Analytical Lab Supervisor

Job Description

Job Description

Description

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, you’ll 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 Thorne's 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 Thorne's 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.

• 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.

Education & Experience  

• Bachelor's 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.

• Competitive compensation
• 100% company-paid medical, dental, and vision insurance coverage for employees
• Company-paid short- and long-term disability insurance
• Company- paid life insurance
• 401k plan with employer matching contributions up to 4%
• Gym membership reimbursement
• Monthly allowance of Thorne supplements
• Paid time off, volunteer time off and holiday leave
• Training, professional development, and career growth opportunities