Full-time
Global R&D QA, R&D Quality Biotech Manager
Posted by Chiesi Group • Parma, Emilia-Romagna, Italy
About the Role
Who we are looking for
This is what you will do
Guarantee the compliance with EU and US regulations related to the application of the Good Manufacturing Practices for gene editing and biological products for clinical trials.
You will be responsible for
- QA GMP reference in Project Teams related to gene editing/biological products for clinical trials
- QA oversight on quality documentation (review and approval of master batch record, executed batch record) related to the project assigned
- QC oversight on external su...
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