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The role involves preparing documentation, monitoring technical project progress, and ensuring compliance with regulatory requirements in the biopharma sector.
Candidates should have 5-7 years of relevant experience and a strong understanding of quality and validation processes.
This position offers a dynamic work environment with the potential for contract extension beyond 12 months. xcfaprz
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Remote working/work at home options are available for this role.
Sprachkenntnisse
- English
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