Qualified Person (QP) – Pharmaceutical Manufacturing & Quality

Industry: Global Pharmaceuticals / Life Sciences

Location: London, United Kingdom (On-site / Manufacturing & Corporate Quality Office)

Type: Full-Time, Permanent

Salary Band: £90,000 – £110,000 + Benefits

Experience 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 Directives
• Ensure manufacturing and testing activities comply with GMP and Marketing Authorisations
• Oversee internal and third-party manufacturing partners

Quality Systems & Compliance Leadership:

• Own and maintain the Quality Management System (QMS)
• Lead governance of:
• Deviations
• CAPAs
• Change Controls
• Risk Assessments
• Annual Product Reviews (APR)
• Self-Inspections & Audits

Regulatory & Authority Engagement:

• Act as a senior quality interface with MHRA and EU regulatory bodies
• Support inspections, manufacturing line approvals, and regulatory submissions

Cross-Functional Leadership:

• Partner with QA, Manufacturing, Regulatory Affairs, and Supply Chain teams
• Lead GMP training and SOP development across UK/EU operations

Quality Risk & Patient Safety:

• Own recall processes and escalation pathways
• Proactively identify and mitigate quality risks impacting patient safety

Must-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 environments
• Degree in Pharmacy, Chemistry, Biology, or related life sciences
• Deep hands-on experience with: GMP manufacturing operations; Batch certification and regulatory documentation; Pharmaceutical Quality Systems
• Experience within large or multi-site pharmaceutical organisations

Nice-to-Haves:

• UK/EU multi-site manufacturing oversight
• Third-party manufacturer and Quality Agreement management
• Regulatory audit leadership

Work Environment:

• On-site role spanning manufacturing facilities and corporate quality office (London)
• Close collaboration with production, QA, regulatory, and leadership teams
• 2–3 stage interview process, including technical and compliance assessment

Compliance & Eligibility:

• UK Citizens / Permanent Right to Work required
• Notice Period: 30–45 days preferred
• This 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