Job Description:

QC Analyst | London | Pharmaceutical Manufacturing

Smart4Sciences is partnering with a pharmaceutical manufacturer in London to recruit an experienced QC Analyst to join their Quality Control team.

This is an excellent opportunity for a detail-oriented analytical professional with experience in a GMP-regulated environment, who is passionate about laboratory testing, product quality and regulatory compliance.

Key Responsibilities:

• Perform routine testing of raw materials and finished products using analytical techniques such as HPLC, GC, UV, FTIR and titration.

• Conduct method validation, method transfer and method development in line with relevant regulatory guidelines.

• Review analytical data, raw data and batch documentation to ensure compliance with cGMP requirements.

• Support stability studies, OOS investigations, deviations and CAPA implementation.

• Prepare, review and update SOPs, product specifications and controlled quality documentation.

• Perform raw material sampling, visual inspections and material release activities.

• Maintain laboratory equipment and support equipment qualification and routine maintenance.

• Monitor environmental and microbial data, prepare trend reports and maintain accurate records.

• Support change controls, supplier management, quality investigations and continuous improvement initiatives.

What We're Looking For:

• Experience in a pharmaceutical or GMP-regulated laboratory environment.

• Practical experience with analytical techniques such as HPLC, GC, UV, FTIR or titration.

• Knowledge of cGMP and laboratory documentation requirements.

• Experience in method validation, stability testing, OOS investigations and CAPA is advantageous.

• Strong analytical skills, attention to detail and excellent documentation practices.

If you're looking for your next opportunity in pharmaceutical Quality Control, we'd love to hear from you!