Job Title: Analyst Location: Brimsdown World-changing careers, enabled by Johnson Matthey. With more than 200 years history, join us and help to accelerate the transition to net-zero! As an Analyst, you'll contribute to JM's mission as a world leader in sustainable technology, transforming energy and reducing carbon emissions for a cleaner, brighter future. The role: As a Analyst, you will help drive our goals by: To analyse samples submitted using approved procedures. To ensure the work is performed at minimum cost by making efficient use of time, equipment and materials. To ensure all regulations with regard to Environment Health & Safety and security are strictly observed. To attend approved training courses as requested, complete on-line L&D courses as well as actively participate in receiving analytical skills training and assessment. Ensure required standards of housekeeping and workplace efficiency are maintained using 5S and Lean methodology as appropriate. Establish and maintain all necessary communication links within and outside the Laboratory to help ensure good customer service is maintained. Key skills that will help you succeed in this role: Degree or HNC (or equivalent) in Chemistry or related subject. Been trained and assessed in Laboratory Skills. Experience in Analytical Chemistry is advantageous. Understanding of the requirements of ISO9001, ISO14001, ISO17025 is desirable. Strong safety awareness. Good organisational skills and ability to prioritise. What we offer: We make sure salaries are fair, competitive and aligned to individual roles, experience and responsibilities. We are also supportive of hybrid and flexible working and where applicable, offer life, medical and other benefits that support our employees' financial and physical wellbeing, such as: Retirement savings Share plans Saving accounts House saving funds Life and disability insurance Commuter allowances and loans Medical plans / health assessments Fitness discounts Ready to make a meaningful impact on your career and the environment? Join us and help shape a sustainable future while advancing your career! At JM, inclusivity is central to our values. We create an environment where everyone can thrive, embracing diverse perspectives to tackle challenges and ensure all colleagues feel valued and connected. For any queries or accessibility requirements, please contact (url removed). We will work with you to make suitable adjustments at any stage of the recruitment process. All conversations are confidential, and your feedback is welcome to help us provide an accessible and positive recruitment experience. Closing date for applications: This job advertisement will be posted for a minimum of 2 weeks, early application is advised. To submit your application, please click the "Apply" button online. All applications are carefully considered and your details will be stored on our secure Application Management System. This is used throughout Johnson Matthey for the selection of suitable candidates for our vacancies as they arise.Johnson Matthey respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice: Johnson Matthey Privacy Notice . By applying for this role and creating an account you are agreeing to the notice. Johnson Matthey Plc is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
May 07, 2026
Full time
Job Title: Analyst Location: Brimsdown World-changing careers, enabled by Johnson Matthey. With more than 200 years history, join us and help to accelerate the transition to net-zero! As an Analyst, you'll contribute to JM's mission as a world leader in sustainable technology, transforming energy and reducing carbon emissions for a cleaner, brighter future. The role: As a Analyst, you will help drive our goals by: To analyse samples submitted using approved procedures. To ensure the work is performed at minimum cost by making efficient use of time, equipment and materials. To ensure all regulations with regard to Environment Health & Safety and security are strictly observed. To attend approved training courses as requested, complete on-line L&D courses as well as actively participate in receiving analytical skills training and assessment. Ensure required standards of housekeeping and workplace efficiency are maintained using 5S and Lean methodology as appropriate. Establish and maintain all necessary communication links within and outside the Laboratory to help ensure good customer service is maintained. Key skills that will help you succeed in this role: Degree or HNC (or equivalent) in Chemistry or related subject. Been trained and assessed in Laboratory Skills. Experience in Analytical Chemistry is advantageous. Understanding of the requirements of ISO9001, ISO14001, ISO17025 is desirable. Strong safety awareness. Good organisational skills and ability to prioritise. What we offer: We make sure salaries are fair, competitive and aligned to individual roles, experience and responsibilities. We are also supportive of hybrid and flexible working and where applicable, offer life, medical and other benefits that support our employees' financial and physical wellbeing, such as: Retirement savings Share plans Saving accounts House saving funds Life and disability insurance Commuter allowances and loans Medical plans / health assessments Fitness discounts Ready to make a meaningful impact on your career and the environment? Join us and help shape a sustainable future while advancing your career! At JM, inclusivity is central to our values. We create an environment where everyone can thrive, embracing diverse perspectives to tackle challenges and ensure all colleagues feel valued and connected. For any queries or accessibility requirements, please contact (url removed). We will work with you to make suitable adjustments at any stage of the recruitment process. All conversations are confidential, and your feedback is welcome to help us provide an accessible and positive recruitment experience. Closing date for applications: This job advertisement will be posted for a minimum of 2 weeks, early application is advised. To submit your application, please click the "Apply" button online. All applications are carefully considered and your details will be stored on our secure Application Management System. This is used throughout Johnson Matthey for the selection of suitable candidates for our vacancies as they arise.Johnson Matthey respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice: Johnson Matthey Privacy Notice . By applying for this role and creating an account you are agreeing to the notice. Johnson Matthey Plc is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
