304 Quality Control Analyst jobs in the United Kingdom

• Job Title: QC Analyst – Biosafety
• Location: Speke, Liverpool.
• Contract: until 31/7/26
• Rate: £14 p/h
• Hours: 37.5 per week

SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some GMP experience to further their career.

Main responsibilities:

• Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
• Performing routine QC testing
• Documenting laboratory results in an accurate and timely manner.
• Complying with GMP regulatory requirements at all times.

Key requirements:

• Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
• Biological background either from university degree or relevant work in the field
• Computer skills, excel, word, outlook

Preferrable

• Experience within cell cultures and/or assay testing.
• LIMS and SAP

• Perform a range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, dissolution testing).
• Ensure all testing is conducted in accordance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines.
• Prepare reagents, standards, and samples accurately for testing.
• Calibrate and maintain laboratory equipment, ensuring it is in optimal working order.
• Validate analytical methods and document results thoroughly.
• Analyze and interpret test results, identifying any deviations or out-of-specification (OOS) results.
• Investigate OOS results and contribute to the development of corrective and preventative actions (CAPAs).
• Maintain accurate and detailed laboratory records, including raw data, calculations, and reports.
• Contribute to the continuous improvement of QC processes and laboratory efficiency.
• Ensure compliance with all relevant regulatory requirements (e.g., MHRA, FDA).
• Participate in internal and external audits as required.
• Collaborate effectively with other departments, including Production, Quality Assurance, and Research & Development.

• Bachelor's degree or higher in Chemistry, Pharmacy, Biochemistry, or a related life science discipline.
• Proven experience working in a pharmaceutical Quality Control laboratory environment.
• Hands-on experience with analytical instrumentation such as HPLC, GC, dissolution apparatus, and spectrophotometers.
• Solid understanding of GMP, GLP, and relevant pharmaceutical regulations.
• Excellent analytical, problem-solving, and data interpretation skills.
• High level of attention to detail and accuracy in all aspects of work.
• Proficiency in laboratory information management systems (LIMS) is advantageous.
• Strong written and verbal communication skills.
• Ability to work independently and as part of a collaborative team.
• Good organizational skills and the ability to manage multiple tasks efficiently.
• Experience with method validation is desirable.

• Perform quantitative and qualitative analyses of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, KF).
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Operate, calibrate, and maintain laboratory equipment, troubleshooting issues as they arise.
• Review and approve analytical data, ensuring accuracy and compliance with specifications.
• Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
• Maintain accurate and comprehensive laboratory records, including test results, instrument logs, and deviations.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements.
• Contribute to internal and external audits by providing documentation and expertise.
• Assist in the training and mentoring of junior laboratory personnel.
• Stay updated on new analytical technologies and regulatory changes impacting quality control.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
• Significant experience as a Quality Control Analyst in the pharmaceutical industry.
• Proficiency with a range of analytical instruments (HPLC, GC, etc.) and associated software.
• Thorough understanding of GMP regulations and quality management systems.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong attention to detail and accuracy.
• Effective written and verbal communication skills.
• Ability to work independently and collaboratively in a fast-paced laboratory environment.
• Experience with method validation and OOS investigations is highly desirable.

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Prepare samples and reagents for testing according to established procedures.
• Operate and maintain laboratory equipment, ensuring calibration and suitability for use.
• Record all test results accurately and contemporaneously in laboratory notebooks and electronic systems.
• Review and interpret analytical data, identifying deviations or out-of-specification results.
• Investigate and document any deviations or out-of-specification (OOS) results, participating in root cause analysis.
• Ensure compliance with GLP, GMP, and other relevant regulatory requirements.
• Maintain laboratory cleanliness and organization.
• Participate in method validation and verification activities.
• Assist in the preparation of quality control reports and documentation.
• Stay updated on current scientific literature and industry best practices.

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related life science discipline.
• Previous experience in a pharmaceutical quality control laboratory is highly desirable.
• Proficiency in analytical techniques such as HPLC, GC, and wet chemistry methods.
• Familiarity with GLP and GMP regulations.
• Strong attention to detail and accuracy in record-keeping.
• Excellent problem-solving and analytical skills.
• Ability to work effectively both independently and as part of a team.
• Good understanding of laboratory safety procedures.
• Proficiency in Microsoft Office Suite.

