Qualified Person (QP) – QA Operations Manager

Qualified Person (QP) – QA Operations Manager

Qualified Person (QP) – QA Operations Manager

2 weeks ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Direct message the job poster from Meet Life SciencesQA Operations Manager and Qualified Person (QP)Location:

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

Pharmaceutical ManufacturingEmployment Type:

Full-timeAbout the RoleWe are partnering with a well-established pharmaceutical manufacturing company to hire a

QA Operations Manager and 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 ResponsibilitiesAct as Qualified Person (QP) for batch release of sterile pharmaceutical productsLead and mentor two QA Associates to ensure efficient and compliant operationsOversee QA processes, including deviation handling, CAPA, change control, and QMS updatesEnsure site-wide GMP compliance and support audit readiness activitiesRepresent QA during external inspections and audits (approximately 4–5 per year)Collaborate cross-functionally with manufacturing, supply chain, and regulatory teamsRequired QualificationsCurrent eligibility to act as a Qualified Person (QP) in the UK3–4 years of active QP experienceStrong background in quality assurance within a GMP-regulated environmentExperience in sterile manufacturing is essentialSolid understanding of QMS, batch documentation, and regulatory requirementsPrior experience managing or mentoring junior QA team membersAbility to work on-site three days per week as part of a hybrid modelPreferred QualificationsFamiliarity with MHRA and EMA regulatory expectationsExperience representing QA during external audits or inspectionsExposure to sterile fill/finish operations or aseptic processesStrong communication, leadership, and problem-solving skillsAdditional InformationHybrid working model: minimum 3 days per week on-siteStart 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 levelEmployment type

Employment type Full-timeJob function

Job function Quality Assurance and ManufacturingIndustries Pharmaceutical Manufacturing and Biotechnology ResearchReferrals increase your chances of interviewing at Meet Life Sciences by 2xGet notified about new Quality Assurance Operations Manager jobs in

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