Responsibilities may include the following and other duties may be assigned:
Act as a senior technical authority and subject-matter expert for medical device development, leading complex product development projects from initiation through commercialization
Develop and review system architectures, product requirements, design concepts, specifications, and technical documentation, ensuring engineering decisions are based on sound technical principles, risk management, usability, reliability, and patient safety
Provide technical mentorship and coaching to engineers and project team members; provide day-to-day work direction for the team focused on maintaining steady workflow, effective resource allocation, and productivity; and lead engineering activities in accordance with applicable medical device regulations, standards, and company quality systems
Lead cross-functional projects and develop project plans, schedules, budgets, resource requirements, milestones, and deliverables in collaboration with stakeholders; monitor and communicate project progress; identify risks and dependencies; and implement corrective actions
Represent Articulating Technologies as a primary contact, communicating with internal and external customers and vendors at various levels, and drive project meetings, design reviews, technical reviews, and management updates
Escalate critical issues and make recommendations regarding project priorities and resource allocation, while leading technical problem-solving and decision-making in complex or ambiguous situations
Collaborate closely with Quality, Regulatory Affairs, Clinical, Manufacturing, Supply Chain, Product Management, and Commercial teams to translate business and customer needs into robust technical solutions and build alignment among stakeholders with competing priorities
Collaborate with Manufacturing and Operations to transition products into production, supporting process development, design transfer, production readiness, and supplier qualification activities
Represent Engineering in cross-functional and executive-level meetings, providing technical leadership and facilitating effective communication, stakeholder alignment, and execution across the organization.
Required Knowledge and Experience
Master’s degree in in Mechanical Engineering/Biomedical Engineering/Industrial Engineering or similar
> 7 years proven experience managing complex projects or programs in research and product development in the in the medical device industry preferably in the field of precision mechanics
Experience with product and process development aligned with ISO 13485 requirements
Good analytical and problem-solving skills, strong attention to detail and accuracy
Mastering the Dutch & English language.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
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Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Netherlands: 87,200.00 EUR - 130,800.00 EUR |
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
