Senior Designer – Design Verification & Validation

Stark Pharma Solutions Inc
  • Irvine, CA
  • Quick Apply
8 days ago

Job 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.

Numbers & Facts

LocationIrvine, CA

Skills

  • Biomedical Engineeringunmatched
  • Cross-Functionalunmatched
  • Design Verificationunmatched
  • Document Managementunmatched
  • Documentationunmatched
  • Educational Technologyunmatched
  • Engineering Drawingunmatched
  • Equipment Validationunmatched
  • Experiment Designunmatched
  • Geometric Dimensioning and Tolerancingunmatched
  • Manufacturingunmatched
  • Manufacturing Engineeringunmatched
  • Manufacturing Equipment Maintenanceunmatched
  • Manufacturing/Industrial Processesunmatched
  • Mechanical Engineeringunmatched
  • Medical Equipmentunmatched
  • Medical Productsunmatched
  • Problem Solving Skillsunmatched
  • Process Failure Mode and Effects Analysis (PFMEA)unmatched
  • Process Improvementunmatched
  • Process Validationunmatched
  • Product Developmentunmatched
  • Project Designunmatched
  • Project/Program Managementunmatched
  • Requirements Managementunmatched
  • Requirements Validation/Verificationunmatched
  • Software Administrationunmatched
  • Software Validationunmatched
  • SolidWorksunmatched
  • Technical Writingunmatched
  • United States Department of Energy (DOE)unmatched
  • Validation Documentationunmatched
  • Validation Planunmatched
  • Validation Testingunmatched
  • Windchill PLM Softwareunmatched

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