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Sr. Manufacturing Engineer - Metals

Employment contract On-site work

Publication date: 30/08/2026

The Sr. Manufacturing Engineer provides leadership in the engineering, design and development of new products or changes to existing products, processes, and equipment. Interfaces with and furnishes scientific knowledge to multi-disciplinary teams overseeing development of neurovascular devices. Provide engineering support on existing devices for manufacturing. Develop, configure, and troubleshoot processing and test equipment. Research, identify and evaluate automated processing equipment. Specify fixtures/tooling for automated equipment support.

Responsibilities

Provides leadership in the engineering, design and development of new products or changes to existing products, processes, and equipment; Develop new processes for medical devices and components; Create drawings for Production and Research and Development; Manage projects as a Project Leader within a multidisciplinary project team; Provide technical support and perform tasks within multidisciplinary project team; Document manufacturing and production development process through lab notebooks, engineering protocols, and engineering reports; Identify and utilize vendors in the development of processes for Penumbra, Inc. products; Perform research and integrate new technologies into existing and future products and processes; Train engineers, technicians and assemblers in new processes and methods; Evaluate and troubleshoot problems to assess root cause and corrective action; Interpret and communicate test results; Document findings and recommendations; Create and modify product design specifications; Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures.

Requirements

Bachelor’s degree in engineering or related technical field with 4+ years of engineering level experience, preferably in the medical device industry, or an equivalent combination of education and experience; 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; Willingness and ability to work on site; Business travel from 0% - 10%; Ability to lift and move up to 25 pounds

Nice to have

Master’s degree

Benefits

Collaborative teamwork environment where learning is constant and performance is rewarded; Opportunity to be part of the team revolutionizing the treatment of some of the world's most devastating diseases; Medical, dental, vision, life, AD&D, short and long-term disability insurance; 401(k) with employer match; Paid parental leave; Eleven paid company holidays per year; Minimum of fifteen days of accrued vacation per year, which increases with tenure; Paid sick time
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