Quality Engineering Intern

Creation TechnologiesRochester, NY
20h

About The Position

It's fun to work in a company where people truly BELIEVE in what they're doing! We're committed to bringing passion and customer focus to the business. Has primary responsibility for development and maintenance of production quality standards and documentation. Collaborates on continuous improvement activities through problem prevention and mitigation, leads corrective actions through data analysis trending, and support external audits and the internal audit program. This includes but is not limited to support of defining quality requirements for new products and preparing/maintaining necessary documentation, monitor production quality performance to identify opportunities for improvement, complete, review and maintain quality records for compliance to creation’s quality system, as well as support customer and regulatory compliance requirements. Supports quality inspections and audit preparation. Supports customers under close supervision. Manages specific customers/serves as the quality representative within an assigned customer focus team or designated functional area. Quality Engineering Intern The Quality Engineering Intern will support Quality Engineering in product quality improvements, and monitoring and reporting quality performance. This person will provide immediate quality support to production, inspection and other support teams as required.

Requirements

  • Current College Student in either a 2-year or 4-year program, preferrable related to Engineering/Manufacturing.
  • Computer skills including proficiency in Microsoft Office Tools
  • Basic knowledge for use of standard measuring equipment
  • Experience with spreadsheets and databases; ability to organize data efficiently and effectively into inspection reports
  • Strong communication, analytical and problem-solving skills
  • Highly organized with positive attitude and willingness to learn

Responsibilities

  • Corrective Action and Non-conformance support
  • Administer and facilitate Non-Conformance (NCR)
  • Support processing product Purges
  • Audit and confirm Corrective action Verifications
  • Data analysis of defect reports for actionable trends
  • Quality Audits
  • Perform various process audits
  • Audit compliance to recently implemented CAPAs
  • Work on Document control projects
  • Complete the adoption of the global core documents
  • Periodic review on all local QMS documents
  • Merging the ROC QMS documents into Doc Bank

Benefits

  • Apply classroom learning, experience team collaboration, build industry connections, and explore career growth opportunities
  • Experience working for one of the largest global electronics manufacturing service companies
  • Experience in interpretation of drawings and other manufacturing materials
  • Gain knowledge of industry standards such as ISO 9001, AS 9100, ISO 13485, ISO 80079-34 (ATEX), or 21 CFR part 820 (FDA)
  • Gain knowledge of electronic components and assemblies
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