record and report analytical findings, ensuring data integrity. Maintain and calibrate laboratory equipment, ensuring it is in good working order. Adhere strictly to UKAS accreditation requirements, company procedures, and health and safety guidelines. Participate in internal and external quality control programs.
Jul 17, 2025
Full time
Asbestos Lab Analysts - Manchester What's in store for you? Competitive salary up to 30,000, depending on skills and experience 23 days annual leave plus Bank Holidays Pension scheme Overtime work available Staff Referral Incentive Scheme Training opportunities to enhance Employee development Come be part of our expanding Lab team at a well-established, UKAS accredited asbestos consultancy. Due to significant contract wins in the North West, specifically related to domestic housing stock, and a relocation to an office twice the size, we are seeking talented individuals to join our team. We are looking for dedicated and P401 qualified Asbestos Lab Analysts to join our growing operations. In this vital role, you will contribute directly to ensuring public safety and regulatory compliance through accurate analysis. Key Responsibilities of a BOHS P401 Asbestos Analyst: Receive and log asbestos samples into the laboratory management system. Prepare asbestos samples for analysis using appropriate techniques. Undertake microscopic analysis of bulk materials for the presence of asbestos fibres. Identify and quantify asbestos fibre types (Chrysotile, Amosite, Crocidolite) to BOHS P401 standards. Accurately record and report analytical findings, ensuring data integrity. Maintain and calibrate laboratory equipment, ensuring it is in good working order. Adhere strictly to UKAS accreditation requirements, company procedures, and health and safety guidelines. Participate in internal and external quality control programs.
Gap Technical Ltd
QC Section Leader
Gap Technical Ltd Wrexham, Clwyd
QC Section Leader Competitive Salary + Benefits Wrexham Days Only gap technical are proud to be representing this global manufacturing business in their search for a QC Section Leader to work at their facility based near Wrexham Performance Objectives To manage the analytical testing of solid dose products. To ensure that all testing is carried out within the requirements of cGMP, Health and Safety and COSHH. To critically review analytical data, and where specifications are met, approve products for further processing. In this role, you will be responsible for leading a team of analyst and ensuring that release of our product meet the highest standards of quality and consistency. You will be a key player in driving continuous improvement and ensuring compliance with industry regulation and company polices. Person Specification Science degree in Chemistry or equivalent qualification. Previous experience within a pharmaceutical or equivalent laboratory environment is essential. A thorough understanding of current GMP, Health and Safety and COSHH regulation and sound supervisory and interpersonal skills. Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules. Previous experience in leading OOS/OOT investigations and deviations is essential. Previous experience in leading a team is preferred. Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affair department is essential Experience in leading the analytical method transfer, verification and validation is preferred Apply Please send your CV via the Apply now option on the website If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch This vacancy is being advertised on behalf of gap technical who are operating as an employment agency. gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Closing Date: 16/08/2025 "By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy."
Jul 17, 2025
Full time
QC Section Leader Competitive Salary + Benefits Wrexham Days Only gap technical are proud to be representing this global manufacturing business in their search for a QC Section Leader to work at their facility based near Wrexham Performance Objectives To manage the analytical testing of solid dose products. To ensure that all testing is carried out within the requirements of cGMP, Health and Safety and COSHH. To critically review analytical data, and where specifications are met, approve products for further processing. In this role, you will be responsible for leading a team of analyst and ensuring that release of our product meet the highest standards of quality and consistency. You will be a key player in driving continuous improvement and ensuring compliance with industry regulation and company polices. Person Specification Science degree in Chemistry or equivalent qualification. Previous experience within a pharmaceutical or equivalent laboratory environment is essential. A thorough understanding of current GMP, Health and Safety and COSHH regulation and sound supervisory and interpersonal skills. Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules. Previous experience in leading OOS/OOT investigations and deviations is essential. Previous experience in leading a team is preferred. Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affair department is essential Experience in leading the analytical method transfer, verification and validation is preferred Apply Please send your CV via the Apply now option on the website If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch This vacancy is being advertised on behalf of gap technical who are operating as an employment agency. gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Closing Date: 16/08/2025 "By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy."
Broughton Group
Scientist - Student Placement
Broughton Group Skipton, Yorkshire
Main Purpose of the Role The Laboratory Analyst is principally responsible for performing chemical analyses on customers' products within agreed deadlines and quality standards. Location and Hours Either at Skipton, BD23 or Earby BB18 Hours of work - 40 hours per week, 8am - 4.30pm Monday - Friday. Key tasks and responsibilities Perform chemical analysis to produce high-quality, compliant data for clients within the agreed timeframes. Prepare reagents, samples, and standards used in testing. Employ instrument techniques including HPLC, LC-MS, GC-FID, GC-MS, CETI-8. Maintain the standards of housekeeping required in a laboratory. Produce data in accordance with the Quality Management System. Adhere to the principles of GMP / GLP applicable. Follow test methods/study plans, document deviations, and communicate directly with line or study managers. Key Person Specification Student of Chemistry or related Analytical Chemistry subject. Good technical problem-solving skills. Good verbal reasoning and negotiation skills. Proficient IT skills, including Microsoft applications. Right to work in the UK. Able to commit to and complete a 12-month placement contract.
