Quality Assurance Officer

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Quality Assurance Officer

Who are we?

A leading cell and gene therapy development organisation is creating life-changing therapies through innovation and collaboration.

Why join us?

  • Fast-growing company offering career development opportunities.
  • Competitive salary and generous benefits package.
  • 31 days of annual leave + public holidays.
  • Attractive pension scheme and life cover.
  • Private healthcare and mental health support.
  • Flexible benefits, including retail discounts and Cycle2Work scheme.

Your new role

  • Write, review, and update SOPs to align with regulatory standards.
  • Approve quality documentation like Incident Reports and Change Controls.
  • Conduct internal audits and ensure GMP compliance.
  • Evaluate suppliers and assist with audits.
  • Support audits and regulatory inspections.
  • Deliver training on quality topics and monitor QMS metrics.

    About you

    • Strong knowledge of cGMP principles.
    • Proficient with Microsoft Office and quality management systems.
    • Excellent communication and decision-making skills.
    • Proactive and adaptable, able to work independently.

    Qualifications

    • Degree in Life Science or 2+ years’ industry experience.

#J-18808-Ljbffr”, “datePosted”: “2026-03-28”, “hiringOrganization”: { “@type”: “Organization”, “name”: “Barrington James Limited”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__394262583__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861&geoID=8” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “Scotland” } } }
Company: Barrington James Limited
Apply for the Quality Assurance Officer
Location: Scotland
Job Description:

Quality Assurance Officer

Who are we?

A leading cell and gene therapy development organisation is creating life-changing therapies through innovation and collaboration.

Why join us?

  • Fast-growing company offering career development opportunities.
  • Competitive salary and generous benefits package.
  • 31 days of annual leave + public holidays.
  • Attractive pension scheme and life cover.
  • Private healthcare and mental health support.
  • Flexible benefits, including retail discounts and Cycle2Work scheme.

Your new role

  • Write, review, and update SOPs to align with regulatory standards.
  • Approve quality documentation like Incident Reports and Change Controls.
  • Conduct internal audits and ensure GMP compliance.
  • Evaluate suppliers and assist with audits.
  • Support audits and regulatory inspections.
  • Deliver training on quality topics and monitor QMS metrics.

    About you

    • Strong knowledge of cGMP principles.
    • Proficient with Microsoft Office and quality management systems.
    • Excellent communication and decision-making skills.
    • Proactive and adaptable, able to work independently.

    Qualifications

    • Degree in Life Science or 2+ years’ industry experience.

#J-18808-Ljbffr…

Posted: March 28th, 2026