$117,895 – $152,570
Listed on Gilead Sciences’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role supports the commercial lifecycle of combination drug-device products, handling design transfer, regulatory compliance, and post-launch engineering activities. It suits engineers with medical device manufacturing experience who want to work on established products rather than early-stage development.
Our summary, not Gilead Sciences’s wording. The full posting is on their site.
Skills this role names
- Change Management
- Design of Experiments (DOE)
- ISO 13485
- Onshape
- Risk Management
- Root Cause Analysis
- SolidWorks
- Statistical Analysis
Log in to see which of these are already on your profile.
What they ask for
Required
- 5+ years relevant experience with BS/BA, or 3+ years with MS
- Medical device development and manufacturing per ISO 13485
- Risk management per ISO 14971
Nice to have
- Root cause analysis, deviation management, and investigations
- Lifecycle change control for combination products
- Complaint management experience
- Vendor and contract manufacturer collaboration
- Process characterization study design and execution
- Design transfer to manufacturing sites
- Knowledge of mechanical assembly for injection/delivery systems
- CAD experience with Solidworks, Onshape, or Fusion 360
- ICH Q7, Q8, Q9, Q10 familiarity
- Project management methods and tools
- Basic statistical methods including design of experiments and statistical tolerancing