Offer summary

Qualifications:

Bachelor's degree in a relevant field such as life sciences or engineering., Experience in regulatory affairs for medical devices is essential., Strong understanding of FDA and international regulations., Excellent communication and analytical skills are required..

Key responsibilities:

Ensure compliance with regulatory requirements for medical devices.

Prepare and submit regulatory documentation to authorities.

Collaborate with cross-functional teams to support product development.

Provide guidance on regulatory strategy and risk management.

Diapharm (www.diapharm.com) is a leading global consulting firm and service provider for the consumer healthcare and pharmaceutical industry. With around 100 employees at seven locations in Germany, the Netherlands, Austria and China, Diapharm provides consulting services to clients in strategic matters, assumes responsibility for regulatory, medical and scientific tasks, as well as for quality assurance. Diapharm supports manufacturers and distributors of medicinal products, medical devices and healthcare products throughout the world. Legal notice: https://www.diapharm.com/en/contact/legal-notice/ Privacy policy: https://www.diapharm.com/en/contact/privacy-policy/

Required profile