At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services, and care across the entire healthcare journey. Guided by our vision—“Creating a future worth living. For patients. Worldwide. Every day.”—we work with purpose and compassion, supported by a global team of over 110,000 employees.
Within our Care Enablement segment, we develop and provide life-sustaining medical products, digital health solutions, and therapies that empower clinical teams and improve patient outcomes. Our FME Reignite strategy drives transformation through innovation, efficiency, and sustainable growth.
Our values guide how we work:
We Care for our patients, each other, and our communities
We Connect across teams and borders to deliver excellence together
We Commit to doing things the right way— growing with purpose and leading kidney care with integrity and innovation
Systems, Quality & Regulatory (SQR), a global function within Care Enablement ensuring Fresenius Medical Care’s products meet the highest standards of quality, safety, and regulatory compliance throughout the entire product lifecycle. The team supports market access, innovation, and patient safety by driving excellence across manufacturing and supply chain, overseeing post-market surveillance, and promoting continuous improvement and system harmonization. SQR also manages regulatory and quality data governance and provides critical product-related business services across global operations. Join our passionate team and help shape healthcare worldwide!
Your Purpose As Director of the Global Biocompatibility and Toxicology Competence Center, you will be responsible for establishing and leading a globally aligned, high-performing team of experts. Your mission is to define and implement FME’s overarching biocompatibility strategy across medical devices and primary packaging materials, ensuring regulatory compliance and product safety in line with the highest standards of patient care.
Your tasks:
Build, lead, and develop the Global Biocompatibility and Toxicology Competence Center, both professionally and disciplinary.
Derive overarching biocompatibility strategy for all relevant products of Care Enablement, i.e., medical devices and primary packaging materials for drugs.
Process-owner for biocompatibility SOP package within FME’s QMS.
Strong involvement and integration in development and sustaining projects with the team’s expertise.
Professional and transparent resource management and prioritization of tasks
Derive an overarching strategy biocomp strategy (sampling, testing, evaluation etc.) with all verticals.
Align sampling and testing strategies and support product responsibles/product development groups to apply them.
Qualification of test laboratories and subsequent alignment of requirements for studies, e.g., AET, test methods, etc.
Support evaluation of analytical and biological results gained by internal or external testing labs.
Oversee the creation of biocomp files including BEP (biological evaluation plant), BER (biological evaluation report) TRA (toxicological risk evaluation) and risk assessments.
Agree strategy with regulatory agencies and notified bodies.
Actively work in standard committees and create network to agencies and experts in the field of biocompatibility.
Manage interfaces and stakeholder relations with R&D teams within CE Verticals, incl. communication of global biocompatibility and toxicology strategy and priorities.
Your profile:
7–10 years of hands‑on experience in the biocompatibility evaluation of medical devices and/or drug packaging materials
Sound expertise in biocompatibility testing methodologies; laboratory management experience is a strong asset
In-depth knowledge of the ISO 10993 series; relevant certifications and training preferred
Knowledge in toxicology and risk management is a plus
Strong leadership experience in an international context and matrix environment, supporting and fostering performance culture and individual and team accountability
Strategic and visionary personality able to balance short‑term priorities and long‑term vision
Excellent project management and organizational skills; structured and detail oriented.
Strong communication and stakeholder management skills; capable of handling complex topics with clarity and confidence
Advanced experience with PTC Windchill PDM; working knowledge of Polarion ALM is a plus
Proficient in Microsoft Office and related business tools
Committed to continuous learning and able to thrive in a dynamic environment.
Fluent in business English; additional languages (e.g., German, French, Italian) are a plus
Our offer for you:
The opportunity to work in a hybrid model
Whether in front of or behind the scenes - you will help to make better medicine accessible to more and more people around the world
Individual opportunities for self-determined career planning and professional development
A corporate culture in which there is enough room for innovative thinking - to find the best solution together, not the quickest one
A large number of committed people with a wide range of skills, talents and experience
The benefits of a successful global corporation with the collegial culture of a medium-sized company
We are committed to diversity and equal opportunities and welcome applications from people with disabilities.
Director Global Biocompatibility and Toxicology Competence Center (m/w/d) in Poznań – pracodawca: Fresenius Medical Care AG
Fresenius Medical Care AG to firma, która stawia na rozwój swoich pracowników, oferując im wsparcie w osiąganiu celów zawodowych i osobistych. Pracownicy są kluczowym elementem sukcesu firmy, a kultura organizacyjna opiera się na wartościach takich jak troska, łączenie ludzi i zaangażowanie. Dzięki temu, Fresenius Medical Care AG zapewnia stabilne środowisko pracy oraz możliwości rozwoju kariery.
Dane kontaktowe:
Zespół rekrutacyjny Fresenius Medical Care AG
