Website GE Healthcare
The Systems Engineer is responsible for driving technical design proposal & execution on Installed Base projects and products for the Maternal & Infant care group. The systems engineer identifies opportunities in existing products, prepares design proposals to deliver lower cost design solutions and provide technical solutions for product quality improvements. works closely with LPI, Product Sourcing Leader,PM & cross-functional teams to execute the IB programs & to ensure best practices
Duties include (but are not limited to):
Work as the technical leader for the products he/she owns.
Identifies technical unknowns and risks, creates mitigation plans and works closely with LPI and cross functional teams to mitigate them.
Ensuring that projects and processes abide to the business Engineering Quality Procedures, Phased Review Discipline, Supplier Transfer Work Instructions and regulatory needs of the applicable markets.
Developing strong stakeholder relationships and working with cross-functional teams, to drive program execution on-time and within spec
Working with functional managers to ensure right design quality within each function
Bring in Electrical, Embedded and Electronics Design Experience to the Variable Cost Productivity (Product cost reduction) programs.
Design Change Management – Implementing design changes for cross functional effectiveness. Transfer of designs to manufacturing teams and service teams to implement in production and post market service.
Bachelor’s Degree in electronics/electrical, Embedded or biomedical Engineering with experience in medical equipment development a must.
4+ years’ experience in hardware design (electrical and electronics) within a development, research or manufacturing environment.
Demonstrated ability to build lasting cross-functional relationships, including strong influential, communication, and collaboration skills.
Demonstrated understanding/experience with the product life cycle, transfer programs, product cost reduction programs or other productivity projects.
Highly developed problem solving skills
Experience working with foreign and domestic regulatory agencies
Quality Specific Goals
Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.
Complete all planned Quality & Compliance training within the defined deadlines.
Identify and report any quality or compliance concerns and take immediate corrective action as required.
Ensure compliance/closure of Regulatory and Quality requirements before approving technical and program milestones.
Lead continuous improvement activities by driving the implementation of process and product quality improvement initiatives.
Knowledge of GE Healthcare tools and processes (engineering, sourcing, supply chain)
Previous healthcare experience developing products within an FDA regulated environment
Hands on board design experience in a product development environment
Masters in Electronics and electrical, Embedded , bio-medical engineering or equivalent.
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