Qualified Person (QP) – QA Operations Manager

Company: Meet Life Sciences
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Location: London
Job Description:

Qualified Person (QP) – QA Operations Manager

Qualified Person (QP) – QA Operations Manager

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QA Operations Manager & Qualified Person (QP)

Location: United Kingdom (Hybrid – 3 days on-site)

Industry: Pharmaceutical Manufacturing

Employment Type: Full-time

About the Role

We are partnering with a well-established pharmaceutical manufacturing company to hire a QA Operations Manager & Qualified Person (QP) to join their UK-based team. This is a key position supporting GMP compliance and sterile manufacturing operations, with direct responsibility for batch release and leadership of the site’s quality operations.

You’ll lead day-to-day QA activities, manage a small quality team, and ensure ongoing compliance with regulatory requirements. This hybrid role offers both strategic and hands-on responsibilities in a high-impact environment.

Key Responsibilities

  • Act as Qualified Person (QP) for batch release of sterile pharmaceutical products
  • Lead and mentor two QA Associates to ensure efficient and compliant operations
  • Oversee QA processes, including deviation handling, CAPA, change control, and QMS updates
  • Ensure site-wide GMP compliance and support audit readiness activities
  • Represent QA during external inspections and audits (approximately 4–5 per year)
  • Collaborate cross-functionally with manufacturing, supply chain, and regulatory teams

Required Qualifications

  • Current eligibility to act as a Qualified Person (QP) in the UK
  • 3–4 years of active QP experience
  • Strong background in quality assurance within a GMP-regulated environment
  • Experience in sterile manufacturing is essential
  • Solid understanding of QMS, batch documentation, and regulatory requirements
  • Prior experience managing or mentoring junior QA team members
  • Ability to work on-site three days per week as part of a hybrid model

Preferred Qualifications

  • Familiarity with MHRA and EMA regulatory expectations
  • Experience representing QA during external audits or inspections
  • Exposure to sterile fill/finish operations or aseptic processes
  • Strong communication, leadership, and problem-solving skills

Additional Information

  • Hybrid working model: minimum 3 days per week on-site
  • Start date: ASAP (ideally within the next couple of months)

This is an excellent opportunity to lead quality operations in a dynamic and fast-paced sterile manufacturing environment. If you’re a Qualified Person ready for the next step in your career, apply today!

Seniority level

  • Seniority level

    Mid-Senior level

Employment type

  • Employment type

    Full-time

Job function

  • Job function

    Quality Assurance and Manufacturing

  • Industries

    Pharmaceutical Manufacturing and Biotechnology Research

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Posted: August 14th, 2025