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The job in short
Pharma and medical device quality assurance validation documentation.
Compliance
Details
- Found
- 9 d ago · posted 2026-10-14
- Location as listed
- Pardi, Gujarat, India
- Role
- Quality Engineer
- Source
- The company’s own careers site
Full description
0-2
year experience in Medical Device/Pharma industry.
Job
Responsibility
- Monitoring
of qualification and validation activities.
- Preparation
of technical files and related documentation.
- Preparation
and review of qualification & validation protocols and reports.
- Review
of raw data, including analytical reports, BMRs, job cards, batch release
certificates, data mapping reports, etc.
- Support validation
activities across multiple manufacturing segments
Requirements
•
Qualification & Validation (IQ/OQ/PQ)
•
Technical Documentation & Technical File Preparation
•
Protocol and Report Preparation & Review
•
Data Review & Documentation Verification
•
GMP Compliance & Regulatory Documentation
•
Batch Manufacturing Records (BMR) & Analytical Report Review
•
Cross-functional Coordination & Validation Support