Analytical Science Data Review Group Leader

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.

Responsibilities

• 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
• 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

Requirements

• 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

Schedule

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.

Pay

Hourly rate is between $28.50 - $34.75 based on education and experience.

Benefits

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Candidates located within a commutable distance to Rensselaer, New York, are strongly encouraged to apply.