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11565en
- Contract
- English
- Associate
- Research & Development
- Zug
- Healthcare & Life Sciences
- Regulatory Affairs, Medical Device, H
This vacancy has now expired
For our client, one of the leading Healthcare & Life Sciences companies based in Zug, Swisslinx is seeking a highly motivated individual to take on a challenging role as a Senior Regulatory Affairs Manager. This is a contract position for at least 1 year with the option of extension.
Your responsibilities:
- Responsible for Project Lead Regulatory, within the scope of a project for new products or during the product lifecycle:
- Ensure the interface function between employer and Regulatory Affairs teams for the product approval/clearance in the country of interest.
- Education of staff members of R&D and Portfolio Management on regulatory related topics (e.g. Regulations or changes in the regulations)
- Monitor regulatory requirements, including communication and distribution in a level appropriate manner
Your skills/experience:
- Minimum Bachelor’s degree in the Healthcare & Life Sciences field
- Experience in Medical device, particularly in hard and software (in vitro)
- 3-4 years of experience with regulatory strategy
- Fluent in English, German is preferred but not a must
Candidates must have a valid Swiss or European permit or work rights to be considered for this position. If you would like to be considered for the role, please apply directly or send your CV to fiona.maqi@swisslinx.com.
We look forward to hearing from you!
Your responsibilities:
- Responsible for Project Lead Regulatory, within the scope of a project for new products or during the product lifecycle:
- Ensure the interface function between employer and Regulatory Affairs teams for the product approval/clearance in the country of interest.
- Education of staff members of R&D and Portfolio Management on regulatory related topics (e.g. Regulations or changes in the regulations)
- Monitor regulatory requirements, including communication and distribution in a level appropriate manner
Your skills/experience:
- Minimum Bachelor’s degree in the Healthcare & Life Sciences field
- Experience in Medical device, particularly in hard and software (in vitro)
- 3-4 years of experience with regulatory strategy
- Fluent in English, German is preferred but not a must
Candidates must have a valid Swiss or European permit or work rights to be considered for this position. If you would like to be considered for the role, please apply directly or send your CV to fiona.maqi@swisslinx.com.
We look forward to hearing from you!
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