Regulatory Affairs Intern
- Gurgaon, Haryana
- Training
- Full-time
1. Tracking and establishing Process of PC& PNDT (Pre Conception & Pre Natal Diagnostic Techniques) regulations at the District / State level for the sale / supply / demonstration of medical devices that come under PC& PNDT regulations.
2. Tracking and establishing Process of AERB (Atomic Energy Regulatory Board) regulations at the District / State level for the sale / supply / demonstration of medical devices that come under PC& PNDT regulations.
3. Consolidating, Reviewing and Establishing activities under Regulatory Affairs function of Philips India Ltd (HS).You're the right fit if:
1. You are pursuing a degree in Life Sciences, Bio Technology.
2. You can commit for Sep- Dec 2025 for 5 days a week
3. Based out of Delhi /NCR as we require 3 days in-office presence.How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.Indicate if this role is an office/field/onsite role.About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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