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 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 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 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
Team Leadership & Workforce Management
• Lead, schedule, and supervise laboratory personnel to ensure coverage and performance targets are consistently met
• Conduct interviews, evaluate candidates, and make hiring decisions for direct-report positions
• Deliver structured onboarding and ongoing training for assigned staff on test methods, SOPs, ISO requirements, and laboratory policies
• Conduct annual performance reviews and provide continuous coaching and feedback to foster team development
• Foster a culture of morale, teamwork, and accountability that reflects Eurofins' mission and values Laboratory Operations & Quality Assurance
The Laboratory Operations Manager provides operational leadership for Eurofins Microbiology laboratory functions, acting with sufficient authority from the Business Unit Manager to ensure the highest standards of quality, compliance, and team performance. This role serves as a backup to the Business Unit and Quality Manager and has the authority to initiate work stoppages in response to quality failures and to reinstate operations once issues are resolved.
• Assist the Business Unit Manager in managing daily microbiology laboratory operations, including scheduling, supervision, and performance of manual and instrumental analyses
• Ensure all analytical work complies with ISO requirements, applicable government regulations, and Eurofins quality standards
• Review and evaluate test data for technical accuracy, SOP compliance, and test method adherence; apply basic statistical tools to assess data quality
• Investigate non-conformances, determine root causes, implement corrective actions, and verify resolution
• Maintain authority to execute a work stoppage upon quality failure and to reinstate operations upon resolution
• Create and review laboratory reports and maintain accurate, complete records of work performed Equipment & Facility Management
• Establish and implement procedures ensuring all equipment is properly cleaned, calibrated, and maintained in good working order
• Maintain equipment operating instructions, manuals, and required logbooks
• Troubleshoot instruments and equipment; perform minor repairs and coordinate major repairs with qualified service personnel Compliance & Continuous Improvement
• Adhere to and enforce all Quality System documentation including the Quality Manual, SOPs, and applicable test methods
• Apply quality measures that meet or exceed standards set by government regulations and company requirements
• Maintain a working knowledge of technical, industry, and regulatory advancements as directed by the Business Unit Manager
• Adhere to all company health, safety, and environmental regulations
• Promote the Eurofins brand through ethical, professional business practices with clients and the public
• Perform other duties as assigned
QualificationsEducation & Experience
• Bachelor's degree in a scientific discipline or closely related field
• Minimum 3–5 years of supervisory experience, preferably in a laboratory environment
• Demonstrated ability to organize and lead laboratory personnel in alignment with corporate goals and productivity objectives Technical Skills
• Hands-on experience with laboratory procedures, data analysis, computer operations, and technical/business writing
• Experience with PCR, ELISA, and cultural confirmation of foodborne pathogens including Salmonella, Listeria, and E. coli O157:H7
• Strong computer proficiency and organizational skills Core Competencies
• Exceptional leadership, initiative, and team-building capabilities • Strong written and verbal communication skills with high attention to detail
• Ability to work independently and collaboratively; self-motivated with a positive, adaptable mindset
• Capacity to learn new techniques, manage multiple tasks simultaneously, and comply with company policies
• Flexible availability including evenings, weekends, and holidays as needed
What we Offer:
Excellent full-time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidays Read LessEurofins 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 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 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 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job DescriptionThe Laboratory Operations Manager provides operational leadership for Eurofins Microbiology laboratory functions, acting with sufficient authority from the Business Unit Manager to ensure the highest standards of quality, compliance, and team performance. This role serves as a backup to the Business Unit and Quality Manager and has the authority to initiate work stoppages in response to quality failures and to reinstate operations once issues are resolved.
