Manufacturing Scientist

As an MSAT Scientist within our Bio-Engineering team, you are a technical owner of the manufacturing processes behind our IVD blood-transfusion products. Working at the interface between manufacturing, quality and regulatory (IVDR, ISO 13485, GMP), your mission is to keep our processes robust, compliant and under control — investigating non-conformities, driving CAPAs, leading projects, and assessing the regulatory impact of changes.

Your impact: 

• Manage non-conformities (NC): lead technical investigations using structured root-cause methodologies (Ishikawa, 5-Why, FMEA) and define effective corrective and containment actions.
• Drive CAPAs: own corrective and preventive actions from definition to effectiveness check within cross-functional teams.
• Master change control (CC): author, review and approve change requests, and assess their process, validation and regulatory impact.
• Lead manufacturing projects: manage scope, timelines, risk and stakeholders from initiation to close.
• Own process knowledge: maintain deep understanding of the processes and their control strategy across the product lifecycle, identifying key sources of variability and root causes of failures.
• Author technical documentation: sampling plans, SOPs, risk assessments, protocols and technical reports — clear and audit-ready.
• Communicate effectively: summarise complex technical and quality issues for diverse audiences to support sound decision-making.

What you bring:

• Degree in Life Sciences — Biology, Biochemistry, Chemistry or equivalent (Dipl. Ing., M.Sc.).
• Minimum 3-5 years of experience in the diagnostics or pharmaceutical industry, with hands-on knowledge of biology, biochemistry and/or immunology techniques and automation. Knowledge in immune-hematology a plus.
• Strong scientific background and analytical capabilities, with robust investigation methodologies (root-cause analysis, risk assessment).
• Technical and laboratory skills for investigation: hands-on bench work is part of the role to characterise issues, run tests and verify hypotheses.
• Solid understanding of the IVD regulatory framework (IVDR, ISO 13485, GMP) and the ability to assess the regulatory impact of changes.
• Structured, methodical and rigorous, with strong project-management and synthesis/communication skills.
• Fluent in French and English, German a plus.

About us: For 70 years, Bio-Rad has been committed to innovation and transformation in the fields of science and healthcare. As one of the five largest companies in the life sciences sector, we are leaders in the development, production and marketing of a wide range of research and clinical diagnostic products. Our raison d'être is to help people live longer, healthier lives.

Bio-Rad offers the opportunity to work with teams around the world. Here, management helps you build your career step by step, and you are encouraged to implement changes that will have a real impact.

• a competitive salary
• annual bonus and salary review
• training and development programs, with access to LinkedIn Learning

Equal opportunities: Bio-Rad is committed to preventing discrimination and promoting equal opportunities. All our positions are open to people with disabilities. Don't hesitate to apply!

Non-solicitation: Bio-Rad does not accept agency CVs unless the agency has been authorized by a Bio-Rad recruitment representative. Please do not submit resumes unless authorized. Bio-Rad will not pay any fees related to unsolicited resumes.