QC Analyst III

We’re seeking an experienced QC Analyst III to join a high-performing Quality Control team within a GMP-regulated environment. This is an exciting opportunity for an analytical scientist with strong hands‑on laboratory experience who enjoys working across development, manufacturing, quality, and client-focused projects
.

As a QC Analyst III, you’ll perform and lead analytical testing activities supporting programs from early-stage development through commercial manufacturing
. You’ll play a key role in ensuring product quality, data integrity, and compliance with cGMP and regulatory requirements.

The role offers exposure to a broad range of analytical testing, laboratory investigations, troubleshooting, technical documentation, and continuous improvement initiatives.

• Perform routine and non-routine testing of raw materials, in-process samples, stability samples, and finished products
• Conduct analytical testing using techniques including HPLC/UPLC, GC, UV-Vis, qPCR, ELISA, gel electrophoresis, microscopy
  , and other relevant methods
• Support environmental monitoring and raw material testing
• Review and verify laboratory data in accordance with GMP and data integrity requirements
• Author and revise SOPs, analytical methods, protocols, specifications, and technical reports
• Lead and support investigations involving deviations, OOS, OOT, and CAPAs
• Troubleshoot analytical methods, laboratory equipment, and testing processes
• Maintain accurate laboratory documentation in line with cGMP and GDP
• Collaborate closely with QA, Manufacturing, Development, and Project Management
• Communicate technical findings, testing results, and quality issues to key stakeholders
• Support regulatory inspections, client audits, and quality initiatives
• Contribute to continuous improvement across laboratory processes and quality systems

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences
  , or a related scientific discipline
• 5+ years of experience in a GMP-regulated QC laboratory
• Strong hands‑hands on experience with HPLC, ELISA, and qPCR
• Experience with UPLC, GC, UV-Vis, gel electrophoresis, and microscopy is highly desirable
• Strong knowledge of cGMP, GDP, data integrity, and laboratory compliance
• Familiarity with FDA, ICH, and EU regulatory requirements
• Experience with laboratory investigations, troubleshooting and CAPAs
• Strong technical writing skills, including SOPs, methods, protocols, and reports
• Previous CDMO/CMO experience is preferred
• Excellent analytical, problem‑solving, and communication skills
• Highly organised, detail‑oriented, and able to manage multiple priorities in a fast‑paced environment