QA Release & Compliance Technician (Medical Devices, GMP)

Automation Personnel Services, Inc.; Marietta (GA); On-site; USD 28,000 - 39,000; Full time

Benefits offered by this job

Weekly Pay

Medical, dental, vision, short-termdis

Life insurance

401(k) Retirement Plan

6 paid Holidays

$50 referral bonus

Job summary

Automation Personnel Services, Inc. in Marietta, GA, is seeking a detail-focused Quality Assurance Technician for a respected medical device manufacturer.

This role provides hands-on experience in a regulated environment, supporting product quality, compliance, and patient safety. You will verify labels and lot information, perform release inspections, review batch records, and manage product release in Epicor from start to finish, including verifying labeling before startup and final sign-off

Qualifications

• High School diploma required; some college preferred.
• 2–3 years of recent quality inspector experience.
• Medical manufacturing experience preferred.
• Experience with GMP procedures.
• Strong attention to detail and documentation accuracy.
• Ability to read, write, and communicate effectively in English.
• Drug screening and background check required.

Responsibilities

• Verify labels, cartons, products, and other materials for correct lot information during first-off quality release.
• Perform release inspections and collect random in-process samples to confirm products meet specified criteria.
• Review Device Batch Records for completeness and GMP documentation compliance.
• Manage product release in Epicor from start to finish, including verifying production labeling before startup and signing off on the release.

Skills

Attention to detail

Documentation accuracy

Quality inspection

English communication

Education

HS diploma

Some college preferred

Tools

Epicor

Job description

Automation Personnel Services, Inc. in Marietta, GA, is seeking a detail-focused Quality Assurance Technician for a respected medical device manufacturer.

This role provides hands-on experience in a regulated environment, supporting product quality, compliance, and patient safety. You will verify labels and lot information, perform release inspections, review batch records, and manage product release in Epicor from start to finish, including verifying labeling before startup and final sign-off