Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Чёткая зона ответственности на уровне руководителя в регулируемом производстве медизделий даёт серьёзный масштаб задач, но работа на площадке и периодическая поддержка вне обычных часов ограничивают гибкость.
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Работа вне графика
Чёткая зона ответственности
Медтех-направление
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Director, Operations Inhealth Technologies (Medical Devices): Leading manufacturing operations for a regulated medical device production site with an accent on safety, quality, delivery, cost, compliance, and continuous improvement. Focus on directing multi-shift teams, driving lean manufacturing and process improvement, managing budgets and CAPEX, and ensuring compliance with FDA, ISO 13485, and EU MDR requirements.
Location: Carpinteria, California, United States; onsite manufacturing environment with frequent walking and standing, cleanrooms, PPE/gowning areas, and occasional off-hours, weekend, or emergency support.
Salary: $120,000–$150,000 annually, depending on skills, experience, and qualifications.
Company
hirify.global operates in the medical device and regulated manufacturing sector.
What you will do
Lead site manufacturing operations across production, scheduling, and support functions to achieve safety, quality, delivery, cost, and continuous improvement targets.
Oversee department planning, goal setting, performance management, and operations across multiple shifts or production units.
Direct and develop the Operations team, including leadership pipeline and succession planning.
Collaborate with Product Development, Quality, Regulatory, and Finance leaders to ensure operational readiness and business alignment.
Drive lean manufacturing, process improvement, employee engagement, regulatory compliance, and operational excellence.
Lead operational budget planning, cost management, CAPEX investments, KPI reporting, and improvement actions.
Requirements
Bachelor’s degree in Engineering, Operations, Business, or a related field.
10+ years of manufacturing operations experience, including at least 5 years in a senior leadership capacity.
Deep knowledge of global regulatory requirements, including FDA, ISO 13485, EU MDR, and CFDA.
Proven success leading multi-shift teams in a regulated production environment.
Advanced business and financial acumen, including operational budget and CAPEX project management.
Strong cross-functional leadership, decision-making, and stakeholder management skills.
Proficiency in ERP systems, preferably SAP, Microsoft Office, and data-driven performance management.
Ability to walk and stand frequently, occasionally lift up to 30 pounds, work in cleanrooms and PPE/gowning areas, and support occasional off-hours, weekend, or emergency production needs.
Nice to have
Graduate degree in Operations, Engineering, Business, or a related field.
Lean Six Sigma Black Belt certification.
Experience in medical devices, life sciences, or other regulated industries.
Culture & Benefits
Full-time employment in an onsite manufacturing environment.
Work includes controlled manufacturing areas, cleanrooms, and PPE/gowning requirements.
Occasional off-hours, weekend production, and emergency escalation support is required.
Freudenberg is committed to equal employment opportunity, diversity, and inclusion.
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