Inspector, Quality Control

Portland, TX - USA

Monthly Salary: Not Disclosed

Posted on: 3 hours ago

Vacancies: 1 Vacancy

Job Summary

Job Title: Inspector Quality Control
Location (On-site Remote or Hybrid): Portland OR (onsite)
Contract Duration: Contract until 11/04/2026
Working hours: 8a - 4:30p
Total hours: 40

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.

Common Educational/Experience Requirements:

High school diploma or equivalent is required. Associates or Bachelors 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.

Job Title: Inspector Quality Control Location (On-site Remote or Hybrid): Portland OR (onsite) Contract Duration: Contract until 11/04/2026 Working hours: 8a - 4:30p Total hours: 40 Description: The Inspector performs basic routine inspection of electronic electro-mechanical and/or mechanical ...

Job Title: Inspector Quality Control
Location (On-site Remote or Hybrid): Portland OR (onsite)
Contract Duration: Contract until 11/04/2026
Working hours: 8a - 4:30p
Total hours: 40

Description:

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.

Common Educational/Experience Requirements:

High school diploma or equivalent is required. Associates or Bachelors 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.