Senior Regulatory Affairs Administrator, Central Europe (EU)

Viatris; Viseu; On-site; EUR 42,000 - 64,000; Full time

Job summary

Viatris is seeking a Senior Regulatory Affairs Administrator to support regulatory activities across Europe, ensuring compliance with European and local requirements. The role collaborates with internal stakeholders and affiliate teams to maintain marketing authorisations and manage regulatory tasks.

The ideal candidate has a solid administrative background in pharma or life sciences, strong communication skills, and fluency in English.

Qualifications

• Previous administrative experience, ideally within pharmaceuticals, healthcare, life sciences, or a regulated environment.
• A strong interest in Regulatory Affairs and the pharmaceutical industry.
• Excellent organisational skills and attention to detail.
• Strong communication and stakeholder management skills.
• Fluent English, both written and spoken.
• Regulatory Affairs experience is advantageous but not essential.

Responsibilities

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

Skills

Administrative experience

Fluent English

Regulatory affairs

Job description

Viatris is seeking a Senior Regulatory Affairs Administrator to support regulatory activities across Europe, ensuring compliance with European and local requirements. The role collaborates with internal stakeholders and affiliate teams to maintain marketing authorisations and manage regulatory tasks.

The ideal candidate has a solid administrative background in pharma or life sciences, strong communication skills, and fluency in English.