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AI based regulatory approval software for medical device companies

Regulatory Affairs Manager (Medical Device or Pharma)

₹60,000 – ₹1L
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The Regulatory Affairs Manager will play a key role in research and synthesis of medical device and pharmaceutical registration guidelines globally. The individual will work with the lead technical analyst.

Duties & Responsibilities:
• Hire and manage team of regulatory experts in India.
• Conduct research into regulatory requirements for medical devices, cosmetics, and pharmaceuticals in countries around the world.
• Read the regulations and summarize key elements in a particular format.
• Drive content development. Leverage external network of local regulatory
consultants to fill any gaps in the data.
• Analyze changes in device requirements and communicate changes to the
development team.
• Manage contracts with local experts, budget follow-up and monitoring.

RegDesk at a glance

AI based regulatory approval software for medical device companies

RegDesk focuses on Biotechnology, Healthcare, Pharmaceuticals, and Medical Devices. Their company has offices in Philadelphia. They have a small team that's between 11-50 employees.

You can view their website at http://www.regdesk.co or find them on Twitter and LinkedIn.

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