Biomaterials IRM & QC Lifecycle Specialist

Eurofins Group; Netherlands; Remote; EUR 60,000 - 90,000; Full time

Job summary

Eurofins Scientific invites applications for a Specialist to join the ATS-Bio Technical Life Cycle Management Biomaterials team. You will manage the Integrated Risk Management program, build risk overviews for biomaterials, and perform in-depth data analysis to mitigate supply risks while supporting assay reliability.

The role emphasizes collaboration across QC sites and international teams, documentation, and ongoing biomaterial lifecycle improvements, with a focus on ensuring robust QC

Qualifications

• Bachelor, Masters or PhD in Biology, Biochemistry, Biotechnology, Chemistry, Pharmacy or equivalent laboratory experience.
• 2–5 years hands-on experience in pharma/biological QC, R&D, or related lab environments with biomaterials or biological QC assays.
• Hands-on knowledge of techniques such as ELISA, immunoassays, virus titration, cell culture, antibody/antigen handling, protein purification, conjugation, serum processing, or stability/qualification testing.
• Experience in project/program management and communicating with stakeholders is a strong plus.
• Good communication and collaboration skills, with ability to document and present technical information clearly.
• English proficiency and preferably Dutch; experience with LIMS and Excel is advantageous.

Responsibilities

• Support the Integrated Risk Management (IRM) program by collecting and structuring technical information for critical biomaterials, including use, availability, criticality, qualification status and supply risks.
• Compile data to identify risks and help plan a mitigation roadmap with stakeholders.
• Assist in documentation gathering, protocol writing, data evaluation and report writing for IRM activities.
• Support characterization and qualification activities for new, replacement, or transferred biomaterials, including data generation and evaluation.
• Support biomaterial transfers and routine replacements for inline QC bioassays.
• Contribute to continuous improvement by standardizing procedures and reducing variability in biomaterial handling.
• Help establish realistic replacement timelines and minimum stock levels for biomaterials.
• Assist investigations and troubleshooting by analyzing assay data and supporting CAPA implementations.

Skills

Project management

Communication

Team collaboration

English language

Education

Biology/Biochemistry/Biotechnology/Chemistry/Pharmacy degree

Tools

LIMS

Excel

Data analysis tools

Job description

Eurofins Scientific invites applications for a Specialist to join the ATS-Bio Technical Life Cycle Management Biomaterials team. You will manage the Integrated Risk Management program, build risk overviews for biomaterials, and perform in-depth data analysis to mitigate supply risks while supporting assay reliability.

The role emphasizes collaboration across QC sites and international teams, documentation, and ongoing biomaterial lifecycle improvements, with a focus on ensuring robust QC