Global Regulatory Affairs Associate — Central Europe (EU)

Viatris; Lisboa; Presencial; EUR 25 000 - 40 000; Tempo integral

Resumo da oferta

Viatris seeks a Regulatory Affairs Associate to support a diverse European portfolio from its Lisbon office. This early‑career role offers exposure to submissions, renewals, and licensing activities across multiple markets in a global pharmaceutical company.

You will work with European affiliates and cross‑functional teams to maintain compliance, coordinate national submissions, and manage regulatory databases, contributing to efficient, compliant product launches and lifecycle management.

Qualificações

• Degree in Pharmacy, Biotechnology, Life Sciences or related field.
• 0–2 years in Regulatory Affairs or regulated healthcare environment.
• Strong communication and stakeholder management skills.
• Excellent organizational skills and attention to detail.
• Fluent English (written and spoken).

Responsabilidades

• Support regulatory activities for a diverse portfolio across Europe.
• Assist with preparation and submission of variations, renewals, and post-approval activities.
• Maintain marketing authorisations and regulatory compliance.
• Coordinate regulatory submissions with local affiliate teams.
• Keep Regulatory Information Management (RIM) systems up to date and accurate.
• Collaborate with cross-functional teams to meet regulatory objectives.

Conhecimentos

Regulatory Affairs

Communication

Stakeholder management

Attention to detail

Organization

Fluent English

Formação académica

Pharmacy

Biotechnology

Life Sciences

Descrição da oferta de emprego

Viatris seeks a Regulatory Affairs Associate to support a diverse European portfolio from its Lisbon office. This early‑career role offers exposure to submissions, renewals, and licensing activities across multiple markets in a global pharmaceutical company.

You will work with European affiliates and cross‑functional teams to maintain compliance, coordinate national submissions, and manage regulatory databases, contributing to efficient, compliant product launches and lifecycle management.