Principal Systems Engineer

Posted Yesterday
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McHenry, IL, USA
In-Office
140K-140K Annually
Expert/Leader
Healthtech • Pharmaceutical • Manufacturing
The Role
Leads system architecture, requirements development, integration, verification, validation, risk management, and technical documentation for complex electromechanical medical devices. Collaborates across mechanical, electrical, software, and cross-functional teams to define interfaces, connected-device technologies, and technical direction. Supports FDA-regulated product development, design controls, audits, and international market requirements while providing hands-on systems engineering leadership.
Summary Generated by Built In

Principal Systems Engineer-Medical Devices

Location: McHenry, IL

Hybrid Work Schedule: Three days a week on-site in McHenry and two days from home office

Salary starting at $140K plus bonus


Are you an experienced hands-on Systems Engineer who enjoys solving complex technical challenges, developing innovative medical devices and bringing together multiple engineering disciplines to create successful products?


Medela LLC, in McHenry, IL is seeking a Principal Systems Engineer to provide hands-on technical and architectural leadership for its Maternity Care and NICU product portfolio. This is an opportunity for a hands-on engineer who thrives on solving complex problems, influencing technical decisions and collaborating with talented engineering professionals.


The ideal candidate brings strong experience in complex electromechanical medical devices, systems architecture and requirements development, along with an understanding of embedded software and connected device technologies.


This is a highly collaborative, hands-on technical leadership position with the opportunity to influence product development across a diverse medical device portfolio.


What You'll Do-Principal Systems Engineer, Medical Devices
  • Lead the development of system architectures for complex electromechanical medical devices, including new product development, existing product improvements and system integration initiatives.
  • Translate customer, clinical and business needs into clear, measurable system and subsystem requirements.
  • Develop and maintain system architectures, interface specifications and technical documentation across hardware, software and connected technologies.
  • Provide expertise with object-oriented development methodologies, networks, data storage, data modeling, data ontologies, wireless communication and security architectures.
  • Collaborate with mechanical, electrical and software engineers to evaluate technical alternatives, resolve integration challenges and establish effective engineering solutions.
  • Define interfaces that enable medical devices to communicate with external systems, including hospital networks and cloud-based platforms.
  • Serve as a principal technical resource, providing guidance on architectural decisions and resolving complex engineering challenges.
  • Partner with engineering leadership and cross-functional teams to establish technical direction and gain alignment on design decisions.
  • Review verification and validation strategies to ensure products meet system requirements, performance expectations and applicable regulatory standards.
  • Support risk management, design controls and technical documentation for regulatory submissions and audits.
  • Hands-on involvement in engineering activities throughout the product development lifecycle.
  • Provide technical oversight and guide engineering personnel in resolving varied technical/scientific problems with systems engineering principles

Qualifications for the Principal System Engineer, Medical Devices

  • Bachelor's degree in Systems Engineering, Electrical Engineering, Mechanical Engineering, Biomedical Engineering or a related technical discipline.
  • Extensive experience developing complex electromechanical systems, diagnostic equipment, or connected medical technologies within the medical device industry.
  • Strong background in embedded software, firmware or software-intensive electromechanical systems.
  • Demonstrated experience translating user needs into system requirements and developing system-level architectures.
  • Strong understanding of hardware and software integration, system interfaces and technical requirements management.
  • Experience leading complex engineering initiatives and influencing multidisciplinary teams without direct reporting authority.
  • Hands-on experience developing technical specifications, resolving system integration challenges and supporting product development.
  • Solid understanding of verification and validation, risk management and regulated product development.
  • Experience defining interfaces between physical devices and external systems, including hospital networks and cloud platforms.
  • Familiarity with APIs, interface control documents (ICDs) and wireless communication technologies.
  • Working knowledge of FDA design controls, ISO 13485, ISO 14971 and IEC 60601.
  • Experience with model-based systems engineering (MBSE), SysML or related systems engineering tools.
  • Experience developing medical devices for international markets.

What we offer our Principal Systems Engineer, Medical DevicesComprehensive benefits plan401K with matchPension Plan16-week Paid Parental LeaveGenerous PTO package, plus 14 paid holidaysA great place to work! At Medela, you will be joining a global community of colleagues, united by the purpose that drives our business: helping people. Medela exists to advance human health and well-being through knowledge-based and innovative human milk and medical vacuum solutions. This is not a job description. More details will be provided regarding the functions of this position. As an EEO/Affirmative Action Employer, all qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, citizenship, sex, protected veteran status, age, physical or mental disability, medical condition, HIV/AIDs status, marital status, domestic partner status, sexual orientation, gender identity (transgender status), weight, height or any other characteristic protected by federal, state, or local law or ordinance.https://mandatoryview.com/?LicenceId=e7c44cfe-6946-4b77-9939-493d186ba760&ProductType=OnlineApplicant&SubType=PG  

Skills Required

  • Bachelor's degree in Systems Engineering, Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or a related technical discipline.
  • Extensive experience developing complex electromechanical systems, diagnostic equipment, or connected medical technologies within the medical device industry.
  • Strong background in embedded software, firmware, or software-intensive electromechanical systems.
  • Experience translating user needs into system requirements and developing system-level architectures.
  • Strong understanding of hardware and software integration, system interfaces, and technical requirements management.
  • Experience leading complex engineering initiatives and influencing multidisciplinary teams without direct reporting authority.
  • Hands-on experience developing technical specifications, resolving system integration challenges, and supporting product development.
  • Understanding of verification and validation, risk management, and regulated product development.
  • Experience defining interfaces between physical devices and external systems, including hospital networks and cloud platforms.
  • Familiarity with APIs, interface control documents, and wireless communication technologies.
  • Working knowledge of FDA design controls, ISO 13485, ISO 14971, and IEC 60601.
  • Experience with model-based systems engineering, SysML, or related systems engineering tools.
  • Experience developing medical devices for international markets.
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The Company
HQ: Baar
1,241 Employees
Year Founded: 1961

What We Do

Through advancing research, observing natural behavior, and listening to our customers, Medela turns science into care while nurturing health for generations. Medela supports millions of moms, babies, patients, and healthcare professionals in more than 100 countries all over the world. As the healthcare choice for more than 6 million hospitals and homes across the globe, Medela provides the leading research-based breast milk feeding and baby products, healthcare solutions for hospitals, and clinical education. A family-owned company, Medela has 20 subsidiaries in Europe, the Americas, Asia and Australia, three production and warehouse facilities in Switzerland, the U.S and China and a worldwide distribution network in over 100 countries. With more than 1,500 employees, Medela is dedicated to developing breakthrough innovations that build better health outcomes and improve the lives of moms, babies and patients. Founded in 1961 by Olle Larsson, his son Michael Larsson serves as Chairman of the Board of Directors since 2001. Annette Brüls is the CEO of the company since 2018. Medela is committed to providing equal employment opportunity (EEO) to all persons regardless of race, religion, color, national origin, ancestry, citizenship, sex, protected veteran status, age, physical or mental disability, medical condition, HIV/AIDS status, marital or domestic partner status, sexual orientation, gender identity, or any other characteristic protected by federal, state, or local law or ordinance

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