Sr Medical Systems Engineer

Global Connect Technologies; Milwaukee (WI); On-site; USD 95,000 - 125,000; Full time

Job summary

A global technology firm is seeking a Team Lead for Systems Engineering. This role involves leading systems engineering processes to define product features, collaborating with cross-functional teams, and implementing enhancements. Qualifications include a Bachelor's degree in Engineering, 7+ years in systems engineering, and proficiency in ALM tools. Ideal candidates will have a strong background in medical devices and regulatory standards. This is a full-time, mid-senior level position located in Milwaukee, Wisconsin.

Qualifications

• 7+ years of systems engineering experience required.
• Experience with medical device regulatory and safety standards is a plus.
• Minimum 3 years of experience with ALM tools.

Responsibilities

• Lead definition of incremental features within SEALM/Jama Connect.
• Collect and triage user feedback for process improvements.
• Develop training materials and deliver training.

Skills

Systems engineering

Cross-functional teamwork

Communication of technical information

Mentoring and influencing

Education

Bachelor’s degree in Engineering or related field

Tools

ALM tools (e.g., Jama, DOORS)

Job description

Team Lead at Global Connect Technologies

Job Description:

The Systems Engineering Design Leader will be responsible for leading systems engineering processes and feature definitions for GE Healthcare products using the SEALM (Systems Engineering Application Lifecycle Management) tool, specifically Jama Connect. The role involves defining standards, gathering stakeholder input, supporting tool implementation, and driving process adoption across global cross-functional teams.

Responsibilities:

• Lead definition of incremental features such as essential characteristics, accessories, and alarms within SEALM/Jama Connect
• Gather stakeholder inputs and best practices from key product teams
• Develop “standard work” proposals including process definitions, training materials, and tool configurations
• Refer to applicable GEHC internal standards, work instructions, and external regulatory standards
• Identify corner-case users and validate standard work proposals to establish MVP processes
• Communicate new processes to the broader user community
• Collect and triage user feedback into must‑fix issues, productivity improvements, and optional enhancements
• Submit formal change requests and manage them through deployment
• Create summaries explaining triage decisions and tailoring guidelines
• Develop and deliver training for each implemented feature
• Monitor enhancement requests after deployment and iterate improvements
• Work with design leads to identify and align feature clusters
• Collaborate with teams to address country‑specific scope including language and regulatory requirements

Qualifications / Requirements:

• Bachelor’s degree in Engineering or related field
• Minimum 7 years of systems engineering experience
• Minimum 3 years of experience working with ALM tools (e.g., Jama, DOORS)
• Minimum 3 years of design engineering/product development experience
• Experience working in cross‑functional, global teams
• Familiarity with regulatory, design, and safety standards

Desired Qualifications:

• Master’s degree in Engineering or related field
• 10+ years of experience in design/product development of medical devices
• Strong knowledge of medical device regulatory and safety standards (ISO, FDA, IEC 60601 series)
• Experience working with external partners and universities
• Ability to communicate complex technical information clearly
• Demonstrated ability to mentor, influence, and teach systems engineering concepts

Seniority Level

• Mid‑Senior level

Employment Type

• Full‑time

Job Function

• Medical Equipment Manufacturing and Medical Practices