Senior Human Factors Engineer

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!

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.

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.