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4 дня назад

Quality Technician (Medical Devices/Pharma)

44 800 - 61 600$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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 Technician (Medical Devices/Pharma): Supporting quality systems, inspections, documentation control, inventory management, and functional testing in medical device and pharmaceutical manufacturing with an accent on process compliance, product quality, and regulatory procedures. Focus on performing audits and in-process inspections, troubleshooting quality issues, analyzing data, and improving manufacturing processes across Drug Delivery and Penicillin facilities.

Location: Round Lake, Illinois, United States; onsite work on 12-hour night shifts

Salary: $44,800–$61,600 annually

Company

hirify.global develops and manufactures healthcare products focused on saving and sustaining lives.

What you will do

  • Support quality systems, label copy control, sample management, documentation review, and floor shop oversight.
  • Perform routine inspections, quality checks, in-process product inspections, and process compliance audits across manufacturing areas.
  • Analyze observations and data, interpret results, troubleshoot issues, and make decisions under established procedures.
  • Manage controlled-material equipment and inventory, including monthly cycle counts and variance follow-up.
  • Perform functional product testing for equipment validations and identify process improvements.
  • Collaborate with manufacturing and supervision to resolve quality and batch-related concerns.

Requirements

  • High school diploma or equivalent.
  • Six months of manufacturing or quality experience is preferred.
  • Basic science, mathematics, computer, Microsoft Word, and Microsoft Excel skills.
  • Strong writing, verbal communication, problem-solving, attention-to-detail, and organizational skills.
  • Experience with current Good Manufacturing Practices and Good Documentation Practices in medical device or pharmaceutical manufacturing is desirable.
  • Must be authorized to work for any employer in the United States; visa sponsorship is not available. Must not be allergic to penicillin or cephalosporin drugs.

Culture & Benefits

  • Work with manufacturing and quality teams in a fast-paced environment with minimal direct supervision.
  • Flexible hours, some weekend or Saturday work, and overtime may be required.
  • Medical, dental, and vision coverage starting on day one.
  • Paid time off, paid holidays, paid parental leave, and 401(k) matching.
  • Employee stock purchase program, tuition reimbursement, and educational assistance.

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