Compliance Documentation Lead - Greece - 12-Month Contract
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Compliance Documentation Lead 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.

REQUIREMENTS:

Solid technical background and experience
5 years minimum experience in brown field projects
Pharma experience preferred, not a requirement
Work experience with Kneat or similar test documentation systems
Good communication skills in Danish and English
If this role is of interest to you, please apply now!
The candidate must have the rights to work in the location stated in the job advert.
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Provide engineering support related the day-to-day activities within Plant Engineering, including, support of CMMS Work Orders, Requests, update Job Plan’s and changes.
Support of TrackWise, change orders, deviations and CAPA’s.
Drive the interaction with FDBD Quality department through approval process of documents and Change Management requests.
Support transfer of test documentation to Kneat.