Regulatory Affairs Freelancer/Contractor, Pre-Approval

Regulatory Affairs Freelancer/Contractor, Pre-Approval, Flexible Hours

We are currently looking for an experienced regulatory affairs professional to join a development team with a number of new Biotech products in early development. Critical to this role will be having someone with experience in regulatory biologics in development covering critical CTAs/INDS/IMPD submissions and HA meetings, who understands working with the EMA/FDA.

The contract can be flexible in length and timing for the right candidate. For people don't own their own Swiss entity, NonStop is a licensed labour provider in Switzerland and we can offer payroll options that in essence, offer the benefits of permanent work (Contract, holiday, sickness pay etc). If you are interested in 'principle', then please contact me.

Key Requirements:

• Regulatory pre-approval experience with the EMA in Pharma Rx for Biologics
• At least 10 years pharma regulatory affairs expeirence
• HA experience
• Life science degree
• Ability to work in the Basel area
• Fluency in English

For a confidential discussion about regulatory affairs, or to apply, then send your CV to m.beedle@nonstop-recruitment.com or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41435 080817. For regular job updates and market information please join the Switzerland regulatory affairs linked-in group. https://www.linkedin.com/groups/4550988

I am a specialist headhunter(recruiter) for regulatory affairs in the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on the Swiss regulatory affairs market as well as ATMP(Advanced Therapeutics) and biological regulatory professionals worldwide. Please refer to ch.linkedin.com/in/regulatoryaffairsswitzerland for references.