Fortress Diagnostics Ltd is seeking a Laboratory Analyst to join its clinical testing team. This role requires a strong blend of skills, as the successful candidate will be responsible for conducting precise sample tests and accurately recording the results. Attention to detail and the ability to follow detailed instructions are essential. If you have the skills and experience needed, we encourage you to apply! Job Summary- Responsibilities and Duties: The preparation and handling of samples and diagnostic reagents Ensuring that the integrity of all samples is adhered to at all times The performance of various analytical procedures, including various manual screening and automated methods covering a wide variety of clinical diagnostic tests The operation of various automated analytical systems The routine maintenance and calibration of analytical instrumentation The accurate maintenance of analytical records in line with the UKAS quality system requirements. Ensure all records meet the requirements for UKAS/ISO 17025 accreditation. Strict adherence to Chain of Custody procedures throughout the analytical process Stock Management Perform Troubleshooting on Technical issues associated with Clinical Diagnostic Testing Ensuring that all the necessary Quality Control checks are completed daily and that they meet internal criteria Participation in internal & external audits Recording and Monitoring of Temperature for Laboratory and Equipment Participate in additional duties to support laboratory operations and compliance. Undertake any other tasks or duties the Technical Manager or Team Leader assign to support laboratory functions. Experience Specification (essential): Ideally a BSc in Biomedical Science and Diploma in Professional Practice. Alternatively, qualified to at least degree standard in Biochemistry or a Life Science (Minimum 2:1) Possess excellent communication skills (written and verbal) Possess excellent organisational and time management skills Be computer literate with a working knowledge of the Microsoft Office Suites Ability to work independently and within a team and under pressure Highly motivated, independent, accurate and proactive Understanding of chemistry principles and analysis Working knowledge of quality systems i.e. ISO 17025 Working knowledge of communication and data management software (e.g. MiddleWare, LIMs etc). 1+ years' experience in a similar role within the clinical diagnostic industry Manage Consent
May 07, 2026
Full time
Fortress Diagnostics Ltd is seeking a Laboratory Analyst to join its clinical testing team. This role requires a strong blend of skills, as the successful candidate will be responsible for conducting precise sample tests and accurately recording the results. Attention to detail and the ability to follow detailed instructions are essential. If you have the skills and experience needed, we encourage you to apply! Job Summary- Responsibilities and Duties: The preparation and handling of samples and diagnostic reagents Ensuring that the integrity of all samples is adhered to at all times The performance of various analytical procedures, including various manual screening and automated methods covering a wide variety of clinical diagnostic tests The operation of various automated analytical systems The routine maintenance and calibration of analytical instrumentation The accurate maintenance of analytical records in line with the UKAS quality system requirements. Ensure all records meet the requirements for UKAS/ISO 17025 accreditation. Strict adherence to Chain of Custody procedures throughout the analytical process Stock Management Perform Troubleshooting on Technical issues associated with Clinical Diagnostic Testing Ensuring that all the necessary Quality Control checks are completed daily and that they meet internal criteria Participation in internal & external audits Recording and Monitoring of Temperature for Laboratory and Equipment Participate in additional duties to support laboratory operations and compliance. Undertake any other tasks or duties the Technical Manager or Team Leader assign to support laboratory functions. Experience Specification (essential): Ideally a BSc in Biomedical Science and Diploma in Professional Practice. Alternatively, qualified to at least degree standard in Biochemistry or a Life Science (Minimum 2:1) Possess excellent communication skills (written and verbal) Possess excellent organisational and time management skills Be computer literate with a working knowledge of the Microsoft Office Suites Ability to work independently and within a team and under pressure Highly motivated, independent, accurate and proactive Understanding of chemistry principles and analysis Working knowledge of quality systems i.e. ISO 17025 Working knowledge of communication and data management software (e.g. MiddleWare, LIMs etc). 1+ years' experience in a similar role within the clinical diagnostic industry Manage Consent
A leading Life Sciences company based in Oxford is seeking a Lab Assistant for a 6-month fixed-term contract. The role requires strong analytical chemistry skills and offers responsibilities such as sample preparation, technical support in the lab, and maintenance of lab systems. Candidates should have GCMS experience and a relevant degree. Benefits include 25 days of holiday plus bank holidays and enhanced pension. The position is full-time and onsite at the laboratory.
