Verfora SA
Villars-sur-Glâne und Worb
Regulatory Affairs Specialist / Manager (m/f/d) 80%-100%
- 09 October 2026
- 80 – 100%
- Villars-sur-Glâne und Worb
Job summary
Join our team to drive regulatory compliance in pharmaceuticals. Enjoy a collaborative work environment with great benefits.
Tasks
- Ensure regulatory compliance from development to product lifecycle.
- Prepare and submit regulatory documentation, maintaining compliance.
- Collaborate with teams, identifying regulatory requirements and risks.
Skills
- Degree in pharmacy, chemistry, biology, or related fields required.
- Fluent in German and French; proficient in English for documentation.
- Strong analytical skills to address complex regulatory issues.
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About the job
What you can achieve
- You ensure the regulatory compliance of your portfolio of medicinal products, dietary supplements and medical devices from development to the end of the product lifecycle
- You create, write and submit regulatory documentation and keep dossiers as well as product labelling up to date according to applicable requirements
- You develop project-specific submission strategies and coordinate these directly with authorities and partners in Switzerland and internationally
- You accompany development teams early on, identify regulatory requirements and risks and derive viable courses of action from them
- You work closely with Quality, R&D, Marketing and Medical Affairs and contribute your regulatory perspective to portfolio decisions
- You monitor regulatory and scientific developments, especially in the pharmaceutical sector as well as, depending on the portfolio, in herbal medicinal products and phytotherapy
What you bring with you
- You have a university degree in pharmacy, chemistry, biology, biomedical sciences or a comparable scientific discipline
- You have very good professional German and French language skills, both spoken and written, and can work independently in both languages
- You have good English skills for scientific and regulatory documentation as well as for communication with international partners
- You analyse complex scientific and regulatory issues precisely and represent your position clearly to internal teams, partners and authorities
- You reliably organise multiple priorities, recognise challenges early and develop pragmatic solutions
- You have a special affinity for herbal medicinal products, herbal substances or phytotherapy; experience in this area is an advantage
- Ideally, you bring around two years of experience in Regulatory Affairs in the pharmaceutical industry
5 weeks holiday, with the option to purchase up to 10 additional holiday days or take unpaid leave
Pension fund with favourable premium sharing - approx. 2/3 are covered by us
Various discounts in our pharmacies and with other top brands
Expand skills through funded and supported training and further education as well as internal development opportunities
Family-friendly with 16 weeks maternity leave (100% salary) and 20 days paternity leave (100% salary), as well as participation in child funds
Registered shares at preferential prices - not only engage professionally for Galenica but also invest
Mobile and flexible working in agreement with the team
