Industrial Engineer II

Roseville, CAfull timeOn Site

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mid

$90k–$120k

H1B: no

Penumbrainc Industrial Engineer II focused on eliminating waste and improving productivity, quality, and efficiency in manufacturing processes. The role involves Lean Manufacturing implementation and mentoring engineers.

Responsibilities

Review production schedules, engineering specifications, process flows, work instructions, and other information to understand methods and activities in manufacturing and services.
Drive efforts to analyze systems and determine how to manufacture parts or products with maximum efficiency and quality, with minimal supervision.
Work with manufacturing, quality, and R&D engineers to identify equipment and process improvement opportunities, and improvements in layout of workspaces.
Drive Time Study Analysis and identification of Value / Non-Value-added activities during these studies and subsequent presentation of findings, planning, and implementation of improvement plans.
Develop Systems, Processes and Procedures that enable the Industrial Engineering Group to function at a high level.
Develop, Support and be able to train Penumbra Employees on programs that support Lean Manufacturing Implementation.
Mentor and Train Industrial Engineers, help advance appropriate skill sets and understanding of Lean Manufacturing Concepts and Techniques.
Ensures facility efficiency and workplace safety, maintaining a safe and compliant work environment.
Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures.
Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company.
Ensure other members of the department follow the QMS, regulations, standards, and procedures.
Perform other work-related duties as assigned.

Qualification

Excellent oralMedical deviceWillingness and ability to work on site

Required

Excellent oral, written, and interpersonal communication skills with the ability to present findings and recommendations to diverse audiences
High degree of accuracy and attention to detail
Proficiency with standard office tools including Word, Excel, and PowerPoint
Excellent organizational skills with ability to prioritize assignments while handling various projects simultaneously
Medical device, pharmaceutical, biotech, or other regulated industry experience desired
2+ years of experience in a medical device industry role desired
General office and cleanroom environments
Willingness and ability to work on site. May have business travel from 0% - 10%
Potential exposure to blood-borne pathogens
Requires some lifting and moving of up to 25 pounds
Must be able to move between buildings and floors.
Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day.