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Eurofins
Analytical Science Data Review Group Leader
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What they do
A Data Scientist utilizes skills and experience to systematically answer questions using data to provide actionable recommendations. Commonly utilizes advanced statistical analysis and machine learning techniques. Common responsibilities also include data cleaning and data management.
$116,614 / year median in New York
+10% projected growth
Job Description
Company DescriptionAt 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.
Job DescriptionWe 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 ResponsibilitiesData Review & ComplianceReview GMP analytical data for accuracy, completeness, and compliance with governing proceduresVerify logbook entries for completeness and correctnessConfirm chain of custody integrity for all tested samplesReview audit trails to ensure proper execution and adherence to procedural timelinesCommunicate efficiently with laboratory personnel to resolve discrepancies, annotations, and correctionsApply Good Documentation Practices (GDP) in all records, including logbooks, notebooks, and electronic systemsPerform laboratory safety and compliance walkthroughs and document observationsComplete all required safety and procedural trainingsLeadership & Team ManagementLead, manage, and develop a team of data reviewersCoordinate team workload and ensure timely completion of deliverablesManage cross-training initiatives and team capacity planningTrack, monitor, and report productivity and quality metricsServe as a proactive and effective point of contact for client and internal teamsConduct routine safety walkthroughs and employee compliance checksParticipate in hiring, onboarding, and training of new team membersDeliver training programs for new hires and existing staffSupport scheduling needs, including overtime and weekend coverage as requiredQualificationsBS in Chemistry or related field2+ years of cGMP experience + 2+ years of leadershipExperience with HPLC/UPLC, UV-Vis, and LC data analysisExposure to ELISA, MCE, or iCIEFStrong communication, organization, and attention to detailHigh integrity with a focus on data quality and complianceAbility to multitask in a fast-paced environment and work independently or on a teamAble to lift 25 lbs and stand/walk for extended periodsMust be authorized to work in the U.S. without sponsorshipAdditional InformationThis 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysHourly rate is between $28.50 - $34.75 based on education and experience
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.
Job DescriptionWe 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 ResponsibilitiesData Review & ComplianceReview GMP analytical data for accuracy, completeness, and compliance with governing proceduresVerify logbook entries for completeness and correctnessConfirm chain of custody integrity for all tested samplesReview audit trails to ensure proper execution and adherence to procedural timelinesCommunicate efficiently with laboratory personnel to resolve discrepancies, annotations, and correctionsApply Good Documentation Practices (GDP) in all records, including logbooks, notebooks, and electronic systemsPerform laboratory safety and compliance walkthroughs and document observationsComplete all required safety and procedural trainingsLeadership & Team ManagementLead, manage, and develop a team of data reviewersCoordinate team workload and ensure timely completion of deliverablesManage cross-training initiatives and team capacity planningTrack, monitor, and report productivity and quality metricsServe as a proactive and effective point of contact for client and internal teamsConduct routine safety walkthroughs and employee compliance checksParticipate in hiring, onboarding, and training of new team membersDeliver training programs for new hires and existing staffSupport scheduling needs, including overtime and weekend coverage as requiredQualificationsBS in Chemistry or related field2+ years of cGMP experience + 2+ years of leadershipExperience with HPLC/UPLC, UV-Vis, and LC data analysisExposure to ELISA, MCE, or iCIEFStrong communication, organization, and attention to detailHigh integrity with a focus on data quality and complianceAbility to multitask in a fast-paced environment and work independently or on a teamAble to lift 25 lbs and stand/walk for extended periodsMust be authorized to work in the U.S. without sponsorshipAdditional InformationThis 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysHourly rate is between $28.50 - $34.75 based on education and experience