Europe Regulatory Affairs Associate – Central CRA

1100 Mylan Pharmaceuticals Inc.; Lisboa; Presencial; EUR 28 000 - 38 000; Tempo integral

Resumo da oferta

Viatris is seeking an Associate Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe. You will support regulatory submissions, maintain product licences, and ensure compliance across multiple European markets.

Ideal candidates have a degree in Pharmacy or Life Sciences, fluent English, and 0-2 years in regulatory affairs or a regulated healthcare environment. Collaboration with European affiliates is essential.

Qualificações

• Strong interest in regulatory affairs and the pharmaceutical industry.
• 0-2 years of regulatory affairs experience or regulated healthcare environment.
• Excellent communication and stakeholder management skills.

Responsabilidades

• Support regulatory activities for a diverse portfolio of pharmaceutical products across Europe.
• Assist with variations, renewals and other post-approval regulatory activities.
• Maintain marketing authorisations and regulatory compliance activities.
• Coordinate regulatory submissions with local affiliate teams.
• Maintain Regulatory Information Management (RIM) systems.
• Collaborate with Supply Chain, Quality, Finance and Product Launch teams.
• Support regulatory administration and fee management.

Conhecimentos

Regulatory Affairs

English fluency

Stakeholder management

Communication

Attention to detail

Formação académica

Pharmacy degree

Life sciences degree

Descrição da oferta de emprego

Viatris is seeking an Associate Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe. You will support regulatory submissions, maintain product licences, and ensure compliance across multiple European markets.

Ideal candidates have a degree in Pharmacy or Life Sciences, fluent English, and 0-2 years in regulatory affairs or a regulated healthcare environment. Collaboration with European affiliates is essential.