QA Specialist

4732172
  • Job type

    Permanent
  • Location

    Maidenhead
  • Working Pattern

    Full-time
  • Specialism

    Quality Assurance And Validation
  • Industry

    Scientific and R&D
  • Pay

    £43,000 - £58,000

Quality Assurance Specialist – GMP/GDP | UK Hybrid | Global Pharma

About the Opportunity
A leading global pharmaceutical organisation is seeking a Quality Assurance Specialist to join their UK-based team. This company is committed to regulatory excellence and continuous improvement in the commercialisation of medicinal products. With a strong international footprint and a focus on high-quality standards, they collaborate closely with health authorities, contract manufacturers, and internal stakeholders to ensure compliance across the product lifecycle.

Key Responsibilities
  • Lead product release and compliance activities, ensuring documentation accuracy and adherence to GMP/GDP standards.
  • Maintain and improve Quality Systems including Change Control, Deviations, Complaints, Product Quality Reviews (PQRs), Recalls, and Returns.
  • Act as a key liaison with Health Authorities, ensuring timely incident reporting and regulatory compliance.
  • Conduct risk assessments, support technical knowledge-sharing, and contribute to quality documentation.
  • Implement and monitor Corrective and Preventative Actions (CAPAs), track effectiveness, and report outcomes to senior leadership.
  • Drive continuous improvement initiatives to enhance operational quality and efficiency.
What You’ll Bring
  • A degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Biochemistry, or a related discipline.
  • 5+ years’ experience in Quality Assurance, Quality Control, or a similar function within the pharmaceutical or healthcare sector.
  • Certifications in GMP and GDP.
  • Strong knowledge of regulatory affairs, pharmaceutical guidelines, and quality systems.
  • Proven experience in compliance activities including CAPAs, Change Control, and Deviations.
  • Exposure to regulatory audits and interactions with Health Authorities is highly desirable.
  • A proactive mindset with a passion for quality improvement and operational excellence.
Why Apply?
  • Join a global leader in pharmaceutical innovation.
  • Work in a collaborative and quality-driven environment.
  • Be part of a team that values regulatory integrity and continuous improvement.

Apply for this job

Talk to Aleksandra Topalovic, the specialist consultant managing this position

Located in London-City, 5th Floor, 107 Cheapside, Telephone +44 333 010 4702
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