Group Leader- Data Review
Eurofins BioPharma Product Testing North America · Columbia, MO · 1 mo ago
On-siteScienceFull-time
About the role
Eurofins Scientific is an international life sciences company providing analytical testing services across multiple industries to ensure product safety, authenticity, and compliance. The Eurofins network operates 900 laboratories in over 54 countries, employing 58,000 staff and offering over 200,000 analytical methods. In 2024, Eurofins generated total revenues of €6.515 billion.
Responsibilities
- Data Review & Compliance: Review GMP data 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 metrics
- Serve 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
Requirements
- BS in chemistry, biology, biochemistry or related field
- 2+ years of cGMP experience
- 2+ years of leadership experience
- 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
- Must be authorized to work in the U.S. indefinitely without sponsorship
Schedule
- Full-Time, Second Shift, Monday–Friday 12:00 PM–8:00 PM
- Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply
- 25% travel may be required
- This position is NOT remote
Benefits
- Comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays