Job Information
Eurofins US Network QC Utilities & Raw Materials Team Lead in Rensselaer, New York
Rensselaer, NY, USA
Full-time
Company Description
At 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 Description
The 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 Responsibilities
Laboratory & Technical Responsibilities
Perform QC Utilities and Raw Materials testing, including:
pH
Conductivity
Nitrate identification
Total Organic Carbon (TOC)
Appearance testing
Receive, handle, log, and dispose of samples in accordance with GMP requirements
Calibrate and verify calibration of laboratory instruments and equipment prior to use
Accurately document test results and investigate or escalate quality anomalies as needed
Utilize LIMS for sample management, data entry, and documentation
Maintain laboratory supplies, reagents, and inventory; perform general laboratory housekeeping
Comply with all applicable regulatory, safety, and data integrity standards
Participate in required training and continuous improvement initiatives
Communicate testing results, trends, and recommendations during group meetings
Independently investigate quality deviations and implement corrective actions to prevent recurrence
Schedule testing activities on a weekly, monthly, and quarterly basis
Team Lead & Leadership Responsibilities
Support, monitor, and coordinate the daily activities of the Utilities and Raw Materials QC team
Assist with onboarding and training of new hires, including GMP-related responsibilities
Coordinate and maintain training plans and competency documentation
Perform peer review of analytical data and documentation
Assist with scheduling, task allocation, and resource planning
Support equipment maintenance and calibration coordination
Participate in interviews and hiring activities, as needed
Disseminate administrative and quality-related communications
Promote teamwork, accountability, and adherence to company values
Meet or exceed quality, productivity, and compliance metrics
Work Environment & Physical Requirements
This 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 products
Short, clean, unadorned nails
No jewelry (exceptions for medical alert items and one smooth ring)
Hair and facial hair must be secured with appropriate coverings
Physical requirements include:
Lifting 25 lbs. or more
Standing and walking for extended periods
Pushing or pulling carts and drums
Bending, reaching, and handling laboratory materials
Qualifications
Required
Bachelor’s degree in Life Sciences or a related scientific discipline (or equivalent experience)
1+ years of cGMP laboratory experience
1+ years of leadership or team lead experience
Strong attention to detail and documentation practices
Excellent written and verbal communication skills
Ability to multi-task, plan proactively, and work independently or collaboratively
Authorization to work in the U.S. without sponsorship
Preferred
Experience with utilities or raw materials testing
Experience using LIMS
Prior work in a regulated biopharmaceutical manufacturing environment
Additional Information
What to Expect in the Hiring Process:
10-15 Minute Phone Interview with Region Recruiter
45-60 Minute Virtual Interview with Manager and/or Group Leader
30 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 options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Hourly rate is between $28-$33, depending on education and experience
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.