S'INSCRIRE

Offres d'emploi

Trouvez des postes près de chez vous, sur site, hybrides ou à distance.
  • Emplois similaires à : Staff Software QA Engineer
XX
Staff Embedded Software EngineerAbbott Laboratories company • Alameda, California, United States
Postuler Maintenant
XX

Staff Embedded Software Engineer

Abbott Laboratories company
  • US
    Alameda, California, United States
  • US
    Alameda, California, United States
Postuler Maintenant

À propos

The Opportunity This position works out of our Alameda, CA location in the Abbott Diabetes Care Division, where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informaded decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.
This Staff Embedded Software Engineer works independently on the design, development, and maintenance of embedded firmware for an innovative and exciting new venture investigating and commercializing novel technologies and biomarkers that will give people and the professionals who treat them new insights into their health, physical and mental performance. They will work independently on identifying new technologies for implementation into new product development and process improvement for both commercial and medical products. This person also exercises independent judgment in identifying, recommending, and implementing significant and/or complex new tools/process improvements to support the sensor technology that helps people understand what their body is telling them and how they can translate these insights into meaningful action so that they can lead a healthier life.
What you’ll work on
Lead software development, verification, and validation; responsible for on-time delivery of high-quality embedded software products that meet budgetary objectives.
Design and implement software in current programming languages (e.g., C, C++, C#, Python), practical experience with embedded C development.
Identifies parameters, structure, and critical test components. Writes, updates, or executes test design, cases, as well as procedures and reports results.
Working from requirement specifications, develops, maintains, and updates detailed design and interface specifications.
Participates in and supports the implementation, development, enhancements, and modifications to software source code, scripts, and procedures.
Debugs, troubleshoots, and isolates software problems as well as offers strategic solutions, analysis, and advice regarding identified issues for future development.
Assist in the evaluation of selected designs through testing and full documentation of the results.
Working on complex problems where analysis of situations or data requires evaluation of identifiable factors.
Exercise judgment within defined procedures and practices to determine appropriate action.
Contributes to and supports gathering, analyzing, and validating requirements;
Contributes to and supports writing, updating, developing and maintaining Hazard/Risk analysis specifications;
Contributes to and supports root-cause analysis of failures.
Participate in software development, verification and validation following the guidance of software lead.
Follow approved Design Control procedures for software development in accordance with FDA guidelines.
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
At this level, it is expected the candidate will have proficiency in software implementation.
Interacts with QA engineers to ensure that software products are robust and of very high quality.
Actively participates in product development teams for the development of new products and services.
Readily adjusts priorities and works within team environment for timely completion of common objectives for multiple projects.
Resolve significant and/or complex technical issues to empowering health through breakthrough technology.
Required Qualifications
Bachelor of Science in Electrical Engineering, Computer Science, or equivalent. MS desired.
8 to 15 years experience in software engineering required. Some experience in software engineering management.
Excellent written and verbal communication skills.
Expert knowledge in current programming languages (e.g., C, C++, C#, Python, etc.).
Expert knowledge with current development tools (IDEs, debuggers, unit test frameworks and source control management).
Experience with software testing.
Experience with software development life cycle processes.
Good knowledge of software engineering principles are required.
Demonstrated success in technical proficiency, creativity, and independent thought.
Experience with structured software development and/or Object Modeling Design experience required.
Experience with software development of embedded systems for safety-critical products required.
Strong debugging techniques and experience on using debugger in an embedded environment is required.
Excellent troubleshooting skills are a must.
Knowledgeable of microprocessor architecture is required.
Ability to multi-task and prioritize responsibilities.
Demonstrated ability in providing guidance to junior team members.
Preferred Qualifications
Solid knowledge of design controls and regulations for medical device development, (EN460001, ISO13485, FDA) is desirable.
Experience in model-based design (UML or SysML), is highly desirable.
Cross-platform development experience is preferred.
Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement and process is desirable.
Good knowledge of and experience in RF and WiFi software design, device driver configuration, and test is preferred.
Experience with Bluetooth and Bluetooth Low-Energy is highly preferred.
Experience with Source Control Management is highly preferred.
Experience with testing of embedded devices is a strong plus.
What We Offer
Training and career development, with onboarding programs for new employees and tuition assistance.
Financial security through competitive compensation, incentives and retirement plans.
Health care and well-being programs including medical, dental, vision, wellness and occupational health programs.
Paid time off.
401(k) retirement savings with a generous company match.
The stability of a company with a record of strong financial performance and history of being actively involved in local communities.
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.
#J-18808-Ljbffr
  • Alameda, California, United States

Compétences linguistiques

  • English
Avis aux utilisateurs

Cette offre provient d’une plateforme partenaire de TieTalent. Cliquez sur « Postuler maintenant » pour soumettre votre candidature directement sur leur site.