AbbVie Posted June 29, 2026

Senior Electrical Engineer, Combination Product Development

North Chicago, IL Full-time
Manufacturing & CMC Senior

AbbVie is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Company Description

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 at  www.abbvie.com . Follow @abbvie on  LinkedIn,   Facebook ,  Instagram ,  X  and  YouTube.

Job Description

Sr. Electrical Engineer, Combination Product Development, R&D

We are seeking an experienced Sr. Electrical Engineer to support the development of innovative drug-device combination products within our Combination Product Development team in R&D. In this role, you will lead electrical system design efforts for clinical development of advanced drug delivery systems, including on-body injectors, subcutaneous ambulatory infusion pumps, and other electromechanical systems.

This role will contribute to the development of new device and platform technologies, maintaining technical rigor and ensuring compliance with regulatory standards.  This role will work closely with engineering colleagues in R&D and cross-functional colleagues in a global organization as well as maintaining strong working relationships with external development partners throughout the product development process.

Responsibilities

Design and Development Leadership:

Work closely with external development partners through design and development efforts associated with electronic components of drug delivery systems

Execute feasibility and initial development activities including needs definition, requirements, assessment of design fundamentals, and technology landscaping

Conduct system architecture evaluation, including assessment of system design, testing, and analysis of electrical components

Perform electronics design assessments including circuit design, PCB assessment, circuit analysis, evaluation of design margins, and testing requirements definition

Technical Analysis and Validation:

Support system integration activities, reliability assessments, verification testing, and design validation to ensure products are technically robust and meet reliably goals

Provide engineering analysis and design history file documentation to support development activities, including Design Inputs, Design Outputs, Protocols, Task Analysis, and risk assessments

Support the lab and design verification teams with test plans, test setups, methods, investigations, and engineering confidence tests

Cross-Functional Collaboration:

Engage and collaborate with clinical, project development, regulatory, quality, and operations teams, as well as external engineering partners to ensure alignment throughout device development

Work across engineering disciplines (mechanical, software, systems engineering) to drive consensus and support execution on technical solutions

Partner with cross-functional stakeholders to ensure development deliverables and timelines meet regulatory standards and quality expectations

Professional Development and Process Improvement:

Establish and maintain working knowledge of technology trends and assess their relevance to combination product development

Partner with external vendors to understand and evaluate future technology roadmaps

Participate in and drive department continuous improvement initiatives focused on maximizing process efficiencies and enhanced collaboration

Use appropriate project management techniques and stage/gate processes to ensure successful completion of assigned projects

Qualifications

Education and Experience:

BS in Electrical Engineering or equivalent discipline, with typically 10+ years of relevant industry experience; MS in Electrical Engineering with typically 8+ years of relevant experience;

Demonstrated experience in medical devices or combination product development

Prior experience with subcutaneous injection devices, electromechanical devices, or digital/connected health technologies is highly desirable

Technical Skills and Knowledge:

Demonstrated expertise in electrical system design for drug delivery systems

Advanced understanding of circuit design, PCB design, and embedded systems; experience having designed and developed electrical systems from concept through product launch is a plus

Proficiency with design tools, simulation software, and analytical modeling techniques

Solid knowledge of applicable global regulatory requirements and industry standards (e.g., 21 CFR 820.30, ISO 13485, MDR)

Understanding of modern, lean product development methodologies and stage/gate processes

Experience with design verification and validation protocols in regulated environments

Competencies and Attributes:

Demonstrated ability to function as a technical leader, generating original technical ideas and development strategies

Possesses strong technical judgment and ability to work on problems of complex scope with competing factors

Excellent ability to work collaboratively with diverse groups within engineering and maintain strong working relationships with internal and external partners

Outstanding written and verbal communication skills with ability to clearly articulate technical challenges and solutions to stakeholders

Demonstrated project management capability and ability to balance multiple priorities

Proactive approach to identifying and resolving technical and project risks

Self-motivated with ability to operate independently

Key Stakeholders and Working Relationships

R&D team members (mechanical engineering, software engineering, systems engineering)

Regulatory and Quality Assurance functions

Operations and Supply Chain teams

Clinical and Commercial teams

External development partners

Project management and cross-functional leadership

Additional Information

Travel (domestic and/or international) may be required depending on project assignments (estimated 5%-10%)

This role requires strong attention to detail and commitment to quality and regulatory compliance

The successful candidate will demonstrate a passion for advancing innovative drug delivery technologies

Additional Information

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

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

This job is eligible to participate in our short-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of  any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable 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.

US & Puerto Rico only - to learn more, visit  https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Job details

Seniority
Senior
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
North Chicago, IL
Employment type
Full-time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 373 comparable Senior Manufacturing & CMC roles across 53 biopharma companies.

373Comparable roles tracked
344Currently active
53Companies hiring similar roles
20Countries represented

Salary context

174 of 373 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $96,500/yr – $183,500/yr
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $222,900 (median $142,388)

Where these roles are based

Top locations among the 373 comparable roles

United States267
India37
Ireland10
Singapore10
Netherlands7
Switzerland6

+ 14 more countries

Seniority mix

373 of 373 peers have a known seniority level

Senior250
Principal79
Associate Director44

Therapeutic area mix

0 of 373 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly San Diego, California, United States of America Senior
Same function Same seniority Same country
60%similar
Merck Rahway, New Jersey, United States of America Senior
Same function Same seniority Same country
60%similar
Seagen Inc Washington – Bothell, United States Senior
Same function Same seniority Same country
60%similar
Pfizer Groton, United States Senior
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Senior
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Senior
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Sr. Scientist - Lab Automation Scientist
Lilly · San Diego, California, United States of America · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist, Process Development
Pfizer · Groton, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist, Biologics Purification II
AbbVie · North Chicago, IL · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist I, Production and Characterization
AbbVie · Worcester, MA · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.