Quality System Compliance Specialist I

📍 Location: Roswell, GA 🕒 Full-time | Entry-Level 💼 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.