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Magle Group isgrowing and we are looking Regulatory Affairs Specialist who is looking for a new challenge and who want to be part of a small butdynamic regulatory team. Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology.his role will focus on supporting ourmedical devices business and assure wecomply with all regulatory standards and guidelines applicable in our active markets. The Regulatory Affairs Specialist plays acrucial role in the submission, registration, and lifecycle management of our medical device products.
Key Responsibilities:
Qualifications:
Meriting:
If you find the above position interesting, itfits your experience and you want to join a company who has interesting journey ahead, we would love to hear from you. We are a value driven organization and we expectyou to share our passion to make an impact by making life better, therefore we also look to find a person who not only fit the qualifications but also shares our values and fit our organisation personal wise.
In this process we will have an continuous recruitment, please submit your CV and a short cover letter telling us why you find the position interesting. The position is placed at our office in Malmö and will be a full time position. To find out more about us please visit our group webb page. www.maglegroup.com