Qualified Person (QP) - Pharmaceutical Manufacturing
Core
Ensuring quality, safety, and compliance of medicinal gases manufactured at the Templemars site in France.
Role type
Qualified Person (QP) for pharmaceutical manufacturing
Builds
Medicinal gases for commercial distribution
Domain
Pharmaceutical manufacturing / Industrial gases
Required skills
EU GMP knowledge, batch certification, regulatory inspection coordination, quality management system maintenance, cross-functional collaboration
Preferred skills
Experience with CE-marked medical devices, stakeholder management
Technologies
GMP systems, Pharmaceutical Quality Management System
Responsibilities
Certifying and releasing batches of medicinal gases, ensuring compliance with EU/French regulations, leading internal and external audits, preparing for regulatory inspections, maintaining the Pharmaceutical Quality Management System, escalating quality issues to the Pharmacien Responsable
Seniority
Mid-level, hands-on IC
