GMP Analytical Data Review Supervisor
About The Position
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, apply with us today! Position Overview We are seeking a GMP Analytical Data Review Supervisor with proven leadership experience to oversee a team dedicated to ensuring data integrity and compliance in a regulated pharmaceutical environment. This role combines technical expertise with strong people management skills to maintain the highest standards of quality and operational excellence.
Requirements
- Bachelor’s degree in Chemistry, Life Sciences, or related field.
- Minimum 3 years of leadership experience managing technical teams in a GMP-regulated pharmaceutical or biopharma environment.
- Strong understanding of analytical techniques and data integrity principles.
- Demonstrated ability to coach, mentor, and develop team members while driving operational excellence.
- Proven success in managing compliance-driven processes and leading cross-functional initiatives.
- Must be authorized to work in the United States indefinitely without restriction or sponsorship.
Responsibilities
- Lead and develop a high-performing team of data reviewers in a GMP-regulated laboratory setting.
- Oversee the review of analytical data (LC, MCE, ELISA) for completeness, accuracy, and compliance with industry standards.
- Ensure adherence to FDA, ICH, and GMP guidelines throughout all data review processes.
- Drive team engagement through coaching, mentoring, and performance management.
- Manage workflow, scheduling, and resource allocation to optimize efficiency and maintain compliance.
- Collaborate with laboratory operations to resolve discrepancies and implement corrective actions.
- Serve as a liaison between internal teams and external clients, ensuring timely and accurate deliverables.
- Apply Lean principles to improve processes and foster continuous improvement.
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Manager
Number of Employees
5,001-10,000 employees