May 05, 2026
Full time
A leading Life Sciences company based in Oxford is seeking a Lab Assistant for a 6-month fixed-term contract. The role requires strong analytical chemistry skills and offers responsibilities such as sample preparation, technical support in the lab, and maintenance of lab systems. Candidates should have GCMS experience and a relevant degree. Benefits include 25 days of holiday plus bank holidays and enhanced pension. The position is full-time and onsite at the laboratory.
Summary: The Laboratory Quality Analyst for Nijhuis Saur Industries in Stoke is responsible for ensuring the laboratory and Riventa business unit operate to the highest quality standards by managing accreditation compliance, internal and external audits, QA/QC processes, instrument calibration, data analysis, and documentation control. The role provides technical guidance to staff, supports method development, oversees customer satisfaction and performance metrics, leads accreditation audit representation, and manages non conformance investigations. It also involves collaborating with management and customers, producing performance reports, supporting routine and specialised testing, and maintaining ISO 9001 and ISO 17025 quality systems for both laboratory and manufactured parts environments. Duties and Responsibilities: Ensure compliance with laboratory accreditation, regulatory standards and provide guidance to staff to ensure that quality policies, processes and procedures are established, current and adhered to by all laboratory staff. Oversee laboratory internal audit processes, external proficiency testing programs, document control systems, competency assessment, training, and other quality processes. Support the development of instrument techniques, ensuring adequate calibrations and QC are in place. Monitor customer satisfaction and performance metrics of the laboratory. Liaise with management throughout the business as well as customers when reporting on quality and statistical data. Oversee the Riventa business unit quality system including manufactured parts QA/QC process, calibration of temperature probes to approved methods, warranty, repair and returns process for Riventa parts. Maintain a quality management system for Riventa. Work to the global NSI ISO 9001 accredited quality management system. Work to the NSI WTL ISO 17025 accredited quality management system. Manage, document and audit the Riventa incoming and assembled products/parts testing and acceptance QA/QC process at the Stoke facility, in collaboration with the Riventa team. Manage, document and audit the Riventa temperature and pressure probe calibration process to relevant standards. Conduct lab testing to high standards through busy periods or during periods of absence of Laboratory Analyst or Develop Analysts. Audit the analytical performance of the analysts, content of laboratory methodology and documentation to ensure compliance with the quality system. Represent the laboratory during annual accreditation audits. Oversee the laboratories non conformance log to ensure its appropriate use and investigations are completed in full, with appropriate actions. Analyse data, identify trends, monitor prevention and correction of quality deviations, and develop reports for management utilising regulatory knowledge, technical knowledge and laboratory experience. To provide quality support to the laboratory for routine testing when required as well as providing quality support to the Technical Development Scientist and the wider technical team with specialised testing and the growth of these methods. Report periodically to management, customers on the quality performance of the laboratory. Presenting data to stakeholders on laboratory performance statistics. Support the creation and reviewing of validation reports for new and current tests. Perform Uncertainty of Measurement calculations when required. This is not a fully comprehensive list of responsibilities, and other duties will be expected to be completed within the limits of the position. Required Skills/Qualifications (Essential): Knowledge and experience of quality management systems such as ISO 9001 and ISO 17025 and quality improvement tools and techniques Knowledge and experience of UKAS accreditation and audits is advantageous. Experienced in the auditing of quality systems and laboratory testing procedures. Experience working with a QC process for manufactured parts. Working knowledge of accreditation standards, practices, and guidelines sufficient to advise and