Qualification: B.Pharm/M.Pharm/Life Sciences/Medical Devices or any relevant Science graduate.
Required Skills:
✔ ISO 13485
✔ EU MDR (2017/745)
✔ CDSCO Regulations
✔ ISO 14971 (Risk Management)
✔ Technical File & Device Master File (DMF) Preparation
If you're passionate about Medical Device Regulatory Affairs, we'd love to hear from you
Pay: ₹500,000.00 - ₹650,000.00 per year
Advantages:
- Provident Fund
Ability to commute/relocate:
- Chakan, Pune, Maharashtra: Reliably commute or planning to relocate before starting work (preferred)
Experience:
- ISO 13485: 8 years (preferred)
- EU MDR: 8 years (preferred)
- CDSCO Regulation: 8 years (preferred)
- SO 14971: 8 years (preferred)
- Manufacturing: 8 years (preferred)
- Medical Device: 5 years (preferred)