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Medical Device Regulatory Consultant
2 months ago
Indegene is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Medical Device Regulatory Consultant, you will be responsible for providing expert regulatory advice to our clients and ensuring compliance with UK medical device regulations.
Key Responsibilities- Provide guidance on UK medical device promotion regulations and standards.
- Review and approve medical device promotional and non-promotional materials for compliance with UK regulations.
- Collaborate with internal and external stakeholders to ensure regulatory requirements are met.
- Analyze complex regulatory issues and propose effective solutions.
- Life science graduate or post-graduate degree.
- Regulatory Affairs/Compliance professional with experience in medical device regulations and standards.
- Strong foundation in medical device regulatory affairs, with experience working with a range of medical devices.
- Ability to build and maintain strong working relationships with internal and external contacts.
- Ability to analyze complex regulatory issues and propose effective solutions.
Indegene is a technology-led healthcare solutions provider that partners with life science organizations to provide effective, AI-enabled material review and compliance solutions. We offer comprehensive medical, regulatory, and editorial review services, as well as operations support through a team of 350+ experienced professionals.