guide the laboratory manager and laboratory team as they implement new methodology and maintain accreditation. Working knowledge of computer and analytical software programs sufficient for the evaluation of electronic data, data interpretation, and report development (A good understanding of the Microsoft Office Suite would be advantageous). Experience working with LIMS. Excellent organisational skills allowing the coordination of multi faceted QA activities. Experience in performing data analysis such as uncertainty of measurement. Working experience of overseeing the development of new analytical techniques. Good awareness of all HSE aspects in a laboratory environment (i.e., COSHH, RA). Required Skills/Qualifications (Desirable): Degree/HND in Biochemistry/Chemistry or related science (Highly Desirable) Consideration will be given to applicants with Certifications in Quality (Highly Desirable) Consideration will be given to those candidates with 2 years' experience in a similar position (Highly desirable) Knowledge and/or previous experience of GC FID, Ion chromatography, FT IR, wet chemistry, spectrophotometry experience of water, wastewater, cooling water and boiler water in the Oil & Gas, Petrochemical, food & beverage industries (Highly desirable). Working for us means: The salary is between £33,000 & £38,000 per year, depending on your professional experience. Hours of Work - 40 hours per week, Monday to Friday Holidays - 25 days + 8 statutory days (pro-rata) Probationary Period - 6 months. Pension - Can join immediately or auto enrolled after 3 months - Employee 5% and Employer 5% via salary sacrifice. Eligible to join Private Healthcare after successfully completing probation. Enrolled in Group Income Protection and Death in Service (4 x basic salary) upon commencement of employment. Notice - 1 Week during probation, increasing to 1 months thereafter. Nijhuis Saur Industries UK & Ireland are committed to maintaining Environmental & Social Impact goals: To reach Net Zero emissions across our value chain by 2040. To continuously meet high standards of social and environmental performance, transparency, accountability, maintaining B Corp Certification. To be a socially responsible company creating a positive impact to all stakeholders including workers, communities, customers, and our planet. Nijhuis Saur Industries UK & Ireland are an equal opportunity employer; we are committed to providing equal opportunities in all aspects of employment in line with the Equality Act 2010.
May 05, 2026
Full time
Summary: The Laboratory Quality Analyst for Nijhuis Saur Industries in Stoke is responsible for ensuring the laboratory and Riventa business unit operate to the highest quality standards by managing accreditation compliance, internal and external audits, QA/QC processes, instrument calibration, data analysis, and documentation control. The role provides technical guidance to staff, supports method development, oversees customer satisfaction and performance metrics, leads accreditation audit representation, and manages non conformance investigations. It also involves collaborating with management and customers, producing performance reports, supporting routine and specialised testing, and maintaining ISO 9001 and ISO 17025 quality systems for both laboratory and manufactured parts environments. Duties and Responsibilities: Ensure compliance with laboratory accreditation, regulatory standards and provide guidance to staff to ensure that quality policies, processes and procedures are established, current and adhered to by all laboratory staff. Oversee laboratory internal audit processes, external proficiency testing programs, document control systems, competency assessment, training, and other quality processes. Support the development of instrument techniques, ensuring adequate calibrations and QC are in place. Monitor customer satisfaction and performance metrics of the laboratory. Liaise with management throughout the business as well as customers when reporting on quality and statistical data. Oversee the Riventa business unit quality system including manufactured parts QA/QC process, calibration of temperature probes to approved methods, warranty, repair and returns process for Riventa parts. Maintain a quality management system for Riventa. Work to the global NSI ISO 9001 accredited quality management system. Work to the NSI WTL ISO 17025 accredited quality management system. Manage, document and audit the Riventa incoming and assembled products/parts testing and acceptance QA/QC process