Abbott Posted October 4, 2026

Reliability Engineer II

Alameda, California, United States FULL_TIME
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About this opportunity

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.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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 a high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

Join us at Abbott Diabetes Care (ADC) in our mission to help individuals with diabetes lead active, fulfilling lives. We’re focused on helping people manage their health more effectively and comfortably, with life-changing products that provide accurate data to drive better-informed decisions.

The Reliability Engineer II is an individual contributor with deep expertise in electrical engineering, software development principles, and project management. This role executes complex investigations and projects, adapting traditional approaches to develop innovative solutions. The position is responsible for maintaining programs for systematic monitoring and evaluation of product reliability and quality standards, ensuring compliance with regulatory and internal requirements.

This is an onsite opportunity based out of Alameda, CA.

What You’ll Work On

Perform detailed failure analysis investigations on returned ADC products (readers and sensors), including hardware and embedded software components.

Lead and support medium-sized projects, applying project management methodologies to ensure timely completion.

Collaborate with cross-functional teams to address recurring reliability issues in both hardware and software domains.

Conduct sustaining activities such as process improvements, tooling updates, and software reliability enhancements.

Apply quality principles and perform complex analysis of quality records and reports to recommend improvements.

Document reliability issues and performance measures for management review.

Provide technical guidance to engineers in the lab and mentor on best practices for hardware/software integration.

Liaise with external vendors and internal design teams to resolve technical challenges.

Required Qualifications

Bachelor’s degree in a technical (e.g. electrical/mechanical/software) or scientific (e.g. statistics/math) discipline.

Or an equivalent combination of education and work experience

Equivalent experiences is defined as five years in a role responsible for product engineering, ideally in a medical device industry.

Experience in product failure analysis, hardware/software integration, and reliability investigations.

Experience supporting CAPA activities and nonconforming product/procedure investigations

Knowledge of embedded systems, and electrical design principles.

Excellent problem-solving and critical thinking skills.

Ability to manage complex technical investigations and adapt solutions.

Project management and organizational skills, with the ability to manage multiple priorities and meet deadlines.

Strong technical writing and presentation skills, including the preparation of investigation reports and the communications of findings to management and stakeholders

Preferred Qualifications

Knowledge of FDA Quality System Regulations (21 CFR Part 820) and ISO 13485.

Proficiency with data analysis and statistical tools (e.g., Power BI, Python) to evaluate reliability trends, identify patterns, and determine root causes.

Experience with Failure Modes and Effects Analysis (FMEA) and Root Cause Analysis (RCA) methodologies, including 5 Whys and Fishbone analysis.

Demonstrated ability to work effectively within cross-functional teams, including Quality Assurance, R&D, and Manufacturing.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

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.

The base pay for this position is $81,500.00 – $141,300.00. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Alameda, California, United States
Employment type
FULL_TIME

How this role compares

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

We currently track 1369 comparable Quality roles across 143 biopharma companies.

1369Comparable roles tracked
1242Currently active
143Companies hiring similar roles
52Countries represented

Salary context

230 of 1369 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QA - Stat Sort Specialist · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Highest disclosed · Vice President, Quality Assurance - GMP · Exelixis Inc $315,500/yr – $366,500/yr
Peer group range $55,037 – $341,000 (median $129,052)

Where these roles are based

Top locations among the 1369 comparable roles

United States553
Ireland82
China62
France58
Germany51
India50

+ 46 more countries

Seniority mix

625 of 1369 peers have a known seniority level

Manager183
Senior166
Intern/Fellow/Postdoc73
Associate68
Associate Director35
Director35
Principal30
Senior Director28
Executive/VP7

Therapeutic area mix

1 of 1369 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1

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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.

40%
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Function Therapeutic area Seniority Country
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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.