Senior CQV Coordinator
Our client is preparing a major wave of qualification activities across three aseptic filling lines and is seeking an experienced CQV Coordinator to oversee planning, execution, and cross‑functional alignment. You will act as the central point of coordination for a team of around 10 engineers/technicians, ensuring qualification activities run smoothly, deviations are managed proactively, and communication flows clearly between stakeholders.
This role is ideal for someone who thrives in fast‑moving GMP environments, understands the realities of aseptic operations, and can represent senior leadership in key meetings.
Key Responsibilities
- Coordinate all qualification activities across three aseptic filling lines.
- Lead and organise daily/weekly planning with CQV, production, QA, and engineering teams.
- Represent the project lead in critical meetings, including:
- Qualification feedback sessions
- Planning and scheduling meetings
- Deviation and non‑conformity reviews related to qualification
- Ensure alignment between teams and maintain clear communication channels.
- Track progress, risks, and resource needs across the 10‑person CQV team.
- Support documentation, readiness checks, and inspection‑aligned qualification standards.
- Maintain a strong on‑site presence to ensure issues are escalated and resolved quickly.
Profile
- Strong experience in CQV, aseptic operations, or sterile manufacturing.
- Proven ability to coordinate multi‑line qualification activities.
- Comfortable managing or guiding a team of ~10 people.
- Excellent communication and stakeholder‑management skills.
- Fluent French is mandatory.
- Able to be on‑site most of the week (with some flexibility).
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