Senior Clinical Engineer — Robotic Surgery Systems

Biopharma Careers; Cincinnati (OH); In loco; USD 120.000 - 160.000; Tempo pieno

Vantaggi offerti da questo lavoro

Travel up to 15%

Descrizione del lavoro

Johnson & Johnson in Cincinnati seeks a Senior Clinical Engineer to lead clinical input for the OTTAVA Robotic Surgical System. You will collaborate with physicians to define device performance, assess risks, and guide product development through FDA-aligned validation and pre-clinical activities.

The role requires a strong engineering background (Bachelor's plus 5+ years in medical devices), cross-functional leadership, and effective communication to ensure patient safety and regulatory

Competenze

• Bachelor's degree in engineering with 5+ years in medical device industry.
• Experience collaborating with physicians to gather clinical performance feedback.
• Experience designing and conducting pre-clinical engineering studies.

Mansioni

• Apply clinical, technical, and design control knowledge to collaborate with a cross-functional team to discover, define, develop, and validate a new product.
• Partner with physicians and clinical users to develop device performance and gather feedback.
• Develop bench models and metrics to evaluate prototype designs for clinical performance.
• Create and execute Design Validation plans, protocols, and testing as per FDA requirements.
• Support pre-clinical studies and initial product launch activities.

Conoscenze

Clinical knowledge

Cross-functional collaboration

Regulatory risk analyses

Design Validation

Data analysis

Programming (MATLAB)

Programming (Python)

Formazione

Bachelor's degree in Engineering

Advanced degree preferred (MS/PhD/MD)

Strumenti

MATLAB

Python

Descrizione del lavoro

Johnson & Johnson in Cincinnati seeks a Senior Clinical Engineer to lead clinical input for the OTTAVA Robotic Surgical System. You will collaborate with physicians to define device performance, assess risks, and guide product development through FDA-aligned validation and pre-clinical activities.

The role requires a strong engineering background (Bachelor's plus 5+ years in medical devices), cross-functional leadership, and effective communication to ensure patient safety and regulatory