Quality System Compliance Specialist I
StimLabsRoswell, GA
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Job Description
đź“Ť Location: Roswell, GA
đź•’ Full-time | Entry-Level
đź’Ľ Industry: Biologics | Medical Devices | Regulated Manufacturing
StimLabs is on a mission to push the boundaries of regenerative medicine —and quality is at the heart of everything we do. We're looking for a Quality System Compliance Specialist I to join our dynamic team and support the systems that ensure we meet the highest standards of excellence.
What You’ll Do:
- Provide essential Quality support across departments
- Review and finalize batch records for regulatory compliance
- Facilitate corrections and clarifications of records
- Assist with audits, CAPAs, deviations, complaints, and product releases
- Support document control and quality record management
- Participate in improvement initiatives and quality education efforts
- Contribute to a range of cross-functional projects under guidance from Quality leadership
What You Bring:
- Bachelor’s degree in a technical or related field preferred (not required)
- Up to 1 year of experience in Quality Assurance or Quality Control in a regulated environment (pharmaceutical, medical device, biologics, or tissue banking)
- Familiarity with FDA regulations (21 CFR 1271, AATB, ISO13485, cGTP, cGMP) is a plus
- Detail-oriented mindset and collaborative attitude
- Eagerness to learn and grow in a quality-driven field
At StimLabs, you’ll join a passionate, fast-paced team where your work directly impacts patient outcomes. This is an ideal role for recent graduates or early-career professionals looking to break into the world of regulatory compliance and quality systems in a high-growth industry.