3 дня назад
Senior Operations Manager (MedTech)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Operations Manager (MedTech): Establishing and scaling a new manufacturing value stream for surgical vision care with an accent on safe, compliant, and reliable production across quality, delivery, cost, people, and EHS. Focus on optimizing capacity, staffing, equipment, materials, and inventory, leading Lean and Six Sigma improvements, and ensuring FDA QSR, ISO 13485, and EU MDR compliance.
Location: Jacksonville, Florida, United States of America; manufacturing site. Up to 50% travel may be required during the first 6–9 months.
Company
Johnson & Johnson MedTech develops healthcare and surgical vision care solutions through medical technology innovation.
What you will do
- Establish and scale a new manufacturing value stream and build a high-performing operations organization.
- Lead supervisors, process teams, support teams, and cross-functional stakeholders across safety, quality, delivery, cost, people, and compliance objectives.
- Develop capacity, staffing, process continuity, equipment, maintenance, safety, and operational readiness plans.
- Manage budgets and headcount while optimizing labor, materials, inventory, equipment, and production capacity.
- Lead continuous improvement and Kaizen initiatives to simplify work, remove non-value-added activities, and reduce costs.
- Support new-product initiatives and collaborate with Supply Chain stakeholders through the S&OP process.
Requirements
- Bachelor’s degree in engineering, science, operations management, supply chain, or a related field; an advanced degree is preferred.
- 10+ years of progressive manufacturing or operations experience, including 5+ years in people management or operations leadership within a regulated environment.
- Experience in the medical device or pharmaceutical industry is required.
- Strong expertise in Lean Manufacturing, Six Sigma, productivity, operational excellence, and cost-reduction methodologies.
- Working knowledge of GMP and quality and regulatory requirements for regulated manufacturing, including FDA QSR, ISO 13485, and EU MDR.
- Strong communication, presentation, interpersonal, influencing, and team leadership skills.
Nice to have
- Advanced degree.
- Experience with Agile Manufacturing, Value Stream Mapping, Validation Master Plans, and Manufacturing Science and Technology.
Culture & Benefits
- Full-time employment in an inclusive work environment.
- Focus on employee development, required training, engagement, recognition, and challenging assignments.
- Strong emphasis on environmental, health, safety, industrial hygiene, sustainability, and ISO 14001 compliance.
- Equal opportunity employment with an inclusive interview process and applicant accommodation support.
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