at the Stoke facility, in collaboration with the Riventa team. Manage, document and audit the Riventa temperature and pressure probe calibration process to relevant standards. Conduct lab testing to high standards through busy periods or during periods of absence of Laboratory Analyst or Develop Analysts. Audit the analytical performance of the analysts, content of laboratory methodology and documentation to ensure compliance with the quality system. Represent the laboratory during annual accreditation audits. Oversee the laboratories non conformance log to ensure its appropriate use and investigations are completed in full, with appropriate actions. Analyse data, identify trends, monitor prevention and correction of quality deviations, and develop reports for management utilising regulatory knowledge, technical knowledge and laboratory experience. To provide quality support to the laboratory for routine testing when required as well as providing quality support to the Technical Development Scientist and the wider technical team with specialised testing and the growth of these methods. Report periodically to management, customers on the quality performance of the laboratory. Presenting data to stakeholders on laboratory performance statistics. Support the creation and reviewing of validation reports for new and current tests. Perform Uncertainty of Measurement calculations when required. This is not a fully comprehensive list of responsibilities, and other duties will be expected to be completed within the limits of the position. Required Skills/Qualifications (Essential): Knowledge and experience of quality management systems such as ISO 9001 and ISO 17025 and quality improvement tools and techniques Knowledge and experience of UKAS accreditation and audits is advantageous. Experienced in the auditing of quality systems and laboratory testing procedures. Experience working with a QC process for manufactured parts. Working knowledge of accreditation standards, practices, and guidelines sufficient to advise and guide the laboratory manager and laboratory team as they implement new methodology and maintain accreditation. Working knowledge of computer and analytical software programs sufficient for the evaluation of electronic data, data interpretation, and report development (A good understanding of the Microsoft Office Suite would be advantageous). Experience working with LIMS. Excellent organisational skills allowing the coordination of multi faceted QA activities. Experience in performing data analysis such as uncertainty of measurement. Working experience of overseeing the development of new analytical techniques. Good awareness of all HSE aspects in a laboratory environment (i.e., COSHH, RA). Required Skills/Qualifications (Desirable): Degree/HND in Biochemistry/Chemistry or related science (Highly Desirable) Consideration will be given to applicants with Certifications in Quality (Highly Desirable) Consideration will be given to those candidates with 2 years' experience in a similar position (Highly desirable) Knowledge and/or previous experience of GC FID, Ion chromatography, FT IR, wet chemistry, spectrophotometry experience of water, wastewater, cooling water and boiler water in the Oil & Gas, Petrochemical, food & beverage industries (Highly desirable). Working for us means: The salary is between £33,000 & £38,000 per year, depending on your professional experience. Hours of Work - 40 hours per week, Monday to Friday Holidays - 25 days + 8 statutory days (pro-rata) Probationary Period - 6 months. Pension - Can join immediately or auto enrolled after 3 months - Employee 5% and Employer 5% via salary sacrifice. Eligible to join Private Healthcare after successfully completing probation. Enrolled in Group Income Protection and Death in Service (4 x basic salary) upon commencement of employment. Notice - 1 Week during probation, increasing to 1 months thereafter. Nijhuis Saur Industries UK & Ireland are committed to maintaining Environmental & Social Impact goals: To reach Net Zero emissions across our value chain by 2040. To continuously meet high standards of social and environmental performance, transparency, accountability, maintaining B Corp Certification. To be a socially responsible company creating a positive impact to all stakeholders including workers, communities, customers, and our planet. Nijhuis Saur Industries UK & Ireland are an equal opportunity employer; we are committed to providing equal opportunities in all aspects of employment in line with the Equality Act 2010.
