- 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
- 2 year experience in Medical Device / Pharma industry.
Job Summary
Senior Officer QA - Pardi, Gujarat, India. 0-2 year experience in Medical Device/Pharma industry.
Responsibilities
- 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
Job Type
Full time
Location
Pardi, Gujarat, India
Industry
Medical Device
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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