Now’s our time to inspire the future of healthcare together.
Siemens Healthineers is a leading global medical technology company with over 170 years of experience and 18,000 patents. More than 48,000 dedicated colleagues in over 70 countries are driven to shape the future of healthcare. We stand with our customers around the world to support them in delivering high quality care to their patients. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. This is what truly matters to us.
Join our team now at Siemens Healthineers as a Cardiovascular Chief Engineer!
This is a role well suited to an experienced professional looking to make a business-level impact as a Cardiovascular Chief Engineer:
In this senior individual contributor role, you will be responsible for leading the technical teams responsible for Siemens Ultrasound Cardiovascular product development projects; for producing Cardiovascular products with high quality, high customer satisfaction, and high business impact; and ensuring the teams maintain compliance to medical device standards and regulations.
You will proactively collaborate with senior leaders from Product Management, Quality and Regulatory, Implementation Engineering, Systems Engineering, and other Chief Engineers to define portfolio plans, technology strategies, and product/technology roadmaps.
You will proactively collaborate with product managers, project engineers, clinicians, project managers, quality engineers, and implementation engineers to ensure successful feature definition and execution for each Cardiovascular product releases.
You will collaborate with Advanced Development on future clinical solutions, including clinical understanding, system design, technical verification, and clinical validation, in preparation for formal product development. The clinical solutions could be Cardiovascular well as other areas such as OB/GYN and Radiology.
Your engineering background and experience will be utilized to define customer, product, and system requirements, and use them to guide the project release teams. Your customer-facing experience will be used in discussions with clinicians and customers at external sites, and in reviews of customer complaints.
Your background and expertise in Design Controls and other Medical Device standards will be utilized to guide the teams during product lifecycles from concept definition through post-market surveillance.
You will be responsible for cross-Agile-SAFe-release-train and cross-platform coordination of technical and feature definition and designs.
Your experience in cross-site development will be utilized to lead and coordinate technical teams in multiple countries with different cultures, languages, and development environments.
Other desired experience and skills:
You are a motivated individual who strives for excellence and inspires others. You always want to do better.
You are driven by a desire to develop products that help and improve the clinical outcomes of patients.
One of your strongest attributes is influencing other individuals for whom you would not have a direct reporting relationship.
You believe that sharing knowledge strengthens the Organization and leads to better outcomes.
Willing to travel up to 10%, including internationally.
Required experience and skills to have for the success in this role:
Bachelors, Masters, or Doctorate in Engineering or Physics or related field.
20+ years’ experience in Ultrasound Engineering, Systems Engineering, Electrical Engineering, Mechanical Engineering, Software Engineering, Biomedical Engineering, Biophysics, or related experience in a regulated industry.
10+ years’ experience in medical devices, preferably medical imaging and ultrasound.
Strong and practical understanding of medical device development, product definition, Design Controls, and engineering methodologies.
Experience applying medical device standards to a complex medical product development. Should be able to demonstrate knowledge and understanding of a Quality Management System and Regulatory processes including 21 CFR 820, ISO 13485, IEC 60601-1, IEC 62366, and IEC 62304 standards
At Siemens Healthineers, we value those who dedicate their energy and passion to a greater cause. Our people make us unique as an employer in the med-tech industry. What unites and motivates our global team is the inspiration of our common purpose: To innovate for healthcare, building on our remarkable legacy of pioneering ideas that translate into even better healthcare products and services. We recognize that taking ownership of our work allows both us and the company to grow. We offer you a flexible and dynamic environment and the space to move beyond your comfort zone to grow both personally and professionally.
If you want to join us in transforming the way healthcare is delivered, visit our career site at https://usa.healthcare.siemens.com/careers.
If you wish to find out more about the specific position before applying, please visit: https://usa.healthcare.siemens.com/about.
As an equal-opportunity employer we are happy to consider applications from individuals with disabilities.
Organization: Siemens Healthineers
Company: Siemens Medical Solutions USA, Inc.
Experience Level: Experienced Professional
Job Type: Full-time
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