Regulatory Affairs Manager vacancy for our Glattpark (Opfikon) based client in the Pharma sector.

Your tasks:

• Support regulatory activities related to the development, registration, and life cycle management of vaccine candidates in Europe.
• Manage assigned regulatory projects, including support for dossier/Marketing Authorization Application (MAA) submissions.
• Ensure all necessary applications are filed and maintained in compliance with applicable regulations.
• Provide regulatory oversight for assigned clinical trials conducted in the region.
• Collaborate with global regulatory counterparts to ensure alignment and execution of regulatory strategy.

Your experience/knowledge:

• A minimum of 6 years of pharmaceutical industry experience, including 3 years of regulatory experience.
• Experience in managing filings to EMA via Centralised Procedure resulting in first-time approval.
• Vaccines and/or biologics experience is essential.
• Language skills: English – fluent

Your soft skills:

• Strong oral and written communication skills.
• Excellent organisation skills and attention to detail.
• Proactive in identifying regulatory issues and offering creative solutions.

Location: Glattpark (Opfikon), Switzerland
Work setting: Hybrid
Sector: Pharma
Start: 02/03/2026
Duration: 6+ months
Workload: 100%
Ref.Nr.: BH 23699

Take the next step and send us your resume along with a daytime phone number where we can reach you.

Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens, and current work-permit holders for Switzerland.

We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application.

As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.