European Regulatory Affairs Associate — CRA

Viatris; Almada; On-site; EUR 26,000 - 38,000; Full time

Job summary

Viatris in Caparica, Portugal, is seeking an Associate Regulatory Affairs Executive to support regulatory submissions across Europe and help maintain product licences in a fast‑paced global pharma environment.

You will collaborate with local affiliates and cross‑functional teams including Quality, Supply Chain and Product Launch, while developing practical Regulatory Affairs expertise and ensuring ongoing regulatory compliance.

Qualifications

• Excellent communication and stakeholder management skills.
• Fluent English for written and spoken communication.
• Degree in Pharmacy, Biotechnology, Life Sciences or related field.
• 0-2 years of Regulatory Affairs experience or experience in a regulated healthcare/pharmaceutical environment.

Responsibilities

• Support regulatory activities for a diverse portfolio of pharmaceutical products across Europe.
• Assist with the preparation and submission of variations, renewals, and other post-approval regulatory activities.
• Support the maintenance of marketing authorisations and regulatory compliance activities.
• Collaborate with local affiliate teams to coordinate regulatory submissions and national regulatory activities.
• Maintain Regulatory Information Management (RIM) systems and regulatory databases.
• Work cross-functionally with teams including Supply Chain, Quality, Finance, and Product Launch to ensure successful delivery of regulatory objectives.

Skills

Excellent communication

Stakeholder management

Organisational skills

Fluent English

Education

Degree in Pharmacy, Biotechnology, Life Sciences

Job description

Viatris in Caparica, Portugal, is seeking an Associate Regulatory Affairs Executive to support regulatory submissions across Europe and help maintain product licences in a fast‑paced global pharma environment.

You will collaborate with local affiliates and cross‑functional teams including Quality, Supply Chain and Product Launch, while developing practical Regulatory Affairs expertise and ensuring ongoing regulatory compliance.