22 часа назад
Project Manager Global Engineering (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Project Manager Global Engineering (Medical Devices): Leading cross-functional engineering projects for new products, technologies, equipment, and process improvements with an accent on integrated planning, process development, equipment qualification, and regulated manufacturing. Focus on coordinating technical scope, DOE and statistical analysis, design controls, manufacturing transfer, risk mitigation, and commercialization.
Location: Ballina, Ireland; occasional on-site manufacturing activities and business travel may be required.
Company
is an independent, employee-owned healthcare company developing, manufacturing, and marketing ostomy care, continence care, and critical care products worldwide.
What you will do
- Lead cross-functional and cross-geographical teams delivering new products, technologies, equipment, and process improvements.
- Develop and manage integrated project plans, schedules, budgets, resource plans, ROI assessments, and risk mitigation strategies.
- Define technical scope, process concepts, specifications, validation plans, and acceptance testing.
- Oversee process development, characterization, testing, equipment qualification, and manufacturing transfer.
- Coordinate engineering, operations, quality, suppliers, regulatory, marketing, and market access stakeholders.
- Report project status and milestones to leadership while supporting capacity planning, cost reduction, mentoring, and continuous improvement.
Requirements
- Bachelor’s degree and 5–8 years of related engineering experience.
- At least 3 years of project or program management experience, preferably in a regulated industry.
- Experience with automated production equipment, DOE methods, statistical analysis, process development, equipment qualification, and design controls.
- Knowledge of project management methodologies, structured problem-solving, Lean, Six Sigma, or continuous improvement.
- Strong communication, stakeholder management, technical writing, critical thinking, business acumen, and data-driven decision-making skills.
- Ability to work at a computer for extended periods and participate in occasional on-site manufacturing activities and travel.
Nice to have
- Engineering or related technical degree; advanced degree preferred.
- PMP or equivalent certification.
- Experience in medical devices, pharmaceuticals, or FDA-regulated environments.
Culture & Benefits
- Employee-owned organization guided by a mission to make life more rewarding and dignified.
- Work with cross-functional teams across engineering, operations, quality, regulatory, and commercial functions.
- Opportunities to mentor colleagues and contribute to organizational capability building.
- International operating environment with manufacturing and distribution centers across three continents.
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