Senior Portfolio Owner Regulatory Affairs (m/f/d)
This benefits not only our partners, but also patients around the world. We are proud that our specialised business model has enabled us to become one of the world's leading companies in the acquisition of original preparations within 20 years, and we continue to grow. The aspiration of our approximately 800 employees: Together, we want to ‘ACHIEVE MORE’.
What makes your day with us special:
Strategic Product & Regulatory Ownership
End-to-end responsibility for all regulatory and product-related activities within the portfolio, ensuring a sustainable product strategy that supports compliance, product availability, patient safety, and effective risk management.
Regulatory Strategy & Compliance Management
Develop and drive the global regulatory strategy while overseeing all submission activities, agency interactions, and regulatory processes across the entire product lifecycle. Ensure compliance with all relevant national and international regulatory requirements.
Team Leadership & Operational Management
Provide disciplinary and functional leadership to the product team, including task prioritization, resource allocation, budget responsibility, and the continuous development of team capabilities and expertise.
Cross-Functional Coordination & Stakeholder Management
Ensure strong cross-functional alignment with internal departments, particularly SCM, Therapeutic Areas, and IMO, while acting as the central escalation point (SPOC) for regulatory and product-related topics.
Risk Management & Strategic Decision-Making
Assess complex regulatory and business risks and develop sustainable solutions under uncertain conditions with medium- and long-term impact on products, markets, and business objectives.
External Partner & Outsourcing Oversight
Lead and oversee external service providers and outsourcing activities, ensuring quality, compliance, performance, and professional communication with authorities and external stakeholders.
Innovation, Governance & Continuous Improvement
Continuously evaluate regulatory developments, market trends, and available methodologies to improve processes, strengthen governance structures, and support long-term organizational effectiveness.
What sets you apart:
Academic Qualification & Industry Expertise
Master’s degree in a relevant scientific or pharmaceutical discipline combined with more than 10 years of professional experience in Regulatory Affairs within the pharmaceutical industry.
Leadership & Organizational Management
More than 10 years of proven leadership experience managing large, cross-functional Regulatory Affairs organizations at senior management level, including extensive experience leading global and international teams.
Conflict Resolution & Stakeholder Management
Strong ability to manage and resolve conflicts at high organizational and political levels while maintaining effective collaboration across complex stakeholder environments.
Communication & Influencing Skills
Excellent indirect leadership, communication, and influencing skills across multiple hierarchical levels and in interactions with external stakeholders and regulatory partners.
What we offer you besides the job:
Corporate culture & internationality
A growing company with a diverse, open working environment and employees from around 40 countries.
Flexible working models & work-life balance
Individually customisable working models, including the option to work from another EU country for up to two months per year. Working time account with compensatory time off and 30 days of holiday.
Individual benefits & pension provision
Flexible benefits budget, e.g. for increased company pension provision, fitness and health offers or subsidies for travel and meal costs.
Discounts & additional benefits
Access to the corporate benefits platform with discounts at hundreds of partner companies.
Further development & team culture
Internal and external training courses tailored to personal goals, as well as company and team events to strengthen cohesion and celebrate successes together.
We look forward to receiving your detailed application! Please only use the ‘Apply now!’ function to submit your application.
Your contact person:
- Nadine Gustke
- Talent Acquisition Partner
- nadine.gustke@cheplapharm.com
