456 Quality Control Analyst jobs in the United Kingdom

Quality Control Analyst (Pharmaceutical)

25,000 - 30,000 + Training + Progression + Company Benefits + Bonus

Sandwich, Kent

Are you a Quality Control Analyst within a laboratory environment and are looking to join a tight-knit, family run pharmaceutical business offering guided training and clear progression routes into senior positions?

On offer is a varied role where you will perform physical and analytical testing on Active Pharmaceutical Ingredients (API) and manufactured products using techniques such as HPLC, GC and wet chemistry. You will be supporting both Production and Quality Assurance departments, ensuring compliance with GMP and international regulatory standards.

This company has been established for over 10 years and operates in a highly regulated, niche pharmaceutical sector, supporting critical global healthcare supply chains. They pride themselves on their investment in people, structured training, and opportunities for career advancement.

This role would suit a QC Analyst with laboratory experience, ideally within pharmaceuticals, who is looking for a technically challenging and rewarding position with guided training and clear routes to progress into senior roles across Quality and Production.

The Role:

Perform analytical and physical testing (HPLC, GC, wet chemistry, microbiological checks)

Support manufacturing and ongoing studies with accurate test data

Maintain laboratory housekeeping and ensure equipment is calibrated, validated and fit for use

Adhere to GMP, QMS requirements and SOPs

The Person:

Quality Control Analyst or similar with a background in Pharmaceutical

Degree in Science related Degree

Knowledge of GMP and laboratory equipment calibration/validation advantageous

Reference: BBBH21793

Keywords: QC, Quality Control, Analyst, Chemistry, Analytical Chemistry, HPLC, GC, Wet Chemistry, Pharmaceutical, GMP, Laboratory, Testing, Sandwich, Kent

• Perform routine and non-routine quality control testing on raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, spectroscopy, wet chemistry).
• Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines (e.g., MHRA, FDA).
• Calibrate, maintain, and troubleshoot laboratory equipment to ensure accurate and reliable results.
• Prepare and standardize reagents and solutions required for testing.
• Accurately record all test results, observations, and deviations in laboratory notebooks and electronic systems.
• Analyze and interpret test data, identifying any out-of-specification (OOS) results and initiating investigations as per SOPs.
• Participate in method validation and transfer activities.
• Contribute to the continuous improvement of quality control processes and laboratory operations.
• Maintain a clean and organized laboratory environment.
• Collaborate with production, R&D, and regulatory affairs teams to resolve quality issues.
• Prepare Certificates of Analysis (CoAs) for released products.
• Adhere to all safety protocols and hazardous material handling procedures.

• A Bachelor's degree in Chemistry, Pharmacy, Pharmaceutical Science, or a related scientific discipline.
• Proven experience in a pharmaceutical quality control laboratory environment.
• Hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, etc.
• Strong understanding of GMP principles and regulatory requirements in the pharmaceutical industry.
• Excellent laboratory technique, data recording, and analytical skills.
• Proficiency in documentation and report writing.
• Meticulous attention to detail and a commitment to accuracy.
• Ability to work independently and as part of a team.
• Good problem-solving skills and the ability to investigate deviations effectively.
• Familiarity with LIMS (Laboratory Information Management System) is a plus.

• Perform a variety of chemical and physical tests on pharmaceutical products using sophisticated analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).
• Analyze raw materials, intermediates, and finished goods to confirm identity, purity, and potency.
• Prepare reagents and solutions required for testing procedures.
• Accurately document all test results, observations, and deviations in laboratory notebooks and electronic systems.
• Calibrate and maintain laboratory equipment, ensuring it is in optimal working condition.
• Follow Standard Operating Procedures (SOPs) meticulously and ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
• Investigate out-of-specification (OOS) results and deviations, contributing to root cause analysis.
• Participate in method validation and transfer activities.
• Contribute to internal audits and regulatory inspections.
• Maintain a clean and organized laboratory workspace.

• Bachelor's degree in Chemistry, Pharmaceutical Science, Biochemistry, or a related scientific discipline.
• Minimum of 2 years of experience in pharmaceutical quality control or a related analytical laboratory role.
• Hands-on experience with analytical instrumentation such as HPLC, GC, spectroscopy techniques.
• Proficiency in GMP and other relevant regulatory guidelines.
• Strong understanding of pharmaceutical testing methodologies.
• Excellent attention to detail and accuracy in data recording and reporting.
• Ability to interpret analytical data and identify potential issues.
• Good problem-solving skills and the ability to work independently.
• Effective written and verbal communication skills.
• Familiarity with laboratory information management systems (LIMS) is a plus.

• Perform chemical and physical analysis on raw materials, intermediates, and finished pharmaceutical products.
• Utilize various analytical techniques including HPLC, GC, FTIR, UV-Vis, and wet chemistry.
• Ensure all testing is conducted in compliance with GMP, GLP, and relevant pharmacopoeial standards.
• Accurately document all experimental data, observations, and results in laboratory notebooks and LIMS.
• Calibrate, maintain, and troubleshoot laboratory equipment.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Prepare and standardize reagents and solutions.
• Contribute to method validation and transfer activities.
• Maintain a clean and organized laboratory environment.
• Participate in internal and external audits.

• Bachelor's degree in Chemistry, Pharmaceutical Science, or a related field.
• Proven experience in a pharmaceutical Quality Control laboratory setting.
• Hands-on experience with HPLC, GC, and other relevant analytical instrumentation.
• Knowledge of GMP and GLP regulations.
• Familiarity with pharmacopoeial methods (BP, USP, EP).
• Strong understanding of analytical chemistry principles.
• Excellent documentation skills and attention to detail.
• Ability to work independently and as part of a team.
• Good problem-solving skills.

• Perform a variety of analytical tests on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Prepare reagents, solutions, and standards required for analytical testing.
• Operate and maintain laboratory equipment, ensuring proper calibration and functionality.
• Accurately document all testing procedures, results, and observations in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Analyze and interpret test data, identifying deviations and out-of-specification results.
• Investigate deviations and non-conformances, contributing to root cause analysis.
• Write and review analytical test methods and validation reports.
• Maintain a clean and organized laboratory environment, adhering to safety protocols.
• Participate in internal audits and inspections.
• Collaborate with R&D, production, and regulatory affairs departments to resolve quality-related issues.

• Bachelor's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline.
• Proven experience working in a pharmaceutical QC laboratory environment is essential.
• Hands-on experience with common analytical instruments like HPLC, GC, and UV-Vis spectrophotometers.
• Strong understanding of analytical chemistry principles and techniques.
• Familiarity with GMP, GLP, and relevant regulatory guidelines (e.g., ICH).
• Excellent attention to detail and accuracy in data recording and analysis.
• Strong written and verbal communication skills.
• Ability to work effectively both independently and as part of a team.
• Proficiency in using laboratory information management systems (LIMS) is an advantage.
• A proactive approach to problem-solving and continuous improvement.

Quality Control Analyst (Pharmaceutical)

£25,000 - £30,000 + Training + Progression + Company Benefits + Bonus

Sandwich, Kent

Are you a Quality Control Analyst within a laboratory environment and are looking to join a tight-knit, family run pharmaceutical business offering guided training and clear progression routes into senior positions?

On offer is a varied role where you will perform physical and .

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