Medical device regulatory affairs recruitment is one of three core areas of business for Elemed. We are proud to work with some of the leading medical device and IVD companies in Europe, and have spent the last 7 years forming long-lasting partnerships which have continued to secure them with the most exciting talent in the market.
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What medical device regulatory affairs recruitment services do we offer?
Elemed is a recruitment agency that is dedicated to finding exceptional regulatory affairs professionals for medical device and IVD organisations. We offer services including permanent recruitment, headhunting, executive search and consulting.
One of the reasons why we’re such a successful regulatory affairs medical device recruitment agency is that we work in close collaboration with our clients’ internal teams, from human resources and talent acquisition to the team managers and regulatory affairs directors.
Some of companies we work with include:
- Global MedTech corporations
- International MedTech organisations
- Medical device and IVD manufacturers
- Startups and SMEs
- Contact research organisations
- Notified Bodies
Our dedication to working exclusively with the medical device and IVD industry also means that we are experts in the complexities and nuances of regulatory affairs. We know CE marking from PMA submissions and MDD from MDR. We understand the various therapeutic areas relating to medical devices and IVDs, and what our regulatory affairs candidates’ experience means for the companies we represent and the roles we recruit for.
What types of medical device and IVD regulatory affairs jobs do we recruit for?
We specialise in medical device regulatory affairs recruitment for all kinds of regulatory affairs jobs, with a dedicated team of recruiters who know the medical device and IVD industry inside out. We have a network of 1000s of talented, qualified regulatory affairs professionals across all seniorities, which means we’re able to recruit for the most difficult-to-fill roles with truly exceptional regulatory affairs talent. Our ever-expanding database of the world’s leading medical device and IVD regulatory affairs professionals means that we can source and present fantastic candidates for regulatory affairs jobs at the following seniority levels and functions:
Medical device and IVD regulatory affairs roles and seniorities:
- Global Director Regulatory Affairs
- Vice President Regulatory Affairs
- Regulatory Affairs Director
- Head of Regulatory Affairs
- Regulatory Affairs Specialist
- Regulatory Affairs Associate
- Senior Regulatory Affairs Manager
- Regulatory Affairs Manager
- Remote Regulatory Affairs
- Risk Management Specialist
- Regulatory Affairs IVD Consultant
- Product Assessor
- RAQA Manager
- Regulatory Affairs Team Manager
- Clinical & Regulatory Affairs Administrator
- Global Regulatory Intelligence Manager
Medical device and IVD product types:
- Class I, II, III medical devices
- Software as a medical device and digital health
- Active and non-active medical devices
Why should I use Elemed as my medical device regulatory affairs recruitment agency?
Unlike other recruitment agencies, we only have one industry focus – medical devices and IVDs. This 100% focus on medical technology means that there is no one else recruiting deeper into the MedTech skillsets of regulatory, quality and clinical.
Our network of medical device regulatory professionals is vast – we work with thousands of exceptional regulatory affairs professionals who are actively looking for their next role or who will be ready to pursue something new if it’s the right role for them.
Not sure whether permanent or interim medical device regulatory affairs recruitment is right for your company? We can also help connect you with fantastic regulatory affairs consultants and freelancers via our Elemed Interim division.
We are also award winners, having been recognised as the Best International Recruitment Agency at the Recruiter Awards 2021
Latest medical device regulatory affairs jobs
CLOSED - Executive Director Regulatory Affairs - Lead International RA for a major Corporation! REMOTE IN United Kingdom, France, Netherlands, Germany, Italy or Spain GBRActive
CLOSED - Senior Regulatory Affairs Specialist Remote, ISLActive
PMS Director- Lead Global Projects Zürich, ZHActive
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