Job Information
ThermoFisher Scientific QC Finished Product Supervisor in High Point, North Carolina
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products 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 by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Position Summary
The Finished Product / Stability QC Supervisor is responsible for leading a Quality Control team in a cGMP-regulated environment, ensuring compliance with all regulatory requirements and internal quality standards. This role provides technical leadership and oversight of laboratory operations supporting pharmaceutical manufacturing, including finished product release and stability testing programs.
The supervisor drives operational excellence through team development, workflow optimization, and continuous improvement initiatives, while maintaining a strong focus on quality, compliance, and data integrity.
Key Responsibilities
Lead and supervise QC analysts supporting finished product release and stability testing
Ensure compliance with cGMP, FDA regulations, ICH guidelines, and internal quality systems
Oversee laboratory operations including scheduling, resource allocation, and workload prioritization
Provide technical expertise in analytical testing methods (e.g., HPLC, GC, dissolution)
Manage and prioritize stability testing programs to meet critical deadlines
Review and approve laboratory data, investigations, and technical documentation
Lead and support OOS, OOT, deviations, and root cause investigations
Mentor, coach, and develop team members to foster a strong quality culture
Support regulatory inspections and audits, ensuring inspection readiness at all times
Drive continuous improvement initiatives to enhance efficiency, compliance, and data quality
Ensure adherence to data integrity principles and proper documentation practices
Collaborate cross-functionally with Manufacturing, QA, and other stakeholders
Utilize LIMS and quality systems for data tracking, reporting, and compliance
Minimum Qualifications
Education & Experience:
Advanced degree with 3+ years of relevant experience, or
Bachelor’s degree with 5+ years of experience in pharmaceutical/biotech QC
Minimum 2 years of leadership or supervisory experience
Field of Study:
Chemistry, Biology, Biochemistry, Microbiology, or related scientific discipline
Preferred Qualifications
Certifications in quality systems, regulatory compliance, or project management
Experience with LIMS and quality management systems
Experience supporting regulatory audits and inspections
Required Skills & Competencies
Strong knowledge of cGMP, FDA regulations, and ICH guidelines
Expertise in release chemistry and stability testing requirements
Proficiency with analytical instrumentation (HPLC, GC, dissolution, etc.)
Strong technical writing skills (SOPs, investigations, regulatory documents)
Proven leadership and team development capabilities
Excellent problem-solving and root cause analysis skills
Strong organizational and project management abilities
Effective communication and interpersonal skills across all organizational levels
Working knowledge of data integrity and documentation practices
Ability to manage multiple priorities while maintaining high-quality standards
Proficiency in Microsoft Office applications
Flexibility to support manufacturing schedules as needed
Work Environment & Expectations
Operates in a regulated laboratory environment supporting pharmaceutical manufacturing
Requires adaptability to shifting priorities and production timelines
Strong emphasis on quality, compliance, and continuous improvement
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.