6 дней назад
Quality Lab Supervisor (Manufacturing)
95 591 - 116 834$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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 operations.
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