Reference Number: JO-1908-435297
Regulatory Affairs Specialist
Job Type: Permanent
Job Title Regulatory Affairs Specialist
Location Leuven, Belgium (Office Based)
Are you a customer focused with strong communication skills?
Are you result driven?
This may be the right position for you!
Is one of larger company leading the market forward within the production, development & distribution of dental products. Looking for Regulatory Affairs Specialist to grow with the company and take into the future.
Responsible for legal product information and keeping this available when required
Working alongside with R&D department with new and existing product development
Maintaining CE marketing & QA departments under regulatory supervision
Aiding the company growth into the future with R&D department developing a product addressing the regularity strategies
Performing vigilance activities when required
Skills required & desired
Masters degree chemistry, biology, pharmacy, engineering
3 years experience in a similar role
Extensive knowledge of current mandatory legal documents
Knowledge of ISO standards (13485) (desired FDA CFR title 21)
MS Office alliterate
Fluent English required (additional language is a bonus)
Strong communication skills & customer focused
If you are successful you will receive a competitive salary & extra company benefit
All Candidates must have the right to work documents applicable to this role.
If you are interested in this role please apply using the link below or send your CV to Louise.King@medtechclinicalprofessionals.com
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