GMP Scientific Data Review Lead at Eurofins

Rensselaer, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

01 Jan, 26

Salary

33.0

Posted On

03 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP, Analytical Science, Data Review, Team Leadership, Compliance, ELISA, MCE, iCIEF, Documentation Standards, Safety Walkthroughs, Mentoring, Capacity Planning, Quality Metrics, Collaboration, Continuous Improvement, Organizational Skills

Industry

Medical and Diagnostic Laboratories

Description

Company Description Make an Impact with Eurofins At Eurofins, your work helps ensure the safety and effectiveness of life-saving therapies. As a global leader in laboratory services, we support the pharmaceutical industry with cutting-edge science and unwavering commitment to quality. Join a team where your expertise in GMP and analytical science drives real-world impact—and where your career can grow with purpose. Job Description We’re seeking a GMP Scientific Data Review Lead to oversee the integrity and compliance of analytical data generated in a GMP-regulated clinical biochemistry environment. This leadership role blends scientific rigor with operational oversight, ensuring data quality, team performance, and regulatory alignment. What You’ll Do: Scientific & Compliance Oversight Lead the review of analytical data from assays such as ELISA, MCE, and iCIEF. Ensure data accuracy, completeness, and compliance with GMP and GDP standards. Confirm sample chain of custody and audit trail integrity. Collaborate with analysts to resolve discrepancies and uphold documentation standards. Conduct routine safety walkthroughs and escalate concerns appropriately. Team Leadership & Development Manage and mentor a team of scientific reviewers. Coordinate workload distribution, cross-training, and capacity planning. Monitor and report on productivity and quality metrics. Support hiring, onboarding, and training of new team members. Foster a culture of compliance, collaboration, and continuous improvement. Qualifications Bachelor’s degree in Life Sciences or related field. Minimum 2 years of GMP experience and 2 years of leadership experience. Hands-on experience with ELISA, MCE, and/or iCIEF techniques. Strong organizational, communication, and computer skills. Ability to meet physical demands (lifting up to 25 lbs, standing/walking for extended periods). Authorization to work in the U.S. without restriction or sponsorship. Additional Information Why Join Eurofins? Growth & Purpose Be part of a mission-driven company impacting global health. Collaborate with top scientific minds in a supportive, growth-focused environment. Enjoy clear career advancement pathways and ongoing professional development. What to Expect in the Hiring Process 10–15 Minute Phone Interview with a Regional Recruiter 45–60 Minute Virtual Interview with the Hiring Manager and/or Group Leader Schedule: Full-time, Monday–Friday, 8:00 AM–4:00 PM Candidates currently living within a commutable distance to Rensselaer, NY are encouraged to apply. Benefits & Compensation Medical Coverage: Comprehensive medical insurance options Dental & Vision: Full dental and vision coverage available Life & Disability Insurance: Employer-sponsored plans Retirement: 401(k) plan with company match Paid Time Off: Vacation days, paid holidays, and additional PTO options Compensation: $28.00 – $33.00 per hour Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

The GMP Scientific Data Review Lead oversees the integrity and compliance of analytical data in a GMP-regulated environment. This role includes leading data reviews, ensuring compliance with standards, and managing a team of scientific reviewers.