Head of Team Regional Regulatory Leads

Boehringer Ingelheim; Ingelheim am Rhein; Vor Ort; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

Boehringer Ingelheim is seeking a Team Leader for Regional Regulatory Leads in the EUCAN region. This role involves managing regulatory strategies, ensuring compliance, and leading development projects in the pharmaceutical industry. Candidates must possess advanced degrees in pharmacy or life sciences, significant regulatory affairs experience, and strong leadership skills.

Qualifikationen

• Long-term experience in the pharmaceutical industry, especially in Regulatory Affairs.
• Several years of practical experience in Oncology development projects.
• In-depth knowledge of EUCAN regulatory requirements.

Aufgaben

• Lead and manage a team of Regional Regulatory Leads for EUCAN.
• Ensure delivery of robust regulatory strategies while maintaining compliance.
• Monitor team development and support in strategic objectives establishment.

Kenntnisse

Leadership

Regulatory Affairs

Project Management

Cross-functional Collaboration

Fluent English

Ausbildung

Doctoral Degree (e.g. PhD, MD) in Pharmacy or Life Sciences

Master's Degree in Pharmacy or Life Sciences

Specialized Pharmacist or Master of Drug Regulatory Affairs

Jobbeschreibung

You will lead and manage a team of Regional Regulatory Leads (RRL) for EUCAN Region.

Tasks & responsibilities

• In your new role, you will lead and manage a Team of Regional Regulatory Leads responsible for steering and coordination of regional regulatory activities for the EUCAN region required for development, maintenance, and expansion of world-wide marketing authorizations for the assigned BI's global human pharma portfolio.
• With your expertise, you will ensure the delivery and execution of robust regional regulatory strategies for the EUCAN region, while ensuring our regulatory compliance.
• You will monitor and enhance the functional and personal development of the team members to drive the team goals.
• Furthermore, you will provide support to the Head of RA in establishing objectives, strategies, and priorities for the complete EUCAN team under consideration of the overall objectives.
• You will also lead assigned development projects as well as general projects, while additionally contributing to our common standards and procedures within the group.

Requirements

• Doctoral Degree (e.g. PhD, MD) and / or Master's Degree in pharmacy or life sciences. Further degrees, e.g., Specialized Pharmacist or Master of Drug Regulatory Affairs are appreciated
• Long-term experience in the pharmaceutical industry in Regulatory Affairs, and ideally also in functions outside Regulatory Affairs (e.g. research and development)
• Several years of practical experience in development projects in Oncology in the EUCAN region, with a special focus on the EU regulatory strategy
• In depth knowledge of international regulatory requirements including the understanding, interpretation, and application of regulatory legislation in the EUCAN region, with focus on EMA (European Medicines Agency)
• Experience with direct Health Authority interactions (e.g. EMA / BfArM) and in handling new developments, registrations and maintenance of products
• Proven experience in successful leadership of international and cross functional project teams
• Ability to collaboratively work cross-functionally in- and outside of the regulatory affairs organization with a good understanding of different cultures and their impact
• Fluent English skills, both written and spoken

Ready to contact us?

If you have any questions about the job posting or process - please contact our HR Direct Team, Tel : [phone] or via mail : [emailprotected]

Recruitment process :

Step 1 : Online application - application deadline is July 4th, 2025

Step 2 : Virtual meeting in the period from beginning till mid of July

Step 3 : On-site interviews end of July