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Analytical Lab Supervisor

Thorne

Job Location:

Summerville, SC - USA

Monthly Salary: Not provided by the employer

Posted: 3 July 2026 (30+ days ago)

Application Deadline: 4 October 2026

Vacancies: 1 Vacancy

Job Summary

At Thorne we work to deliver high-quality science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. At Thorne youll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage.

The Analytical Lab Supervisor oversees the day-to-day operations of Thornes Analytical Laboratory ensuring testing activities are performed safely efficiently and in compliance with applicable quality and regulatory standards. This role leads laboratory personnel manages daily workflows and supports the timely delivery of accurate analytical results that are essential to product quality manufacturing operations and regulatory compliance.

Working closely with Quality Control Quality Assurance Manufacturing Regulatory Affairs and other cross-functional teams the Analytical Lab Supervisor ensures laboratory operations adhere to Laboratory Standard Operating Procedures (SOPs) Good Laboratory Practices (GLP) current Good Manufacturing Practices (cGMP) ISO 17025 requirements and Thornes Hazardous Material Safety Program. The ideal candidate is a hands-on laboratory leader with strong technical expertise a commitment to quality and data integrity and a passion for developing high-performing teams while driving continuous improvement across laboratory operations.

RESPONSIBILITIES

Lead the day-to-day operations of the Analytical Laboratory ensuring testing activities are completed safely efficiently and in accordance with established priorities and quality standards.
Supervise train mentor and develop laboratory personnel ensuring employees receive timely training on analytical methods laboratory procedures safety requirements Good Laboratory Practices (GLP) current Good Manufacturing Practices (cGMP) and applicable Standard Operating Procedures (SOPs).
Oversee laboratory workflows including routine testing stability studies retained sample management documentation and resource planning to support manufacturing and business objectives.
Review analytical data laboratory documentation specifications validation protocols stability protocols investigation reports and Standard Operating Procedures (SOPs) to ensure accuracy completeness and regulatory compliance.
Lead investigations of Out-of-Specification (OOS) and other atypical laboratory results partnering with cross-functional teams to perform root cause analysis implement corrective actions and prevent recurrence.
Partner with the QC Data team to resolve testing issues ensure data integrity and maintain laboratory records in accordance with regulatory requirements and industry best practices.
Ensure laboratory instrumentation equipment and supporting software are properly maintained calibrated and qualified to support reliable analytical testing.
Maintain the Analytical Laboratory in an inspection-ready state by ensuring compliance with GLP cGMP ISO 17025 and applicable federal state and local regulatory requirements.
Support the Quality Control Laboratory Manager in maintaining and continuously improving the laboratory Quality Management System (QMS) including ISO 17025 compliance audit readiness and quality system effectiveness.
Promote a culture of data integrity impartiality confidentiality safety and continuous improvement by identifying risks implementing process improvements and fostering operational excellence across laboratory operations.
Collaborate with Quality Assurance Manufacturing Regulatory Affairs Product Development and other cross-functional teams to support product quality resolve technical issues and achieve organizational objectives.

WHAT YOU NEED

Education & Experience

Bachelors degree in Chemistry or a related scientific discipline required including a minimum of 12 credit hours in college-level chemistry.
Experience in an analytical laboratory operating within a cGMP-regulated environment.
Hands-on experience with at least two of the following analytical techniques:
- High Performance Liquid Chromatography (HPLC)
- Gas Chromatography (GC)
- Inductively Coupled Plasma (ICP) Spectroscopy
- Near Infrared (NIR) Spectroscopy
Previous supervisory or team leadership experience in an analytical laboratory environment preferred.
Experience supporting laboratory investigations method validation stability testing and quality systems is preferred.

Technical Knowledge

Strong knowledge of Good Laboratory Practices (GLP) current Good Manufacturing Practices (cGMP) and laboratory quality systems.
Working knowledge of ISO 17025 requirements laboratory documentation and data integrity principles.
Experience reviewing analytical data laboratory documentation specifications validation protocols stability studies and investigation reports.
Familiarity with laboratory instrumentation calibration maintenance troubleshooting and supporting software applications.
Ability to interpret scientific data technical documentation Standard Operating Procedures (SOPs) and regulatory requirements to support sound technical decision-making.

Core Competencies

Proven leadership skills with the ability to supervise coach mentor and develop high-performing laboratory teams.
Experience managing laboratory workloads prioritizing testing activities and delegating assignments to meet business objectives and testing deadlines.
Strong analytical and problem-solving skills with experience leading investigations root cause analysis and corrective actions.
Excellent verbal and written communication skills with the ability to communicate effectively across Quality Control Quality Assurance Manufacturing Regulatory Affairs and senior leadership.
Strong organizational skills with the ability to manage multiple priorities while maintaining laboratory efficiency and regulatory compliance.
Collaborative leadership style with the ability to build strong cross-functional relationships and drive continuous improvement initiatives.
High attention to detail with a commitment to laboratory excellence data integrity and operational quality.
Demonstrated ability to hire develop evaluate and retain talent while fostering a culture of accountability safety and continuous learning.

WHAT WE OFFER