Job Title: Regulatory Affairs Intern
Location: Gurgaon, India
Summary:
Philips India is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our dynamic team in Gurgaon. This internship offers an exceptional opportunity for students pursuing a degree in Life Sciences or Biotechnology to gain hands-on experience in the regulatory landscape of the medical device industry. As an intern, you will support our Regulatory Affairs department in ensuring compliance with key regulations such as PC-PNDT and AERB, contributing to the smooth and efficient operation of our Health Systems business. If you are a proactive learner with a strong interest in regulatory compliance and are based in the Delhi NCR region, we encourage you to apply!
About Philips India:
Philips is a leading health technology company focused on improving people’s health and enabling better outcomes across the health continuum from healthy living and prevention, to diagnosis, treatment and home care. Philips leverages advanced technology and deep clinical and consumer insights to deliver integrated solutions.
Role Overview:
As a Regulatory Affairs Intern, you will play a vital role in supporting Philips India’s compliance efforts related to medical devices. Your primary focus will be on assisting with regulatory requirements for devices governed by the PC-PNDT Act and AERB regulations. You will be responsible for tracking compliance processes at various levels and supporting the streamlining of Regulatory Affairs activities. This internship will provide you with valuable exposure to the complexities of medical device regulations and the opportunity to contribute to a global leader in health technology.
Key Responsibilities:
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PC-PNDT Compliance Support:
- Track PC-PNDT approval processes at the state and district levels.
- Assist in establishing documentation and workflows for the sale, supply, and demonstration of regulated medical devices.
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AERB Regulatory Process Support:
- Monitor and support approval processes under AERB guidelines.
- Assist in ensuring compliance for radiation-related medical products.
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Regulatory Affairs Operations:
- Consolidate and review compliance-related activities.
- Support ongoing regulatory audits, documentation, and submissions for Philips India Ltd (Health Systems).
Eligibility & Qualifications:
- Currently pursuing a Bachelor’s or Master’s degree in Life Sciences, Biotechnology, or a related field.
- Must be able to commit to a full-time internship (5 days/week) from September–December 2025.
- Must be based in the Delhi NCR region and able to work onsite at our Gurgaon office 3 days per week.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Detail-oriented and highly organized.
- Basic understanding of regulatory principles is a plus.
Work Model:
Philips embraces a collaborative hybrid work model, providing flexibility while fostering teamwork and innovation. For this internship:
- You will be required to work from our Gurgaon office 3 days per week.
- The remaining workdays can be performed remotely.
Why Join Philips India?
This internship offers a unique opportunity to:
- Gain practical experience in the field of medical device regulations.
- Work directly with PC-PNDT and AERB regulatory frameworks.
- Receive mentorship and guidance from experienced regulatory professionals.
- Contribute to a global leader in health technology.
- Develop a strong foundation for a future career in Regulatory Affairs, Quality Assurance, or Compliance.
Application Instructions:
If you meet the qualifications and are excited about the opportunity to contribute to Philips India as a Regulatory Affairs Intern, we encourage you to apply. Please submit your resume and a cover letter highlighting your relevant skills and experience.