Quality Control Technician - GMP/GLP Tester & Auditor

Abbott; Atlanta (GA); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Medical plan

Dental plan

Vision plan

Health Savings Account

Flexible Spending Accounts

Life Insurance

Short/Long Term Disability

401(k)

Job summary

Abbott is seeking a Quality Control Technician to support the Quality Management System in Atlanta, onsite. The role involves product testing, documentation review, inspections, and audits to ensure GMP and GLP compliance. A Bachelor's degree in a scientific/technical field and GMP/GLP knowledge are required.

Preferred one year of QA experience in the medical device industry. The position runs 12 months with 100% onsite work; shift is 2:30 PM – 11:00 PM.

Qualifications

• Bachelor's degree in a scientific or technical field or equivalent combination of education and experience.
• Ability to follow GMP and GLP.

Responsibilities

• Conduct product testing to support complaint investigations and stability verification.
• Generate product testing reports.
• Review production and finished goods batch records (DHRs) for accuracy and completeness.
• Identify, document, and ensure resolution of deviations prior to product approval.
• Conduct spot-check inspections and production audits.
• Participate in internal audit programs.
• Write, review, and approve SOPs.
• Support document control, record retention, and sample retention activities.
• Process returned instruments, including logging, decontamination, inspection, documentation, and preparation for repair.
• Perform other duties as assigned.

Skills

Product Testing

Batch Record Review

GMP & GLP Compliance

SOP Documentation

Internal Auditing

Attention to Detail

Documentation & Record Management

Education

Bachelor's degree in scientific/technical field

Tools

Database software

Inventory software

Spreadsheet software

Microsoft Word

Internet applications

Job description

Abbott is seeking a Quality Control Technician to support the Quality Management System in Atlanta, onsite. The role involves product testing, documentation review, inspections, and audits to ensure GMP and GLP compliance. A Bachelor's degree in a scientific/technical field and GMP/GLP knowledge are required.

Preferred one year of QA experience in the medical device industry. The position runs 12 months with 100% onsite work; shift is 2:30 PM – 11:00 PM.