CQV Quality Lead – Onsite in Limerick (Pharma)
Role Description & Technical Scope
PM Group is seeking an experienced Quality Lead (CQV) to oversee commissioning, qualification, and validation activities onsite in Limerick. The role requires directing QA processes, approving CQV documentation, and ensuring compliance with GMP and regulatory expectations across complex pharma projects.
The ideal candidate has at least 8 years in pharma/biotech manufacturing, a related bachelor’s degree, and strong stakeholder management skills to coordinate cross-functional teams and client
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Key Details
- Date Posted: 25 Oct 2026
- Location: limerick
- Employment: Permanent
- Workplace: Hybrid
- Domain: Business Development & Strategy
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PM-Grou
Verified Tech EmployerEnterprise technology firm or security consultancy operating across the UK digital defense ecosystem.
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