Назад
Company hidden
6 дней назад

Receiving Inspector 2 (Medical Devices)

45 400 - 68 100$
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Receiving Inspector 2 (Medical Devices): Inspecting incoming materials, components, and subassemblies for compliance with engineering drawings, specifications, quality requirements, and manufacturing procedures with an accent on precision measurement, GD&T interpretation, and regulated documentation. Focus on identifying nonconforming materials, completing first article inspections, supporting investigations, and maintaining QMS, GMP, and GDP compliance.

Location: Newark, Delaware, United States

Annual base salary: $45,400–$68,100, bonus eligible.

Company

hirify.global develops and manufactures medical devices and operates in a regulated manufacturing environment.

What you will do

  • Perform incoming inspections of materials, components, and subassemblies using approved procedures, drawings, specifications, and inspection plans.
  • Interpret engineering drawings, GD&T, material specifications, schematics, blueprints, and part lists.
  • Verify dimensional, visual, labeling, and documentation requirements using calipers, micrometers, height gauges, optical comparators, pin gauges, microscopes, scales, and other precision equipment.
  • Record inspection results and complete quality documentation in accordance with Good Documentation Practices.
  • Review supplier Certificates of Conformance, test reports, and inspection records; identify and segregate nonconforming materials.
  • Initiate and support nonconformance events and investigations, perform first article inspections, communicate discrepancies, and meet daily inspection priorities.

Requirements

  • High school diploma or equivalent required; an associate degree is preferred.
  • 1–2 years of experience in medical device manufacturing or another highly regulated manufacturing industry preferred.
  • Strong technical inspection skills and experience using precision measurement and quality control equipment.
  • Ability to read and interpret engineering drawings, GD&T, schematics, blueprints, part lists, and technical data.
  • Working knowledge of Microsoft Office, especially Excel, plus strong written and verbal communication skills.
  • Ability to follow written procedures, maintain detailed documentation, work independently and collaboratively, and work overtime as needed.

Nice to have

  • Experience with Oracle ERP or Agile Product Lifecycle Management System.
  • ASQ Certified Quality Inspector certification.
  • Familiarity with GMP and GDP.

Culture & Benefits

  • Comprehensive onboarding training and continued professional development.
  • Commitment to quality, data integrity, compliance, and continuous improvement.
  • Bonus eligibility in addition to the annual base salary.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →