Quality Control Technician
Job in
Atlanta, Fulton County, Georgia, 30383, USA
Listed on 2026-06-09
Listing for:
Experis/Manpower Group
Full Time
position Listed on 2026-06-09
Job specializations:
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager -
Manufacturing / Production
QA Specialist / Manager
Job Description & How to Apply Below
Location: Atlanta GA (100% Onsite)
Duration: 12 Months
Shift Time: 8am to 5pm
Pay Range : $22/hr to $26/hr (On W2)
We are looking for a "Quality Control Technician" to join one of our Fortune 500 clients.
Job Responsibilities:
- Conduct product testing, including testing to support complaint investigations and stability verification
- Generate product testing results reports
- Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production.
- Review finished goods batch records.
- Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
- Conduct spot-check inspections/audits of production operations
- Participate in the internal audit program
- Write, review and approve Standard Operating Procedures (SOPs) as necessary
- May assist in supporting the Document Control program, record retention areas, and sample retention areas
- May support returned instrument processing
- Log returned instruments from the field.
- Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
- Inspect returned instruments for damage, and performing basic investigation and documenting results prior to second level processing.
- As necessary, process instrument documentation for return to repair facility, and pack instruments as required.
- Other duties as assigned by supervisor Supervisory Responsibilities This job has no supervisory responsibilities.
- The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP
- Education and/or Experience Bachelor's degree in a scientific or technical area or equivalent combination of experience and education.
- At least one year in quality assurance role in medical device industry is preferred.
If you're interested, please click "Apply" button
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