Job Information
ThermoFisher Scientific Team Leader Operations Batch Record Review in Greenville, North Carolina
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond.
Location/Division Specific Information
Greenville, NC
RELOCATION ASSISTANCE IS NOT PROVIDED
Must be legally authorized to work in the United States WITHOUT SPONSORSHIP OF ANY KIND NOW OR IN THE FUTURE.
Must be able to pass a comprehensive background check, which includes a drug screen.
Discover Impactful Work:
In this role, you will support and coordinate Production batch record review activities to ensure accuracy, completeness, and compliance prior to submission to Quality Assurance. You will partner closely with Operations and cross-functional teams to resolve documentation issues, support timely product release, and contribute to a culture of quality and continuous improvement.
A Day in the Life:
Coordinate daily batch record review activities and prioritize team workload
Serve as a point of contact for routine questions, issue resolution, and escalations
Perform detailed batch record review to ensure compliance with procedures and cGMP standards
Identify and resolve documentation errors in collaboration with QA and Production teams
Track key performance metrics and escalate risks to quality or delivery
Support onboarding and training of team members
Maintain knowledge of systems, procedures, and regulatory requirements
Contribute to continuous improvement initiatives and process enhancements
Promote safe work practices and compliance with all safety requirements
Keys to Success:
Education
- Bachelor’s degree in a scientific or related field OR equivalent experience (5+ years)
Experience
2–4 years of experience in pharmaceutical or regulated manufacturing
Experience with batch record review, documentation, or quality operations preferred
Knowledge, Skills, Abilities
Strong attention to detail and commitment to accuracy
Working knowledge of cGMP and regulated environments
Ability to follow procedures and ensure compliant documentation
Strong communication and cross-functional collaboration skills
Problem-solving skills with ability to escalate complex issues
Ability to manage multiple priorities in a fast-paced environment
Strong organizational and time management skills
Ability to maintain confidentiality and exercise sound judgment
Competencies
Customer-focused mindset
Accountability and ownership
Effective communication
Team collaboration
Continuous improvement orientation
Additional Information
Supervisory responsibility for a team of 2–6 employees
Reports to Manager, Operations Support
Ability to work in an aseptic or controlled environment
Ability to stand, walk, and perform physical tasks as required (10–35 lbs occasionally)
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.