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3 дня назад

Quality Control Inspector II (Bioprocessing)

28 - 35$
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
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 Control Inspector II (Bioprocessing): Inspecting incoming materials, machined parts, and manufacturing processes for conformity with drawings, specifications, sampling plans, and regulated quality standards with an accent on precision measurement, GD&T, and quality documentation. Focus on identifying non-conforming materials, supporting First Article Inspection and corrective actions, and collaborating across Operations, Engineering, Supply Chain, and Quality teams.

Location: Waltham, MA, United States

Salary: $28–$35 per hour, plus eligibility for variable cash programs and equity for eligible roles

Company

hirify.global develops technologies and solutions for bioprocessing and the production of biologic drugs.

What you will do

  • Inspect and approve or reject incoming supplier materials and machined parts using documented specifications, sampling plans, and inspection methodologies.
  • Use calipers, Micro-Hite systems, comparators, and other precision measuring equipment to evaluate product conformity.
  • Interpret engineering drawings, purchase orders, statements of work, industry standards, and GD&T requirements.
  • Apply part-number labels to approved materials and accurately document inspection activities and results.
  • Communicate non-conforming material findings and support investigations, corrective actions, deviations, customer complaints, and First Article Inspection activities.
  • Collaborate with Operations, Engineering, Supply Chain, and Quality teams to improve quality processes and operational excellence.

Requirements

  • High school diploma, two-year technical degree, or equivalent education; relevant machine shop, inspection, quality, or industry experience may be considered.
  • At least two years of Quality Assurance experience in an ISO 13485, ISO 9001, or similar regulated Quality Management System environment.
  • Experience with inspection practices in medical device, bioprocessing equipment, aerospace, military, or another highly regulated manufacturing industry is preferred.
  • Working knowledge of GD&T, precision measurement, inspection documentation, and Good Documentation Practices.
  • Proficiency with Microsoft Office applications, including Outlook, Excel, and Word.
  • Strong communication, collaboration, attention to detail, ownership, judgment, and ethical decision-making skills.

Culture & Benefits

  • Leadership behaviors emphasize integrity and compliance, customer focus, collaboration, courage, team empowerment, and accountability.
  • Benefits include paid time off, health, dental, and vision coverage, retirement benefits, and flexible spending accounts.
  • Work includes maintaining a clean, organized, and safe environment and following company safety and quality standards.

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