Jul 16, 2025
Full time
Main Purpose of the Role The Laboratory Analyst is principally responsible for performing chemical analyses on customers' products within agreed deadlines and quality standards. Location and Hours Either at Skipton, BD23 or Earby BB18 Hours of work - 40 hours per week, 8am - 4.30pm Monday - Friday. Key tasks and responsibilities Perform chemical analysis to produce high-quality, compliant data for clients within the agreed timeframes. Prepare reagents, samples, and standards used in testing. Employ instrument techniques including HPLC, LC-MS, GC-FID, GC-MS, CETI-8. Maintain the standards of housekeeping required in a laboratory. Produce data in accordance with the Quality Management System. Adhere to the principles of GMP / GLP applicable. Follow test methods/study plans, document deviations, and communicate directly with line or study managers. Key Person Specification Student of Chemistry or related Analytical Chemistry subject. Good technical problem-solving skills. Good verbal reasoning and negotiation skills. Proficient IT skills, including Microsoft applications. Right to work in the UK. Able to commit to and complete a 12-month placement contract.
Broughton Group
Scientist - Student Placement
Broughton Group Earby, Lancashire
Main Purpose of the Role The Laboratory Analyst is principally responsible for performing chemical analyses on customers' products within agreed deadlines and quality standards. Location and Hours Either at Skipton, BD23 or Earby BB18 Hours of work - 40 hours per week, 8am - 4.30pm Monday - Friday. Key tasks and responsibilities Perform chemical analysis to produce high-quality, compliant data for clients within the agreed timeframes. Prepare reagents, samples, and standards used in testing. Employ instrument techniques including HPLC, LC-MS, GC-FID, GC-MS, CETI-8. Maintain the standards of housekeeping required in a laboratory. Produce data in accordance with the Quality Management System. Adhere to the principles of GMP / GLP applicable. Follow test methods/study plans, document deviations, and communicate directly with line or study managers. Key Person Specification Student of Chemistry or related Analytical Chemistry subject. Good technical problem-solving skills. Good verbal reasoning and negotiation skills. Proficient IT skills, including Microsoft applications. Right to work in the UK. Able to commit to and complete a 12-month placement contract.
Jul 16, 2025
Full time
Main Purpose of the Role The Laboratory Analyst is principally responsible for performing chemical analyses on customers' products within agreed deadlines and quality standards. Location and Hours Either at Skipton, BD23 or Earby BB18 Hours of work - 40 hours per week, 8am - 4.30pm Monday - Friday. Key tasks and responsibilities Perform chemical analysis to produce high-quality, compliant data for clients within the agreed timeframes. Prepare reagents, samples, and standards used in testing. Employ instrument techniques including HPLC, LC-MS, GC-FID, GC-MS, CETI-8. Maintain the standards of housekeeping required in a laboratory. Produce data in accordance with the Quality Management System. Adhere to the principles of GMP / GLP applicable. Follow test methods/study plans, document deviations, and communicate directly with line or study managers. Key Person Specification Student of Chemistry or related Analytical Chemistry subject. Good technical problem-solving skills. Good verbal reasoning and negotiation skills. Proficient IT skills, including Microsoft applications. Right to work in the UK. Able to commit to and complete a 12-month placement contract.
QC Analyst Chemistry - 30h per week
Danone Liverpool, Lancashire
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.
Jul 16, 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.
VRS-UK
Inorganic Analyst
VRS-UK Newmarket, Suffolk
Exciting opportunity for an experienced Inorganic Chemist to progress your career by joining a fast-paced & industry-leading laboratory in Cambridgeshire! As an Inorganic Analyst, you will work under limited supervision carrying out a range of ICP-MS & ICP-OES analyses of various environmental samples. You will hold responsibility for the maintenance and troubleshooting of instrument issues, calling external engineers when necessary to minimise instrument downtime. As the successful candidate you will have: Hands-on experience working with ICP systems Experience with maintenance and troubleshooting of ICP instrumentation. Experience working within an accredited laboratory (GxP or ISO) Applications are also invited from graduates who have completed a placement year and are looking to kick-start their career in Analytical Chemistry! If this sounds like the position for you then apply to VRS today! Key words: ICP-MS, ICPMS, gas chromatography, mass spectrometry, environmental, laboratory, analysis, analytical, chemistry, soil, water, forensic, toxicology, management, Cambridgeshire, Cambridge, East Anglia, Southeast, Newmarket, VRS9065PC Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website
Jul 15, 2025
Full time
Exciting opportunity for an experienced Inorganic Chemist to progress your career by joining a fast-paced & industry-leading laboratory in Cambridgeshire! As an Inorganic Analyst, you will work under limited supervision carrying out a range of ICP-MS & ICP-OES analyses of various environmental samples. You will hold responsibility for the maintenance and troubleshooting of instrument issues, calling external engineers when necessary to minimise instrument downtime. As the successful candidate you will have: Hands-on experience working with ICP systems Experience with maintenance and troubleshooting of ICP instrumentation. Experience working within an accredited laboratory (GxP or ISO) Applications are also invited from graduates who have completed a placement year and are looking to kick-start their career in Analytical Chemistry! If this sounds like the position for you then apply to VRS today! Key words: ICP-MS, ICPMS, gas chromatography, mass spectrometry, environmental, laboratory, analysis, analytical, chemistry, soil, water, forensic, toxicology, management, Cambridgeshire, Cambridge, East Anglia, Southeast, Newmarket, VRS9065PC Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website
CK GROUP
Laboratory Analyst
CK GROUP Redcar, Yorkshire
CK Group are recruiting for a Laboratory Analyst, on behalf of a multinational provider of technical services, to be based at their site in Wilton. Please note this role is a days role, on a 4 on 4 off shift pattern. The shifts are; 3 X 12 hours shifts and 1 X 11.5 hours, starting at 7am. The salary on offer is £30,000 plus a shift allowance. The Company: Our client provides a range of testing services, and they now have a new opportunity for an experienced Laboratory Analyst to join their team. Location: The Laboratory Analyst role is based in Wilton. The Role: Follow laboratory methods and procedures to specification and issue quality assured results to customers. Manage own work by sequencing tasks and priorities in accordance with planned analytical schedules. Liaise with customers, internal and external to determine requirements for non-scheduled activities, identify optimum solutions and ensure financial recovery is made for the services provided. Develop (as appropriate) and carry out SHE, COSHH, Risk Assessment, Safety / Housekeeping and Quality related activities including audits as required by the relevant systems and procedures. Act as the focal point for specific areas within the laboratory and actively manage the delivery and development of that service offering. Check, maintain, overhaul, and liaise with called out analytical instrument engineers to maximise the uptime availability of the laboratory equipment. Support and lead wherever possible the development of new methods and commissioning of new equipment. Your Background: Qualified to HNC / Degree in science discipline. At least 2 years industrial experience in the application of technical skills in an equivalent laboratory role. Good SHE awareness including application of COSHH, Risk Assessments and laboratory standards. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Jul 12, 2025
Full time
CK Group are recruiting for a Laboratory Analyst, on behalf of a multinational provider of technical services, to be based at their site in Wilton. Please note this role is a days role, on a 4 on 4 off shift pattern. The shifts are; 3 X 12 hours shifts and 1 X 11.5 hours, starting at 7am. The salary on offer is £30,000 plus a shift allowance. The Company: Our client provides a range of testing services, and they now have a new opportunity for an experienced Laboratory Analyst to join their team. Location: The Laboratory Analyst role is based in Wilton. The Role: Follow laboratory methods and procedures to specification and issue quality assured results to customers. Manage own work by sequencing tasks and priorities in accordance with planned analytical schedules. Liaise with customers, internal and external to determine requirements for non-scheduled activities, identify optimum solutions and ensure financial recovery is made for the services provided. Develop (as appropriate) and carry out SHE, COSHH, Risk Assessment, Safety / Housekeeping and Quality related activities including audits as required by the relevant systems and procedures. Act as the focal point for specific areas within the laboratory and actively manage the delivery and development of that service offering. Check, maintain, overhaul, and liaise with called out analytical instrument engineers to maximise the uptime availability of the laboratory equipment. Support and lead wherever possible the development of new methods and commissioning of new equipment. Your Background: Qualified to HNC / Degree in science discipline. At least 2 years industrial experience in the application of technical skills in an equivalent laboratory role. Good SHE awareness including application of COSHH, Risk Assessments and laboratory standards. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
CK GROUP
Laboratory Analyst
CK GROUP Redcar, Yorkshire
CK Group are recruiting for a Laboratory Analyst, on behalf of a multinational provider of technical services, to be based at their site in Wilton. Please note this role is a days role, on a 4 on 4 off shift pattern. The shifts are; 3 X 12 hours shifts and 1 X 11.5 hours, starting at 7am. The salary on offer is £30,000 plus a shift allowance. The Company: Our client provides a range of testing services, and they now have a new opportunity for an experienced Laboratory Analyst to join their team. Location: The Laboratory Analyst role is based in Wilton. The Role: Follow laboratory methods and procedures to specification and issue quality assured results to customers. Manage own work by sequencing tasks and priorities in accordance with planned analytical schedules. Liaise with customers, internal and external to determine requirements for non-scheduled activities, identify optimum solutions and ensure financial recovery is made for the services provided. Develop (as appropriate) and carry out SHE, COSHH, Risk Assessment, Safety / Housekeeping and Quality related activities including audits as required by the relevant systems and procedures. Act as the focal point for specific areas within the laboratory and actively manage the delivery and development of that service offering. Check, maintain, overhaul, and liaise with called out analytical instrument engineers to maximise the uptime availability of the laboratory equipment. Support and lead wherever possible the development of new methods and commissioning of new equipment. Your Background: Qualified to HNC / Degree in science discipline. At least 2 years industrial experience in the application of technical skills in an equivalent laboratory role. Good SHE awareness including application of COSHH, Risk Assessments and laboratory standards. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Jul 12, 2025
Full time
CK Group are recruiting for a Laboratory Analyst, on behalf of a multinational provider of technical services, to be based at their site in Wilton. Please note this role is a days role, on a 4 on 4 off shift pattern. The shifts are; 3 X 12 hours shifts and 1 X 11.5 hours, starting at 7am. The salary on offer is £30,000 plus a shift allowance. The Company: Our client provides a range of testing services, and they now have a new opportunity for an experienced Laboratory Analyst to join their team. Location: The Laboratory Analyst role is based in Wilton. The Role: Follow laboratory methods and procedures to specification and issue quality assured results to customers. Manage own work by sequencing tasks and priorities in accordance with planned analytical schedules. Liaise with customers, internal and external to determine requirements for non-scheduled activities, identify optimum solutions and ensure financial recovery is made for the services provided. Develop (as appropriate) and carry out SHE, COSHH, Risk Assessment, Safety / Housekeeping and Quality related activities including audits as required by the relevant systems and procedures. Act as the focal point for specific areas within the laboratory and actively manage the delivery and development of that service offering. Check, maintain, overhaul, and liaise with called out analytical instrument engineers to maximise the uptime availability of the laboratory equipment. Support and lead wherever possible the development of new methods and commissioning of new equipment. Your Background: Qualified to HNC / Degree in science discipline. At least 2 years industrial experience in the application of technical skills in an equivalent laboratory role. Good SHE awareness including application of COSHH, Risk Assessments and laboratory standards. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Senior Analytical Scientist
Viatris
Senior Analytical Scientist page is loaded Senior Analytical Scientist Postuler locations Sandwich, England, United Kingdom time type Temps plein posted on Offre publiée il y a 18 jours job requisition id R Mylan Pharma UK Limited Chez Viatris, nous envisageons la santé non pas telle qu'elle est mais telle qu'elle devrait être. Nous agissons avec courage et notre positionnement unique est source de stabilité dans un monde où les besoins en matière de santé sont en constante évolution. Viatris permet à chacun dans le monde entier de vivre en meilleure santé à chaque étape de sa vie. Via trois axes majeurs: Accès : En fournissant des médicaments de haute qualité et reconnus, quels que soient le lieu de résidence ou la situation de chaque patient. Leadership : En favorisant l'évolution de nos activités de façon durable et le développement de solutions innovantes pour améliorer la santé des patients. Partenariat : En valorisant notre expertise collective afin de donner accès à tous à nos produits et services. Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment. For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here's how the Senior Analytical Scientist role will make an impact: Carry out all analytical activities required to deliver new respiratory products to clinical studies and commercialization Lead the planning and execution of experiments to generate scientific understanding in development of analytical methods, formulations and processes. Perform analyses related to clinical supplies, stability, and process scale up. Process and review data, interpret results and report experimental outcomes to project development team. Lead the troubleshooting of instrumentation and investigation of aberrant sample results. Maintain laboratory documentation in accordance with cGMP documentation practices. Contribute to project delivery by carrying out other tasks (e.g. laboratory housekeeping, ordering, shipping samples) as required. Work with other senior analysts to lead the analytical laboratory operation and identify opportunities for improvements in working practices and procedures. Oversee the day-to-day work of less experienced analytical laboratory staff. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role and any associated responsibilities, including people management where applicable Perform other duties as assigned consistent with the grade of the role About Your Skills & Experience For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences: Minimum of a Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, or substantial practical work experience. Good understanding of laboratory safety and best practice Has a good understanding of basic principles of physical, organic and analytical chemistry, and can demonstrate advanced knowledge in specific areas related to their experience. Highly familiar with calculations used in analytical chemistry and the application of statistics. Has a good understanding and substantial practical experience of modern laboratory techniques, including HPLC. Able to work with others to plan the day-to-day work of a small team Able to work autonomously to deliver multiple tasks, planning own work to consistently achieve output of high quality results in a timely manner. Able to work collaboratively within a multi-disciplinary team environment. Able to lead troubleshooting and investigations Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective verbal and written communication skills Enthusiasm to work in a laboratory based role At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles. Benefits at Viatris At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary: Top Employer Accreditation, demonstrating that we provide excellent people policies and practices Focus on career progression with growth and development opportunities Emphasis on Health & Wellness programmes 100% paid medical insurance and Employee Assistance Programme Life cover Excellent employer-matched pension scheme with Viatris contributing up to 11% 2 paid volunteer days per year Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit Chez Viatris, nous proposons des salaires compétitifs, des bénéfices et un environnement inclusif au sein duquel vous pouvez mettre à profit votre expérience, vos perspectives et vos compétences pour aider à avoir un impact positif sur la vie des autres.
Jul 09, 2025
Full time
Senior Analytical Scientist page is loaded Senior Analytical Scientist Postuler locations Sandwich, England, United Kingdom time type Temps plein posted on Offre publiée il y a 18 jours job requisition id R Mylan Pharma UK Limited Chez Viatris, nous envisageons la santé non pas telle qu'elle est mais telle qu'elle devrait être. Nous agissons avec courage et notre positionnement unique est source de stabilité dans un monde où les besoins en matière de santé sont en constante évolution. Viatris permet à chacun dans le monde entier de vivre en meilleure santé à chaque étape de sa vie. Via trois axes majeurs: Accès : En fournissant des médicaments de haute qualité et reconnus, quels que soient le lieu de résidence ou la situation de chaque patient. Leadership : En favorisant l'évolution de nos activités de façon durable et le développement de solutions innovantes pour améliorer la santé des patients. Partenariat : En valorisant notre expertise collective afin de donner accès à tous à nos produits et services. Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment. For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here's how the Senior Analytical Scientist role will make an impact: Carry out all analytical activities required to deliver new respiratory products to clinical studies and commercialization Lead the planning and execution of experiments to generate scientific understanding in development of analytical methods, formulations and processes. Perform analyses related to clinical supplies, stability, and process scale up. Process and review data, interpret results and report experimental outcomes to project development team. Lead the troubleshooting of instrumentation and investigation of aberrant sample results. Maintain laboratory documentation in accordance with cGMP documentation practices. Contribute to project delivery by carrying out other tasks (e.g. laboratory housekeeping, ordering, shipping samples) as required. Work with other senior analysts to lead the analytical laboratory operation and identify opportunities for improvements in working practices and procedures. Oversee the day-to-day work of less experienced analytical laboratory staff. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role and any associated responsibilities, including people management where applicable Perform other duties as assigned consistent with the grade of the role About Your Skills & Experience For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences: Minimum of a Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, or substantial practical work experience. Good understanding of laboratory safety and best practice Has a good understanding of basic principles of physical, organic and analytical chemistry, and can demonstrate advanced knowledge in specific areas related to their experience. Highly familiar with calculations used in analytical chemistry and the application of statistics. Has a good understanding and substantial practical experience of modern laboratory techniques, including HPLC. Able to work with others to plan the day-to-day work of a small team Able to work autonomously to deliver multiple tasks, planning own work to consistently achieve output of high quality results in a timely manner. Able to work collaboratively within a multi-disciplinary team environment. Able to lead troubleshooting and investigations Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective verbal and written communication skills Enthusiasm to work in a laboratory based role At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles. Benefits at Viatris At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Some of our benefits include the following on top of a competitive salary: Top Employer Accreditation, demonstrating that we provide excellent people policies and practices Focus on career progression with growth and development opportunities Emphasis on Health & Wellness programmes 100% paid medical insurance and Employee Assistance Programme Life cover Excellent employer-matched pension scheme with Viatris contributing up to 11% 2 paid volunteer days per year Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit Chez Viatris, nous proposons des salaires compétitifs, des bénéfices et un environnement inclusif au sein duquel vous pouvez mettre à profit votre expérience, vos perspectives et vos compétences pour aider à avoir un impact positif sur la vie des autres.
