Regulatory Affairs Manager, CMC, Austria

€50000 - €60000 per annum + Relocation+ Bonus
Mar 07, 2018
Apr 06, 2018
Matt Beedle
Jobseeker Type
Organization Type
Clinical Practice
Contract Type
Full Time

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

Role Responsibilities:

  • 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

Role Requirements:

  • 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 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.

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