CMC Regulatory Affairs Associate

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11257en
  1. Contract
  2. English
  3. Associate
  4. Legal, Regulatory & Compliance
  5. Basel
  6. Healthcare & Life Sciences

Skills

CMC, Compliance, Regulations

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About our client
For our client, one of the leading Healthcare & Life Sciences companies based in Switzerland, Swisslinx is seeking a highly motivated individual to take on a challenging role in their GDD department.

Your mission:
- Identify required documentation for global submissions and provide timely preparation of high quality CMC regulatory documentation
- Apply agreed CMC global regulatory strategies
- Engage in the process of product lifecycle and prepare CMC responses
- Assure technical congruency and regulatory compliance
- Set up and maintain solid relationships with partners and customers

The ideal candidate:
- Initial professional experience within the Regulatory field, preferably in the Pharmaceutical industry
- Familiar with regulations and guidelines for new chemical entities
- Degree and Advanced Degree in Science (Chemistry, Pharmacy, Biology)
- Ability to multi-task and work independently under pressure of time

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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