Job 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.

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.