Senior Regulatory Affairs Specialist - Europe Central

Viatris; Lisboa; Presencial; EUR 42.000 - 65.000; Jornada completa

Descripción de la vacante

Viatris in Lisbon is seeking a Senior Regulatory Affairs Administrator to support regulatory activities across Europe and ensure products comply with European and local requirements. You will collaborate with internal stakeholders and affiliate teams to drive submissions and manage documentation.

You will coordinate administrative tasks, maintain RIM systems, and assist with post-approval variations and regulatory notifications. Fluent English is essential for this role.

Formación

• Previous administrative experience in pharmaceuticals, healthcare, life sciences or regulated environments.
• Strong interest in Regulatory Affairs and the pharmaceutical industry.
• Excellent organisational skills with attention to detail.
• Strong communication and stakeholder management abilities.
• Fluent English in both writing and speaking.
• Regulatory Affairs experience is advantageous but not required.

Responsabilidades

• Support regulatory activities across Europe for a portfolio of pharmaceutical products.
• Assist with post-approval submissions including variations, renewals and regulatory notifications.
• Coordinate administrative and compliance activities to maintain marketing authorisations.
• Maintain and update Regulatory Information Management (RIM) systems and databases.
• Collaborate with local affiliate teams on regulatory and operational tasks.
• Support regulatory fee processing, purchase orders and other admin duties.
• Liaise with cross-functional teams to ensure timely delivery of regulatory objectives.

Conocimientos

Administrative experience

Regulatory Affairs interest

Organisational skills

Communication & stakeholder management

Fluent English

Regulatory Affairs experience

Descripción del empleo

Viatris in Lisbon is seeking a Senior Regulatory Affairs Administrator to support regulatory activities across Europe and ensure products comply with European and local requirements. You will collaborate with internal stakeholders and affiliate teams to drive submissions and manage documentation.

You will coordinate administrative tasks, maintain RIM systems, and assist with post-approval variations and regulatory notifications. Fluent English is essential for this role.