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Senior QC Analyst

Employer not disclosed

Manchester, Greater ManchesterFull-timePermanent£30,000 – £35,000 a year16 days ago
Medical/Pharmaceutical/Scientific

Job Advertisement: Senior QC Analyst (6-Month FTC Contract Role) Overview Salary £30,000 - £35,000 pro rata We are seeking a highly skilled and experienced Senior QC Analyst for a 6-month fixed-term contract to join a pharmaceutical manufacturing organisation. Reporting directly to the QC Manager, this role is integral to ensuring the quality and compliance of pharmaceutical products. If you are a detail-oriented professional with a strong background in Quality Control and a passion for excellence, we encourage you to apply. Responsibilities As a Senior QC Analyst, your key responsibilities will include: * Supervising and leading a team of analysts in the Quality Control laboratory, ensuring compliance with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP). * Reviewing Batch Manufacturing Documents and analytical test results to facilitate product release. * Performing analytical testing of manufactured product samples for release, stability studies, and validation using techniques such as HPLC and GC. * Assigning duties to analysts based on production release requirements, ensuring efficient laboratory operations. * Reviewing and approving product labels for use by the Production Department. * Preparing and reviewing Standard Operating Procedures, Raw Material Documents, Analytical Test Reports, Validation Protocols, and Reports. * Providing technical support, troubleshooting analytical methods, and maintaining laboratory equipment. * Ensuring laboratory housekeeping is maintained to appropriate standards. * Supporting inspection readiness and promoting a culture of continuous improvement. * Collaborating with Quality Assurance and Production teams to ensure seamless operations. * Reviewing analytical data against pharmacopeial and registered specifications. Qualifications To be successful in this role, you will need: * A degree in Chemical Sciences or equivalent practical experience. * A minimum of 5 years of Quality Control/Analytical experience within a GMP environment. * Proficiency in analytical techniques, including IR and NIR spectroscopy, High-Performance Liquid Chromatography (HPLC), and Gas Chromatography (GC). * Strong analytical thinking, problem-solving, and troubleshooting skills. * Excellent communication skills, both verbal and written, with a keen eye for detail. * Good computer literacy and familiarity with laboratory systems. * A commitment to health and safety practices, including ensuring team members are adequately trained in safety protocols and the use of PPE. Benefits * Competitive compensation for the duration of the 6-month fixed-term contract. * Opportunity to work in a dynamic and well-established pharmaceutical manufacturing environment. * Gain valuable experience in a leadership role within a Quality Control function. * Contribute to the production of high-quality pharmaceutical products that make a difference in people's lives. If you are ready to take on this exciting 6-month fixed-term opportunity and bring your expertise to our team, we look forward to receiving your application. Note: No sponsorship is available for this position

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