Qa Executive

Role summary

• 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, professional
• Analysing and Logical sequencing ability
• Knowledge on Regulatory Guidelines

Experience:

• 2-5 years of experience in Medical Device and Pharma documentation