Regulatory Affairs Specialist
vor 1 Woche
Job Summary:
We are seeking a highly experienced Global Regulatory Affairs Manager to join our team at Elemed. As a key member of our global regulatory team, you will be responsible for enabling and navigating product launches in various markets globally, with a focus on international markets.
Key Responsibilities:
- Keep yourself and your colleagues up-to-date with the latest regulatory developments in key global markets (Asia-Pacific, North America, and the EU)
- Identify, review, advise, and present plans of action to internal teams globally of the latest regulatory changes in the market and their wider impact on market access and product compliance
- Create internal and external reports for the global headquarters
Requirements:
- At least 12 years' experience in Regulatory Affairs with a Medical Devices Manufacturer
- Experience within the medical device industry is required
- Fluent written and spoken English
About Elemed:
We serve within the Medical device, diagnostic, and combination device arena, working with managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow.
What We Offer:
We are a leading recruitment agency in the medical device industry, and we are committed to finding the best talent for our clients. We offer a unique opportunity to work with a global team of experts and to contribute to the development of innovative medical devices.
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