Consent Cookie Name : Google Analytics What it does: Data Collection, Configuration, Data Processing and Reporting Why is it used: Tracks and Reports Traffic (Anonymised) for Web Analytics How long it lasts: At least 25 Months . Enquiries When contacted with an enquiry, we will hold the entity name and contact details only for the purposes of handling the enquiry. recognise you whenever you visit this website (this speeds up your access to the website as you do not have to log in each time); obtain information about your preferences, online movements and use of the internet; carry out research and statistical analysis to help improve our content, products and services and to help us better understand our customer requirements and interests; target our marketing and advertising campaigns more effectively by providing interest-based advertisements that are personalised to your interests; make your online experience more efficient and enjoyable.Senior GC Analyst (Team Lead) page is loaded Senior GC Analyst (Team Lead)locations: Southampton, UKtime type: Full timeposted on: Posted 2 Days Agojob requisition id: REQ106681 This role is located in Marchwood, within the Cawood Scientific Environment Division. Marchwood, part of Cawood, was established in 1998 and performs a range of specialist analytical testing services to customers operating in the Environmental, Industrial and Agricultural Sectors from its three laboratories based in the South and North of England. As a leading UK Dioxin and Furans analysis laboratory and the UK's leading specialist laboratory for independent occupational hygiene analysis, Marchwood offers a range of services for the environmental, occupational and food/feed sectors Job Description: Job Title: Senior GC Analyst (Team Lead) Location: Marchwood Southampton Company: Cawood Job Description: We are seeking a highly skilled and motivated Senior GC Analyst to join our dynamic team within our Dioxins Laboratory. The successful candidate will be responsible for performing routine analysis on customer samples, working to deadlines in accordance with the company Quality Management System and UKAS guidelines. Experience with High Resolution Mass Spectrometry advantages but not essential. Key Responsibilities: Perform routine analysis on customer samples, adhering to deadlines and quality standards (ISO 17025 and MCERTS). Accurately record and analyze data, identifying possible deviations and ensuring compliance with system suitability checks, calibrations, and AQC charts. Undertake and assist with the investigation of queries and non-conformance. Perform routine and non-routine instrument maintenance, troubleshooting, identifying root causes, and implementing corrective actions to minimize unplanned instrument downtime. Plan and perform validation work to improve existing methods and develop new methods to support client requests and company growth strategy. Assist with the validation of new instruments as required. Effectively communicate with co-workers and local management. Prepare standards and solutions and aid in the preparation/extraction of samples if required. Maintain a high standard of personal knowledge and skills relevant to the role through company-led and self-directed learning. Work with minimal supervision, prioritizing and managing workload for self and a small team of analysts. Act as a coach and mentor for less knowledgeable colleagues in areas of subject matter expertise. Comply with company health and safety requirements, adopting a proactive safety attitude to ensure the safety of self and others. Participate in wider laboratory support teams such as spill team, fire warden, first aid team, HS rep, quality team, or internal audit team. Qualifications: Bachelor's degree in Chemistry/Scientific discipline or equivalent experience within similar role. Proficiency in GC analysis and relevant software such as Xcalibur, Masslynx, Chromeleon or Masshunter. Strong analytical and problem-solving skills. Excellent communication and teamwork abilities. Knowledge of ISO 17025 and MCERTS standards.
May 05, 2026
Full time
Consent Cookie Name : Google Analytics What it does: Data Collection, Configuration, Data Processing and Reporting Why is it used: Tracks and Reports Traffic (Anonymised) for Web Analytics How long it lasts: At least 25 Months . Enquiries When contacted with an enquiry, we will hold the entity name and contact details only for the purposes of handling the enquiry. recognise you whenever you visit this website (this speeds up your access to the website as you do not have to log in each time); obtain information about your preferences, online movements and use of the internet; carry out research and statistical analysis to help improve our content, products and services and to help us better understand our customer requirements and interests; target our marketing and advertising campaigns more effectively by providing interest-based advertisements that are personalised to your interests; make your online experience more efficient and enjoyable.Senior GC Analyst (Team Lead) page is loaded Senior GC Analyst (Team Lead)locations: Southampton, UKtime type: Full timeposted on: Posted 2 Days Agojob requisition id: REQ106681 This role is located in Marchwood, within the Cawood Scientific Environment Division. Marchwood, part of Cawood, was established in 1998 and performs a range of specialist analytical testing services to customers operating in the Environmental, Industrial and Agricultural Sectors from its three laboratories based in the South and North of England. As a leading UK Dioxin and Furans analysis laboratory and the UK's leading specialist laboratory for independent occupational hygiene analysis, Marchwood