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Philips India is inviting applications for the role of Regulatory Affairs Intern in Gurgaon. This is a unique opportunity for Life Sciences and Biotechnology students to gain hands-on experience with regulatory processes in the healthcare and medical devices sector.
As a global leader in health technology, Philips is dedicated to improving lives through meaningful innovation. This internship will expose you to regulatory frameworks such as PC&PNDT and AERB regulations, making it an ideal steppingstone for those aspiring to work in Regulatory Affairs for medical devices.
Key Responsibilities
As a Regulatory Affairs Intern at Philips India, your role will include:
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- Tracking and establishing processes for PC&PNDT regulations at district and state levels for the sale, supply, and demonstration of medical devices.
- Tracking and establishing processes for AERB regulations at district and state levels for medical devices governed under PC&PNDT guidelines.
- Consolidating, reviewing, and supporting activities under the Regulatory Affairs function of Philips India Ltd (Health Systems division).
Who Can Apply?
You’re the right fit if you meet the following criteria:
- Currently pursuing a degree in Life Sciences or Biotechnology.
- Able to commit from September to December 2025, 5 days a week.
- Based in Delhi/NCR (3 days in-office presence required).
Benefits of Joining Philips India
- Work with a global healthcare technology leader.
- Gain real-world exposure to Indian regulatory frameworks.
- Enhance your career prospects in Regulatory Affairs.
- Hybrid experience: 3 days in-office, 2 days remote.
Application Process
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