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:
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Perform routine testing of raw materials and finished products using analytical techniques such as HPLC, GC, UV, FTIR and titration.
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Conduct method validation, method transfer and method development in line with relevant regulatory guidelines.
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Review analytical data, raw data and batch documentation to ensure compliance with cGMP requirements.
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Support stability studies, OOS investigations, deviations and CAPA implementation.
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Prepare, review and update SOPs, product specifications and controlled quality documentation.
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Perform raw material sampling, visual inspections and material release activities.
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Maintain laboratory equipment and support equipment qualification and routine maintenance.
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Monitor environmental and microbial data, prepare trend reports and maintain accurate records.
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Support change controls, supplier management, quality investigations and continuous improvement initiatives.
What We're Looking For:
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Experience in a pharmaceutical or GMP-regulated laboratory environment.
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Practical experience with analytical techniques such as HPLC, GC, UV, FTIR or titration.
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Knowledge of cGMP and laboratory documentation requirements.
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Experience in method validation, stability testing, OOS investigations and CAPA is advantageous.
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Strong analytical skills, attention to detail and excellent documentation practices.
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Contact Details:
Science Solutions Recruitment Ltd Recruitment Team
