Deputy Qualified Person (QP) – Sterile Manufacturing

About the role

We are seeking an experienced Deputy Qualified Person to support batch certification and release in a sterile manufacturing environment. This hands‑on position works closely with production, quality control and release teams, offering high visibility across the site.

Key responsibilities

• Support the QP in batch certification and release, including batch record review and GMP documentation approval.
• Manage deviations, investigations, CAPAs and Change Controls, ensuring GMP compliance.
• Provide senior QA support to sterile/aseptic manufacturing operations and contribute to continuous improvement on the shop floor.
• Assist with inspections, customer audits and inspection readiness, acting as the quality interface between Production, QC, QA, Release and external customers.

Required profile

• Several years of operational QA experience in pharmaceutical manufacturing, with recent sterile/aseptic experience.
• Substantial experience in batch review, disposition and release, and prior involvement in QP activities.
• Strong knowledge of deviations, CAPA, Change Control and GMP compliance.
• Fluent French and good professional English.

Required skills

• Batch certification and release
• GMP documentation and batch record review
• Deviation, CAPA and Change Control management
• Sterile/aseptic manufacturing processes