Quality Systems Coordinator - Denmark - 12 Months Contract
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Quality Systems Coordinator to join their new and exciting large-scale CAPEX investment programme. With a mission to provide process development and cGMP production in cell culture, microbial fermentation, and gene therapies, this is an outstanding opportunity make a genuine contribution to the biopharmaceutical industry.
Responsibilities include:
- Vendor Assessment program management
- Support vendor PQA visit plan development
- Follow up with outstanding items.
- Support vendor visit summary report process.
- Monitoring and reporting of change control completion
- Maintenance of Quality Risk Register
- Development and maintenance of Quality metrics and trending
- Coordinate internal and external training.
- General support for PQA organisation (eg. audit readiness, tasks to support the different PQA Leads)
- Action tracking from team meetings
Key requirements include:
- Knowledge of ASTM- E2500 or similar qualification projects preferable
- Knowledge of Biopharmaceuticals beneficial
- General computer experience including Excel and PowerPoint
- Experience with complex projects and working in or around operating facilities.
If this role is of interest, please apply now!
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