Specialist - Large Molecule Biocritical Reagents

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 62,000 staff across a network of more than 1000 independent companies in over 62 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

In 2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client' site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!

Job Description

We are looking for a Specialist to join the ATS-Bio Technical Life Cycle Management Biomaterials team. The ATS-Bio Technical Life Cycle Management Biomaterials team supports the establishment and execution of harmonized lifecycle management for critical biomaterials used in LM QC assays.

Biomaterials are biological reagents playing a critical role in bioassays, which are produced in-house or purchased commercially,  Due to their critical role in bioassays, biomaterials are considered critical assets and an Integrated Risk Management (IRM) program was initiated.

Main responsibilities for this Specialist role, will be to manage the Integrated Risk Management (IRM) program together with relevant QC sites, establishing a detailed risk overview per biomaterial, followed by additional in depth data evaluation of the QC test in which the biomaterial is used, and where needed, defining a roadmap to mitigate these risks and support in execution thereof.

In this Specialist role, you contribute to reliable assay performance, reduced biomaterial-related supply risk, and consistent, on-time product supply.

Key responsibilities

• Support the IRM program by collecting and structuring technical information for critical biomaterials, including current use, availability, criticality, qualification status, documentation gaps, replacement readiness, and supply continuity risks.
• Contribute to detailed risk identification and mitigation by compiling critical biomaterial and assay data, followed by defining, planning and monitoring of  a mitigation roadmap with relevant stakeholders.
• IRM risk mitigation activities including for example, supporting in documentation gathering, protocol writing, data evaluation and report writing.
• Support characterization (e.g., biological, chromatographical) and qualification activities for new, replacement, or transferred biomaterial batches, including data generation & evaluation, and documentation of results.
• Support biomaterial transfers and routine replacements for inline QC bioassays.
• Contribute to continuous improvement by identifying opportunities to standardize procedures, improve documentation quality, reduce variability, and strengthen biomaterial robustness and supply continuity.
• Contribute to biomaterial lifecycle management by establishing realistic replacement timelines and minimum stock limits.
• Assist in biomaterial-related investigations and troubleshooting by compiling and analyzing historical and current assay data, i