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360 Resourcing Solutions Logo 360 Resourcing Solutions · Quality Control

Senior QC Analyst

· Job Posted January 22, 2026
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Job Description

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, committed to revolutionising healthcare. As the UK’s leading manufacturer and supplier of unlicensed medicines and hard-to-source products, we serve retail pharmacies, hospitals, pharmaceutical wholesalers, and homecare markets with unmatched expertise and passion. With a diverse team of over 500 professionals, including top pharmacists, skilled technicians, and dedicated support staff, we ensure excellence and innovation in everything we do. We are looking for a Senior QC Analyst to join our growing and forward-thinking team. You will be responsible for performing, reviewing, and leading analytical testing to ensure the quality, safety, and efficacy of pharmaceutical products in accordance with current Good Manufacturing Practices (cGMP), internal procedures, and regulatory requirements. This role provides technical expertise, supports method validation and transfer, and assists in troubleshooting analytical issues while mentoring junior analysts within the QC laboratory.

Job Responsibility

  • Perform qualitative and quantitative chemical and microbiological analyses of raw materials, in-process samples, finished products, and stability samples using validated methods (e.g., HPLC, GC, UV, FTIR, Dissolution)
  • Review and verify analytical data, ensuring accuracy, completeness, and compliance with cGMP and SOPs
  • Lead out-of-specification (OOS), out-of-trend (OOT), and deviation investigations, including root cause analysis and CAPA development
  • Support release testing and timely completion of batch records to ensure uninterrupted product supply
  • Participate in method validation, method transfer, and equipment qualification activities
  • Develop and optimise analytical methods as required to support new product development or process changes
  • Troubleshoot complex analytical and instrumentation issues independently and provide guidance to peers
  • Ensure all activities comply with cGMP and ICH, and other applicable regulatory guidelines
  • Prepare, review, and maintain laboratory documentation including test records, logbooks, and SOPs
  • Support internal and external audits and respond to audit findings
  • Mentor and train junior analysts in analytical techniques, data integrity, and laboratory best practices
  • Participate in continuous improvement initiatives to enhance laboratory efficiency, quality, and safety
  • Collaborate cross-functionally with QA and Production teams to resolve quality issues

Requirements

  • Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field
  • Minimum 5–8 years of QC laboratory experience in the pharmaceutical or biopharmaceutical industry
  • Strong working knowledge of analytical techniques such as HPLC, GC, UV-Vis, FTIR, TOC and dissolution
  • Proven experience in method validation, instrument troubleshooting, and data integrity compliance
  • Excellent understanding of cGMP, GLP, and regulatory requirements
  • Strong attention to detail and analytical thinking
  • Proficiency in laboratory software including Chromeleon
  • Strong communication, leadership, and mentoring skills
  • Ability to work independently and manage multiple priorities under tight timelines

What we offer

  • Active Social and charity committee
  • Cycle to Work Scheme
  • Electric Vehicle Scheme
  • Eye Care Vouchers
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