Senior Device Engineer, Lifecycle Management

AbbVie

Confirmed live yesterday High trust
Hybrid

Quick summary

Work type
Hybrid
Location
North Chicago, IL
Salary
$124,500–$236,500 / yr
Posted
56 days ago
Freshness
Confirmed live yesterday
Closes
Jul 17, 2126

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $187k
This role $180k
$111k most similar roles pay here $250k

This role pays more than 59% of similar roles. Most pay $159,825–$213,375 — the shaded band above. At the midpoint, this role pays about $180k versus about $187k for comparable roles.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 297 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 271 roles with salary data.

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At a glance

TL;DR · Senior Device Engineer, Lifecycle Management

Senior Device Engineer - Lifecycle Management will join a multi-disciplined engineering team to support medical device products from production transfer through end of life. This technical leadership role focuses on the continuous improvement of body contouring products by managing small-scale projects, defining functional requirements, and performing in-depth data analysis to improve software quality. The engineer will design, develop, and support embedded systems, Windows embedded applications, and desktop applications while troubleshooting hardware and software components. Key technical requirements include experience with C#, .NET Framework, and multi-threaded Windows-based applications. Candidates should possess knowledge of PID control algorithms, common protocols like RS232, SPI, and USB, and familiarity with IEC 62304 standards. The role operates within a strictly regulated medical device environment, ensuring all development documentation and processes comply with FDA QSR, ISO13485, and other international regulatory requirements.

What you'll do

  • Lead and manage small-scale projects to ensure timely delivery of product milestones.
  • Define functional requirements and develop technical designs for current generation software systems.
  • Design, develop, and support embedded, Windows embedded, and desktop applications.
  • Perform in-depth data analysis to drive improvements in software and product quality.
  • Interface, integrate, troubleshoot, and debug hardware and software components.
  • Generate required product development documentation including functional specifications and design documents.
  • Execute manual or automated tests for the verification and validation of software applications.
  • Design, code, and validate software tools used in manufacturing and verification processes.

What we're looking for

  • BS in Software Engineering or equivalent degree and/or experience.
  • Advanced degree (preferred).
  • Minimum of 8 years of experience in engineering design.
  • At least 5 years of experience with embedded Windows programming using C# and .NET.
  • At least 3 years of experience in medical devices or a similarly controlled software environment (preferred).
  • Experience developing event-driven, multi-threaded Windows-based applications using .NET Framework and C# (preferred).
  • Required experience in structured software/systems development, including design methodologies, patterns, and component-oriented architecture.
  • Knowledge of PID control algorithms and IEC 62304 lifecycle processes for regulated environments.

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