36 минут назад
JJV Contact Lens Process Engineering Director (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
JJV Contact Lens Process Engineering Director (Medical Devices): Leading the global process engineering organization supporting contact lens manufacturing in Jacksonville and Limerick with an accent on process capability, manufacturing robustness, technology transfer, validation, and regulated performance. Focus on harmonizing engineering standards, developing technical leaders, solving complex process problems, and driving quality, reliability, sustainability, and cost improvements across manufacturing sites.
Location: Jacksonville, Florida, United States, or Limerick, Ireland; up to 25% domestic and international travel may be required.
Company
Johnson & Johnson MedTech develops healthcare and vision solutions, including contact lens products and services.
What you will do
- Set the global process engineering strategy, priorities, operating model, governance, and technical roadmap for contact lens manufacturing.
- Harmonize engineering standards, practices, tools, skills, and ways of working across Jacksonville and Limerick.
- Build and develop a high-performing global engineering organization through coaching, succession planning, and technical career development.
- Partner with R&D, Manufacturing, Operations, Quality, MAKE Engineering, and other stakeholders on technology transfer, risk management, and strategic programs.
- Lead process characterization, validation, FMEA, troubleshooting, data analytics, lifecycle management, and continuous improvement.
- Ensure compliance with procedures, training requirements, GMP expectations, and deviation management practices.
Requirements
- Bachelor’s degree in Engineering or a related technical field; an advanced degree is preferred.
- At least 12 years of relevant experience in Process Engineering, Manufacturing Engineering, Technical Development, R&D, or Quality.
- At least 8 years of people leadership experience, including performance management, talent development, succession planning, and organizational capability building.
- Experience setting strategy and leading cross-site or global technical teams in a matrixed environment.
- Strong knowledge of GMP, regulated manufacturing, process and equipment validation, process characterization, FMEA, risk management, and disciplined engineering practices.
- Strong communication, collaboration, decision-making, project leadership, and management skills.
Nice to have
- Medical device or pharmaceutical experience.
- Six Sigma Green Belt or Black Belt certification.
- FPX or PMP certification.
- Advanced degree in Engineering or a related technical field.
Culture & Benefits
- Work across a global, cross-functional engineering organization.
- Focus on inclusive collaboration and development of current and future technical leaders.
- Opportunity to improve quality, reliability, speed, flexibility, cost effectiveness, and process sustainability.
- Travel across domestic and international manufacturing locations may be required.
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