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QC Analyst

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: Science Solutions Recruitment Ltd
Full Time position
Listed on 2026-10-26
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Data Analyst
Salary/Wage Range or Industry Benchmark: 36000 - 48000 GBP Yearly GBP 36000.00 48000.00 YEAR
Job Description & How to Apply Below

QC Analyst | London | Pharmaceutical Manufacturing

Smart4

Sciences 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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