Regulatory Affairs Specialist: Policy Development and Compliance Expert
hace 1 mes
As a Regulatory Affairs Specialist at Philips, you will play a vital role in shaping the company's regulatory processes and ensuring compliance with medical device regulations.
The ideal candidate will have a strong background in design controls, medical device regulations, and international registrations. Experience in preparation and submission of international documents, as well as supporting international registrations, is also essential.
We offer a competitive salary range of $80,000 - $120,000 per year, depending on experience and qualifications. Additionally, you will have opportunities to develop your full potential with flexibility, encouragement, and opportunities for growth.
About This Role:
This position involves evaluating changes to standards and regulations, informing teams, and maintaining project data. You will also be responsible for implementing medical device standards, organizing archives, and training personnel on regulatory affairs.
Requirements:
- Bachelor's degree in a technical discipline or equivalent experience
- Minimum 3-5 years of experience in the medical device or pharmaceutical industry
- Excellent working knowledge of medical device regulations, FDA Law, MDR, and other global laws
Benefits:
- Meaningful work focused on innovative solutions
- Opportunities to develop your full potential
- Chance to improve the world through your work
About Philips:
Philips is a leading health technology company that creates customer-first health technology solutions. We are committed to creating a healthier society and improving the health and well-being of billions of people.
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