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6 дней назад

Lead Quality Inspector (APU 4 2nd 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 2nd Shift) (Pharmaceutical Manufacturing): Coordinating quality inspection activities and production quality controls in a clean-room pharmaceutical manufacturing environment with an accent on batch release, cGMP compliance, inspection planning, and nonconforming product disposition. Focus on analyzing quality data, reducing internal and external failures, coaching inspectors, and maintaining FDA and ISO requirements during the second shift.

Location: Vernon Hills, Illinois, United States; must be eligible to work in the United States. Onsite clean-room manufacturing role on the second shift, Monday through Friday, 2:00 PM–10:30 PM.

Salary: $20.00–$30.00 USD per hour.

Company

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

What you will do

  • Coordinate Quality Inspector activities, assignments, schedules, and production sequences.
  • Perform quality inspection duties and oversee the evaluation of goods, inspection methods, and sampling plans.
  • Review quality data and documentation, prepare reports, and analyze statistical information.
  • Manage nonconforming product disposition, batch release, CoC/CoA creation, and LRP closure.
  • Support investigations, customer complaint reviews, problem-solving activities, and continuous improvement.
  • Train, coach, and mentor Quality Inspectors while providing performance feedback to management.

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 quality system requirements.
  • Ability to plan and organize work, apply basic mathematical concepts, and use Microsoft Word, Excel, and database software.
  • 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.

Culture & Benefits

  • Full-time hourly employment with a Monday–Friday second-shift schedule.
  • Work in a clean-room manufacturing environment with moderate noise and required cleanroom apparel.
  • Regular movement between office, production departments, and company buildings is required.
  • Equal opportunity employment and US benefits information are provided.

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