Analytical Sciences Lab Lead – HPLC/UPLC & Data Review

We are seeking a hands-on Analytical Sciences Lab Lead with strong expertise in HPLC/UPLC testing and GMP data review to support laboratory operations in a fast-paced, compliance-driven environment.

This role is ideal for a scientist who enjoys staying connected to the bench while playing a critical role in ensuring the accuracy, integrity, and compliance of analytical data. The Lab Lead will be responsible for both executing and reviewing analytical work, with a strong emphasis on data verification, audit trail review, and Good Documentation Practices (GDP).

In addition to technical responsibilities, this individual will lead and develop a team, helping ensure high-quality output, strong compliance practices, and efficient lab operations. The position requires a proactive leader who can bridge hands-on testing with detailed data review oversight.

Key Responsibilities

Analytical Testing & Data Review

• Perform and support HPLC/UPLC and other analytical testing in a GMP laboratory
• Conduct thorough review of analytical data to ensure accuracy, completeness, and compliance with SOPs and regulatory requirements
• Review chromatographic data, calculations, sequences, and system suitability results
• Verify audit trails, integration, and proper system usage
• Ensure chain of custody and sample traceability throughout testing processes
• Review and maintain lab notebooks, logbooks, and electronic records in accordance with GDP
• Identify, investigate, and resolve data discrepancies or deviations in collaboration with lab staff

Leadership & Lab Operations

• Lead, mentor, and develop a team of analysts and data reviewers
• Balance team workload across testing and data review activities
• Support training, onboarding, and skill development, particularly in data integrity and chromatography
• Monitor and report on quality metrics, turnaround times, and productivity
• Serve as a key point of contact between lab staff, management, and clients
• Promote a culture of quality, accountability, and continuous improvement

Compliance & Quality Oversight

• Ensure adherence to cGMP, GLP, and internal procedures
• Perform audit trail reviews and documentation checks to support data integrity initiatives
• Conduct laboratory walkthroughs and compliance checks
• Support internal and external audits as needed
• Maintain a strong focus on data integrity, documentation accuracy, and regulatory readiness

• Bachelor’s degree in Chemistry or related scientific field
• 2+ years of cGMP data review experience (required)
• 2+ years of leadership or team coordination experience
• Strong hands-on experience with HPLC/UPLC and chromatographic data analysis
• Experience with UV-Vis; exposure to ELISA, MCE, or iCIEF preferred
• Deep understanding of data integrity principles, audit trails, and GDP
• Strong attention to detail with the ability to identify inconsistencies in analytical data
• Effective communicator with strong organizational and multitasking skills
• Ability to work both at the bench and in a data review capacity

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 

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