Quality Systems Coordinator- Life Sciences- Contract- Denmark
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Quality Systems Coordinator to join them on their new expansion project. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
As Quality Systems Coordinator, you will be responsible for the delivery of Quality Systems Coordinator activities on a complex drug manufacturing extension project.
Quality Systems Coordinator Responsibilities:
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
About you:
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.
Are you a good fit for a Quality Systems Coordinator? Get in touch with us today.
The candidate must have the rights to work in the location stated in the job advert.
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