Analytical Science Data Review Group Leader

Job Description

We are seeking a driven and detail-oriented Analytical Sciences Data Review Group Leader to support GMP laboratory operations. This role combines hands-on data review responsibilities with team leadership, ensuring high-quality, compliant analytical data while mentoring and developing a high-performing team.

The ideal candidate brings strong cGMP experience, a deep understanding of analytical techniques, and a proactive leadership style focused on quality, accountability, and continuous improvement.

This is a Data Review role, rather than a Data Engineering role 

Key Responsibilities

Data Review & Compliance

• Review GMP analytical data for accuracy, completeness, and compliance with governing procedures
• Verify logbook entries for completeness and correctness
• Confirm chain of custody integrity for all tested samples
• Review audit trails to ensure proper execution and adherence to procedural timelines
• Communicate efficiently with laboratory personnel to resolve discrepancies, annotations, and corrections
• Apply Good Documentation Practices (GDP) in all records, including logbooks, notebooks, and electronic systems
• Perform laboratory safety and compliance walkthroughs and document observations
• Complete all required safety and procedural trainings

Leadership & Team Management

• Lead, manage, and develop a team of data reviewers
• Coordinate team workload and ensure timely completion of deliverables
• Manage cross-training initiatives and team capacity planning
• Track, monitor, and report productivity and quality metrics
• Serve as a proactive and effective point of contact for client and internal teams
• Conduct routine safety walkthroughs and employee compliance checks
• Participate in hiring, onboarding, and training of new team members
• Deliver training programs for new hires and existing staff
• Support scheduling needs, including overtime and weekend coverage as required

Qualifications

• BS in Chemistry or related field
• 2+ years of cGMP experience + 2+ years of leadership
• Experience with HPLC/UPLC, UV-Vis, and LC data analysis
• Exposure to ELISA, MCE, or iCIEF
• Strong communication, organization, and attention to detail
• High integrity with a focus on data quality and compliance
• Ability to multitask in a fast-paced environment and work independently or on a team
• Able to lift 25 lbs and stand/walk for extended periods
• Must be authorized to work in the U.S. without sponsorship

Additional Information

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 based on education and experience 

LinkedIn: #LI-EB1

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Company Description

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.

Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.