Medical, Regulatory Affairs & Quality Director

Medical, Regulatory Affairs & Quality Director

Teva

Bucharest, Romania

About the Role

We are looking for an experienced and strategic Medical, Regulatory Affairs & Quality Director to lead three critical functions within our organization: Medical Affairs, Regulatory Affairs, and Quality. This is a key leadership role with high impact on the business, ensuring compliance with EU and local regulations, scientific accuracy, and high quality standards across all activities.

Key Responsibilities

• Lead and oversee the Medical, Regulatory Affairs, and Quality functions.
• Establish, coordinate, monitor, and update policies and processes in alignment with EU/global guidelines and local legislation.
• Ensure accuracy, clarity, and scientific balance in internal and external medical information.
• Coordinate the Medical Information process for external customers.
• Manage the review and approval of all medical and promotional communications.
• Represent the company before relevant health authorities and regulatory bodies.
• Act as a People Manager and lead the local team.

Ideal Candidate Profile

• Bachelor’s degree in Medicine, Pharmacy, or Dentistry.
• 5–7 years of experience in a similar leadership role within a complex business or pharma environment.
• Strong pharmaceutical business knowledge and the ability to navigate matrix organizations.
• Strategic thinker with strong influencing skills and the ability to work cross functionally.
• Advanced MS Office skills (Word, Excel, PowerPoint).
• Experience in innovative pharma organizations is an advantage.
• Fluent English.