QC Utilities & Raw Materials Team Lead

Company DescriptionAt Eurofins Professional Scientific Services (PSS), the work we do truly matters—and so do our people. We are committed to supporting professional growth, providing hands-on experience within the biopharmaceutical industry, and fostering long-term career development in a collaborative, GMP-driven environment.

Eurofins Scientific is a global leader in laboratory testing services, supporting industries ranging from biopharmaceuticals and food safety to environmental and clinical research. With a strong commitment to scientific excellence, quality, and sustainability, Eurofins helps ensure the safety and integrity of the products that improve lives around the world.

Join a global organization where your work contributes to a safer, healthier, and more sustainable future.

Job DescriptionThe QC Utilities & Raw Materials Team Lead is a hands-on leadership role supporting Quality Control operations within a regulated biopharmaceutical manufacturing environment. This position combines routine QC testing responsibilities with day-to-day team leadership, training coordination, and operational oversight for utilities and raw materials testing.

The ideal candidate brings prior GMP laboratory experience, a strong testing background, and proven ability to support and guide junior staff while maintaining compliance, productivity, and data integrity.

Key ResponsibilitiesLaboratory & Technical ResponsibilitiesPerform QC Utilities and Raw Materials testing, including:pHConductivityNitrate identificationTotal Organic Carbon (TOC)Appearance testingReceive, handle, log, and dispose of samples in accordance with GMP requirementsCalibrate and verify calibration of laboratory instruments and equipment prior to useAccurately document test results and investigate or escalate quality anomalies as neededUtilize LIMS for sample management, data entry, and documentationMaintain laboratory supplies, reagents, and inventory; perform general laboratory housekeepingComply with all applicable regulatory, safety, and data integrity standardsParticipate in required training and continuous improvement initiativesCommunicate testing results, trends, and recommendations during group meetingsIndependently investigate quality deviations and implement corrective actions to prevent recurrenceSchedule testing activities on a weekly, monthly, and quarterly basisTeam Lead & Leadership ResponsibilitiesSupport, monitor, and coordinate the daily activities of the Utilities and Raw Materials QC teamAssist with onboarding and training of new hires, including GMP-related responsibilitiesCoordinate and maintain training plans and competency documentationPerform peer review of analytical data and documentationAssist with scheduling, task allocation, and resource planningSupport equipment maintenance and calibration coordinationParticipate in interviews and hiring activities, as neededDisseminate administrative and quality-related communicationsPromote teamwork, accountability, and adherence to company valuesMeet or exceed quality, productivity, and compliance metricsWork Environment & Physical RequirementsThis role requires extensive time in ISO 8 or higher biopharmaceutical cleanroom environments, with strict adherence to hygiene and gowning requirements, including:

No cosmetics or cosmetic productsShort, clean, unadorned nailsNo jewelry (exceptions for medical alert items and one smooth ring)Hair and facial hair must be secured with appropriate coveringsPhysical requirements include:

Lifting 25 lbs. or moreStanding and walking for extended periodsPushing or pulling carts and drumsBending, reaching, and handling laboratory materialsQualificationsRequiredBachelor's degree in Life Sciences or a related scientific discipline (or equivalent experience)1+ years of cGMP laboratory experience1+ years of leadership or team lead experienceStrong attention to detail and documentation practicesExcellent written and verbal communication skillsAbility to multi-task, plan proactively, and work independently or collaborativelyAuthorization to work in the U.S. without sponsorshipPreferredExperience with utilities or raw materials testingExperience using LIMSPrior work in a regulated biopharmaceutical manufacturing environmentAdditional InformationWhat to Expect in the

Hiring Process:

 10-15 Minute Phone Interview with Region Recruiter45-60 Minute Virtual Interview with Manager and/or Group Leader30 Minute Virtual Interview with Site Director 

Additional Details:

 This is a full-time, onsite position based on a first-shift schedule (Sunday through Wednesday 7am-5:30pm), with overtime required as needed. Candidates located within a commutable distance to Rensselaer, New York, are strongly encouraged to apply. Excellent full-time benefits include:

Comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysHourly rate is between $28-$33, depending on education and experience Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.