- Data collection, analysis and preparation of summaries for PSUR, Adverse Event Data, Literature, etc
- Change control Handling- follow-up until the change control process is complete
- Design and Development File/ Medical Device File : updated and maintained.
- Document and data Control
Skill required
- MS Word, Excel, skilled
- Analysing and Logical sequencing ability
- Knowledge on Regulatory Guidelines
Experience:
- 2-5 years of experience in Medical Device and Pharma documentation
📌 Qa Executive (Padra)
🏢 Care Group
📍 Padra
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