SRG
QC Analyst
SRG Worthing, Sussex
Job Title: QC Analyst Job Type: Contract to End of the Year Employment Start Date: ASAP Hours of work: Mon - Fri Onsite requirement: Fully onsite Industry: Quality Location: Worthing, England Salary: 15.64 per hour - PAYE QC Analyst - Temporary We are currently recruiting QC Analysts to join our Quality Control team at the Worthing Manufacturing site. The role(s) carry out physical and chemical analytical test methods on oral products for release to market and stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of product is of satisfactory quality. Key Responsibilities include: To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets. Calibrate and maintain analytical equipment. Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc). To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required. To check and verify analytical testing and data generated by other analysts To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date. Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC. Supplying data / reports to Value Stream as requested. May be required to communicate with the relevant Value Steam. to progress OOS investigations About You: This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed. About Worthing Manufacturing Site: Manufacturing at the Worthing site is for antibiotics. It is advised that you take this into consideration when deciding to apply for this position. You must disclose if you have a pre-existing penicillin allergy. When applying for this role, please use your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you provide in your CV will be used to assess your application. Basic Qualifications: Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline) Understanding of laboratory analysis Relevant Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Mar 08, 2025
Contractor
Job Title: QC Analyst Job Type: Contract to End of the Year Employment Start Date: ASAP Hours of work: Mon - Fri Onsite requirement: Fully onsite Industry: Quality Location: Worthing, England Salary: 15.64 per hour - PAYE QC Analyst - Temporary We are currently recruiting QC Analysts to join our Quality Control team at the Worthing Manufacturing site. The role(s) carry out physical and chemical analytical test methods on oral products for release to market and stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of product is of satisfactory quality. Key Responsibilities include: To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets. Calibrate and maintain analytical equipment. Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc). To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required. To check and verify analytical testing and data generated by other analysts To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date. Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC. Supplying data / reports to Value Stream as requested. May be required to communicate with the relevant Value Steam. to progress OOS investigations About You: This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed. About Worthing Manufacturing Site: Manufacturing at the Worthing site is for antibiotics. It is advised that you take this into consideration when deciding to apply for this position. You must disclose if you have a pre-existing penicillin allergy. When applying for this role, please use your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you provide in your CV will be used to assess your application. Basic Qualifications: Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline) Understanding of laboratory analysis Relevant Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
The People Pod
Software Tester
The People Pod
Software Tester - LIMS Remote - Work From Home We are looking for a Software Tester to join our growing team, working on Laboratory Information Management Systems (LIMS) . This is a fantastic opportunity for someone with some experience in software testing who is looking to develop their skills further in a highly specialised and regulated industry. If you have a keen eye for detail, strong problem-solving abilities, and an interest in scientific software , this could be the perfect next step for you! Key Responsibilities: Assist in creating and executing test plans, test cases, and test scripts for LIMS software. Perform a range of testing activities, including functional, integration, and user acceptance testing. Identify and document software defects, working closely with developers to resolve them. Verify system performance, reliability, and security across different environments. Ensure compliance with industry standards and regulatory requirements. Collaborate with business analysts, developers, and end-users to ensure the software meets user needs. Support test automation by learning and maintaining automated test scripts where appropriate. Provide clear and structured feedback on testing results to the wider team. Contribute to ongoing process improvements to enhance software quality and testing efficiency. What We're Looking For: Some experience in software testing (manual or automated), ideally within scientific, medical, or regulated industries . A basic understanding of software testing methodologies and tools (e.g., JIRA, TestRail, or similar). Desirable Knowledge of SQL for data validation and back-end testing would be beneficial but not essential. Exposure to automated testing tools such as Selenium or TestComplete is a plus. An interest in learning about compliance and regulatory standards like ISO 17025 and GxP. Strong analytical and problem-solving skills, with great attention to detail . Good communication skills and the ability to work well in a team. A proactive approach, with a willingness to learn and develop new skills. Why Join Us? A chance to work with cutting-edge LIMS software used in laboratories worldwide. Training and development opportunities to help you progress in your software testing career. A supportive and friendly team, offering mentorship and guidance. Flexible remote working. WFH Competitive salary and benefits package. If you're an aspiring Software Tester looking to gain experience in the LIMS and scientific software industry, we'd love to hear from you! Basic Salary 27-32,000 DOE + benefits + ongoing training and development
Mar 08, 2025
Full time
