Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Ram Sasane at email address can be reached on # .
We have Contract role Inspector, Quality Control for our client at Portland OR. Please let me know if you or any of your friends would be interested in this position.
Position Details:
Inspector, Quality Control- Portland OR
Location : Portland OR. 97224
Project Duration : 6+ Months of contract
Pay rate : $ 25/hour on W2
Description:
The Inspector performs basic routine inspection of electronic, electro-mechanical and/or mechanical materials, components and sub-assemblies received, in process of manufacture, or manufactured, for conformance with quality assurance standards.
Key Job Duties and Responsibilities: Inspection & Testing:
- Performs visual and physical inspections of raw materials, in-process components, and finished products to ensure they meet quality specifications. Uses precision measuring tools and lab equipment to verify product dimensions and performance.
Documentation & Compliance:
- Accurately maintains Lot History Records (LHR), batch records, and inspection logs in compliance with Good Documentation Practices (GDP) and FDA regulations.
Defect Management:
- Identifies, classifies, and reports defects. Manages non-conforming material by initiating Non-Conformance Reports (NCR) and assisting with investigations.
Process Control:
- Monitors production processes to ensure adherence to standard operating procedures (SOPs) and Good Manufacturing Practices (GMPs).
Equipment Maintenance:
- Calibrates, cleans, and performs routine maintenance on inspection and testing equipment to ensure accuracy.
- Collaboration: Works with production and engineering teams to support quality improvements, provide feedback on product quality, and ensure regulatory compliance.
- Key Competencies:
- Attention to Detail: High level of accuracy in documentation and inspection.
- Computer Literacy: Proficient in using software like SAP, POMS, or Laboratory Information Management Systems (LIMS).Technical Knowledge: Understanding of ISO 13485 and FDA 21 CFR Part 820 regulations.
- Communication: Ability to clearly report deviations and collaborate in a team environment.
Educational/Experience Requirements:
- High school diploma or equivalent is required. Associate s or Bachelor s degree in a technical field preferred.
Previous experience in manufacturing, particularly in medical device, pharmaceutical, or similar regulated industries is highly desired. 1+ years of experience desired
To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Ram Sasane at email address can be reached on # .
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