Quality System Compliance Specialist I

StimLabs LLC.; Roswell (GA); On-site; Full time

Job summary

A leading company in the biologics and medical devices industry is seeking a Quality System Compliance Specialist I. This entry-level position offers the chance to gain hands-on experience in quality assurance and regulatory compliance, with opportunities for recent graduates or early-career professionals to contribute to meaningful projects in a high-growth environment.

Qualifications

• Up to 1 year of experience in Quality Assurance or Quality Control in a regulated environment.
• Eagerness to learn and grow in a quality-driven field.

Responsibilities

• Provide essential Quality support across departments.
• Review and finalize batch records for regulatory compliance.
• Assist with audits, CAPAs, deviations, complaints, and product releases.

Skills

Detail-oriented

Collaborative attitude

Familiarity with FDA regulations

Education

Bachelor’s degree in a technical or related field

Job description

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

$18 - $22.50 an hour

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.