Advertisement
Philips, a global leader in health technology, is hiring a Regulatory Affairs Specialist in Pune. This role offers an exciting opportunity to be part of a central team driving regulatory compliance, international filings, and dossier preparation for medical devices. If you have 3–5 years of regulatory affairs experience and a passion for improving healthcare access, this position could be the next step in your career.
Key Responsibilities
As a Regulatory Affairs Specialist at Philips, you will:
- Act as a key regulatory point of contact for international submissions and compliance activities.
- Support the centralization of regulatory operations to enhance efficiency and market readiness.
- Prepare and review dossiers for Class I and Class II medical devices.
- Manage multiple projects across geographies while meeting strict timelines.
- Collaborate with cross-functional teams and participate in regular project meetings.
Qualifications
To be considered for this role, you should have:
Advertisement
- Experience: 3–5 years in international regulatory affairs.
- Technical Skills: Expertise in dossier preparation, regulatory submissions, and device classifications (Class I & II).
- Education: Bachelor’s or Master’s degree in Engineering (Biomedical preferred).
- Soft Skills: Strong interpersonal skills and excellent communication abilities.
Benefits of Working at Philips
- Work in a global healthcare technology company committed to improving lives.
- Be part of a Regulatory Affairs Center of Excellence with growth opportunities.
- Hybrid work model (minimum 3 days in office per week).
- Exposure to international regulatory frameworks and market compliance.
How to Apply
Advertisement
