Philips India, a global leader in health technology, is hiring Regulatory Affairs Interns in Gurgaon. This internship offers aspiring life sciences and biotechnology students the chance to gain real-world regulatory affairs experience. You’ll work on compliance with PC&PNDT and AERB regulations, collaborate with expert teams, and help streamline regulatory processes for medical devices.
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If you are looking to build your career in regulatory affairs and contribute to advancing healthcare compliance in India, this role is your perfect opportunity.
Key Responsibilities
As a Regulatory Affairs Intern, you will:
- Track and establish processes for PC&PNDT regulations at district and state levels for medical device sales, supply, and demonstrations.
- Track and establish processes for AERB (Atomic Energy Regulatory Board) regulations at district and state levels.
- Consolidate, review, and establish activities under the Regulatory Affairs function of Philips India Ltd.
- Support documentation, compliance, and coordination across internal teams.
Qualifications
You’re the right fit if:
- You are pursuing a degree in Life Sciences, Biotechnology, or related fields.
- You can commit full-time from September to December 2025 (5 days/week).
- You are based in Delhi/NCR and available for 3 days of in-office presence weekly.
Benefits of Joining Philips India
- Hands-on exposure to healthcare regulations and compliance frameworks.
- Opportunity to work with global regulatory affairs professionals.
- Hybrid working model: 3 days in office, 2 days flexible.
- Experience with leading-edge medical devices and compliance requirements.
- Networking and career growth opportunities in regulatory affairs and medical technology.
How to Apply

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