Location
Irvine, California, United States
Posted
May 16, 2026
Job Description
Job Description:
The Validation Engineer will work under limited supervision to support product validation and engineering activities in a regulated medical device environment. The role focuses on leading Continuous Improvement (CIP) initiatives, supporting process validation, and ensuring compliance with applicable regulatory standards. The engineer will collaborate with internal teams and external suppliers to improve product performance, reduce costs, and ensure robust validation of systems and processes, including those related to product electrical design and functionality.
Responsibilities:
The Validation Engineer will work under limited supervision to support product validation and engineering activities in a regulated medical device environment. The role focuses on leading Continuous Improvement (CIP) initiatives, supporting process validation, and ensuring compliance with applicable regulatory standards. The engineer will collaborate with internal teams and external suppliers to improve product performance, reduce costs, and ensure robust validation of systems and processes, including those related to product electrical design and functionality.
Responsibilities:
- Lead Continuous Improvement (CIP) projects in collaboration with cross-functional internal teams and external suppliers.
- Perform CIP calculations, including supplier quotation evaluations and cost-benefit analysis.
- Develop and manage project budgets covering feasibility stud...