• Perform analytical testing of raw materials, intermediates, and finished products.
• Operate and maintain laboratory equipment, including HPLC, GC, and spectrophotometers.
• Prepare samples, reagents, and standards for analysis.
• Document all test procedures, results, and observations accurately.
• Ensure compliance with GLP, GMP, and other relevant regulatory guidelines.
• Participate in method validation and transfer activities.
• Investigate and report on out-of-specification (OOS) results.
• Maintain a clean, organized, and safe laboratory environment.
• Collaborate with R&D, Production, and Regulatory Affairs teams.
• Contribute to the continuous improvement of QC processes and procedures.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related life science discipline.
• Proven experience working in a pharmaceutical quality control laboratory.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, FTIR, etc.
• Familiarity with pharmacopoeial standards (BP, USP, EP).
• Knowledge of GLP and GMP principles.
• Strong understanding of experimental design and data analysis.
• Excellent problem-solving and critical thinking skills.
• Meticulous attention to detail and accuracy.
• Good written and verbal communication skills.
• Ability to work effectively in a team-oriented environment.

• Perform analytical testing of raw materials, intermediates, and finished pharmaceutical products using methods such as HPLC, GC, UV-Vis Spectroscopy, and titrations.
• Prepare reagents, standards, and samples according to approved procedures.
• Operate and maintain laboratory equipment, ensuring calibration and performance are within specifications.
• Document all testing procedures, results, and observations accurately and comprehensively in laboratory notebooks and electronic systems.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and recommending corrective actions.
• Ensure all activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Participate in method validation and transfer activities.
• Review and approve test data and batch release documentation.
• Contribute to the continuous improvement of laboratory processes and quality systems.
• Maintain a safe working environment by adhering to all safety protocols and procedures.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues.
• Assist in the preparation for internal and external audits.

• Bachelor's or Master's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline.
• Proven experience in pharmaceutical quality control or a related laboratory setting.
• Hands-on experience with analytical instrumentation commonly used in pharmaceutical analysis (e.g., HPLC, GC, Karl Fischer titrator, FTIR).
• Strong understanding of GMP, GLP, and relevant regulatory requirements.
• Excellent data analysis and interpretation skills.
• Proficiency in scientific documentation and record-keeping.
• Strong problem-solving abilities and attention to detail.
• Ability to work independently and manage priorities effectively in a remote work environment.
• Effective communication and teamwork skills, even in a virtual setting.
• Knowledge of pharmacopoeial methods (e.g., USP, EP).
• Commitment to maintaining the highest standards of quality and scientific integrity.

• Performing analytical tests on pharmaceutical products using techniques such as HPLC, GC, UV-Vis, and titration.
• Testing raw materials, intermediates, and finished goods to ensure they meet specifications.
• Accurately documenting all testing procedures, results, and observations in compliance with GMP guidelines.
• Maintaining and calibrating laboratory equipment to ensure accuracy and reliability.
• Investigating out-of-specification (OOS) results and participating in deviation investigations.
• Assisting in the validation of analytical methods and equipment.
• Preparing and reviewing quality control documentation, including reports and certificates of analysis.
• Collaborating with R&D, production, and regulatory affairs departments.
• Staying updated on current Good Manufacturing Practices (cGMP) and relevant regulatory guidelines.

• Perform a range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titration).
• Prepare reagents, solutions, and standards accurately for testing.
• Interpret analytical data, document results meticulously, and compare them against established specifications.
• Identify and investigate any out-of-specification (OOS) results or deviations from standard procedures.
• Maintain laboratory equipment, ensuring proper calibration and functioning.
• Adhere strictly to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and all relevant safety regulations.
• Contribute to the validation and qualification of analytical methods and equipment.
• Write and review standard operating procedures (SOPs) and technical reports.
• Participate in internal audits and support external regulatory inspections.
• Collaborate effectively with production, R&D, and other departments to resolve quality-related issues.

• Bachelor's degree in Chemistry, Pharmaceutical Science, Biotechnology, or a related scientific discipline.
• Proven experience (2+ years) in a Quality Control laboratory environment, preferably within the pharmaceutical or biopharmaceutical industry.
• Strong practical knowledge of analytical instrumentation and techniques commonly used in pharmaceutical QC.
• Familiarity with GMP, regulatory guidelines (e.g., FDA, MHRA), and quality management systems.
• Excellent data recording and documentation skills.
• Strong problem-solving abilities and attention to detail.
• Ability to work independently and as part of a team in a fast-paced laboratory setting.
• Good written and verbal communication skills.
• Proficiency in using laboratory software and Microsoft Office Suite.