Quality Assurance Specialist II
Quality Assurance SpecialistLaboratory & Life Sciences
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Quick Summary
Overview
At Thorne, we work to deliver high-quality, science-backed solutions to empower individuals to take a proactive approach to their well-being.
Technical Tools
Quality Assurance SpecialistLaboratory & Life Sciences
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 Quality Assurance (QA) Specialist II is responsible and accountable for quality tasks and operations. Possesses and applies a broad knowledge of Quality principles, practices, and procedures. Supports Change Control process, Corrective and Preventive Action (CAPA) system, nonconforming material process, , internal audit process and third-party audit process. Works with the Material Review Board, Purchasing, and internal and external partners to resolve product issues. Must be able to lead and work with cross-functional teams and track projects to completion. Requires experience in a cGMP manufacturing environment plus demonstrated familiarity with standard quality concepts, practices, and procedures.
The Quality Assurance (QA) Specialist II is responsible and accountable for quality tasks and operations. Possesses and applies a broad knowledge of Quality principles, practices, and procedures. Supports Change Control process, Corrective and Preventive Action (CAPA) system, nonconforming material process, , internal audit process and third-party audit process. Works with the Material Review Board, Purchasing, and internal and external partners to resolve product issues. Must be able to lead and work with cross-functional teams and track projects to completion. Requires experience in a cGMP manufacturing environment plus demonstrated familiarity with standard quality concepts, practices, and procedures.
Location & Eligibility
Where is the job
Summerville, United States
On-site at the office
Who can apply
US
About this job
- Who can apply
- United States
- Posted
- 156 days ago
Listing Details
- First seen
- May 20, 2026
- Last seen
- October 24, 2026
Posting Health
- Days active
- 156
- Repost count
- 0
- Trust Level
- 18%
- Scored at
- October 24, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
External application
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