Team Leadership & Workforce Management
• Lead, schedule, and supervise laboratory personnel to ensure coverage and performance targets are consistently met
• Conduct interviews, evaluate candidates, and make hiring decisions for direct-report positions
• Deliver structured onboarding and ongoing training for assigned staff on test methods, SOPs, ISO requirements, and laboratory policies
• Conduct annual performance reviews and provide continuous coaching and feedback to foster team development
• Foster a culture of morale, teamwork, and accountability that reflects Eurofins' mission and values Laboratory Operations & Quality Assurance
• Assist the Business Unit Manager in managing daily microbiology laboratory operations, including scheduling, supervision, and performance of manual and instrumental analyses
• Ensure all analytical work complies with ISO requirements, applicable government regulations, and Eurofins quality standards
• Review and evaluate test data for technical accuracy, SOP compliance, and test method adherence; apply basic statistical tools to assess data quality
• Investigate non-conformances, determine root causes, implement corrective actions, and verify resolution
• Maintain authority to execute a work stoppage upon quality failure and to reinstate operations upon resolution
• Create and review laboratory reports and maintain accurate, complete records of work performed Equipment & Facility Management
• Establish and implement procedures ensuring all equipment is properly cleaned, calibrated, and maintained in good working order
• Maintain equipment operating instructions, manuals, and required logbooks
• Troubleshoot instruments and equipment; perform minor repairs and coordinate major repairs with qualified service personnel Compliance & Continuous Improvement
• Adhere to and enforce all Quality System documentation including the Quality Manual, SOPs, and applicable test methods
• Apply quality measures that meet or exceed standards set by government regulations and company requirements
• Maintain a working knowledge of technical, industry, and regulatory advancements as directed by the Business Unit Manager
• Adhere to all company health, safety, and environmental regulations
• Promote the Eurofins brand through ethical, professional business practices with clients and the public
• Perform other duties as assigned
QualificationsEducation & Experience
• Bachelor's degree in a scientific discipline or closely related field
• Minimum 3–5 years of supervisory experience, preferably in a laboratory environment
• Demonstrated ability to organize and lead laboratory personnel in alignment with corporate goals and productivity objectives Technical Skills
• Hands-on experience with laboratory procedures, data analysis, computer operations, and technical/business writing
• Experience with PCR, ELISA, and cultural confirmation of foodborne pathogens including Salmonella, Listeria, and E. coli O157:H7
• Strong computer proficiency and organizational skills Core Competencies
• Exceptional leadership, initiative, and team-building capabilities
• Strong written and verbal communication skills with high attention to detail
• Ability to work independently and collaboratively; self-motivated with a positive, adaptable mindset
• Capacity to learn new techniques, manage multiple tasks simultaneously, and comply with company policies
• Flexible availability including evenings, weekends, and holidays as needed
What we Offer:
Excellent full-time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidays Read LessEurofins 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 believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to ca. 63,000 staff across a decentralized and entrepreneurial network of more than 950 laboratories in 60 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.
In 2025, Eurofins generated total revenues of EUR 7.296 billion ($8.596 billion), and has been one of the best performing stocks in Europe over the past 20 years.
Job DescriptionRole Summary:
The Clinical Trial Laboratory Director provides scientific, medical, and regulatory leadership for high‑complexity laboratories supporting clinical research and clinical trials. This role ensures full compliance with CLIA requirements, including director qualifications and oversight responsibilities—and maintains CAP accreditation standards while meeting state-specific director/licensure requirements in multiple states, including Pennsylvania, New York, Rhode Island, Maryland, and California.
The Director ensures assay validity, data integrity, patient‑subject safety, GDP, GLP. and GCP/GCLP‑aligned laboratory conduct throughout the lifecycle of clinical trials.
