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Posted on 15 Apr, 2026
In Office
Job Description | Responsibilities
- To ensure cGMP compliance requirement as per Schedule M, WHO, other MO and regulated market guideline.
- Prepare and review of SOP, test protocols, reports, BMR/BPR/MFR, qualification protocol/report and other relevant document required for execution of manufacturing.
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Other
- Job Role - Other
- Employment type - Full Time
- Work Mode - In Office
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Assistant Manager
Monthly Closing
Finance Reporting
