Quality Control Sampling Group Leader
Eurofins
Posted: April 10, 2026
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Quick Summary
The Quality Control Sampling Group Leader is responsible for ensuring the accuracy and quality of samples in the biopharmaceutical industry, working closely with cross-functional teams to identify and resolve quality issues, and implementing processes to improve overall quality.
Required Skills
Job Description
The work we do at Eurofins Professional Scientific Services (PSS) matters—and so do our employees. At Eurofins PSS, we invest in professional growth by providing hands-on experience, strong team support, and clear development pathways within the biopharmaceutical industry. We are committed to helping employees build long-term careers while maintaining work-life balance and offering competitive benefits.
Eurofins Scientific is an international life sciences company providing a comprehensive range of analytical testing services across industries including pharmaceuticals, biopharmaceuticals, food, environmental, cosmetics, and agroscience. Our work helps ensure products are safe, authentic, and accurately labeled—contributing to a safer, healthier, and more sustainable world.
Join Eurofins and be part of a global team driving scientific excellence.
The Quality Control Sampling Group Leader is a hands-on leadership role responsible for overseeing raw material and container sampling activities within a GMP-regulated biopharmaceutical manufacturing environment. This role combines routine laboratory sampling responsibilities with oversight of daily team operations, training, scheduling, and compliance.
Laboratory Responsibilities
• Perform all duties associated with Quality Control sampling activities in support of manufacturing operations
• Collect solid and/or liquid samples from raw materials and manufacturing components
• Handle, document, and manage samples in compliance with GMP and site SOPs
• Perform quality inspections and analysis of containers and materials
• Calibrate or verify calibration of instruments and devices prior to use
• Gown and work within ISO 8+ cleanroom environments using proper sterile technique
• Maintain laboratory areas, supplies, reagents, media, and sampling equipment
• Use the Laboratory Information Management System (LIMS) for sample tracking and documentation
• Schedule sampling and lab activities on a weekly, monthly, and quarterly basis
• Participate in investigations of quality deviations and implement corrective actions to prevent recurrence
• Communicate findings, deviations, and recommendations during group meetings
• Participate in and/or lead cross-functional initiatives to support optimal client services
• Maintain compliance with regulatory agency and company requirements
• Participate in required training activities and maintain complete training records
• Support physical demands of the role, including lifting 25 lbs or more, standing/walking for extended periods, and handling carts, drums, and materials
Leadership Responsibilities
• Support and monitor the performance of a team of Quality Control Sampling employees
• Coordinate daily work assignments, scheduling, and workload allocation
• Train and onboard new employees and support ongoing technical and GMP training
• Conduct peer review of analytical and sampling documentation
• Assist with equipment maintenance coordination and calibration activities
• Support interviews and hiring activities as needed
• Disseminate administrative and operational communications
• Promote company values, quality culture, and teamwork
• Ensure team meets quality, productivity, and compliance metrics
• Coordinate and maintain the group training program
Important Role Information
This position requires significant time working in ISO 8+ biopharmaceutical cleanroom environments with strict hygiene and gowning requirements, including:
• No cosmetic products permitted in cleanroom areas
• Nails must be short, clean, and unadorned
• No jewelry permitted except medical alerts and one smooth ring band
• Hair must be secured in a hairnet; facial hair must be contained in a beard cover
• Strict adherence to site hygiene policies is required
Ideal Candidate:
• Laboratory experience in a regulated environment
• 1+ year of cGMP experience
• Strong organizational, scientific, and computer skills
• Excellent written and verbal communication skills
• High attention to detail and documentation accuracy
• Ability to work independently and collaboratively in a client-facing environment
• Ability to multitask, prioritize work, and adapt to evolving priorities
• Experience with LIMS preferred
Minimum Qualifications:
• Bachelor’s degree in Life Sciences or a related scientific field (or equivalent relevant experience)
• 1+ year of prior leadership or lead-level experience
• Authorization to work in the United States without sponsorship
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 (Monday through Friday, 8am to 4pm), 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.