offers a range of services for the environmental, occupational and food/feed sectors Job Description: Job Title: Senior GC Analyst (Team Lead) Location: Marchwood Southampton Company: Cawood Job Description: We are seeking a highly skilled and motivated Senior GC Analyst to join our dynamic team within our Dioxins Laboratory. The successful candidate will be responsible for performing routine analysis on customer samples, working to deadlines in accordance with the company Quality Management System and UKAS guidelines. Experience with High Resolution Mass Spectrometry advantages but not essential. Key Responsibilities: Perform routine analysis on customer samples, adhering to deadlines and quality standards (ISO 17025 and MCERTS). Accurately record and analyze data, identifying possible deviations and ensuring compliance with system suitability checks, calibrations, and AQC charts. Undertake and assist with the investigation of queries and non-conformance. Perform routine and non-routine instrument maintenance, troubleshooting, identifying root causes, and implementing corrective actions to minimize unplanned instrument downtime. Plan and perform validation work to improve existing methods and develop new methods to support client requests and company growth strategy. Assist with the validation of new instruments as required. Effectively communicate with co-workers and local management. Prepare standards and solutions and aid in the preparation/extraction of samples if required. Maintain a high standard of personal knowledge and skills relevant to the role through company-led and self-directed learning. Work with minimal supervision, prioritizing and managing workload for self and a small team of analysts. Act as a coach and mentor for less knowledgeable colleagues in areas of subject matter expertise. Comply with company health and safety requirements, adopting a proactive safety attitude to ensure the safety of self and others. Participate in wider laboratory support teams such as spill team, fire warden, first aid team, HS rep, quality team, or internal audit team. Qualifications: Bachelor's degree in Chemistry/Scientific discipline or equivalent experience within similar role. Proficiency in GC analysis and relevant software such as Xcalibur, Masslynx, Chromeleon or Masshunter. Strong analytical and problem-solving skills. Excellent communication and teamwork abilities. Knowledge of ISO 17025 and MCERTS standards.
We are currently looking for a Senior LC-MS Analyst to join a growing laboratory in the South East. The role: As a Senior Laboratory Analyst you will carry out a range analysis using techniques such as LC, HPLC, LC-MS and LC-MS/MS Duties include: Set up and run analytical experiments to test for a wide range of samples. Carry out HPLC, LC-MS and LC-MS/MS analysis. Follow SOPs and ensure work is carried out to UKAS and ISO 17025 guidelines. Troubleshoot analytical instrumentation and perform calibrations. Ideal candidates will be degree qualified in a Chemistry subject and have laboratory experience as an Analytical Chemist/ Laboratory Analyst running LC and LC-MS analysis. For further details on the Laboratory Analyst/ Analytical Chemist role please contact Peter at Rowland Talent Solutions. Please note my client is not able to sponsor a visa for these positions so full eligibility to work in the UK is required. Key words: Lab Technician, Laboratory, Analyst, Analytical Chemist, Science, GC, HPLC, Chemistry, LC-MS, UKAS, Analytical Chemist, Senior, Scientist
Oct 07, 2025
Full time
We are currently looking for a Senior LC-MS Analyst to join a growing laboratory in the South East. The role: As a Senior Laboratory Analyst you will carry out a range analysis using techniques such as LC, HPLC, LC-MS and LC-MS/MS Duties include: Set up and run analytical experiments to test for a wide range of samples. Carry out HPLC, LC-MS and LC-MS/MS analysis. Follow SOPs and ensure work is carried out to UKAS and ISO 17025 guidelines. Troubleshoot analytical instrumentation and perform calibrations. Ideal candidates will be degree qualified in a Chemistry subject and have laboratory experience as an Analytical Chemist/ Laboratory Analyst running LC and LC-MS analysis. For further details on the Laboratory Analyst/ Analytical Chemist role please contact Peter at Rowland Talent Solutions. Please note my client is not able to sponsor a visa for these positions so full eligibility to work in the UK is required. Key words: Lab Technician, Laboratory, Analyst, Analytical Chemist, Science, GC, HPLC, Chemistry, LC-MS, UKAS, Analytical Chemist, Senior, Scientist
We are seeking a Graduate QC Analyst to join our client's quality team in Lanarkshire, Scotland. The successful candidate will be responsible for conducting high-quality analytical testing of raw materials, intermediates, and finished products within a GMP-regulated environment. You will assist with validation, maintain laboratory equipment, and ensure compliance with industry standards. The role involves organising sample testing activities, updating documentation, and supporting batch release processes, with the aim of maintaining exemplary quality standards and efficient laboratory operations. BSc in Chemistry or equivalent Experience in a laboratory environment, GMP experience is advantageous Knowledge of EU GMP and analytical chemistry principles Attention to detail, problem-solving, and organisation skills Computer literacy and practical laboratory skills In return, you will enjoy excellent benefits. This permanent role offers ongoing development opportunities within a highly-regulated pharmaceutical environment, fostering growth in your analytical expertise and quality assurance skills.
