Global Regulatory Affairs Manager – EU/UK/Türkiye

Abbott; Thatcham; Vor Ort; GBP 90.000 - 130.000; Vollzeit

Zusammenfassung

Abbott seeks a Regulatory Affairs leader to drive strategy and activities across EU/EFTA, UK, Region East, and Region Türkiye. You will ensure regulatory compliance, market access, and lifecycle management while guiding cross-functional teams and engaging with authorities.

The role requires experience in IVD or related industries, strong leadership, and excellent communication in English. You will back up country regulatory activities and work across multiple markets to maintain timelines and

Qualifikationen

• Fluent in English (written and spoken).
• Strong communication skills are essential for cross-functional collaboration and regulatory interactions.
• Project management and negotiation skills are required for leading regulatory initiatives.
• Experience in IVD or similar industry with exposure to international markets is preferred.
• Leadership and ability to drive compliance within cross-functional teams.

Aufgaben

• Lead regulatory strategy and lifecycle management across assigned markets.
• Interact with regulatory authorities and trade associations to determine compliance approaches.
• Provide regulatory leadership to commercial and cross-functional teams.
• Act as regulatory lead and backup across regions to ensure continuity.
• Develop and execute regulatory strategies for registrations, promotional review, and DOA requirements.
• Drive collaboration and capability development within the regulatory team.

Kenntnisse

Fluent English

Strong communication

Project management

Negotiation skills

Independent work

PC and internet applications

Leadership skills

Ausbildung

Degree in Medicine, Biology, Chemistry or similar

Experience in IVD or similar industry

International work experience

Jobbeschreibung

Abbott seeks a Regulatory Affairs leader to drive strategy and activities across EU/EFTA, UK, Region East, and Region Türkiye. You will ensure regulatory compliance, market access, and lifecycle management while guiding cross-functional teams and engaging with authorities.

The role requires experience in IVD or related industries, strong leadership, and excellent communication in English. You will back up country regulatory activities and work across multiple markets to maintain timelines and