Senior Human Factors Engineer — Device Usability Leader

Amgen Inc.; Thousand Oaks (CA); In loco; USD 120.000 - 180.000; Tempo pieno

Vantaggi offerti da questo lavoro

Retirement & Savings Plan

Health, Dental & Vision

Stock-based incentives

Flexible work models

Award-winning time-off plans

Descrizione del lavoro

Amgen Inc. seeks a Senior Human Factors Engineer to lead HFE/UE planning, research, development, and continuous improvement of drug delivery devices. You will collaborate across functions to ensure safe and effective device interfaces and support regulatory submissions.

The role requires expertise in HF methodologies, risk analysis, and strong cross-functional communication. Up to 20% travel may be needed, with competitive benefits and a focus on patient safety.

Competenze

• Doctorate or Master’s with HF/UE experience in Biomedical/Pharmaceutical/Medical Device Field.
• Bachelor’s with HF/UE experience in Biomedical/Pharmaceutical/Medical Device Field.
• Associate’s with HF/UE experience in Biomedical/Pharmaceutical/Medical Device Field.
• High school diploma with 10 years of HF/UE experience.

Mansioni

• Lead and coordinate human factors studies from planning to reporting.
• Develop and maintain device user interfaces to minimize use errors.
• Support regulatory submissions with HF documentation and analyses.
• Collaborate with engineering, regulatory, quality, and clinical teams.
• Communicate findings and recommendations to internal and external partners.

Conoscenze

HFE planning

Usability studies

Cross-functional collaboration

Regulatory knowledge

Task analysis & URRA

Formazione

Doctorate degree

Master’s degree + 2 years HF/UE experience

Bachelor’s degree + 4 years HF/UE experience

Associate’s degree + 8 years HF/UE experience

High school diploma + 10 years HF/UE experience

Strumenti

FDA HF Guidance

Descrizione del lavoro

Amgen Inc. seeks a Senior Human Factors Engineer to lead HFE/UE planning, research, development, and continuous improvement of drug delivery devices. You will collaborate across functions to ensure safe and effective device interfaces and support regulatory submissions.

The role requires expertise in HF methodologies, risk analysis, and strong cross-functional communication. Up to 20% travel may be needed, with competitive benefits and a focus on patient safety.