CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Regulatory Affairs(m/w/x)
Full-timeWith HomeofficeSenior
Greifswald, Berlin, Binningen
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CHCHEPLAPHARM Arzneimittel GmbH
Global Head of Regulatory Affairs(m/w/x)
Greifswald, Berlin, Binningen
Full-timeWith Home OfficeSenior
Nejo AI Summary
Leading a global team of 80 regulatory professionals for a specialty pharma company. Driving regulatory strategies for product integration and lifecycle management. Master's degree and 10+ years of global regulatory expertise required. Work from another EU country up to 2 months/year, 30 days holiday.
Requirements
- Master’s degree in relevant scientific or pharmaceutical discipline
- More than 10 years professional experience in Regulatory Affairs
- Deep expertise in global regulatory requirements
- Deep expertise in submission processes across multiple markets
- Proven track record leading large regulatory organizations
- At least 10 years leadership experience
- Leadership experience in international and globally distributed teams
- Strong ability to build and maintain long-term relationships with regulatory authorities
- Strong ability to build and maintain long-term relationships with external partners
- Excellent communication skills
- Excellent leadership skills
- Indirect management across different hierarchical levels
Tasks
- Lead a global organization of 80 regulatory professionals
- Drive regulatory strategies for the product portfolio
- Focus on product integration and lifecycle management
- Ensure sustained market supply and portfolio continuity
- Support financial objectives through regulatory contributions
- Maintain global regulatory compliance and market authorizations
- Oversee regulatory assessments during due diligence
- Evaluate regulatory risks, timelines, and integration feasibility
- Make high-impact regulatory and strategic decisions
- Guide cross-functional teams for effective lifecycle management
- Foster alignment with enabling functions for regulatory operations
- Develop and lead a global regulatory team
- Promote collaboration, accountability, and operational excellence
- Ensure efficient use of enterprise systems and processes
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Individually customisable working models
- Working time account
Workation & Sabbatical
- Work from another EU country (up to 2 months/year)
More Vacation Days
- Compensatory time off
- 30 days of holiday
Additional Allowances
- Flexible benefits budget
- Subsidies for meal costs
Retirement Plans
- Company pension provision
Healthcare & Fitness
- Fitness and health offers
Public Transport Subsidies
- Subsidies for travel costs
Corporate Discounts
- Corporate benefits platform access
- Discounts at partner companies
Learning & Development
- Internal training courses
- External training courses
Team Events
- Company events
- Team events
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CHEPLAPHARM Arzneimittel GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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CHCHEPLAPHARM Arzneimittel GmbH
Global Head of Regulatory Affairs(m/w/x)
Greifswald, Berlin, Binningen
Full-timeWith Home OfficeSenior
Nejo AI Summary
Leading a global team of 80 regulatory professionals for a specialty pharma company. Driving regulatory strategies for product integration and lifecycle management. Master's degree and 10+ years of global regulatory expertise required. Work from another EU country up to 2 months/year, 30 days holiday.
Requirements
- Master’s degree in relevant scientific or pharmaceutical discipline
- More than 10 years professional experience in Regulatory Affairs
- Deep expertise in global regulatory requirements
- Deep expertise in submission processes across multiple markets
- Proven track record leading large regulatory organizations
- At least 10 years leadership experience
- Leadership experience in international and globally distributed teams
- Strong ability to build and maintain long-term relationships with regulatory authorities
- Strong ability to build and maintain long-term relationships with external partners
- Excellent communication skills
- Excellent leadership skills
- Indirect management across different hierarchical levels
Tasks
- Lead a global organization of 80 regulatory professionals
- Drive regulatory strategies for the product portfolio
- Focus on product integration and lifecycle management
- Ensure sustained market supply and portfolio continuity
- Support financial objectives through regulatory contributions
- Maintain global regulatory compliance and market authorizations
- Oversee regulatory assessments during due diligence
- Evaluate regulatory risks, timelines, and integration feasibility
- Make high-impact regulatory and strategic decisions
- Guide cross-functional teams for effective lifecycle management
- Foster alignment with enabling functions for regulatory operations
- Develop and lead a global regulatory team
- Promote collaboration, accountability, and operational excellence
- Ensure efficient use of enterprise systems and processes
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Individually customisable working models
- Working time account
Workation & Sabbatical
- Work from another EU country (up to 2 months/year)
More Vacation Days
- Compensatory time off
- 30 days of holiday
Additional Allowances
- Flexible benefits budget
- Subsidies for meal costs
Retirement Plans
- Company pension provision
Healthcare & Fitness
- Fitness and health offers
Public Transport Subsidies
- Subsidies for travel costs
Corporate Discounts
- Corporate benefits platform access
- Discounts at partner companies
Learning & Development
- Internal training courses
- External training courses
Team Events
- Company events
- Team events
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CHEPLAPHARM Arzneimittel GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
CHEPLAPHARM Arzneimittel GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globales und wachsendes Specialty Pharmaunternehmen mit einem außergewöhnlichen, nachhaltigen Geschäftsmodell.
Not a perfect match?
- CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Regulatory Affairs(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Pharmacovigilance(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Science Affiliates(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Knowledge Hub(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Quality(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin, Binningen