Job Description
Batch record review and support of the release process.
Quality on the Shopfloor
Approval of CAPAs & Deviations, you are responsible for managing minor deviations and resulting CAPAs, ensuring compliance with GMP
standards, and supporting quality investigations. You play a key role in executing structured simple Root Cause Analyses (RCA), tracking CAPA
effectiveness, and supporting audit readiness. Your work contributes to maintaining product quality, reducing recurring issues, and ensuring continuous
process improvements within the organization.
Responsibilities:
1. Batch Record Review
- Batch record review
2. Release Preparation
- Support the release preparation activities, in order to generate a complete batch dossier package
3. Deviation Management
- Review, assess, and close minor deviations. - Perform basic Root Cause An...
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