Group Leader- Data Review

Eurofins; Columbia Township (MO); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins USA BioPharma Services in Columbia, MO seeks a Data Review & Compliance Leader to oversee a team of data reviewers, ensure GMP data accuracy, and maintain GDP standards across all records.

The role covers staff development, workflow coordination, regulatory adherence, and collaboration with lab personnel and clients. Requires a BS in chemistry/biology/biochemistry, 2+ years of cGMP and leadership, and on-site second shift.

Qualifications

• Experience leading data review teams in cGMP environments.
• Strong documentation and compliance mindset.
• Excellent written and verbal communication.
• Ability to multitask in fast-paced settings.

Responsibilities

• Lead, manage, and develop a team of data reviewers.
• Coordinate workload and ensure timely deliverables.
• Manage cross-training and capacity planning.
• Track productivity and quality metrics.
• Serve as point of contact for clients and internal teams.
• Oversee safety and training; participate in hiring and onboarding.
• Deliver training programs for staff.
• Support scheduling, including overtime and weekends.
• Direct and monitor work assigned to team members.
• Understand regulatory requirements.
• Communicate with staff and other departments.

Skills

Leadership

Regulatory knowledge

Data integrity

Communication

Team management

Multitasking

Education

BS in chemistry, biology, biochemistry or related field

Job description

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Data Review & Compliance

• Review GMPdata 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

Leadership & Team Management

• 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 metricsServe 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
• Ability to direct and monitor work assigned to team members.
• Understanding of regulatory requirements.
• Communicate effectively with staff and members of other departments.

Qualifications

• BS in chemistry, biology, biochemistryor related field
• 2+ years of cGMP experience and2+ years of leadership
• 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
• MUSTbe authorized to work in the U.S. indefinitely without sponsorship

Additional Information

Working schedule will beFull-Time, Second Shift, M-F 12pm-8pm. Candidatescurrently living within a commutable distance of Columbia, MOare encouraged to apply. No relocation assistance will be given.25% travel may be required. This position isNOTremote.

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.