Senior Manufacturing Engineer - Lead Medical Device Automation

Penumbra, Inc.; Roseville (CA); On-site; USD 113,000 - 157,000; Full time

Benefits offered by this job

Healthcare benefits

401(k) with employer match

Paid holidays and vacation

Job summary

Penumbra, Inc. seeks a Senior Manufacturing Engineer to lead design and development of new products and changes to existing processes. You will oversee manufacturing support, troubleshoot equipment, and drive automation and improvements in a regulated medical-device environment.

You will create production drawings, lead multidisciplinary projects, and ensure QMS compliance. On-site work in California with travel up to 10% may be required; a strong background in GMP and clean-room practices is

Qualifications

• Bachelor’s degree in engineering or related technical field with 4+ years of engineering experience
• Master’s degree preferred
• Detailed knowledge of GMP/Quality System Regulations and clean room environment practices
• Demonstrated knowledge of engineering and scientific principles
• High proficiency with computers and software applications

Responsibilities

• Create drawings for Production and Research and Development
• Manage projects as a Project Leader within a multidisciplinary project team
• Provide technical support within multidisciplinary project team
• Document manufacturing and production development process through lab notebooks, engineering protocols, and reports
• Identify and utilize vendors in the development of processes
• Train engineers, technicians and assemblers in new processes and methods
• Adhere to the Company’s Quality Management System (QMS) and regulations

Skills

GMP knowledge

Engineering principles

Computer proficiency

Medical device experience

Education

Bachelor's degree in engineering

Master's degree preferred

Job description

Penumbra, Inc. seeks a Senior Manufacturing Engineer to lead design and development of new products and changes to existing processes. You will oversee manufacturing support, troubleshoot equipment, and drive automation and improvements in a regulated medical-device environment.

You will create production drawings, lead multidisciplinary projects, and ensure QMS compliance. On-site work in California with travel up to 10% may be required; a strong background in GMP and clean-room practices is