More jobs:
Quality Control Technician
Job in
New Lenox, Will County, Illinois, 60451, USA
Listed on 2026-02-12
Listing for:
Intellectt Inc
Full Time
position Listed on 2026-02-12
Job specializations:
-
Quality Assurance - QA/QC
Quality Control / Manager, Quality Engineering, Quality Technician/ Inspector, QA Specialist / Manager
Job Description & How to Apply Below
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Direct message the job poster from Intellectt Inc
Employment Type: Long-Term Contract (W2)
Industry: Medical Devices / Pharmaceuticals
Job Summary:
We are seeking a Quality Control Technician to join our team at Abbott Park, IL. The ideal candidate will support quality inspection, testing, and compliance activities to ensure products meet regulatory and company standards. This role involves working within a cGMP-compliant environment, conducting quality assessments, and collaborating with cross-functional teams.
Key Responsibilities:
- Perform incoming, in-process, and final inspections on raw materials, components, and finished products.
- Utilize measuring instruments such as calipers, micrometers, gauges, and CMM to verify product specifications.
- Conduct analytical and physical testing following standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).
- Maintain detailed records of inspections and test results in compliance with FDA, ISO 13485, and GMP standards.
- Support investigations of non-conforming materials and assist in corrective and preventive actions (CAPA).
- Work closely with engineering, production, and regulatory teams to ensure quality standards are met.
- Operate within SAP and other quality management systems (QMS) for documentation and reporting.
- Adhere to safety protocols, environmental policies, and company quality policies.
Required Qualifications:
- Associate’s or Bachelor’s degree in a technical field (e.g., Engineering, Life Sciences, or related discipline) preferred.
- 2+ years of experience in quality control or quality assurance within a medical device, pharmaceutical, or biotech industry.
- Experience with inspection tools (e.g., calipers, micrometers, CMM, height gauges).
- Proficiency in reading engineering drawings, GD&T, and technical specifications.
- Familiarity with ISO 13485, FDA 21 CFR Part 820, and GMP guidelines.
- Strong attention to detail, documentation skills, and problem-solving abilities.
- Experience with SAP, QMS, LIMS, or similar systems is a plus.
- Entry level
- Contract
- Engineering and Quality Assurance
- Medical Equipment Manufacturing
- Pharmaceutical Manufacturing
- Biotechnology Research
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