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Posted on 18 Mar, 2024
- Maintain pharmaceutical industry guidelines/trends, regulatory requirements, and applicable pharmacopoeia
- QC testing of raw materials / investigation / SAP protocol and Implement QC laboratory CAPAs
-Supervise, interprets and executes policies.
- Provide technical and compliance guidance to the QC laboratory analytical techniques and troubleshooting skills in UPLC/HPLC/AAS/UV/IR/KF/PSD etc.
- Must know cGMP, ICH, FDA, USP, EP guidelines.
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO, Biotech / Biopharmaceuticals
- Functional Area - Production / Manufacturing, Plant Engineering / Maintenance / Utility
- Job Role - Quality Assurance / Control - Manager
- Job level - Top Management
- Employment type - Full Time
- Work Mode - In Office
- Other Employee Benefits - NA
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
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