Regulatory Affairs Manager (Ref. 2715) – Permanent Role - Zurich / Fluency in German

AurigaVision AG
Baarerstrasse 139, 6300 Zug
NEU
  • 22.01.2026
  • 80 - 100%
  • Führungsposition
  • Festanstellung

Regulatory Affairs Manager (Ref. 2715) – Permanent Role - Zurich / Fluency in German

Our client is an established, innovation-focused pharmaceutical company with a strong presence in the Swiss market. The organization operates internationally and is active in several therapeutic areas with a clear commitment to high-quality regulatory standards. For their Swiss affiliate, we are currently seeking a

Regulatory Affairs Manager (Ref. 2715) – Permanent Role

Zurich / Fluency in German

In this role, you will be responsible for managing regulatory activities for assigned medicinal products in Switzerland, including new market authorizations and lifecycle management. You will collaborate closely with Swissmedic as well as European and global Regulatory Affairs teams. Cross-functional cooperation with departments such as Medical, Quality, Supply Chain, and Commercial will be part of your daily work.

Your main tasks

  • Serve as the primary regulatory contact for Swissmedic for assigned products
  • Prepare and manage regulatory submissions for new marketing authorisations and lifecycle changes
  • Develop and implement regulatory strategies for Switzerland in coordination with international teams
  • Ensure compliance with national and international regulatory requirements
  • Maintain product licences, including variations, renewals, and safety submissions
  • Provide regulatory support for product launches and supply-related topics
  • Monitor regulatory developments and inform internal stakeholders accordingly

Your profile

  • Solid knowledge of Swiss regulatory requirements and Swissmedic procedures
  • At least 5 years of professional experience in Regulatory Affairs within the pharmaceutical industry (ideally Specialty Care/Oncology)
  • Focus on pre-submission and post-approval activities
  • University degree in Pharmacy, Medicine, Life Sciences, or a related discipline
  • Experience with marketing authorisation applications and lifecycle management
  • Strong communication and stakeholder management skills
  • Structured, independent, and reliable working style
  • Fluency in German and English; additional languages are an advantage

Domagoj Odrljin is looking forward to receiving your application documents via our job portal (CV, diploma, reference letters; no motivational letter necessary).

Full discretion is guaranteed and we will gladly answer any additional questions.

Kontakt

Auriga Vision AG
AurigaVision AG