5 дней назад
Director, Enterprise Manufacturing Applications (MES/SCADA)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Director, Enterprise Manufacturing Applications (MES/SCADA): Defining the global strategy, roadmap, and lifecycle performance of manufacturing applications across 16+ sites with an accent on MES, SCADA, CMMS, calibration systems, and digital manufacturing platforms. Focus on global standardization, predictive and prescriptive KPI dashboards, regulatory compliance, enterprise integrations, and leading implementation and continuous improvement programs.
Location: Fort Worth, Texas, United States
Company
develops products and solutions focused on improving eye health and operates more than 25,000 associates across global manufacturing sites.
What you will do
- Define the global strategy and long-term roadmap for MES, SCADA, CMMS, calibration systems, and related manufacturing OT platforms across 16+ sites.
- Own the design, capability development, compliance, performance, adoption, budgeting, and lifecycle management of global manufacturing applications.
- Lead deployments, upgrades, migrations, integrations, and optimization programs, ensuring quality, on-time delivery, and budget control.
- Drive workflow and data harmonization, predictive analytics, digital workflows, IIoT connectivity, and process automation.
- Develop standardized KPI dashboards and reporting for PPV, inventory, yield, OEE, schedule attainment, and other operational metrics.
- Lead a global team and partner with manufacturing, engineering, quality, supply chain, IT, cybersecurity, validation, compliance, and site leadership.
Requirements
- Bachelor’s degree or equivalent directly related experience; alternative experience combinations are accepted.
- At least 10 years of relevant experience and 6 years of demonstrated leadership.
- Fluent English communication skills in reading, writing, comprehension, and speaking.
- Experience with enterprise manufacturing applications, system architecture, governance, integrations, and global program delivery.
- Ability to work with regulatory and security requirements including FDA, EU MDR, GxP, 21 CFR Part 11, and data integrity.
Nice to have
- Experience in medical device, pharmaceutical, or highly regulated manufacturing environments.
- Knowledge of ISA-95, ISA-88, cloud-hosted architecture, IIoT platforms, and advanced analytics.
- Experience building business cases, managing vendors, and working with major MES, SCADA, and OT providers.
Culture & Benefits
- Inclusive environment focused on transparency, collaboration, innovation, and customer focus.
- Career growth and development opportunities.
- Health, life, retirement, flexible time off, and other benefits.
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