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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
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.
Lead and perform deviation and investigation writing/review, including thorough root cause analysis and CAPA development/effectiveness checks
Review and approve quality agreements and ensure alignment with regulatory and client requirements
Host and support external audits, including regulatory agency inspections and client audits
Conduct internal audits, walkthrough inspections, and ensure audit readiness across laboratory operations
Perform and support risk assessments to proactively identify and mitigate quality risks
Drive data integrity compliance initiatives, ensuring adherence to ALCOA+ principles
Manage and support change control processes, ensuring impact assessments and compliance with procedures
Review and approve SOPs, analytical methods, protocols, and reports
Release and ensure accuracy of analytical reports
Contribute to monthly and quarterly quality metrics reporting
Identify and implement continuous improvement opportunities within QA and laboratory functions
Partner cross-functionally with laboratory staff, clients, and leadership to ensure quality objectives are met
Maintain a strong commitment to safe, compliant, and efficient operations
Bachelor's degree in Chemistry, Biology, Biochemistry, or related scientific discipline
4+ years of QA experience within a pharmaceutical or regulated laboratory environment
Proven experience with:
Investigations and CAPA management
Audit hosting (client and/or regulatory)
Quality systems (change control, deviations, document control)
Data integrity principles and compliance expectations
Strong working knowledge of GxP (GMP/GLP) regulations
Excellent written and verbal communication skills
Ability to confidently interact with clients, auditors, and internal stakeholders
Proficiency in Microsoft Office (Excel, Word, PowerPoint)
Authorization to work in the U.S. without sponsorship
Position is full time, Monday to Friday, 8AM - 5PM. Candidates currently living within a commutable distance of Portage, MI are encouraged to apply.
Excellent full time benefits including
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.