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6 дней назад

Quality Lab Supervisor (Manufacturing)

95 591 - 116 834$
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
Quality Lab Supervisor (Manufacturing): Leading quality control and wastewater laboratory operations in an onsite manufacturing environment with an accent on technician supervision, training, safety, environmental compliance, and continuous improvement. Focus on coordinating production-driven testing, developing lab capabilities, reducing costs, and leading Lean, 5S, kaizen, and equipment reliability initiatives.

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

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

Company

hirify.global develops technology, materials, and products across global manufacturing and technical operations.

What you will do

  • Lead quality control and wastewater laboratory operations, including technician scheduling and shift coverage.
  • Coordinate sample testing priorities between production and wastewater operations based on production and shipment needs.
  • Oversee technician onboarding, qualification, training progression, and training documentation.
  • Support safety, environmental, HRP, EHS audit, and compliance activities within the laboratory.
  • Identify cost-reduction opportunities and improve the use of labor, materials, equipment, and external services.
  • Lead Lean, 5S, standard work, daily audits, kaizen events, continuous improvement projects, and equipment preventive-maintenance practices.

Requirements

  • High school diploma or GED completed and verified before starting.
  • At least three years of experience in manufacturing, quality, research and development, or laboratory work.
  • Prior experience supervising individual contributors is beneficial.
  • Knowledge of routine testing, equipment validation, measurement systems, testing, and calibration is beneficial.
  • 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.

Nice to have

  • Bachelor’s degree or higher in science or engineering.
  • Medical product or quality management system experience, including FDA QSR or ISO.
  • Experience leading continuous improvement projects and kaizen events.

Culture & Benefits

  • Safety and environmental health are core operating priorities.
  • Benefits may include medical, dental, vision, health savings accounts, flexible spending accounts, disability and life insurance, paid absences, and retirement benefits.
  • Opportunities to collaborate with technical teams across global hirify.global operations.

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