Regulatory Affairs Specialist - Ettlingen, Deutschland - NonStop Consulting
Beschreibung
This Medical Device company has recently been bought by new owners who are heavily investing in them. Opening new locations, state-of-the-art clean rooms, and are now focusing on digitalisation.Join this stable and secure company, and help make an impact
The role will be based on the creation and maintenance of technical documentation. Focusing on product approvals and monitoring/tracking the approval status. You'll be involved in maintaining and improving the labelling process and working with various teams in respect to labelling.
What're we looking for?
University degree (Uni, FH) with a technical orientation or comparable professional experience in the field of regulatory affairs
Minimum of 1 year of experience working in Regulatory Affairs in the Medical Devices industr
German and English fluency, both spoken and written (Documents are in German)
What we can offer you:
A secure job in a growing medium-sized company with an international focus
High design options and flat hierarchies
With us you can make a real contribution
Flexible working hours and working models
An intensive on-boarding and training program
For further details, please don't hesitate to reach out and contact Billy O'Brien, through the below channels, who is more than happy to answer any questions you may have
Recruiter:
Mr. Billy O'Brien
Phone:
EXT:
3369
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