A leading global vaccines organisation is seeking an experienced Regulatory Affairs professional to support key European registration activities on an initial six-month contract.

This opportunity offers the chance to work within a highly respected Global Regulatory Affairs team, supporting regulatory strategies and submissions across multiple European markets.

Key Responsibilities

- Develop and execute regulatory strategies.
- Prepare and submit regulatory applications.
- Manage variations, renewals and authority responses.
- Maintain regulatory compliance across EU, UK and Switzerland.
- Support interactions with health authorities.
- Collaborate with quality, medical, commercial and development teams.

Experience Required
- Degree in Life Sciences,



Pharmacy or related field.
- Regulatory Affairs experience.
- Strong EU, UK and Swiss regulatory experience.
- Experience managing regulatory submissions and lifecycle activities.
- Excellent stakeholder management skills.
- Fluent English.

Desirable
- Vaccines experience.
- Biologics experience.
- Veeva exposure.

Location Siena, Italy preferred (hybrid working 3 days per week). Candidates based in the Netherlands will also be considered.

If you would like to discuss this opportunity confidentially, please get in touch.

📌 Regulatory Affairs Principal Associate (Contract) (Siena)
🏢 Haybury
📍 Siena