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Posted on 19 Aug, 2025
In Office
Job Description | Responsibilities
- Ensure QMS and cGMP compliance in PDL
- Support scale-up,validation and placebo batch execution
- Handle tech transfer from regulated sites to plant
- Review BMRs,protocols,deviations and reports
- Coordinate with QA,QC,production,R&D and Planning
- Monitor new product launch and trail batches
- Manage data and e-DMS/e-TMS systems
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Production / Manufacturing, IT Software Programming / Analysis / Quality / Testing / Training
- Job Role - Team Lead / Tech Lead, Head - Product Design & Development
- Employment type - Full Time - Permanent
- Work Mode - In Office
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
QMS
cGMP
Tech Transfer
Vlidation
BMR
Deviation
e-DMS