Senior Designer – Design Verification & Validation

Stark Pharma Solutions Inc

  • Irvine, CA
  • 8 days ago

    Highlights

    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.

    Numbers & Facts

    LocationIrvine, CA

    Description

    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.

    Similar Jobs

    See more jobs