Hybrid Senior Quality Engineer — Medical Device CSV Lead

Tempus AI; Aliso Viejo (CA); Hybrid; USD 90,000 - 150,000; Full time

Benefits offered by this job

Incentive compensation

Restricted stock units

Medical benefits

Job summary

Tempus AI is seeking a Senior Quality Engineer to lead verification, validation, and maintenance of host systems for Tempus Medical Device software. You will drive CSV strategies, risk assessments, and design controls in line with FDA QSR, ISO 13485, and GAMP5.

You will mentor teams, author validation deliverables, and collaborate across disciplines to ensure regulatory compliance and continuous improvement. This hybrid role requires three days in the office in CA or Chicago.

Qualifications

• BA/B.S. or higher preferred in Computer Science, Software Engineering, Informatics, Biomedical, or relevant engineering disciplines.
• 5+ years experience in FDA regulated domain (e.g. medical device, pharma, biotech)
• 3+ years experience in Computer System Validation (CSV).
• Experience with industry standards and best practices for Medical device software and CSV such as Design Controls, GAMP 5, FDA 21 CFR Part 11, FDA (QSR) FDA 21 CFR 820.30, Medical device software (QMS) ISO 13485:2016, FDA 21 CFR 820, and Software life cycle processes (IEC 62304:2006).
• Knowledge of quality system principles, practices, and standards for the life science industry.
• Ability to deliver quality outputs without directions or under minimal supervision.

Responsibilities

• Lead verification, validation and maintenance of host systems supporting Tempus Medical Device(s).
• Lead risk assessments to determine testing strategies.
• Be involved in the medical device software design controls activities, in accordance with the FDA Quality System Regulation, ISO 13485, GAMP5, Computer System Validation (CSV) standards and FDA guidance, other applicable regulatory requirements, as well as best practices in the software industry.
• Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and computer systems against user, functional and regulatory requirements.
• Support regulatory compliance of the host system operating with Tempus Medical Device(s).
• Develop and maintain CSV policies, procedures, templates and work instructions.
• Lead risk-based approach to host / computer system validation (HSV/CSV), SDLC and design controls activities.
• Perform validation, re-validation and change controls of various AI, SaaS, and Tempus in-house developed software.
• Author and review software validation deliverables, including Risk Assessments, Validation Plans, Requirements (URS), Validation Protocols (IQ, OQ, PQ), UAT (User Acceptance Test), and Validation Reports.
• Collaborate with cross-functional teams in developing test-driven system/functional requirements, defining testing strategies and participating in test execution.
• Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance and continuous improvement.
• Provide support to Quality and IT organizations in maintaining compliance to various policies, procedures and activities, including support during internal/external inspections and regulatory and customer audits.
• Provide CSV guidance, coaching, mentorship, and training to test engineers within the team.

Skills

FDA regulations

CSV validation

Quality systems

Regulatory compliance

Leadership

Education

Bachelor's degree in Computer Science/Engineering/biomedical

Tools

Design Controls

GAMP 5

Job description

Tempus AI is seeking a Senior Quality Engineer to lead verification, validation, and maintenance of host systems for Tempus Medical Device software. You will drive CSV strategies, risk assessments, and design controls in line with FDA QSR, ISO 13485, and GAMP5.

You will mentor teams, author validation deliverables, and collaborate across disciplines to ensure regulatory compliance and continuous improvement. This hybrid role requires three days in the office in CA or Chicago.