DescriptionThe Quality Assurance (QA) Specialist II 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:- Managing supplier relationships and ensuring compliance with quality requirements
- Conducting supplier audits (on-site and remote)
- Supporting CAPA, change control, and nonconformance processes
- Leading supplier qualification and maintaining approved supplier lists
- Investigating product complaints and coordinating corrective actions
- Supporting regulatory inspections and internal audits
- Reviewing SOPs and maintaining compliance with cGMP standards
- Driving process improvements and quality initiatives across teams
This individual will collaborate with cross-functional teams including Procurement, Engineering, Quality, and Manufacturing to ensure product quality and regulatory compliance.
Required Skills & Qualifications1. 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
3. Communication & Cross-Functional Collaboration-Strong verbal and written communication skills
-Ability to work cross-functionally with Procurement, Engineering, Manufacturing, and Quality teams
-Clearly present audit findings, compliance updates, and quality initiatives
Additional Skills and Qualifications - Bachelor's degree + 4+ years of relevant experience OR equivalent
- Strong understanding of cGMP, FDA, and regulatory compliance
- Experience working with contract manufacturers and suppliers
- Excellent communication and documentation skills
- Ability to work independently and manage multiple priorities
- Willingness to travel up to 50%
Job Type & LocationThis is a Permanent position based out of Charleston, SC.
Pay and BenefitsThe pay range for this position is $85000.00 - $90000.00/yr.
Full Benefits - Medical, Dental, Vision, 401k Match, etc
Workplace TypeThis is a fully onsite position in Charleston,SC.
Application DeadlineThis position is anticipated to close on Aug 21, 2026.
About TEKsystemsWe're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
About TEKsystems and TEKsystems Global Services We're a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We're a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We're strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We're building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
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