Quality Control Inspector

El Paso, TX, US • Posted 3 days ago • Updated 3 days ago
Contract Corp To Corp
Contract W2
On-site
$45 - $48/hr
Company Branding Image
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Auditing
  • ISO 13485
  • Regulatory Compliance
  • Root Cause Analysis
  • Inspection
  • FDA 21
  • GDP
  • CAPA activities
  • Quality Control
  • medical device industry

Summary

Role: Quality Control Inspector

Location: El Paso, TX Onsite

Must Have Technical Functional Skills Perform incoming| in process| and final inspections of components| sub-assemblies| and or finished goods in accordance with approved inspection plans| drawings| and specifications. Conduct inspections using visual| dimensional| and functional methods| utilizing calibrated measurement tools such as calipers| micrometers| and gauges. Ensure compliance with ISO 13485| FDA 21 CFR Part 820|. Accurately document inspection results in quality records| travelers| and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify| document| and escalate nonconforming material| supporting containment actions and investigations. Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis| CAPA activities| and continuous improvement initiatives as required. Support readiness for internal| customer| and regulatory audits. Collaborate with Manufacturing| Engineering| and Supplier Quality teams to resolve quality issues in a timely manner Roles Responsibilities Perform incoming| in process| and final inspections of components| sub-assemblies| and or finished goods in accordance with approved inspection plans| drawings| and specifications .Conduct inspections using visual| dimensional| and functional methods| utilizing calibrated measurement tools such as calipers| micrometers| and gauges. Ensure compliance with ISO 13485| FDA 21 CFR Part 820| and Supplier Quality requirements. Accurately document inspection results in quality records| travelers| and or electronic quality systems in accordance with Good Documentation Practices (GDP).Identify| document| and escalate nonconforming material| supporting containment actions and investigations .Support lot release activities and ensure full traceability of inspected materials. Participate in root cause analysis| CAPA activities| and continuous improvement initiatives as required. Support readiness for internal| customer| and regulatory audits. Collaborate with Manufacturing| Engineering.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91163888
  • Position Id: 8934848
  • Posted 3 days ago

Company Info

About Vankay Systems

Vankay Systems Inc is a Software Solution Development and Information Technology Consulting Company which provides services to many businesses around the United States and India led by certified professionals with expertise in Research, Design, Development and Delivery of high-end Technology Solutions. Our core competency, developed through extensive worldwide exposure to a variety of business processes, industries, and technologies, lies in providing client focused Business Consulting and Re-Engineering of IT Services.

Vankay Systems Inc weaves together innovative thinking, deep technology skills and strong industry and domain knowledge to help create world class solutions for our clients. We are passionate about delivering great work, exceeding client expectations and helping the client achieve success.

Our strategy is to form long-term relationships with our clients and offer quality end-to-end complete lifecycle solutions to our clients. We introduce unique perspective and inventive business consulting solutions that can leverage the best of our client`s processes.

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