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As a Biosafety Team Leader, you will support the leadership of the Biosafety and Chemical Compliance team. You will combine technical biosafety expertise with day‑to‑day people coordination—helping the team deliver on time, collaborate closely with HQ, and prioritize tasks in line with the global direction. Currently, we are looking for a new Team Leader for a temporary contract (approximately 16 months).
Job Responsibility
Coordinate the assigned team to ensure timely, high‑quality delivery of projects and activities
Support clear communication and alignment between CPBC and HQ Biosafety and Chemical Compliance teams
Support competence development within the Biosafety and Chemical Compliance team, in line with guidance from the Head of Biosafety and Chemical Compliance
Coordinate and support delivery of biosafety input for Coloplast products, ensuring compliance for new and existing medical devices
Facilitate knowledge transfer and information sharing between HQ and CPBC teams to support the agreed task split and processes
Provide input and coordination related to toxicology, chemicals, and people safety
Participate in cross‑functional and global projects related to biosafety and chemical safety
Requirements
Experience in team management
Master's degree in a relevant scientific field (e.g., biology, chemistry, biochemistry, pharmacology, toxicology)
Familiarity with relevant regulations and standards (e.g., ISO 10993, ISO 13485, MDR, FDA requirements)
Basic knowledge of biocompatibility, toxicology, or related areas within medical devices is an advantage
Good understanding of chemical safety and European chemical legislation is an advantage
Fluency in spoken and written English
Good analytical skills and ability to work with scientific data
Structured and result oriented approach
Strong collaboration and communication skills
Ability to work across functions and cultures
Sense of ownership and responsibility
Ability to prioritize and manage multiple tasks
Nice to have
Basic knowledge of biocompatibility, toxicology, or related areas within medical devices is an advantage
Good understanding of chemical safety and European chemical legislation is an advantage
What we offer
Temporary contract (approx. 16 months)
Hybrid / onsite work from our office in Szczecin
Flexible working hours, Mon-Fri
International work environment with Scandinavian culture
Opportunity to use and develop foreign languages in daily work
Fantastic work atmosphere full of respect and partnership