eTeam
Overview
Pharmaceutical Talent Acquisition SME | eTeam Description:
Location: Sunnyvale, CA 94043 • Duration: 12 Months Responsibilities
As part of the Intuitive Human Factors team, the Sr. Human Factors Design Controls Engineer works closely with HF team members, department leadership, clinical engineers, interaction designers, system and software engineers, product managers, project management, technical publications, regulatory and quality. Responsible for informing, guiding development of, and maintaining usability engineering documentation produced during projects within Design Controls. Implement summaries of known use problems reports, task analyses, risk analyses, design inputs, and usability validation test cases. Support the Human Factors Engineering team with expertise in design controls and content creation in tools such as Polarion and Agile, contributing to usability engineering documentation required for submission to global medical device reg. Provide dedicated support and subject matter expertise to the broader human factors engineering team serving all business units and report to a Sr. Human Factors Manager. Business unit descriptions follow. Digital Business Unit: Focus on User Experience with software and web-based products integrated with Intuitive products. ION System Business Unit: Supports development of products for systems, software and instruments with specialized users in pulmonary/endoluminal treatment modalities. Da Vinci Multiport RAS Business Unit: Supports a wide array of products and services focusing on user interface, workflow and safety. Da Vinci Single Port RAS Business Unit: Supports new and sustaining product development on a growing RAS platform. Roles and Responsibilities (continued)
Min 5 Years of experience. Qualifications
Skills:
Risk analysis, usability engineering, design control process, tools - Polarion/Agile/Python/Smartsheets Minimum Education: BS in Human Factors Engineering, Biomedical Science or Engineering, Systems Engineering, Quality Engineering, Information and Data Science, Cognitive Psychology, Computer Science with HCI, Human Centered Design, or related field. Minimum of 8 years of related experience with a bachelor’s degree (in engineering, design controls, medical device product development or related field). Excellent verbal communication and presentation skills in a highly structured environment using multiple channels. Experience with Digital project collaboration tools (e.g., Polarion, Agile, Python, Smartsheets). Ability to collaborate across groups and levels of management to solve complex usability issues involving risk analysis. Ability to travel internationally and domestically up to 15% onsite if remote. Medical device background or regulated industry background is required and mandatory. Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under applicable laws. We will consider qualified applicants with arrest and conviction records in accordance with fair chance laws. Senior/Employment Details
Seniority level: Mid-Senior level Employment type: Contract Job function: Human Resources, Engineering, and Design Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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Pharmaceutical Talent Acquisition SME | eTeam Description:
Location: Sunnyvale, CA 94043 • Duration: 12 Months Responsibilities
As part of the Intuitive Human Factors team, the Sr. Human Factors Design Controls Engineer works closely with HF team members, department leadership, clinical engineers, interaction designers, system and software engineers, product managers, project management, technical publications, regulatory and quality. Responsible for informing, guiding development of, and maintaining usability engineering documentation produced during projects within Design Controls. Implement summaries of known use problems reports, task analyses, risk analyses, design inputs, and usability validation test cases. Support the Human Factors Engineering team with expertise in design controls and content creation in tools such as Polarion and Agile, contributing to usability engineering documentation required for submission to global medical device reg. Provide dedicated support and subject matter expertise to the broader human factors engineering team serving all business units and report to a Sr. Human Factors Manager. Business unit descriptions follow. Digital Business Unit: Focus on User Experience with software and web-based products integrated with Intuitive products. ION System Business Unit: Supports development of products for systems, software and instruments with specialized users in pulmonary/endoluminal treatment modalities. Da Vinci Multiport RAS Business Unit: Supports a wide array of products and services focusing on user interface, workflow and safety. Da Vinci Single Port RAS Business Unit: Supports new and sustaining product development on a growing RAS platform. Roles and Responsibilities (continued)
Min 5 Years of experience. Qualifications
Skills:
Risk analysis, usability engineering, design control process, tools - Polarion/Agile/Python/Smartsheets Minimum Education: BS in Human Factors Engineering, Biomedical Science or Engineering, Systems Engineering, Quality Engineering, Information and Data Science, Cognitive Psychology, Computer Science with HCI, Human Centered Design, or related field. Minimum of 8 years of related experience with a bachelor’s degree (in engineering, design controls, medical device product development or related field). Excellent verbal communication and presentation skills in a highly structured environment using multiple channels. Experience with Digital project collaboration tools (e.g., Polarion, Agile, Python, Smartsheets). Ability to collaborate across groups and levels of management to solve complex usability issues involving risk analysis. Ability to travel internationally and domestically up to 15% onsite if remote. Medical device background or regulated industry background is required and mandatory. Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under applicable laws. We will consider qualified applicants with arrest and conviction records in accordance with fair chance laws. Senior/Employment Details
Seniority level: Mid-Senior level Employment type: Contract Job function: Human Resources, Engineering, and Design Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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