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Safety Engineer (Mission Critical)
Aldridge Group
Montgomery, AL
- $70,000 to $90,000 USD / year
Aldridge is seeking an Safety Engineer (Mission Critical) to join our dynamic and energetic team in Montgomery, AL.
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Sr AI/ML Engineer - Remote Nationwide or Office-Based in MN/DC/NJ
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Minnetonka, MN
- $120,100 to $214,500 USD / year
Design and build REST and GraphQL APIs in Java, integrating with high-performance MySQL database schemas optimized for high-volume transactional workloads
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Quality Systems and Compliance Engineer
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Added 1 min ago
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Lead AI/ML Engineer - Office-Based in Eden Prairie, MN
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Eden Prairie, MN
- $145,500 to $249,500 USD / year
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Lead Electrical Engineer -Water Technologies
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Trevose, PA
- $110,000 to $125,000 USD / year
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Service Market Engineer
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Greensboro, NC
- $96,000 to $118,500 USD / year
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Senior Platform Software Engineer - OCI
Oracle
Raleigh, NC
- $92,500 to $209,500 USD / year
Oracle Cloud Infrastructure (OCI) is looking for a Senior Platform Software Engineer to join the PKI team responsible for building and operating cloud-scale Public Key Infrastructure…
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Staff Full-stack Engineer - Shopping (Remote-eligible)
Capital One
Raleigh, NC
As a Staff Engineer at Capital One, you will be part of a community of technical experts working to define the future of banking in the cloud. You will work alongside our talented team of…
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Lead Data Engineer-Snowflake
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Abbott

Senior Systems Engineer

Alameda, CA, United States

The base pay for this position is $114,000.00 – $228,000.00.

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Job details

Pay: The base pay for this position is $114,000.00 – $228,000.00.
Experience: 8+ years of experience in systems engineering for regulated environments, ideally in medical devices or software as a medical device.
Posting language: English
Posted: Nov 4, 2026

Original job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Job Description

Meet Lingo, a new biosensing technology that provides users a window into their body. Lingo tracks key biomarkers such as glucose, ketones, and lactate to help people make better decisions about their health and nutrition. Biowearable technology will digitize, decentralize and democratize healthcare, enabling consumers to take control of their own health.

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the Freedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU (https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html) education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

THE OPPORTUNITY

This Senior Systems Engineer position works onsite in our Alameda, CA location for Lingo.

We are seeking a Systems Engineer to lead design and development efforts across our cloud, and mobile platforms within a regulated medical device environment. This role is based in Alameda, CA, and plays a critical role in ensuring product quality, regulatory compliance, and scalable delivery.

What You’ll Work On

Define and support software system architecture, safety classification, and system design to enable compliant, high-quality product development.
Create and maintain interface control documentation to ensure robust integration between hardware, and data systems.
Lead risk management activities, identifying hazards, defining mitigations, and ensuring traceability throughout design and development.
Partner with QA/RA to maintain compliance with relevant standards, including FDA 21 CFR 820.30, ISO 13485, ISO 14971, IEC 60601, and IEC 62304.
Support verification and validation (V&V) processes which includes planning, execution, and documenting system tests to confirm requirements are met.
Facilitate design reviews, coordinate multidisciplinary technical decisions, and champion systems thinking in everyday engineering.
Maintain documentation for design history files (DHFs) and ensure full requirements traceability across the product lifecycle.
Support defect analysis and disposition while ensuring alignment with safety and risk management processes.
Support audits, regulatory submissions, SDLC process definition, non-product software validation, configuration management, and change control activities for software systems.

Required Qualifications

8+ years of experience in systems engineering for regulated environments, ideally in medical devices or software as a medical device.
Strong technical breadth across software, IoT systems, with the ability to communicate effectively across disciplines.
Hands‑on experience with requirements definition/management tools (Jama, ALM, DOORS, Polarion, Ketryx, or similar) and interface control documentation.
Hands‑on experience with requirements definition/management tools (Jama, Ketryx, or similar) and interface control documentation.
Knowledge of core regulatory and quality standards for medical devices (FDA 21 CFR 820, ISO 13485, ISO 14971, IEC 62304, IEC 60601).
Familiarity with risk management best practices for medical devices and maintaining hazard analysis/FMEA documentation.
Demonstrated systems thinking skills, understanding how individual components affect safety, performance, and usability of the overall system.
Excellent communication, collaboration, and documentation skills.

Preferred Qualifications

Experience with Model‑Based Systems Engineering (MBSE) tools such as Cameo Systems Modeler or Enterprise Architect.
Background in biosensor, digital health, or IoT medical device development.
Exposure to design history file creation, regulatory submissions, and audits.
Experience integrating cloud‑based services with medical devices in compliance with security/privacy standards (HIPAA, GDPR).
Familiarity with design controls for consumer medical or multifunction devices.
Experience with Human Factors Engineering (IEC 62366).
Experience with project-management and agile tools (e.g., Jira).

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal

#software

The base pay for this position is $114,000.00 – $228,000.00. In specific locations, the pay range may vary from the range posted.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email corpjat@abbott.com

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More about this job

Skills

Biomarkers
Abbott
Regulatory compliance
Documentation
Risk management
Systems thinking
Medical devices
Communication skills
Collaboration
Project management
Jira

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