Description
Regulatory Affairs Manager wanted for our Zug based client in the pharma sector.Your experience/skills:
- Degree in Pharmacy, Life Sciences or equivalent and solid experience in Swissmedic
- 3+ years of extensive work experience in regulatory affairs or drug development in the pharmaceutical industry
- Expertise in regulatory management, life cycle management, quality assurance and in development of new products as well as maintenance of the existing portfolio
- Languages: fluent German, English both written and spoken, conversational French
Your tasks:
- Maintaining and sustaining relevant contacts to health authorities as well as supporting the product development team in organizing the Swissmedic meetings
- Collaborating with Swissmedic and upgrading internal processes along with monitoring changes related to regulatory issues
- Developing and establishing Swiss-specific parts of regulatory dossiers such as information for professionals and patient / packaging information
- Evaluating status of local post-approval commitments and ensuring their delivery time
- Cooperating with the relevant line functions to assure optimal launch preparation for new products besides
- Assuring proper handling of deviations and CAPA handling regarding RA related compliance issues and reporting adverse event / technical quality complaint to the related safety desk
Start:
Duration: 03MM++
Location: Zug, Switzerland
Ref.Nr.: BH10129
Does that sound interesting? Does that sound like a challenging opportunity to you? Then take the next step and send us your CV as a Word Document and a daytime contact telephone number.
Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.
Going the extra mile…
New to Switzerland? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more