Regulatory Affairs Professional

Nemensis

  • Basel-Stadt
  • Unbefristet
  • Vollzeit
  • 1 Tag her
  • Einfach bewerben
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 availableBuilding Our Regulatory Affairs Talent NetworkWe 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 ForLife Sciences or related degree (Pharmacy, Chemistry, Biology, Medicine) with regulatory focus3+ years of regulatory affairs experience in pharmaceutical, biotech, or medical device industryStrong knowledge of ICH guidelines and regulatory requirements (EMA, FDA, Swissmedic)Experience with eCTD submissions and regulatory database managementExcellent English and German skills; French or other European languages advantageousStrategic thinking abilities with attention to regulatory detail and complianceCross-functional collaboration experience with clinical, quality, and commercial teamsProject management skills for complex regulatory timelines and deliverablesWhy Join Our Regulatory Affairs Networknemensis AG is your specialised recruitment partner in Life Sciences with headquarters in BaselPriority consideration for new Regulatory Affairs opportunities as they ariseComprehensive career consultation and regulatory market insights from our experienced consultants
Access to our extensive client network and exclusive positions in Northwestern SwitzerlandProactive career support through individual guidance and strategic career planningReady 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.Branche: Pharma-IndustrieFunktion: Forschung und EntwicklungAnstellungsart: FestanstellungKarrierestufe: Angestellte/r

Nemensis