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Penumbra Inc

Neurovascular and peripheral medical devices manufacturer

Manufacturing Engineer 3 - Electronics

Manufacturing EngineeringUpdated on Nov 11
Full-timeAlameda, CA, USA

About the Job

Requirements

  • A bachelor's degree in Electrical, Biomedical, Mechanical, Chemical, Materials, or Industrial Engineering, or a related degree, with at least 4 years of relevant engineering experience; an equivalent combination of education and experience is also accepted.
  • Engineering experience in a manufacturing environment is recommended, and medical device industry experience is preferred.
  • Proficiency in Word, Excel, PowerPoint, Access, and other computer applications is required.
  • Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing processes is desired.
  • Ability to work on site and travel for business 0%–10%.
  • Ability to lift and move up to 25 pounds, move between buildings and floors, remain stationary and use standard office equipment for extended periods, and read and prepare emails, documents, and spreadsheets.

Responsibilities

  • Support capital equipment manufactured through contract manufacturers, including working directly with suppliers on manufacturing, quality, and technical issues.
  • Navigate and execute within a quality management system environment, including nonconformances, corrective and preventive actions, deviations, change controls, supplier corrective actions, and design and manufacturing documentation.
  • Design, execute, and document test plans for qualification of printed circuit board assembly components.
  • Evaluate and qualify alternate electronic components for printed circuit board assemblies by comparing electrical, mechanical, functional, reliability, and lifecycle specifications against existing components to ensure form, fit, function, and performance equivalency.
  • Execute detailed root cause analyses and recommend vetted solutions.
  • Communicate and explain problems and solutions cross-functionally and interdepartmentally.
  • Collaborate with suppliers, communicate updates promptly, and request necessary changes respectfully.
  • Manage nonconformances, deviations, engineering change orders, and supplier documentation using a quality management system to support continuous improvement and compliance.
  • Troubleshoot electromechanical products using failure analysis and problem-solving techniques, and recommend and implement effective solutions.
  • Lead supplier-level project implementation, manage communications related to test plans, monitor timelines, and ensure milestones are met.
  • Support production; create and maintain product and process documentation; monitor process and equipment performance; and identify and implement improvements to optimize yield, efficiency, or throughput.
  • Apply an understanding of quality, operational, and financial systems, company products, customer requirements, business objectives, and cross-functional impacts to projects and products.
  • Test processes, equipment, raw materials, and products; perform process validations; author test protocols; write reports; and draw conclusions or make recommendations based on test results.
  • Plan, schedule, conduct, and coordinate detailed phases of engineering work as part of a project or as a total project.
  • Develop, characterize, and optimize processes using statistical techniques and engineering knowledge and experience.
  • Coordinate with suppliers and other external resources needed to develop and implement process improvement plans.
  • Participate in project planning and scheduling.
  • Train assemblers, quality control staff, and technicians, as necessary, on processes, equipment, and documentation.
  • Adhere to the company's quality management system and applicable domestic and global quality system regulations, standards, and procedures.
  • Understand and adhere to applicable security, privacy, and compliance principles, regulations, standards, and procedures.
  • Ensure other department members follow the quality management system, regulations, standards, and procedures.
  • Perform other work-related duties as assigned.

Desired Qualifications

  • Engineering experience in a manufacturing environment is recommended.
  • Medical device industry experience is preferred.
  • Leadership skills are desired.
  • Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing processes is desired.

About the Company

Penumbra Inc

Neurovascular and peripheral medical devices manufacturer

Penumbra Inc. designs, develops, and sells medical devices for neurovascular and peripheral vascular conditions. Its products are used by doctors in hospitals and clinics and work by being inserted into blood vessels to remove clots, support catheter-based procedures, or help reconstruct vessels. The company differentiates itself with a broad, integrated portfolio across neurovascular and peripheral interventions and a global sales network that serves Europe and the Americas. Its goal is to improve patient outcomes through high-quality tools and ongoing research and development to expand capabilities.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Alameda, CA
Founded
2004

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