Abbott Posted November 6, 2026

Development Quality Engineer I

Sylmar, California, United States FULL_TIME
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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.

A healthy heart is essential to good health. That's why we're committed to advancing treatments for people with cardiovascular disease. As a global leader in Cardiac Rhythm Technologies, our breakthrough medical technologies help restore people's health so they can get back to living their best lives, faster. We focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

“We are seeking an experienced, high caliber Data Scientist, I for our Sylmar, CA .

Responsible for ensuring the requirements for Device/Combination Products through the execution of Abbott standard operating procedure and Product Lifecycle Management.

WHAT YOU’LL DO

Particularly skilled in quantitative analysis and data management

Utilize technologies to collect, clean, analyze, predict, and effectively communicate information

Able to examine and interpret relevant data to quickly develop an analysis plan that will answer key business questions and create value for the organization.

Understanding of machine learning algorithms and advanced statistics such as: regression, time-series forecasting, clustering, decision trees, exploratory data analysis methodology, simulation, scenario analysis, modeling, optimization

Analyze data, draw insights, and present results in a cohesive, intuitive, and simplistic manner to site and executive management.

Ability to work with cross-functional teams to devise test methodologies to ensure validity of the data models being presented.

Work closely with the business to understand the domain and iteratively refine analyses

Identifies opportunities to improve the efficiency and effectiveness of the systems and process being examined (process improvement/reengineering projects).

Identify and implement continuous improvement opportunities throughout the data lifecycle.

Act as Subject Matter Expert in cross functional team meetings as well as internal and external audits.

Ensure compliance with associated regulations, standards, and site procedures.

May demonstrate basic project management skills by acting as a project lead on small, well defined project. Influence exerted at peer level and occasionally at first levels of management.

Qualifications

Bachelors Degree (± 16 years) Engineering, Life Sciences, or Physical Sciences OR an equivalent combination of education and work experience

Experience:

Minimum 1 year

1-2 years experience in pacing industry. Quality experience desired. Must have demonstrated written and verbal communication, interpersonal, presentation, analytical, organizational skills, and the ability to meet deadlines.

Must be able to work effectively with engineers, technical specialists, vendors, and customers to achieve assigned goals; must be capable of coordinating multiple assignments simultaneously and effectively.

Must possess demonstrated personal computer skills (experience with Microsoft Office or equivalent required) in graphics, word-processing, databases, authoring programs, etc., to develop presentation materials.

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

Ability to work in a highly matrixed and geographically diverse business environment.

Ability to work within a team and as an individual contributor in a fast-paced, changing environment.

Ability to leverage and/or engage others to accomplish projects. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.

Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail.

Ability to travel.

0-2 years of experience in Quality Assurance, Technical Quality, or equivalent; Some knowledge in the areas of Design Controls, VV activities, manufacturing practices or processes, and statistical techniques. Drive to learn applicable regulations and standards such as FDA, QSR and ISO regulations. Demonstrated written, oral and interpersonal skills. Strong analytical skills, problem solving techniques and statistical application experience.

Preferred Qualifications:

Bachelors Degree focused in Data Analytics, Data Science or similar discipline including Engineering, Mathematics, Computer science, Statistics or Physics preferred

1-2 years’ of related work experience with a good understanding of specified functional area.

Experience working in life sciences or healthcare industry preferred.

Working experience with database applications including programming experience (e.g. SQL, Python, R, Java, Scala, C++ in Linux/Unix and/or equivalent).

Experience implementing process improvements and efficiencies.

Strong excel skills.

Excellent verbal and written communications skills to explain data analysis findings.

Self-starter who can plan their own work to meet deadlines.

Strong interpersonal skills, be self-motivated, have a strong desire to learn, and be adaptable to a fast paced, ever-changing environment.

WHAT WE OFFER 

At Abbott, you can have a good job that can grow into a great career. 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 t ime 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

Learn more about our benefits that add real value to your life to help you live fully:    www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. 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 and @AbbottGlobal.

The base pay for this position is $73,900.00 – $116,000.00. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Sylmar, 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 1458 comparable Quality roles across 143 biopharma companies.

1458Comparable roles tracked
1336Currently active
143Companies hiring similar roles
53Countries represented

Salary context

256 of 1458 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 · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $120,250)

Where these roles are based

Top locations among the 1458 comparable roles

United States595
Ireland87
France71
Germany68
China66
India56

+ 47 more countries

Seniority mix

712 of 1458 peers have a known seniority level

Manager217
Senior166
Intern/Fellow/Postdoc100
Associate68
Associate Director46
Director45
Principal38
Senior Director25
Executive/VP7

Therapeutic area mix

2 of 1458 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2

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.

40%similar
Lilly Lebanon, Indiana, United States of America Principal
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same country
40%similar
AbbVie North Chicago, IL Director
Same function Same country
40%similar
AbbVie North Chicago, IL Manager
Same function Same country
40%similar
Gilead Sciences, Inc. La Verne, United States
Same function Same country
40%similar
Gilead Sciences, Inc. La Verne, United States Senior
Same function 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.

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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%
Principal Scientist GMP Environmental Monitoring Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
40%
Senior Manager, Clinical Quality Assurance
AbbVie · North Chicago, IL · Manager
Function Therapeutic area Seniority Country
40%
Senior Manager, Quality Assurance
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
40%
Principal QA Validation Specialist, Fill Finish
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Principal
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.