Software Tester - LIMS Remote - Work From Home We are looking for a Software Tester to join our growing team, working on Laboratory Information Management Systems (LIMS) . This is a fantastic opportunity for someone with some experience in software testing who is looking to develop their skills further in a highly specialised and regulated industry. If you have a keen eye for detail, strong problem-solving abilities, and an interest in scientific software , this could be the perfect next step for you! Key Responsibilities: Assist in creating and executing test plans, test cases, and test scripts for LIMS software. Perform a range of testing activities, including functional, integration, and user acceptance testing. Identify and document software defects, working closely with developers to resolve them. Verify system performance, reliability, and security across different environments. Ensure compliance with industry standards and regulatory requirements. Collaborate with business analysts, developers, and end-users to ensure the software meets user needs. Support test automation by learning and maintaining automated test scripts where appropriate. Provide clear and structured feedback on testing results to the wider team. Contribute to ongoing process improvements to enhance software quality and testing efficiency. What We're Looking For: Some experience in software testing (manual or automated), ideally within scientific, medical, or regulated industries . A basic understanding of software testing methodologies and tools (e.g., JIRA, TestRail, or similar). Desirable Knowledge of SQL for data validation and back-end testing would be beneficial but not essential. Exposure to automated testing tools such as Selenium or TestComplete is a plus. An interest in learning about compliance and regulatory standards like ISO 17025 and GxP. Strong analytical and problem-solving skills, with great attention to detail . Good communication skills and the ability to work well in a team. A proactive approach, with a willingness to learn and develop new skills. Why Join Us? A chance to work with cutting-edge LIMS software used in laboratories worldwide. Training and development opportunities to help you progress in your software testing career. A supportive and friendly team, offering mentorship and guidance. Flexible remote working. WFH Competitive salary and benefits package. If you're an aspiring Software Tester looking to gain experience in the LIMS and scientific software industry, we'd love to hear from you! Basic Salary 27-32,000 DOE + benefits + ongoing training and development
NW Recruitment Ltd
Bulk ID Analyst
NW Recruitment Ltd Brighton, Sussex
A leading environmental and laboratory services company are recruiting for a number of p401 qualified Bulk ID Analysts. The successful candidate will: • Responsible for the undertaking sample analysis of the various types of bulk materials • Produce and Compiling and quality assessing reports, ensuring they are delivered promptly to the client • Ensure all associated paperwork is completed, checked and given to the associated office in a timely manner • Ensure all equipment used is within calibration. • Undertake daily quality checks. • Maintain impartiality, integrity and independence throughout • Effectively communicating with Laboratory/Operations Manager • Ensure that all the necessary quality records are completed and made available for regular internal review by a member of the Quality or Management team. This includes all contract review documents, equipment registers and job files.
Mar 06, 2025
Full time
A leading environmental and laboratory services company are recruiting for a number of p401 qualified Bulk ID Analysts. The successful candidate will: • Responsible for the undertaking sample analysis of the various types of bulk materials • Produce and Compiling and quality assessing reports, ensuring they are delivered promptly to the client • Ensure all associated paperwork is completed, checked and given to the associated office in a timely manner • Ensure all equipment used is within calibration. • Undertake daily quality checks. • Maintain impartiality, integrity and independence throughout • Effectively communicating with Laboratory/Operations Manager • Ensure that all the necessary quality records are completed and made available for regular internal review by a member of the Quality or Management team. This includes all contract review documents, equipment registers and job files.
CK GROUP
Stability Analyst
CK GROUP Hull, Yorkshire
CK Group are recruiting for a Stability Analyst, to join a leading healthcare organisation in Hull, on a 6-month contract basis. Salary: £12.96 per hour. The Company: This is an outstanding opportunity to work for a globally recognised company, that has invested heavily into their state of the art R&D and manufacturing facility located in Hull. Having personally visited these facilities, I can say it's one of the most impressive work spaces I have seen, and the company is able to offer a fun and energetic working environment that will appeal to all. Location: This Stability Analyst role is located in the heart of Hull, this city was voted the UK's City of Culture in 2017. Stability Analyst responsibilities will include: Testing of ongoing stability samples within the laboratory. Day-to-day prioritization and organization of individual workload to meet customer service and stakeholder needs. Developing, implementing, and monitoring the progress of their individual Personal Development Plan. Ensuring relevant data is checked, approved, recorded, and available for inspection in accordance with Good Manufacturing & Good Laboratory Practices. Performing responsible operator tasks for basic equipment within the laboratory, including SOP writing and maintenance. Your Background: Degree level qualification and / or relevant and appropriate demonstrable skills & experience. Excellent delivery of core skills. Demonstrable or transferable skills relevant to the delivery of OGS activities. Demonstrable skills in working within a multi-level team environment. Ability to work on own initiative and within a team of people. Can offer a dynamic and flexible attitude to facilitate a fast-moving operation. Apply: It is essential that applicants hold the entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Mar 06, 2025
Full time
CK Group are recruiting for a Stability Analyst, to join a leading healthcare organisation in Hull, on a 6-month contract basis. Salary: £12.96 per hour. The Company: This is an outstanding opportunity to work for a globally recognised company, that has invested heavily into their state of the art R&D and manufacturing facility located in Hull. Having personally visited these facilities, I can say it's one of the most impressive work spaces I have seen, and the company is able to offer a fun and energetic working environment that will appeal to all. Location: This Stability Analyst role is located in the heart of Hull, this city was voted the UK's City of Culture in 2017. Stability Analyst responsibilities will include: Testing of ongoing stability samples within the laboratory. Day-to-day prioritization and organization of individual workload to meet customer service and stakeholder needs. Developing, implementing, and monitoring the progress of their individual Personal Development Plan. Ensuring relevant data is checked, approved, recorded, and available for inspection in accordance with Good Manufacturing & Good Laboratory Practices. Performing responsible operator tasks for basic equipment within the laboratory, including SOP writing and maintenance. Your Background: Degree level qualification and / or relevant and appropriate demonstrable skills & experience. Excellent delivery of core skills. Demonstrable or transferable skills relevant to the delivery of OGS activities. Demonstrable skills in working within a multi-level team environment. Ability to work on own initiative and within a team of people. Can offer a dynamic and flexible attitude to facilitate a fast-moving operation. Apply: It is essential that applicants hold the entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
