обновлено 10 дней назад
Manufacturing Engineering Manager (MedTech)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Manufacturing Engineering Manager (MedTech): Leading manufacturing engineering teams and improving regulated medical-device production through process robustness, yield improvement, equipment reliability, validation, and technical investigations with an accent on GMP/ISO compliance and operational performance. Focus on developing engineers, prioritizing complex engineering programs, executing FAT/IQ/OQ/PQ validation, and driving root-cause analysis and continuous improvement.
Location: Añasco, Puerto Rico, United States; fully onsite. Requires up to 10% travel.
Company
Johnson & Johnson MedTech develops innovative, less invasive, and personalized healthcare and vision treatments.
What you will do
- Lead, coach, and develop the manufacturing engineering team while establishing priorities, accountability, and leadership routines.
- Set engineering standards and governance for manufacturing areas, including line-side support, escalation, and structured problem solving.
- Drive yield, UPPH, uptime, OEE, process reliability, and productivity improvements through trend analysis and risk-based prioritization.
- Lead manufacturing engineering programs and projects, ensuring safety, regulatory compliance, financial discipline, and operational delivery.
- Direct root-cause analysis, non-conformance investigations, corrective and preventive actions, process characterization, and equipment support.
- Develop resource-planning and project-prioritization systems and partner with Operations, Quality, Maintenance, Automation, Facilities, Supply Chain, Finance, Human Resources, and global engineering.
Requirements
- Bachelor’s degree in Engineering is required.
- At least 8 years of relevant experience in manufacturing engineering, maintenance manufacturing, process development, R&D, automation, or regulated manufacturing operations is preferred.
- People leadership or demonstrated technical/team leadership experience is required.
- Experience with GMP/ISO requirements, validation lifecycle, FAT, IQ, OQ, PQ, process characterization, and technical investigations is preferred.
- Strong communication, cross-functional collaboration, decision-making, coaching, and stakeholder management skills are required.
- Medical device or pharmaceutical industry experience, project and financial management, resource planning, optical inspection, automated equipment, and process optimization experience are preferred.
Culture & Benefits
- Work in a regulated GMP/ISO manufacturing environment with a focus on technical excellence and continuous improvement.
- Support is provided for physical, mental, emotional, and financial health programs.
- Employment requires proof of COVID-19 vaccination or an approved accommodation before starting.
- Inclusive and equal-opportunity workplace.
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