Qualified Person (QP) – Pharmaceutical Manufacturing & Quality

Qualified Person (QP) – Pharmaceutical Manufacturing & QualityIndustry: Global Pharmaceuticals / Life SciencesLocation: London, United Kingdom (On-site / Manufacturing & Corporate Quality Office)Type: Full-Time, PermanentSalary Band: £90,000 – £110,000 + BenefitsExperience Level: Senior (8–15 Years)The Role (Why This Exists): We are supporting a global pharmaceutical organisation operating in highly regulated UK and EU markets, seeking a Qualified Person (QP) to take full legal and technical ownership of batch certification, GMP compliance, and regulatory alignment across UK and European operations.This is a hands-on, accountable QP role where you act as the final legal authority between manufacturing and patient release.What You’ll Be Accountable For:Batch Certification & Manufacturing Oversight:Legally certify pharmaceutical batches in line with UK law and EU DirectivesEnsure manufacturing and testing activities comply with GMP and Marketing AuthorisationsOversee internal and third-party manufacturing partnersQuality Systems & Compliance Leadership:Own and maintain the Quality Management System (QMS)Lead governance of:DeviationsCAPAsChange ControlsRisk AssessmentsAnnual Product Reviews (APR)Self-Inspections & AuditsRegulatory & Authority Engagement:Act as a senior quality interface with MHRA and EU regulatory bodiesSupport inspections, manufacturing line approvals, and regulatory submissionsCross-Functional Leadership:Partner with QA, Manufacturing, Regulatory Affairs, and Supply Chain teamsLead GMP training and SOP development across UK/EU operationsQuality Risk & Patient Safety:Own recall processes and escalation pathwaysProactively identify and mitigate quality risks impacting patient safetyMust-Haves (Non-Negotiable):Eligible to act as a Qualified Person under UK law (Directive 2001/83/EC)4–5+ years operating as a named QP in regulated pharmaceutical environmentsDegree in Pharmacy, Chemistry, Biology, or related life sciencesDeep hands-on experience with: GMP manufacturing operations; Batch certification and regulatory documentation; Pharmaceutical Quality SystemsExperience within large or multi-site pharmaceutical organisationsNice-to-Haves:UK/EU multi-site manufacturing oversightThird-party manufacturer and Quality Agreement managementRegulatory audit leadershipWork Environment:On-site role spanning manufacturing facilities and corporate quality office (London)Close collaboration with production, QA, regulatory, and leadership teams2–3 stage interview process, including technical and compliance assessmentCompliance & Eligibility:UK Citizens / Permanent Right to Work requiredNotice Period: 30–45 days preferredThis is a site-based role (not remote / hybrid)Application Process: To apply, please submit your CV and a cover letter detailing your relevant experience and qualifications for the role. Applications will be reviewed on a rolling basis, so early submissions are encouraged.Equal Opportunity Employer: We value diversity and are committed to creating an inclusive work environment. We encourage applicants from all backgrounds to apply.Contact: Elvis Eckardt

Created: 2026-01-18