Principal Electrical Engineer, Connected Systems & Combination Product Development, R&D

AbbVie; Pleasanton (CA); On-site; USD 125,000 - 237,000; Full time

Job summary

AbbVie is seeking an experienced Principal Electrical Engineer in Pleasanton, CA to lead electrical design for drug-device combination products and connected medical technologies. You will drive feasibility, system architecture, and verification activities for wireless, Bluetooth, NFC, NB-IoT-enabled platforms.

Responsibilities include cross‑functional collaboration across R&D, regulatory, and quality teams to ensure compliant, scalable designs from concept through launch.

Qualifications

• BS in Electrical Engineering or equivalent with 10+ years of experience or MS with 8+ years.
• Demonstrated experience in medical devices or regulated electromechanical systems.
• Strong experience from concept to verification, validation and launch.

Responsibilities

• Lead electrical design activities for drug delivery and connected devices.
• Develop and validate electrical systems incorporating wireless tech.
• Evaluate architectures for sensing, power, embedded electronics, and communications.
• Support verification, design validation, and risk assessments.
• Ensure compliance with EMC, safety, and regulatory standards.

Skills

Electrical design

Embedded systems

Bluetooth

NFC

Wi-Fi

NB-IoT

Regulatory standards

Schematic capture

Education

BS in Electrical Engineering or equivalent

MS in Electrical Engineering or equivalent (preferred)

Tools

PCB design

Circuit design

Lab equipment

Job description

Principal Electrical Engineer, Connected Systems & Combination Product Development, R&D

• Full-time
• Salary Min: 124500
• Salary Max: 236500
• Workday Global Grade: 19
• Compensation: USD 124,500 - USD 236,500 - yearly

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com . Follow @abbvie onLinkedIn, Facebook ,Instagram ,X andYouTube.

We are seeking an experienced Sr. Electrical Engineer to support the development of innovative drug-device combination products and connected medical technologies within our Combination Product Development team in R&D. In this role, you will lead and support electrical engineering activities for advanced drug delivery and medical device systems, with particular emphasis on connected and intelligent devices leveraging IoT, AI-enabled engineering approaches, Bluetooth, Wi-Fi, NFC, NB-IoT, and related wireless technologies.

This position will contribute to the development of new device and platform technologies, ensuring strong technical execution and compliance with applicable quality and regulatory requirements. The individual will work closely with cross-functional engineering and development teams, as well as external partners, throughout the product development lifecycle.

Responsibilities

Design and Development

• Lead and support electrical and electronic design activities for drug delivery systems, connected devices, and other electromechanical medical products.
• Execute feasibility and early-stage development activities, including user needs translation, requirements development, concept evaluation, technology assessment, and system architecture definition.
• Evaluate electrical system architectures, including sensing, power, embedded electronics, communications, and subsystem integration.
• Perform electronics design assessments, including circuit design, PCB review, component selection, design margin analysis, and test strategy development.
• Support development of connected device architectures incorporating Bluetooth, NFC, NB-IoT, Wi-Fi and related wireless communication technologies.
• Contribute to robust, manufacturable, scalable designs from concept through clinical development and commercial launch.

Technical Analysis and Validation

• Support system integration, reliability assessments, verification testing, and design validation activities.
• Develop and support engineering documentation, including design inputs, design outputs, protocols, risk assessments, FMEAs, and traceability documentation.
• Partner with lab and verification teams on test methods, test setups, engineering investigations, and confidence testing.
• Review schematics, PCB layouts, and interface definitions to identify technical risks and recommend solutions.
• Support troubleshooting, root cause analysis, complaint investigations, and reliability assessments for development and fielded products.
• Ensure designs address electrical safety, EMC, manufacturability, testability, and long-term reliability.

Connected Systems and Digital Capability

• Drive evaluation and application of connected medical device technologies that improve usability, adherence, data access, and system intelligence.
• Contribute to development of devices that interface with digital health ecosystems, mobile applications, cloud-connected environments, and remote monitoring platforms.
• Apply appropriate IoT architectures, connectivity strategies, and cybersecurity-aware design principles for regulated medical products.
• Provide technical depth in wireless and short-range communication technologies, especially Bluetooth, NFC, Wi-Fi and NB-IoT.
• Evaluate and leverage AI-assisted engineering tools and intelligent development methods to improve design, analysis, prototyping, and testing workflows.

Cross-Functional Collaboration

• Collaborate with clinical, regulatory, quality, operations, software, systems, and mechanical engineering teams, as well as external development partners.
• Work across engineering disciplines to drive technical alignment and execution of integrated product solutions.
• Partner with stakeholders to ensure development deliverables, documentation, and timelines meet quality and regulatory expectations.
• Support technical reviews with suppliers, contract manufacturers, and external partners.
• Maintain awareness of emerging technologies relevant to combination products, connected devices, and digital health.
• Monitor industry trends in IoT, AI-enabled engineering, wireless medical systems, and connected care technologies.
• Contribute to continuous improvement initiatives focused on engineering quality, process efficiency, and innovation.
• Apply appropriate project management and stage-gate development practices to support successful execution.

• BS in Electrical Engineering or equivalent discipline with typically 10+ years of relevant industry experience; or MS in Electrical Engineering or equivalent discipline with typically 8+ years of relevant experience.
• Demonstrated experience in medical devices, drug-device combination products, or other regulated electromechanical systems.
• Strong experience designing and developing electrical systems from concept through verification, validation, and product launch.
• Experience with connected medical devices, digital health technologies, or wireless-enabled products is highly desirable.
• Experience working with external development partners, suppliers, and cross-functional product development teams is preferred.

Technical Skills

• Expertise in analog, digital, and mixed-signal electrical system design.
• Strong understanding of embedded systems, microcontrollers, communication interfaces, and subsystem integration.
• Experience with circuit design, PCB design and review, schematic capture, component selection, and design for manufacturability/testability.
• Strong knowledge of communication protocols such as SPI, I2C, UART/RS-xxx, USB, and related embedded interfaces.
• Experience with wireless and IoT technologies, especially Bluetooth, NFC, Wi-Fi and NB-IoT.
• Experience evaluating or developing connected device architectures in medical or regulated product environments.
• Understanding of IEC 60601, IEC 60601-2-24, 21 CFR 820.30, ISO 13485, ISO14971 and related medical device standards and requirements.
• Experience with design verification and validation in regulated environments.
• Proficiency with engineering tools, lab equipment, simulation tools, and analytical problem-solving methods.
• Experience using AI-assisted tools to enhance engineering productivity is desirable.
• Strong technical leadership and engineering judgment.
• Ability to solve complex problems involving multiple design constraints and tradeoffs.
• Excellent cross-functional collaboration and communication skills.
• Strong project management capability and ability to manage multiple priorities.
• Proactive approach to identifying and resolving technical and project risks.
• Self-motivated with the ability to work independently and effectively within teams.

Key Stakeholders

• R&D engineering teams, including electrical, software, systems, and mechanical engineering
• Regulatory Affairs and Quality Assurance
• Operations, Manufacturing, and Supply Chain
• Clinical and Commercial teams
• External development partners, suppliers, and contract manufacturers
• Project and cross-functional leadership across internal and external development ecosystems in a regulated environment

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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