Regulatory Affairs Professional

Regulatory Affairs Professional (m/w/d)

Navigate Complex Regulatory Landscapes – Join Our Expert Network

• Talent Pool Registration: Building our Regulatory Affairs network 
• Location: Switzerland (Basel, Zurich, Bern region)
• Opportunities: Permanent and temporary positions available

Building Our Regulatory Affairs Talent Network

We are actively building a comprehensive talent pool of Regulatory Affairs professionals for our diverse client portfolio in Switzerland's pharmaceutical, biotech, and medical device sectors. By registering with us, you'll gain priority access to exclusive opportunities with leading companies specialising in drug development, medical technology, and regulatory compliance.

This is not a specific job posting – instead, we want to connect with experienced Regulatory Affairs professionals who are open to new career opportunities and wish to be considered for upcoming positions with our clients across the Swiss life sciences landscape.

What Regulatory Affairs Roles We Recruit For

• Marketing authorisation applications and regulatory submission management for pharmaceuticals and medical devices 

• Global regulatory strategy development across EU, US, and Swiss regulatory frameworks 

• Clinical trial authorisation (CTA) preparation and regulatory interaction management 

• Post-market surveillance and pharmacovigilance regulatory compliance 

• CMC regulatory affairs including manufacturing and quality documentation 

• Labelling and artwork coordination ensuring compliance with local requirements 

• Regulatory intelligence and competitive landscape analysis 

• Health authority interactions including scientific advice and regulatory meetings

Regulatory Affairs Professionals We're Looking For

Life Sciences or related degree (Pharmacy, Chemistry, Biology, Medicine) with regulatory focus 

3+ years of regulatory affairs experience in pharmaceutical, biotech, or medical device industry 

Strong knowledge of ICH guidelines and regulatory requirements (EMA, FDA, Swissmedic) 

Experience with eCTD submissions and regulatory database management 

Excellent English and German skills; French or other European languages advantageous 

Strategic thinking abilities with attention to regulatory detail and compliance 

Cross-functional collaboration experience with clinical, quality, and commercial teams 

Project management skills for complex regulatory timelines and deliverables

Why Join Our Regulatory Affairs Network

nemensis AG is your specialised recruitment partner in Life Sciences with headquarters in Basel 

Priority consideration for new Regulatory Affairs opportunities as they arise 

Comprehensive career consultation and regulatory market insights from our experienced consultants
Access to our extensive client network and exclusive positions in Northwestern Switzerland 

Proactive career support through individual guidance and strategic career planning

Ready to Join Our Regulatory Affairs Talent Network?

This is your opportunity to be part of our exclusive Regulatory Affairs talent pool. At nemensis ag, we have already connected thousands of candidates with their dream jobs, giving them the opportunity to develop further or re-enter the job market.

Register with us today and let us know about your Regulatory Affairs background, therapeutic area expertise, and career aspirations. Whether you're a Regulatory Affairs Manager, Regulatory Submissions Specialist, CMC Regulatory Expert, or Medical Device Regulatory Professional – we want to connect with you and discuss how we can support your next career move.

? Zak Cook, Consultant, Write an email