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4 дня назад

Quality Lab Supervisor (Manufacturing)

95 591 - 116 834$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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 Lab Supervisor (Manufacturing): Supervising quality control and wastewater laboratory operations with an accent on technician leadership, training compliance, safety, and continuous improvement. Focus on coordinating production testing, leading kaizen events, improving laboratory processes, and maintaining equipment and environmental compliance.

Location: Onsite in Cordova, Illinois, United States. Travel may include up to 10%. Relocation assistance is not authorized.

Salary: $95,591–$116,834 annually, including base pay and variable incentive pay if eligible.

Company

hirify.global develops products and technologies across global industrial, healthcare, safety, and consumer markets.

What you will do

  • Oversee quality control and wastewater laboratory operations, including shift coverage and business continuity.
  • Lead laboratory technicians and coordinate sample testing priorities with production and wastewater operations.
  • Manage technician onboarding, qualification, training progression, and training documentation.
  • Support safety, environmental, HRP, EHS audits, and compliance activities within the laboratories.
  • Identify cost-reduction opportunities and improve the use of labor, materials, equipment, and external services.
  • Lead Lean, 5S, standard work, daily audits, kaizen events, preventive maintenance planning, and laboratory improvement projects.

Requirements

  • Bachelor’s degree or higher and seven years of combined experience in manufacturing, quality, research and development, and/or laboratory work; or a high school diploma/GED and at least eleven years of relevant experience.
  • Experience with routine test procedures, equipment validation, measurement systems, testing, and calibration.
  • Strong leadership, decision-making, problem-solving, continuous improvement, and management skills.
  • Must be legally authorized to work in the United States without employment visa sponsorship.
  • Ability to work onsite in Cordova, Illinois, and support around-the-clock laboratory operational needs as required.

Nice to have

  • Bachelor’s degree or higher in science and/or engineering.
  • Medical product or quality management system experience, including FDA Quality System Regulation or ISO.
  • Previous experience supervising individual contributors.
  • Experience leading continuous improvement projects and kaizen events.

Culture & Benefits

  • Collaborative environment with colleagues across global locations, technologies, and products.
  • Medical, dental, and vision coverage.
  • Health Savings Accounts and Health Care and Dependent Care Flexible Spending Accounts.
  • Disability, life insurance, paid absence, voluntary benefits, and retirement benefits.
  • Safety and Environmental Health and Safety are core workplace priorities.

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