QC Inspector (Manufacturing)

job
  • Tekwissen
Job Summary
Location
Union City ,CA 94587
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
27 Nov 2024
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Job Description
Overview
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. This Client is a global animal health company dedicated to supporting customers and their businesses in ever better ways. Building on more than 65 years of experience, it deliver quality medicines, vaccines and diagnostic products, complemented by biodevices, genetic tests and precision livestock farming.
Job Title: QC Inspector (Manufacturing)
Location: Union City, CA 94587
Duration: 6 Months
Job Type: Contract
Work Type: Onsite
Shift: 7:00 am - 3:30 pm (Monday-Friday)
Duties and Responsibilities:
  • Perform inspections of purchased parts according to acceptance criteria using standard sampling plan
  • Physical, mechanical and/or electrical measurements in compliance with the company Quality System
  • Accurately document results of inspection / testing and maintain controlled document files, logs and test records
  • Inspect cables per wiring configuration
  • Initiate non-conformance process and assist in resolving non-conformances
  • Monitor receiving inspection backlog
  • Able to be flexible with the work schedule
  • Process ERP transactions to segregate and disposition non-conforming product
  • Other duties and responsibilities in the Quality Department as assigned
Qualifications:
  • Familiar with measuring equipment such as micrometer, caliper height gauges, plug gauges
  • Able to lift at least 35 lbs.
  • Strong attention to details and ability to understand and follow complex procedures.
  • Working knowledge and experience in basic computer applications such as Microsoft Word, Excel and Outlook.
  • Effective and clear written and verbal communication skills in English language.
Education and Experience:
  • High School Diploma or Equivalent.
  • Preferred one year of experience in an FDA regulated environment and/or ISO 13485 standards in the medical device industry and/or in-vitro diagnostics preferred

TekWissen® Group is an equal opportunity employer supporting workforce diversity
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