At a Glance
- Tasks: Lead a QC team ensuring top-notch quality in pharmaceutical products.
- Company: Join a dynamic pharmaceutical manufacturing organisation with a strong reputation.
- Benefits: Competitive pay, valuable leadership experience, and a chance to make a real impact.
- Other info: Opportunity for growth in a well-established environment.
- Why this job: Be part of a team that ensures the safety and quality of life-changing products.
- Qualifications: Degree in Chemical Sciences and 5 years of QC experience required.
The predicted salary is between 30000 - 35000 £ per year.
Senior QC Analyst (6-Month FTC Contract Role)
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.
Responsibilities
- 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
- 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.
- Note: No sponsorship is available for this position
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Senior QC Analyst in Ringway employer: Nexus Life Sciences
As an Analytical Scientist at our innovative pharmaceutical company, you will thrive in a collaborative work culture that prioritises professional development and mentorship. With competitive salaries and a commitment to GMP compliance, we offer a rewarding environment where your contributions directly impact patient health and safety, all while being part of a vibrant community dedicated to scientific excellence.
