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13 часов назад

Production Supervisor - Packaging

61 558 - 87 940$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Production Supervisor - Packaging (cGMP Manufacturing): Overseeing packaging-line production operations, employee performance, equipment use, documentation, and facility standards with an accent on safety, quality, sanitation, and production targets. Focus on reviewing batch records and work orders, resolving quality issues with Quality Control, maintaining cGMP compliance, and leading continuous improvement initiatives.

Location: Clackamas, Oregon, USA; onsite on the designated shift

Salary: $61,558–$87,940 USD per year

Company

hirify.global develops flavors, fragrances, food ingredients, and health and biosciences solutions, with a focus on sustainable innovation.

What you will do

  • Supervise packaging-line production operations and support shift objectives in a cGMP dietary supplement manufacturing environment.
  • Monitor employees and temporary staff, equipment use, supplies, production orders, work orders, and shift documentation.
  • Review batch records, cleaning and setup records, logs, and other documentation for accuracy, completeness, and compliance.
  • Work with Quality Control to identify, document, and resolve quality, production, and out-of-specification issues.
  • Oversee washroom personnel, including inspections, evaluations, and training related to sanitation and contamination prevention.
  • Lead training, safety activities, task forces, and continuous improvement initiatives within the assigned area.

Requirements

  • College degree, or 5 years of supervisory experience in a manufacturing environment in lieu of a degree.
  • Computer skills, including Microsoft Office and ERP systems.
  • Ability to read, write, and communicate in English.
  • Strong organization, attention to detail, problem-solving, communication, and teamwork skills.
  • Ability to work in a fast-paced, results-oriented manufacturing environment and maintain consistent attendance.
  • Legal right to work in the United States; drug screening and background check required.

Nice to have

  • Experience with FDA and cGMP compliance.
  • Experience identifying deficiencies and implementing corrective actions.
  • Experience leading continuous improvement initiatives.

Culture & Benefits

  • Regular schedule: 6:00 a.m. to 2:30 p.m., Monday through Friday.
  • Hours may exceed 40 per week based on business needs.
  • Inclusive workplace focused on safety, quality, collaboration, and employee contribution.
  • Annual requalification may be required for job-related tests and certifications.

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