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16 часов назад

Quality Inspector (APU 1-C) (Medtech)

21 - 25$
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
France/US/Poland +2 еще
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Quality Inspector (APU 1-C) (Medtech): Inspecting and measuring pharmaceutical drug-delivery device materials and products to verify conformance with specifications, with an accent on lot documentation, dimensional inspection, and quality standards. Focus on analyzing test data, identifying nonconformances, preparing deviation and rework reports, and supporting corrective actions across a 12-hour rotating shift.

Location: Buffalo Grove, Illinois, United States; onsite role with 12-hour rotating shifts from 6:00 PM to 6:15 AM, including every other weekend

Salary: $21.00–$25.00 USD per hour

Company

hirify.global manufactures complex drug delivery systems and provides development, industrialization, manufacturing, and contract manufacturing services for the pharmaceutical industry.

What you will do

  • Inspect, test, and measure materials, products, and work for conformance with specifications.
  • Read and interpret part drawings, manuals, specifications, and inspection procedures.
  • Use rulers, calipers, gauges, micrometers, force gauges, CMM, and optical gaging machines to verify product dimensions.
  • Collect samples, compare products with standards, analyze test data, and calculate test results.
  • Review and approve lot documentation and ensure compliance with procedures and good documentation practices.
  • Document nonconformances, deviations, and rework instructions; communicate inspection results and recommend corrective actions.

Requirements

  • At least 1 year of experience in a quality-related profession is preferred.
  • An associate degree is preferred.
  • Ability to use gauges, inspection fixtures, and leak-testing equipment.
  • Ability to use productivity software and Statistical Process Control tools.
  • Ability to lift up to 30 lb and stand for 75% of the shift.
  • Must be eligible to work in the United States under applicable federal law.

Culture & Benefits

  • Work within an international pharmaceutical manufacturing group focused on improving patients’ lives through drug delivery devices.
  • Follow cGMP, ISO standards, health and safety requirements, continuous improvement practices, and standard work procedures.
  • Collaborate with the Quality Lead, Operational Quality Manager, and other employees to improve product quality and operating-system efficiency.
  • Equal opportunity employment is provided.

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