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Quality Assurance Specialist II

TEKsystems
Location 📍 Summerville, United States
Posted 📅 June 10, 2026
Work Type ⏰ Full-time

Position Overview

The Quality Assurance (QA) Specialist I is responsible for supporting and executing core quality system processes within a cGMP-regulated manufacturing environment. This role focuses heavily on supplier quality management, audit execution, CAPA coordination, and quality systems oversight.
Key responsibilities include:
Top Skills
. Regulated Manufacturing Experience
-Experience in dietary supplements, nutraceuticals, pharmaceuticals, or similar regulated industries
-Strong understanding of cGMP (Current Good Manufacturing Practices), quality systems, and compliance standards
-Hands-on work in regulated environments (pharma, biotech, medical device, etc.)
2. Supplier Quality & Audit Management
-Ownership of supplier quality programs and supplier relationships
-Experience conducting supplier audits (on-site and remote)
-Managing CAPA (Corrective and Preventive Actions) lifecycle, supplier qualification, and compliance oversight
Job Type & Location
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Job Details

Employment Type
Full-time
📊
Category
other-general
🏠
Work Arrangement
On-site
📍
Location
Summerville, United States