Regulatory Affairs Manager, CMC, Austria
Regulatory Affairs Manager, CMC, technical and strategic input, global pharmaceutical company working on products in development and established brands
An excellent opportunity to join a very successful and well developed pharmaceutical team working on regulatory affairs for a strong product pipeline in Oncology and in Biosimilars. In addition to a strong product pipeline, this company typically offers managerial options internally, they are world leaders in many development areas and have significant investment. Given this from a career prospective, the chance to progress internally are fantastic.
Benefits to this position:
- Excellent product pipeline and facilities giving both career progression and safety
- Salzburg is a beautiful location, where the quality of life is amongst some of the highest in Europe! It is perfect for raising a family while also offering a lot in terms of leisure activities and transport.
- A global Pharma company where you will be working in an international atmosphere with coverage for EU and global projects. This gives you a range of future career options while offering you broad experience
- Regulatory compliance and life cycle responsibilities with a focus on CMC documentation
- Input into new strategies
- Act as a 'go to' person for CMC activities
- Mentoring of junior staff
- At least 3 years experience in regulatory affairs for CMC
- A life science degree or relevant study
- A high level in English (written and verbal)
For a confidential discussion about regulatory affairs, or to apply, then send your CV to email@example.com or call me, Matt Beedle, Regulatory Affairs Consultant on +41435 080817 .For regular job updates and market information please join my regulatory affairs linked-in group. https://www.linkedin.com/groups/4550988
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