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Posted on 5 May, 2025
In Office
Job Description | Responsibilities
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Oversee raw material testing and approvals
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Handle OOS/OOT investigations and CAPAs
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Review QC documents and reports
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Support audits and regulatory inspections
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Train and guide QC team
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Ensure safe and compliant lab practices
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Doctors / Medical Professionals / Clinical Research / Pharma Medical Affairs
- Job Role - Manager - Medical Affairs
- Employment type - Full Time - Permanent
- Work Mode - In Office
- Open To Hire - Differently Abled, Retired, Defence Veteran, Government Employees
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Strong knowledge of cGMP
Hands-on experience with HPLC
UPLC
UV
IR
Good communication and team management skills
