Position: Managing Director (m/f/d)
Location:
Cuxhaven, Germany
About Vibalogics GmbH
Vibalogics GmbH is a leading international Contract Development and Manufacturing Organization (CDMO) specializing in biotechnology, with a strong focus on virus research and development (R&D). With approximately 100 employees, we provide innovative solutions to our clients worldwide.
Position Overview
Vibalogics GmbH is seeking a visionary and strategic Managing Director to lead our organization through its next phase of growth and innovation. This role is central to shaping our strategic direction, overseeing operations, and driving business expansion in the field of biotechnology and virus research. The ideal candidate is a dynamic leader with deep industry expertise, a global perspective, and a passion for scientific excellence.
Key Responsibilities:
- Responsible for day-to-day operations at Cuxhaven site to ensure on time delivery of quality service to customers
- Leading the Leadership Team to execute business strategies and local initiatives, delivery of excellent client service, resource management, budgeting, capacity planning, and process improvements
- Ensuring of a good interface between Cuxhaven facility and Recipharm Group
- Leading the leadership team in defining and executing the company's strategic vision and long-term goals
- Motivating, leading, and developing a high-performing, cross-functional team - Maintaining a culture of trust, respect, empowerment, and open communication
- Driving business development and client acquisition efforts to grow market presence
- Ensuring strict adherence to regulatory and quality standards across all functions
- Representing Vibalogics at key industry events, fostering relationships and brand visibility
- Partnering closely with internal and external stakeholders to align on business priorities
- Reporting KPIs to the division and to the Recipharm Group
Qualifications:
- Advanced degree in Biotechnology, Life Sciences, or a related scientific discipline
- At least 10 years’ line management experience in the pharmaceutical manufacturing environment; with ideally 4 years in the biotechnology service sector (CDMO)
- Thorough understanding and experience of applicable EU and US GMP and GLP regulations
- Solid business management skills and understanding of P&L and balance sheet
- Knowledge of labor law and occupational safety
- Proven experience in Safety Quality Delivery and Cost (SQDC) using established methodologies such as LEAN and Six Sigma
- Strategic mindset with excellent decision-making and problem-solving abilities
- Outstanding interpersonal and communication skills
- Demonstrated ability to lead in a complex, international business environment
- Fluent in German and English
- Onsite presence in Cuxhaven at least 4 days a week
What We Offer:
- A high-impact leadership role in a dynamic, science-driven organization
- Opportunities for continued professional and personal development
- A collaborative, innovative, and inclusive work culture
- Competitive compensation and benefits package