Key Responsibilities
1. Regulatory, Trial, and Accreditation Leadership
Serve as the legally accountable CLIA High‑Complexity Laboratory Director and maintain qualifications per 42 CFR §493.1443.Provide executive oversight of CAP accreditation, including biennial inspections, self‑inspections, and adherence to CAP checklist requirements.Ensure all laboratory operations supporting clinical trials meet CLIA, CAP, GLP, ICH‑GCP, and GCLP expectations for accuracy, integrity, and traceability.Oversee trial‑specific regulatory documentation, method validations, equipment qualifications, and assay change controls consistent with CAP validation/verification principles.2. Clinical Trial Scientific Oversight
Review and approve test methods, protocols, analytical plans, policies, procedures, and assay validations specific to clinical trial endpoints.Ensure test systems are suitable for the study population and meet clinical trial protocol requirements, consistent with CLIA’s requirement for appropriate test systems and reliable data.Serve as scientific liaison to sponsors, CROs, principal investigators, and regulatory authorities regarding laboratory capabilities, biomarker strategies, and test result interpretation.3. Quality Management & Data Integrity
Adhere to Quality in accordance with the ECL Quality Management System supporting clinical trial labs, including document control, method validation, instrument qualification, and ongoing competency assessments.Oversee proficiency testing (PT), quality control, and data integrity processes for trial‑critical assays, meeting CLIA/CAP expectations for PT integration and evaluation.Approve CAPA plans and deviations relevant to clinical trials and ensure compliance with protocol‑specific quality and audit requirements.Oversee day to day function of Laboratory and Specimen Management operations.Adhere to adequate Private Health Information (PHI) practices and policies.4. Clinical Trial Operational Oversight
Ensure laboratory workflows support GCP‑compliant chain‑of‑custody, blinding, documentation, metadata capture, and audit trails.Partner with project management teams to ensure lab readiness, study start‑up timelines, sample logistics, and database lock requirements.Oversee Laboratory Information System (LIS) and study‑specific data integrations supporting sample tracking, eCRF data flows, and regulatory compliance, aligned with CAP expectations for LIS management.5. Personnel & Competency
Ensure all laboratory staff involved in clinical trial testing meet CLIA/CAP qualifications and any elevated state requirements (NY CQ categories, CA LFS licensure, etc.).Provide oversight of personnel competency assessments and continuing education tied to trial‑specific techniques. (General competence requirement)Support training in GCP/GCLP, protocol adherence, and data integrity.QualificationsRequired Qualifications
Federal (CLIA High‑Complexity Director Requirements)
Must meet one of the 42 CFR §493.1443 qualification pathways:
MD/DO with state medical license and board certification in anatomic/clinical pathology (ABP/AOBP); orMD/DO/DPM with ≥2 years high‑complexity lab director/supervisor experience + ≥20 CE hours in director responsibilities; orPhD or equivalent with HHS‑approved board certification (e.g., ABB, ABCC, ABMM, ABMLI) + required leadership experience + ≥20 CE hours.State Requirements (must meet the most stringent)
New York: Approved CQ categories for all testing performed; adherence to NY onsite/time requirements and director limits.Pennsylvania: Qualifications per 28 Pa. Code §5.21.California: Active LFS Laboratory Director (or specialty) licensure and personnel equivalency compliance.Clinical Trial–Specific Qualifications
Demonstrated leadership in GCLP/GCP‑aligned clinical trial laboratory operations.Proven experience conducting method validations, instrument qualifications, and assay lifecycle management within regulated trial environments.Prior interaction with sponsors, CROs, monitors, and regulatory audit teams (FDA, EMA, PMDA, CAP).Demonstrated understanding of the EU In Vitro Diagnostic Regulation (IVDR, Regulation (EU) 2017/746) and its impact on the design, validation, documentation, and post‑market oversight of in vitro diagnostic devices and tests.Knowledge, Skills & Abilities
Deep expertise in CAP checklists, CLIA personnel/testing rules, and director responsibilities.Prior success leading CAP inspections under updated personnel rules (Dec 28, 2024 changes).Strong command of GCP/GCLP quality requirements and clinical trial data integrity standards.Ability to communicate scientific, regulatory, and operational requirements effectively to sponsors and internal teams.Leadership skills in fast‑paced, audit‑intensive environments.Experience with global multi‑site or multi‑state clinical trial laboratory networks.Experience overseeing biomarker, pharmacokinetic, immunogenicity, genetic, or flow‑cytometry trial endpoints.Education & Continuing Education
Maintain any state‑specific CE/licensure renewals (NY CQ, CA LFS).As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work!
Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.
We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, vacation, personal days, and dental and vision options.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
All your information will be kept confidential according to EEO guidelines.
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