P
Not Specified Permanent

Alameda, California · USA job

Sr. Industrial Engineer

Penumbra

Alameda, California

Job description

Overview

In this role you help Penumbra optimize production and improve efficiency in a regulated medical-device environment. You will lead cross-functional continuous improvement initiatives and apply lean principles to reduce waste and space, while enhancing productivity and quality. You work closely with Manufacturing, Quality, and R&D to plan, analyze, and implement improvements. This is a hands-on position on-site in Alameda, offering impact through scalable processes and a safety-conscious, QMS-driven culture.

Compensation / Benefits
  • medical, dental, vision
  • life and AD&D
  • short and long-term disability
  • 401(k) with employer match
  • paid parental leave
  • eleven paid holidays per year
Responsibilities
  • Identify opportunities and lead CI projects to optimize costs, manpower, equipment, space and investments
  • Guide the team on lean concepts: flow, standard work, labor analysis, layouts, mistake-proofing, visual controls, and performance metrics
  • Lead productivity gains, reduce lead times, and maximize space through Lean implementation
  • Review schedules, specs, processes, and work instructions to understand manufacturing methods
  • Drive Time Study and Value/Non-Value-Added analyses to improve workflow and space utilization
  • Analyze base operations, quantify improvements, and develop prioritized action plans
  • Collaborate with manufacturing, quality, and R&D to identify improvement opportunities and workspace enhancements
  • Develop detailed cross-functional work plans and strategies for projects
  • Ensure facility efficiency and safety; adhere to QMS and regulatory requirements
  • Promote compliance with security, privacy and applicable regulations across the department
Key requirements
  • Bachelor's degree in Industrial, Manufacturing, or Mechanical Engineering with 4+ years in the medical device or related industry
  • 4+ years of Continuous Improvement experience in a medical device context (preferred)
  • Knowledge of manufacturing processes and clean room practices
  • Ability to design, analyze, and implement industrial engineering techniques
  • Strong analytical, problem-solving, and communication skills; leadership capability desired
  • Proficiency with MS Office (Word, Excel, Visio, PowerPoint, MS Project), AutoCAD, and SAP
  • Excellent interpersonal and organizational skills with ability to multitask
  • Willingness to work on-site and travel 0-5% as needed
  • Awareness of QMS, quality standards, and regulatory compliance
  • strong communication and presentation skills
  • leadership and collaboration across functions
  • creativity and critical thinking
  • Lean manufacturing
  • Time study analysis
  • Value stream mapping

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