Qualified Person (QP) – Pharmaceutical Manufacturing & Quality
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Job Summary
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:Benefits
Experience Level: Senior (815 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 Youll 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)
45 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
23 stage interview process including technical and compliance assessment
Compliance & Eligibility:
UK Citizens / Permanent Right to Work required
Notice Period: 3045 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
Key Skills
- Sales Experience
- B2B Sales
- Primary Care Experience
- Biotechnology
- Account Management
- Territory Management
- Computer Literacy
- Outside Sales
- Biomedical
- Botox Experience
- negotiation
- Compounding Medications
About Company
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