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Working at Meditrade

At Meditrade Group we are proud of the work we do because we develop and distribute products that protect and improves people’s health. Our company fosters a diverse culture where our employees are encouraged to learn, develop professionally, and succeed. At Meditrade Group we value hardworking and ambitious individuals that can share their ideas, skills and knowledge.

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Regulatory Affairs Manager for Medical Devices (m/f/d)

Regulatory Affairs
Berlin, Neubrandenburg
Kiefersfelden

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Responsibilities of the position:

Creation, maintenance and updating of technical documentation for medical devices
Assessment of the conformity of the documentation with the applicable regulations
Independent execution and maintenance of the associated product approval/registration
Internal contact person for regulatory issues
Maintaining and further developing the existing QM system in close cooperation with quality management.

Your profile:

Professional experience in the field of Regulatory Affairs, particularly in relation to working with Class I and IIa medical devices
Extensive knowledge of medical devices and relevant national and international standards and regulations such as EN ISO 13485:2016 or Regulation (EU) 2017/745 (MDR)
Affinity for creating regulatory-relevant documentation
Their work style is characterized by extreme diligence, independence, and a high degree of conscientiousness and responsibility.
Very good MS Office skills
Excellent English skills, both spoken and written.

Our range:

A responsible and challenging role in a quality-conscious family business
Attractive compensation

Please send your complete application documents, including your possible start date and salary expectations, preferably in .pdf format, to Viktoria Burley at viktoria.burley@meditrade.de

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