Senior Human Factors Engineer

Posted 9 Hours Ago
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South San Francisco, CA, USA
In-Office
91K-169K Annually
Senior level
Healthtech • Biotech
The Role
Lead human factors activities for combination products and drug delivery devices: plan and run ethnographic and usability studies, perform use-related risk analysis (uFMEA), author protocols and reports, develop IFUs and training materials, translate user needs into engineering requirements, and analyze qualitative/quantitative data to drive user-centered design.
Summary Generated by Built In

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche!

The Opportunity

In this role, you will provide critical human factors engineering support to cross-functional project teams developing cutting-edge combination products and drug delivery devices for parenteral pharmaceutical therapeutics. You will play a pivotal role in ensuring our innovative products are safe, intuitive, and highly effective by fully accounting for the user, the environment, and the specific drug therapy.

Key Responsibilities:

  • Lead project-level human factors activities throughout the product lifecycle, including ethnographic research, requirements definition, and use-related risk analysis ($uFMEA$).

  • Design, execute, and author protocols and summary reports for formative usability assessments and human factors design validation (summative) studies.

  • Collaborate seamlessly with cross-functional teams spanning device engineering, regulatory affairs, clinical operations, quality assurance, and marketing to shape user-centric product designs.

  • Develop and refine comprehensive instructions for use (IFUs) and quick-reference training materials for clinical trials and commercial distribution.

  • Translate complex, multi-faceted user needs into actionable engineering requirements, delivering thorough and practical solutions to complex design challenges.

  • Analyze qualitative and quantitative usability study data using statistical methods to drive evidence-based design iterations.

Who You Are

You are a highly analytical, detail-oriented, and deeply empathetic professional who puts patients and users at the center of engineering. You thrive in collaborative environments where distinct perspectives are valued, and you possess a strong desire to solve complex healthcare challenges through robust scientific and human-centered design principles.

Qualifications & Experience:

  • Education: A Bachelor's, Master's, or advanced degree in Human Factors Engineering, Cognitive Psychology, Industrial Engineering, Bioengineering, or a related scientific/engineering discipline.

  • Experience: A minimum of 5 years of experience in the bio-pharma industry and/or academia (including advanced studies) after receiving a Bachelor’s degree.

  • Technical Expertise: Demonstrated proficiency in applying human factors standards and regulatory guidances (e.g., FDA Human Factors Guidances, IEC 62366, ANSI/AAMI HE75).

  • Documentation Skills: Proven experience authoring highly technical documents, including usability study protocols, data analysis frameworks, and human factors engineering reports.

  • Collaboration: A track record of collaborating effectively within diverse, multidisciplinary project environments and partnering successfully with external vendors.

Let’s thrive together in a culture built on trust, collaboration, respect, and high performance.

Relocation benefits are available for this job posting.

The expected salary range for this position based on the primary location of South San Francisco, CA is $90,700 - $168,500.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Skills Required

  • Bachelor's, Master's, or advanced degree in Human Factors Engineering, Cognitive Psychology, Industrial Engineering, Bioengineering, or related discipline
  • Minimum of 5 years of human factors experience in the bio-pharma industry and/or academia after receiving a Bachelor's degree
  • Proficiency applying human factors standards and regulatory guidance (FDA Human Factors guidance, IEC 62366, ANSI/AAMI HE75)
  • Experience designing, executing, and authoring formative usability assessments and summative human factors validation studies and protocols
  • Experience performing use-related risk analysis (uFMEA) for medical devices and combination products
  • Proven experience authoring technical human factors documentation, reports, and data analysis frameworks
  • Ability to analyze qualitative and quantitative usability study data using statistical methods
  • Track record of collaborating within multidisciplinary teams and partnering with external vendors
  • Experience developing comprehensive Instructions for Use (IFUs) and training materials for clinical trials and commercial distribution

Genentech Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Genentech and has not been reviewed or approved by Genentech.

  • Healthcare Strength Health coverage is described as comprehensive across medical, dental, vision, mental health, and prescriptions, supported by HSAs/FSAs and broad wellness resources. On‑site fitness and health centers, mental‑health clinicians, and specialized programs like fully covered preventive cancer screenings and menopause support deepen the offering.
  • Retirement Support Retirement benefits feature a 401(k) with up to a 4% company match plus an additional annual 6% company contribution to eligible pay. Additional financial protections such as life and accident insurance complement salary, bonuses, and stock options.
  • Leave & Time Off Breadth Time away includes about 20 paid vacation days, paid holidays, personal days, and a year‑end shutdown. A paid six‑week sabbatical every six years notably expands long‑term time‑off flexibility.

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The Company
HQ: South San Francisco, CA
20,069 Employees
Year Founded: 1976

What We Do

Considered the founder of the industry, Genentech, now a member of the Roche Group, has been delivering on the promise of biotechnology for more than 40 years. Genentech is a biotechnology company dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal. Making a difference in the lives of millions starts when you make a change in yours.

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