QC Utilities & Raw Materials Team Lead

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.