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Biotech Validation Professional
1 week ago
About This Role
Key Responsibilities:- Resolving technical issues encountered during study execution
- Engagement with production, maintenance, and quality representatives in assigned areas of operations during execution of cycle development and performance qualification activities
- Technical input into quality notifications by authoring/reviewing/approving investigations
The successful candidate will have considerable experience in a comparable role, with experience operating as an individual contributor adding value to the business in a GMP manufacturing setting.