Please refer to JobSuchmaschine in your application
Regulatory Affairs Specialist
- Support submission and approval of applications for marketing applications in Switzerland and International - Manage submission and approval of variations in Switzerland Assist/develop regulatory strategies - Participate in due diligence activities - Maintain information on submission status - Assure all regulatory files and HA correspondence are appropriately archived - Support Medical Affairs/Pharmacovigilance activities
Our client is a fast growing Pharmaceutical company
Excellent Regulatory Affairs Specialist opportunity
Minimum 1-2 years experience in regulatory affairs Experience with RA dossiers in Switzerland (experience with oral generics i.e. bioequivalence in Switzerland highly appreciated) Development and preparation of successful regulatory strategies Experience with regulatory agency interactions eCTD experience Experience with Medical Affairs/Pharmacovigilance is a plus Project management skills Pragmatic, focused on results and solutions
Our client is a fast growing Pharmaceutical company.
An excellent opportunity in a fast growing Pharmaceutical company to grow and develop in a Regulatory Affairs Specialist position.