Medical Device Platform Lead - Ocular Port Delivery Device Platform
Genentech
South San Francisco, CA, US
Base: $169,100 to $314,000; bonus/equity: discreti...
Medical device platform leadership
Combination product development
Device lifecycle strategy
The Ocular Port Delivery Platform Lead sets the strategy for the device platform within Roche’s device portfolio responsible for developing, adapting, and maintaining a global device and packaging lifecycle strategy with a 5-10 year planning horizon
Job Summary
The Ocular Port Delivery Platform Lead sets the strategy for the device platform within Roche’s device portfolio responsible for developing, adapting, and maintaining a global device and packaging lifecycle strategy with a 5-10 year planning horizon.
You are responsible for guiding the design and standardization of the Ocular Port Delivery Device platform core technology across all of Roche's drug products, creating a single, integrated pathway from development to commercial manufacturing.
The expected salary range for this position based on the primary location of South San Francisco, California is $169,100 to $314,000, with a discretionary annual bonus and benefits.
Matching Summary
The Ocular Port Delivery Platform Lead sets the strategy for the device platform within Roche’s device portfolio responsible for developing, adapting, and maintaining a global device and packaging lifecycle strategy with a 5-10 year planning horizon.
Salary
Base: $169,100 to $314,000; Bonus/Equity: Discretionary annual bonus; Benefits: Detailed benefits available
Skills & Requirements
Must-have
Medical device platform leadership
Combination product development
Device lifecycle strategy
Design controls expertise
Device manufacturing processes
Technical team management
Nice-to-have
Ophthalmology device experience
Preclinical and clinical device development
Supplier and external partner management
Matrix leadership skills
Pharma/Medtech industry knowledge
Key Requirements
B.S./M.S/Ph.D. in science or engineering
10+ years total work experience
8+ years relevant medical device experience
Experience with Design Controls
Knowledge of GMP quality and regulatory dependencies
Experience in medical device or combination product commercialization