Regulatory Affairs Specialist / Manager (f/m/d) 80%-100%

09 October 2026
80 – 100%
Villars-sur-Glâne et Worb

Job summary

Join our team as a Regulatory Affairs Specialist at Galenica! Enjoy a dynamic work environment with great benefits.

Tasks

Oversee regulatory compliance for a portfolio of drugs and devices.
Prepare and update regulatory submissions and labeling for compliance.
Define submission strategies and liaise with authorities and partners.

Skills

University degree in pharmacy, chemistry, or related field required.
Fluency in French and German, professional level required.
Strong analytical and organizational skills for complex issues.

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About the job

Your scope of action

You assume regulatory responsibility for a portfolio mainly composed of medicines, dietary supplements and medical devices, from development to marketing authorisation, and throughout their entire lifecycle
You prepare, write, submit and update regulatory dossiers as well as labelling to ensure their compliance with applicable requirements
You define submission strategies adapted to projects and interact directly with competent authorities and our partners in Switzerland and internationally
You support development teams from the early phases, identify regulatory requirements and risks, and propose solid and pragmatic options
You collaborate closely with Quality, R&D, Marketing and Medical Affairs teams and contribute to decisions concerning your portfolio
You monitor relevant regulatory and scientific developments, notably in the pharmaceutical field and, depending on your portfolio, for herbal medicines and phytotherapy

Your assets

You hold a university degree in pharmacy, chemistry, biology, biomedical sciences or a comparable scientific discipline
You have professional proficiency in French and German, both spoken and written, and can work independently in both languages
You have a good command of English to handle scientific and regulatory documentation and communicate with international partners
You write precisely, analyse complex scientific and regulatory issues, organise multiple priorities and defend your positions clearly and constructively
You are interested in herbal medicines, plant substances or phytotherapy; experience in this field is an advantage
You ideally have about two years of experience in regulatory affairs within the pharmaceutical industry

5 weeks of holiday, with the possibility to purchase up to 10 additional days of holiday or take unpaid leave

Pension fund with favourable distribution – we cover nearly 2/3 of the contributions

Various discounts in our pharmacies and with other major brands

Opportunity to broaden your skills through encouragement to attend training and development measures as well as internal advancement opportunities

Consideration of family needs, with 16 weeks of maternity leave (100% salary) and 20 days of paternity leave (100% salary), as well as participation in children’s funds

Nominal shares at preferential prices – not only to engage professionally for Galenica but also to invest

Mobile and flexible working in consultation with the team