Oct 05, 2025
Full time
We are seeking a Graduate QC Analyst to join our client's quality team in Lanarkshire, Scotland. The successful candidate will be responsible for conducting high-quality analytical testing of raw materials, intermediates, and finished products within a GMP-regulated environment. You will assist with validation, maintain laboratory equipment, and ensure compliance with industry standards. The role involves organising sample testing activities, updating documentation, and supporting batch release processes, with the aim of maintaining exemplary quality standards and efficient laboratory operations. BSc in Chemistry or equivalent Experience in a laboratory environment, GMP experience is advantageous Knowledge of EU GMP and analytical chemistry principles Attention to detail, problem-solving, and organisation skills Computer literacy and practical laboratory skills In return, you will enjoy excellent benefits. This permanent role offers ongoing development opportunities within a highly-regulated pharmaceutical environment, fostering growth in your analytical expertise and quality assurance skills.
QC Analyst Location: Worthing, West Sussex Salary: £15.64 p/h Employment Type: 6 Month Contract CY Partners have an exciting contract opportunity for a QC Analyst with a background in pharmaceutical analysis. Do you have hands-on expertise with HPLC and other analytical techniques? If so, this could be a fantastic opportunity to further your career within a dynamic and fast-paced QC environment. This is a key role within the Quality function, supporting the release and stability testing of sterile and non-sterile products. Key Responsibilities: Perform physical and chemical testing of production and stability samples, meeting turnaround times and compliance standards. Analyse solid dose and antibiotic formulations using HPLC, Karl Fischer, dissolution, and other wet chemistry techniques. Calibrate, verify, and maintain analytical instruments and systems. Review and verify analytical results, ensuring data integrity and compliance with GMP/GLP. Support investigations into Out-of-Specification (OOS) results, working cross-functionally where needed. Contribute to the validation of analytical methods and equipment. About You: You ll ideally bring a strong background in pharmaceutical quality testing, with sound knowledge of GMP regulations and analytical chemistry. Requirements: HNC, HND, BSc or equivalent in Chemistry or a related scientific discipline. Proven experience in a GMP-regulated lab, with hands-on experience using HPLC. Strong documentation and data reporting skills. Detail-oriented, methodical, and safety-conscious. Able to communicate clearly and work effectively as part of a multidisciplinary team. A proactive, flexible approach to working in a fast-moving manufacturing environment. Whether you re looking to build on your experience or take the next step in your QC career, this is a great opportunity to make a meaningful impact within the pharmaceutical industry.
Sep 23, 2025
Contractor
QC Analyst Location: Worthing, West Sussex Salary: £15.64 p/h Employment Type: 6 Month Contract CY Partners have an exciting contract opportunity for a QC Analyst with a background in pharmaceutical analysis. Do you have hands-on expertise with HPLC and other analytical techniques? If so, this could be a fantastic opportunity to further your career within a dynamic and fast-paced QC environment. This is a key role within the Quality function, supporting the release and stability testing of sterile and non-sterile products. Key Responsibilities: Perform physical and chemical testing of production and stability samples, meeting turnaround times and compliance standards. Analyse solid dose and antibiotic formulations using HPLC, Karl Fischer, dissolution, and other wet chemistry techniques. Calibrate, verify, and maintain analytical instruments and systems. Review and verify analytical results, ensuring data integrity and compliance with GMP/GLP. Support investigations into Out-of-Specification (OOS) results, working cross-functionally where needed. Contribute to the validation of analytical methods and equipment. About You: You ll ideally bring a strong background in pharmaceutical quality testing, with sound knowledge of GMP regulations and analytical chemistry. Requirements: HNC, HND, BSc or equivalent in Chemistry or a related scientific discipline. Proven experience in a GMP-regulated lab, with hands-on experience using HPLC. Strong documentation and data reporting skills. Detail-oriented, methodical, and safety-conscious. Able to communicate clearly and work effectively as part of a multidisciplinary team. A proactive, flexible approach to working in a fast-moving manufacturing environment. Whether you re looking to build on your experience or take the next step in your QC career, this is a great opportunity to make a meaningful impact within the pharmaceutical industry.
