Quality Systems Coordinator
3 weeks ago
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 to 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 (e.g., 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
Seniority levelEntry level
Employment typeContract
Job functionQuality Assurance
IndustriesStaffing and Recruiting
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