Associate Director, Quality Auditor, GVP
GSK · United Kingdom · GB
Quality Improvement
Remote
Pharmacist
Demand72
Career growth68
Healthcare fit62
Remote potential50
5-year outlook
Senior pharmacovigilance quality roles typically offer competitive compensation and can progress toward Director-level QA/compliance positions; exact salary depends on location and experience.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-09-28
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United Kingdom
- License jurisdiction
- GB
- Profession fit
- Pharmacist
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying if you have pharmacovigilance, quality assurance, or clinical research experience and want a senior non-clinical pharma compliance career; otherwise the experience barrier is high.
Who should apply
Pharmacists, physicians, or life sciences graduates with pharmacovigilance, drug safety, clinical research, or quality assurance backgrounds seeking senior pharma QA roles.
CV angle
Frame clinical experience around drug safety, adverse event reporting, regulatory compliance, audit/inspection support, CAPA, and cross-functional collaboration; quantify any quality or compliance projects.
Skills to highlight
- Pharmacovigilance
- GVP
- Quality Auditing
- CAPA
- Regulatory Compliance
- Risk Management
- Stakeholder Management
- Data Analysis
Role summary
Lead global pharmacovigilance audits, ensure compliance with GVP regulations, drive CAPAs and quality improvements, and support regulatory inspections within GSK R&D.
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