Abbott Posted October 5, 2026

Senior Software Design Assurance Engineer

Pleasanton, California, United States FULL_TIME
Quality Senior
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Abbott 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

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.

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 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 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 

The Senior Software Design Assurance Engineer is responsible for supporting product development, executing and maintaining software quality engineering methodologies, and providing quality engineering support for software.   The Senior Software Design Assurance Engineer position focuses primarily on software quality but also supports other aspects of product development based on experience.

What You’ll Work On

Provides technical and quality system guides related to establishing software requirements.

Provide quality oversight for software verification and validation activities for new products in accordance with design planning procedures.  This includes, but is not limited to, reviewing and approving software test case protocols and reports, reviewing software development plans, and reviewing other system and software documentation.

Leads meetings to prioritize, review, and/or approve action plans for addressing issues captured in problem resolution systems during development.

Leads risk evaluation and associated management activities related to software development, including Risk assessments (e.g., FMEA), product risk analysis, and mitigation of software issues.

Participates in technical and management reviews to ensure design plans, product design, and deliverables related to product software are met.  Represent the quality engineering function for the review and approval of designated design outputs.

Provide quality oversight for non-product software validation by assessing the need for validation and preparing and/or supporting protocols, reports, and other documentation as required.

May be involved with supporting product cybersecurity assessments in conjunction with a cross-functional team

Complies with US FDA regulations, other country regulatory requirements, company policies, and procedures.

Maintains a strong, collaborative partnership with cross-functional team members, especially with R&D.

Works as an individual contributor and may provide guidance or oversee the work of other QE team members.

Develop and conduct training of company personnel for the divisional software development and validation program.

Support audits and lead quality system improvement activities.

Additional responsibilities may be assigned as needed.

Required Qualifications:

Bachelor’s degree in engineering or a technical field

Minimum of 5 years related work experience in Quality or a related field.

Knowledge of regulations, standards, and guidance affecting medical software and non-medical device software development.

Strong verbal and written communication with the ability to effectively communicate at multiple levels in the organization.

Preferred Qualifications:

Advanced degree

Previous quality engineering experience and demonstrated use of quality tools/methodologies.

Experience working in a broader enterprise/cross-division business unit model.

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 $78,000.00 – $156,000.00. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
Pleasanton, 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 230 comparable Senior Quality roles across 59 biopharma companies.

230Comparable roles tracked
216Currently active
59Companies hiring similar roles
29Countries represented

Salary context

58 of 230 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 Not listed on this posting
Lowest disclosed · Associate Quality Control Chemist, Senior (Data Review) Mid Shift · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Peer group range $66,560 – $208,845 (median $131,050)

Where these roles are based

Top locations among the 230 comparable roles

United States121
Ireland15
China10
India9
Singapore9
Spain8

+ 23 more countries

Seniority mix

230 of 230 peers have a known seniority level

Senior165
Associate Director35
Principal30

Therapeutic area mix

0 of 230 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
Gilead Sciences, Inc. La Verne, United States Senior
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Senior
Same function Same seniority Same country
60%similar
JuN - Seattle Dexter Seattle 400 Dexter, United States Senior
Same function Same seniority Same country
60%similar
Amgen Inc. Thousand Oaks, United States Senior
Same function Same seniority Same country
60%similar
Novo Nordisk West Lebanon, United States Senior
Same function Same seniority Same country
60%similar
Biogen Research Triangle Park, United States Senior
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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. Quality Assurance Specialist
Gilead Sciences, Inc. · La Verne, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Associate Quality Assurance
Amgen Inc. · Thousand Oaks, United States · Senior
Function Therapeutic area Seniority Country
60%
Sr Associate I, Quality Control Microbiology
Biogen · Research Triangle Park, United States · Senior
Function Therapeutic area Seniority Country
60%
Sr. Associate III, Compliance
Biogen · Research Triangle Park, United States · 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.