FP&A Analyst
Azenta, Inc. Manchester, Lancashire
Company Overview At Azenta Life Sciences, a global leader in the life sciences arena headquartered in Burlington, MA, and operating offices worldwide, the trajectory of our future is shaped by fresh ideas, cutting-edge technologies, and innovative perspectives. Every day our employees support us fulfilling our mission to bring breakthroughs to the market faster. Our organizational culture, firmly grounded in our core values, places the utmost importance on putting people first. Open communication is not just encouraged but embedded in our DNA, fostering an environment where ideas freely flow, and collaboration thrives. Authenticity is not just a principle but a guiding light, encouraging our diverse workforce to bring their true selves to work. This culture empowers our employees to champion innovation and question conventional norms through creative thinking and collaborative work dynamics. Diversity is not just a concept but a cornerstone of our ethos, recognizing that a variety of backgrounds, perspectives, and experiences enhances our collective creativity and success. Leveraging our unmatched expertise, we offer comprehensive services spanning lab analysis, sample management and storage, informatics software, and consumables. Notably, our extensive installed base oversees the management of over 1 billion samples on a global scale. Our Finance team is looking for a new talent, starting at the earliest possible time as FP&A Analyst (m/f/d). hybrid office based in Manchester, UK Permanent, fulltime employment How You'll Add Value This position is within Sample Management Solutions FP&A team and will be responsible for day-to-day activities including data analysis for financial reporting, forecasting, and planning. Support data-driven decision making by providing management reports & analysis of monthly results and forecasts. Perform work to assist in the analysis of cost structure, profitability, and key performance metrics. Support the development of budgets and forecasts for functional spending areas and perform ad hoc analysis, as needed. What You'll Do Serve as a business partner to the operating team to drive business initiatives, growth, and profitability. Provide timely, relevant financial information to develop action plans to meet targets. Financial analysis for Gross Margin, Operating Expenses and Headcount. Trusted finance operations partner to the business leaders and internal support functions (HR, IT, Facilities, Commercial, Legal). Partner with business unit leaders to drive profitability improvements. Analyze and interpret data trends and present results. Improve visibility to costs, lead cost out initiatives. Prepare margin & variance analysis, understand the impact from cost changes, mix etc. Develop and report headlight metrics, perform data analysis on key business metrics. Support development of forecasts, annual operating plan, and multi-year plans. Monthly / quarterly forecasting and monitoring of risk and opportunities. High quality Monthly and quarterly management reporting. Support customer pricing analysis for the division/business units. Engage with commercial team in deal reviews, provide guidance on pricing, payment terms, highlight and address financial risks proactively. Develop business cases for growth initiatives in partnership with the business, functional leads, and commercial team. Drive controllership awareness and compliance with business policies and controls. Ensure compliance with US GAAP and business accounting policies and procedures. Develop and maintain processes to support a strong controls environment. Support internal and external audits. What you will Bring Education: Bachelor's degree in Finance and Accounting, MBA would be a plus. 5+ Years of experience in an FP&A function in a manufacturing environment. Demonstrated track record of business partnership in a dynamic, high-growth environment. Excellent interpersonal, verbal/written communication and presentation skills. Strong process improvement mindset and cross functional engagement. Project management skills. Six Sigma and/or Lean trained would be an added advantage. Highly proficient in ERP & Financial applications (Oracle, OneStream), Excel skills, PowerPoint, data analytics tools (Tableau, Datawarehouse, Sales Force etc.). SQL and VBA skills are a plus. Demonstrate sound work ethic, respect and cultural sensitivity and awareness. Strong analytical/problem solving skills. Detail-oriented with the ability to work independently to meet deadlines. A sense of urgency and self-motivation, with a personal commitment to meeting deadlines. Occasional travel may be required. Our Offer Become part of a company that makes a positive contribution to launching groundbreaking scientific developments and therapies. Contribute to innovative cell therapies and be a part of revolutionary cancer therapies. Flexible working hours are a matter of course for us. Take advantage of the operational opportunities in a growing, modern, and innovative company within the health care/life science industry. Experience an intensive exchange of experiences and close cooperation in a worldwide network with our customers, friends, and partners. We offer participation in national and international company events. After your initial training, you will receive regular training and further education opportunities that are tailored to your needs. A workplace that promotes your maximum. You will participate in capital-forming benefits, numerous corporate benefits. Positive corporate culture and practiced teamwork across all locations. Individual development opportunities of your international competencies and language skills. Our other benefits include: Stock Option program. Profit sharing. LinkedIn Learning cooperation. Corporate Benefits Program (online shopping platform). Contact Azenta Life Sciences Manchester Email: Please apply with your complete application documents (cover letter, detailed CV, references) in English. About us Azenta Life Sciences is a global life sciences leader headquartered in Burlington, MA, with offices and operation sites around the world. We are the market leader in automated biospecimen management solutions and genomic services in areas such as drug development, clinical and novel cell therapies for the world's leading pharmaceutical, biotech, academic and healthcare institutions. Our laboratory analysis, sample management and storage, informatics software and consumables services offer unparalleled capabilities and have the largest installed base managing over one billion samples worldwide. For more information:
