GMP Data Review Group Leader – Analytical Sciences

Company Description

The work we do at Eurofins matters—and so do our employees. We are committed to supporting your professional growth, providing opportunities to enter the biopharmaceutical industry and build a long-term career. Our teams are collaborative, our tools are best-in-class, and we prioritize work-life balance alongside a competitive benefits package.

Eurofins Scientific is a global leader in life sciences testing, delivering a broad range of analytical services across pharmaceutical, biotech, food, environmental, and clinical industries. Our work helps ensure product safety, authenticity, and regulatory compliance—contributing to a safer, healthier world.

Job Description

We are seeking a GMP Data Review Group Leader – Analytical Sciences to support laboratory operations in a regulated environment. This role combines hands-on GMP data review with team leadership , ensuring the delivery of high-quality, compliant analytical data while developing a strong, accountable team.

The ideal candidate brings cGMP expertise , a solid understanding of analytical techniques , and a proactive leadership approach focused on quality, efficiency, and continuous improvement.

Key Responsibilities

Data Review & Compliance

• Perform detailed review of GMP analytical data for accuracy, completeness, and procedural compliance
• Verify logbooks, notebooks, and electronic records for proper documentation practices (GDP)
• Ensure chain of custody is maintained and properly documented
• Review audit trails to confirm compliant execution and timing
• Partner with laboratory staff to investigate and resolve discrepancies, deviations, and corrections
• Conduct laboratory safety and compliance walkthroughs and document findings
• Maintain adherence to all required training, safety, and quality standards

Leadership & Team Management

• Lead, mentor, and develop a team of data reviewers
• Coordinate workload, ensuring timely and high-quality deliverables
• Support cross-training and team capacity planning
• Track and report on productivity, quality, and performance metrics
• Act as a key point of contact for clients and internal stakeholders
• Participate in hiring, onboarding, and training of new team members
• Deliver training programs and reinforce best practices in GMP data review
• Support scheduling needs, including overtime or weekend coverage as required

Qualifications

• Bachelor’s degree in Chemistry or related scientific field
• Minimum 2+ years of cGMP experience and 2+ years of leadership experience
• Hands-on experience with HPLC/UPLC, UV-Vis, and chromatography data analysis
• Exposure to ELISA, MCE, or iCIEF preferred
• Strong knowledge of GMP, GDP, and data integrity principles
• Excellent communication, organization, and attention to detail
• Ability to multitask in a fast-paced environment and work both independently and collaboratively
• Must be able to stand/walk for extended periods and lift up to 25 lbs
• Must be authorized to work in the U.S. without sponsorship

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

This is a full-time, 100% onsite position based on a first-shift schedule (Monday–Friday, 8:30am–4:30pm), 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 $28.50 - $34.75 depending on education and experience