About the Role

An established pharmaceutical manufacturing site is seeking a QC Analyst (Biochemistry) to join its Quality Control team. This role plays a key part in ensuring products meet strict quality, safety, and regulatory standards within a GMP-regulated laboratory environment. You’ll be responsible for performing routine and non-routine analytical testing, maintaining accurate documentation, and supporting continuous improvement across QC operations.

Key Responsibilities

• Perform routine biochemical and analytical testing in line with approved methods and SOPs
• Ensure all testing complies with GMP, GDP, and quality system requirements
• Accurately document results and enter data into LIMS
• Investigate out-of-specification, invalid, or atypical results
• Maintain laboratory equipment, including calibration and troubleshooting
• Support method validation, documentation updates, and continuous improvement initiatives
• Contribute to laboratory safety, housekeeping, and 5S standards
• Collaborate with cross-functional teams to support production and quality outcomes

About You

• Degree in Science, Biochemistry, Chemistry, or a related discipline
• Experience working in a GMP-regulated laboratory (pharma, biotech, or similar)
• Hands-on experience with biochemical or analytical testing techniques
• Strong attention to detail and commitment to quality and compliance
• Comfortable working with documentation, procedures, and regulated systems
• Able to work well in a structured, team-based environment

What’s on Offer

• Join a well-established, regulated manufacturing environment
• Exposure to a broad range of QC activities and techniques
• Supportive team and strong quality culture
• Ongoing training and development opportunities
• Secure, long-term role with stability and career progression

How to Apply
If you’re a QC Analyst looking to grow your experience within a regulated pharmaceutical environment, we’d love to hear from you.
Apply now or reach out for a confidential discussion.