Abbott Posted October 10, 2026

Director, Human Factors Engineering

Milpitas, 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.

WHAT YOU’LL WORK ON:

Provides leadership, vision and direction of the ADC Human Factors Engineering and Usability Function.   Responsible for developing and leveraging product development, data interpretation and establishing external relationships to drive human factors and usability work.  Collaborates across R&D and the division to develop tools to optimize products and development programs strategy and budgets.  Develops processes, tools, and methods that advance evaluation of product designs and concepts at all phases of design. Collaborates with upstream partners (product managers, market research, UX designers, etc.) to streamline development and de-risks development efforts. Responsible for effective people leadership, up to Sr. Manager level staff.  Conduct high level program management coordination and strategic division ownership for a wide range of analytical methodologies, approaches and techniques for product characterization.  Manage direct reports at manager, and administrative levels.  Provide management guidance for their organizations to ensure market leading use of technology and product development.

MAIN RESPONSIBILITIES

Directs activities to ensure new product development activities are achieved within agreed upon scope, timeline, and budget

Recruits, coaches and develops organizational talent

Fosters a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives

Creates an entrepreneurial environment

Provides general direction to managers, exempt specialist and non-exempt support in various areas, groups and/or operations

Keeps the organization’s vision and values at the forefront of decision making and action

Plans and conducts worldwide customer, competitive, and software industry research to identify and prioritize usability improvement possibilities and solutions

Builds strategic partnerships to further departmental and organizational objectives.  Interacts internally and externally with executive level management, outside regulatory agencies, customers, vendors and/or suppliers

Coordinates across functional areas, business units, and/or geographies in order to achieve Division goals

Provides global strategic marketing, engineering management, and staff with training and mentoring on usability

theory, resources, and technology.

Monitors and ensures compliance with company policies and procedures (e.g. compliance with FDA regulations, etc.)

•Makes and executes operational decisions with a strategic perspective

Directs and controls the activities and budget of one or more functional areas, product groups and/or third party vendors.

QUALIFICATIONS:

Bachelor’s or M.S. degree in Human Factors Engineering, Biomedical Engineering, Electrical Engineering, Computer Science, Mechanical Engineering or other scientific or engineering field.

10-15 years of management and technical management experience in the medical device industry with minimum 5 years at a senior management role.

Demonstrated track record of building and driving high performance teams in a highly regulated environment – you have shipped multiple products.

Experience leading Human Factors activities across the product lifecycle, including ethnographic research, user needs identification, workflow and task analysis, requirements development, user interface design, user error analysis, usability and validation testing.

Extensive knowledge of entire medical device development process from needs definition through regulatory approvals, production, launch, and product life cycle maintenance.

Proven ability to work with cross-functional teams and provide technical leadership.

Proven ability to interface with customers in a highly professional manner.

Ability to quickly assimilate advanced domain knowledge.

Self-motivated problem solver who finds pragmatic solutions to highly technical challenges

Excellent verbal and written communication and presentation skills.

Ability and desire to travel, including internationally.

Preferred Qualifications and Education:

Ph.D. degree in one of the above disciplines.

Experience in medical device development especially in system engineering and/or risk management

Working knowledge of cardiac electrophysiology.

Working knowledge of Human Factors/Usability Engineering regulatory standards.

APPLY NOW :

Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.

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 and @AbbottGlobal

The base pay for this position is $172,000.00 – $344,000.00. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Director
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Milpitas, California, United States
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 273 comparable Director Manufacturing & CMC roles across 47 biopharma companies.

273Comparable roles tracked
265Currently active
47Companies hiring similar roles
20Countries represented

Salary context

138 of 273 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
Highest disclosed · Senior Director, Manufacturing Strategy · AbbVie $206,500/yr – $393,000/yr
Peer group range $81,400 – $299,750 (median $194,800)

Where these roles are based

Top locations among the 273 comparable roles

United States206
Netherlands11
India10
Ireland7
Germany6
China5

+ 14 more countries

Seniority mix

273 of 273 peers have a known seniority level

Principal127
Director98
Senior Director48

Therapeutic area mix

5 of 273 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease3
Oncology1
Respiratory1

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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.

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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.