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5 дней назад

Lead Quality Inspector (APU 4 1st Shift) (Pharmaceutical Manufacturing)

20 - 30$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
Lead Quality Inspector (APU 4 1st Shift) (Pharmaceutical Manufacturing): Directing quality inspectors and coordinating inspection, batch release, nonconforming product disposition, and compliance activities in a cleanroom drug-delivery manufacturing environment with an accent on cGMP, FDA, ISO, and statistical quality analysis. Focus on planning inspection schedules, closing LRP records, investigating failures and complaints, and coaching inspectors to maintain production quality.

Location: Vernon Hills, Illinois, United States. Onsite cleanroom manufacturing role on the first shift, Monday through Friday, 6:00 AM to 2:30 PM. Candidates must be eligible to work in the United States.

Salary: $20.00–$30.00 USD per hour.

Company

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

What you will do

  • Direct and coordinate Quality Inspectors and plan inspection schedules, assignments, and production sequences.
  • Perform quality inspection duties and review charts, work orders, records, data, and documentation for accuracy.
  • Analyze inspection methods, sample plans, and statistical data to establish and maintain quality plans.
  • Manage nonconforming product disposition, batch release, CoC/CoA creation, LRP closure, and cGMP compliance.
  • Support investigations, customer complaint reviews, problem solving, quality and safety reporting, and continuous improvement.
  • Train, coach, and mentor inspectors while providing performance feedback to Quality Managers.

Requirements

  • Associate degree or at least three years of related experience, including one year in a leadership role.
  • Ability to perform all Quality Inspector responsibilities and knowledge of raw materials, production processes, inspection tools, and tool maintenance.
  • Knowledge of cGMP, FDA, ISO, health and safety, and company quality-system requirements.
  • Self-directed approach with strong planning, organizing, communication, and basic mathematical skills.
  • Ability to lift up to 35 pounds and sit, stand, or walk for 80% of the shift.
  • Must be eligible to work in the United States and able to travel between office, production departments, and company buildings.

Nice to have

  • Experience with Microsoft Word, Excel, and database software.

Culture & Benefits

  • Cleanroom manufacturing environment with moderate noise and required cleanroom apparel.
  • First-shift schedule with consistent Monday–Friday working hours.
  • Work within a quality-focused pharmaceutical manufacturing operation.
  • U.S. employee benefits are available.

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