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.
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Contact Details:
Science Solutions Recruitment Ltd Recruitment Team
