Philips Regulatory Affairs Specialist 

India, Maharashtra, Pune 

72171999

Your role:

• Be recognized as a key talent in International Regulatory filings and procedures.

• Be considered a key regulatory point person in Centralization of Regulatory Operations and enable the regulatory compliance in Markets where Philips products are commercialized.

• Be an impactful member of the Regulatory Affairs (RA) team and trusted by management as an independent regulatory team member on multiple projects simultaneously.

• Assist in building center of excellence for RA operation with purpose to centralize regulatory operations to enhance compliance, efficiency, and global market readiness.

• Function on a multi-geography basis, prioritize, conduct team meetings, and meet project deadlines.

(4 x bullets max)
1. Experience- 6+yrs of experience in international regulatory affairs
2. Skills- Regulatory Affairs, Dossier Preparation, experience in Class, I, II.
3. Education- Any Engineering Degree, prefer in Biomedical Engineering
4. Anything else-

Good Interpersonal skill, holding strong communication skills.

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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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .