Position: Senior Designer Design Verification & Validation
Location: California
Duration: Long Term
Job Overview
We are seeking an experienced Senior Designer Design Verification & Validation to support design verification, equipment qualification, documentation, and manufacturing process improvement activities in a medical device manufacturing environment. The ideal candidate will have experience with SolidWorks, Windchill, validation documentation, and cross-functional project support.
Key Responsibilities
- Support equipment qualification activities including IQ, OQ, and TMV.
- Create, update, and execute validation and test protocols.
- Develop and revise engineering drawings using SolidWorks.
- Manage document creation, updates, and release through Windchill.
- Support equipment software validation and prepare validation requirements.
- Create and maintain PFMEA, process instructions, and technical documentation.
- Perform GD&T drawing reviews and support design verification activities.
- Develop DOE (Design of Experiments) for process characterization.
- Create and release project deliverables, design specifications, and material specifications.
- Support manufacturing activities, supplier transfers, equipment repairs, and continuous process improvements.
Required Qualifications
- 5 8 years of experience in design verification, validation, or medical device product development.
- Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or a related discipline.
- Strong experience with SolidWorks and Windchill PLM.
- Hands-on experience with IQ/OQ/TMV, design verification, and validation documentation.
- Knowledge of GD&T, PFMEA, and DOE methodologies.
- Experience supporting manufacturing, engineering change documentation, and cross-functional projects.
- Strong technical documentation, problem-solving, and project management skills.
- Experience in a regulated medical device manufacturing environment is preferred.