Teamlead Regulatory Affairs

Our client, a global medical devices producer in east Gelderland, is looking for their next Teamlead Regulatory Affairs.

You would be leading a growing team of 6 and shaping the regulatory processes of the company. The company is very innovative and offers a dynamic and friendly work environment.

Your main tasks:

• Leading and developing a team of 6
• Developing global regulatory strategies and acting as Subject Matter Expert
• Ensuring the compliance of the documentation and processes in the department
• Acting as point of contact for other departments (clinical, quality, production…)
• Staying up to date with international regulations (MDR, FDA, Canada, China etc.)

Your profile:

• You possess a technical or scientific study in a university
• You have at least 5 years experience in Regulatory Affairs for medical devices
• You are an expert in medical devices regulations. Any international regulation is a plus
• You have a first leadership experience and like developping coworkers
• You are fluent in English and like working in international environment

What the company offers:

• 30 days vacation, good company benefits (bonus, pension scheme)
• A dynamic and friendly work atmosphere
• Career and personal developpement trainings

Wenn Sie Interesse an der Stelle haben, schicken Sie mir Ihren CV an claire.renouf@catalystcareers.com oder bewerben Sie sich hier.


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We aim to be an equal opportunity recruiter and we are determined to ensure that no applicant receives less favorable treatment on the grounds of gender, age, disability, religion, belief, sexual orientation, marital status, or race, or is disadvantaged by conditions or requirements.