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Il y a 2 mois
At Indegene, we're committed to creating a dynamic work environment that fosters growth and development. As a Regulatory Affairs Consultant, you'll play a crucial role in supporting our medical device clients with regulatory expertise.
Key Responsibilities:- Provide expert regulatory advice on medical device promotion in France and EU regions
- Review and approve promotional materials for medical devices in France
- Develop and implement regulatory strategies for medical device projects
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements
- Stay up-to-date with changing regulatory landscapes and provide guidance to the team
- Life science graduate or post-graduate degree
- 2-3 years of experience in medical device regulatory affairs, with a strong foundation in device promotion and scientific communication
- Experience with Germany, EU, and global medical device regulations
- Strong analytical and problem-solving skills
- Excellent communication and collaboration skills
We offer a comprehensive benefits package, including medical, regulatory, and editorial review services, as well as operations support from a team of 350+ experienced professionals. If you're passionate about regulatory affairs and want to make a meaningful impact, we encourage you to apply.