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The company is located in Amsterdam and is active in Consumer Health. They have a diverse product portfolio. The company is active in more than 25 countries.
Role Description
We are looking for a full time Quality/Regulatory Affairs Manager for the whole product portfolio who has knowledge in regulations and other standards. You will report directly to the director. The company is a midsize Medical Device company so you will be responsible on a broad aspect. You will collaborate with the Supply Chain department but also with the Sales and R&D department.
Requirements
Your qualifications & experience
You will be responsible for the registrations like MDD, 93/42/EEC, MDR and ISO 13485
Doing the total registrations and create the technical documentations
Build up a network in Notified Bodies and other authorities to create a global market access
guide Audits with the Notified Body and other clients
Your profile:
Master Degree in Pharmaceuticals or Life Science related
8+ years experience in similar role with a preference in Consumer Healthcare
punctual and solution-oriented mind set
Strong interest in consumer healthcare products
Fluent in Dutch and English
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Czy chcesz otrzymywać oferty pracy na podobne stanowiska?