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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.

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