Feb 20, 2025
Full time
Company Overview At Azenta Life Sciences, a global leader in the life sciences arena headquartered in Burlington, MA, and operating offices worldwide, the trajectory of our future is shaped by fresh ideas, cutting-edge technologies, and innovative perspectives. Every day our employees support us fulfilling our mission to bring breakthroughs to the market faster. Our organizational culture, firmly grounded in our core values, places the utmost importance on putting people first. Open communication is not just encouraged but embedded in our DNA, fostering an environment where ideas freely flow, and collaboration thrives. Authenticity is not just a principle but a guiding light, encouraging our diverse workforce to bring their true selves to work. This culture empowers our employees to champion innovation and question conventional norms through creative thinking and collaborative work dynamics. Diversity is not just a concept but a cornerstone of our ethos, recognizing that a variety of backgrounds, perspectives, and experiences enhances our collective creativity and success. Leveraging our unmatched expertise, we offer comprehensive services spanning lab analysis, sample management and storage, informatics software, and consumables. Notably, our extensive installed base oversees the management of over 1 billion samples on a global scale. Our Finance team is looking for a new talent, starting at the earliest possible time as FP&A Analyst (m/f/d). hybrid office based in Manchester, UK Permanent, fulltime employment How You'll Add Value This position is within Sample Management Solutions FP&A team and will be responsible for day-to-day activities including data analysis for financial reporting, forecasting, and planning. Support data-driven decision making by providing management reports & analysis of monthly results and forecasts. Perform work to assist in the analysis of cost structure, profitability, and key performance metrics. Support the development of budgets and forecasts for functional spending areas and perform ad hoc analysis, as needed. What You'll Do Serve as a business partner to the operating team to drive business initiatives, growth, and profitability. Provide timely, relevant financial information to develop action plans to meet targets. Financial analysis for Gross Margin, Operating Expenses and Headcount. Trusted finance operations partner to the business leaders and internal support functions (HR, IT, Facilities, Commercial, Legal). Partner with business unit leaders to drive profitability improvements. Analyze and interpret data trends and present results. Improve visibility to costs, lead cost out initiatives. Prepare margin & variance analysis, understand the impact from cost changes, mix etc. Develop and report headlight metrics, perform data analysis on key business metrics. Support development of forecasts, annual operating plan, and multi-year plans. Monthly / quarterly forecasting and monitoring of risk and opportunities. High quality Monthly and quarterly management reporting. Support customer pricing analysis for the division/business units. Engage with commercial team in deal reviews, provide guidance on pricing, payment terms, highlight and address financial risks proactively. Develop business cases for growth initiatives in partnership with the business, functional leads, and commercial team. Drive controllership awareness and compliance with business policies and controls. Ensure compliance with US GAAP and business accounting policies and procedures. Develop and maintain processes to support a strong controls environment. Support internal and external audits. What you will Bring Education: Bachelor's degree in Finance and Accounting, MBA would be a plus. 5+ Years of experience in an FP&A function in a manufacturing environment. Demonstrated track record of business partnership in a dynamic, high-growth environment. Excellent interpersonal, verbal/written communication and presentation skills. Strong process improvement mindset and cross functional engagement. Project management skills. Six Sigma and/or Lean trained would be an added advantage. Highly proficient in ERP & Financial applications (Oracle, OneStream), Excel skills, PowerPoint, data analytics tools (Tableau, Datawarehouse, Sales Force etc.). SQL and VBA skills are a plus. Demonstrate sound work ethic, respect and cultural sensitivity and awareness. Strong analytical/problem solving skills. Detail-oriented with the ability to work independently to meet deadlines. A sense of urgency and self-motivation, with a personal commitment to meeting deadlines. Occasional travel may be required. Our Offer Become part of a company that makes a positive contribution to launching groundbreaking scientific developments and therapies. Contribute to innovative cell therapies and be a part of revolutionary cancer therapies. Flexible working hours are a matter of course for us. Take advantage of the operational opportunities in a growing, modern, and innovative company within the health care/life science industry. Experience an intensive exchange of experiences and close cooperation in a worldwide network with our customers, friends, and partners. We offer participation in national and international company events. After your initial training, you will receive regular training and further education opportunities that are tailored to your needs. A workplace that promotes your maximum. You will participate in capital-forming benefits, numerous corporate benefits. Positive corporate culture and practiced teamwork across all locations. Individual development opportunities of your international competencies and language skills. Our other benefits include: Stock Option program. Profit sharing. LinkedIn Learning cooperation. Corporate Benefits Program (online shopping platform). Contact Azenta Life Sciences Manchester Email: Please apply with your complete application documents (cover letter, detailed CV, references) in English. About us Azenta Life Sciences is a global life sciences leader headquartered in Burlington, MA, with offices and operation sites around the world. We are the market leader in automated biospecimen management solutions and genomic services in areas such as drug development, clinical and novel cell therapies for the world's leading pharmaceutical, biotech, academic and healthcare institutions. Our laboratory analysis, sample management and storage, informatics software and consumables services offer unparalleled capabilities and have the largest installed base managing over one billion samples worldwide. For more information:

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