QC Analyst - Chemistry (12-month fixed term contract)

We are seeking a QC Analyst - Chemistry to deliver high-quality analytical support for biopharmaceutical products within a cGMP laboratory. The role involves hands-on testing, data review, and technical mentorship, helping to ensure that medicines for people with rare and devastating diseases are safe, consistent, and compliant.

Requirements

• Carry out all laboratory activities in full compliance with cGMP requirements and internal quality standards.
• Complete a range of analytical methods, including Electrophoresis (iCE), HPLC-based assays, protein concentration, and compendial tests.
• Schedule and perform stability testing, ensuring accurate planning, execution, and documentation of all activities.
• Maintain up-to-date training records for all assigned responsibilities and ensure ongoing compliance with training requirements.
• Act as a QC subject matter expert, providing day-to-day technical guidance and support to QC analyst colleagues.
• Perform data review activities, including peer review and logbook review, and authorise results as required by procedures.
• Support the QC management team with operational priorities, problem-solving, and implementation of quality initiatives.
• Lead and complete laboratory investigations and associated CAPAs in a timely and thorough manner, using robust investigation methodologies.
• Serve as training lead for designated assays, coordinating the planning, delivery, and documentation of training for new personnel.
• Drive continuous improvement initiatives within the QC department to improve efficiency, robustness, and compliance.
• Contribute to laboratory housekeeping and 5S activities to sustain an audit-ready environment at all times.

Benefits

• Competitive salary
• Benefits