Quality Control Inspector
Job in
Andover, Essex County, Massachusetts, 05544, USA
Listed on 2026-08-28
Listing for:
MillenniumSoft Inc
Full Time
position Listed on 2026-08-28
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Production QC/QA
Job Description & How to Apply Below
Level Of
Experience:
Mid-Level
Employment Type:
Contract on W2 (Need US Citizens or GC Holders Only)
Shift Timings: 7 to 3:30
Position :
Quality Inspector
Location :
Andover, MA
Duration : 12 Months
Total Hours/week : 40.00
pay rate-$20-30/hr
1st Shift
Client:
Medical Device Company
Job Category:
Quality
Level Of
Experience:
Mid-Level
Employment Type:
Contract on W2 (Need US Citizens or GC Holders Only)
Shift Timings: 7 to 3:30
Job Description- The Quality Inspector is responsible for the inspection of materials, assemblies, work-in-progress and finished medical devices, as well as the completion of documentation to determine conformance to specifications.
- Visual inspections per documented specifications.
- Responsible for the efficient and effective performance of testing in conformance with regulations and standards.
- Inspection, analysis of results, determining final disposition of some product and detecting nonconforming conditions.
- Works within clearly defined SOPs and/or scientific methods.
- Adheres to quality guidelines. Complies with regulations and standards. Identifies basic non-compliance within regulations and standards.
- Proven ability to correctly interpret drawings and geometric dimensions and tolerances.
- Able to use standard measuring equipment including calipers, Random-Access memory (RAM) optic, micrometers, pin gauges, gage blocks, etc.
- Must have attention to detail and be able to work with small components.
- Demonstrated understanding in the use of calibrated equipment and ability to follow equipment manual procedures.
- Previous experience of working in a cleanroom environment and continuous improvement activities.
- 3 or more years of Quality Control Inspection experience, preferably in an ISO 9001, ISO 13485 and/or FDA regulated environment.
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