Industrial Engineer II

Specific Duties and 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.

Position Qualifications Required

• Bachelor's degree required in Industrial, Manufacturing, or Mechanical Engineering or a related discipline, with 2+ years of experience in the medical device or related industry, or an equivalent combination of education and experience
• Creativity, critical thinking, problem solving, and analytical skills 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

Position Qualifications Desired

• Medical device, pharmaceutical, biotech, or other regulated industry experience desired
• 2+ years of experience in a medical device industry role desired

Working Conditions

• 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.
• Must be able to read, prepare emails, and produce documents and spreadsheets.
• Must be able to move within the office and access file cabinets or supplies, as needed.
• Must be able to communicate and exchange accurate information with employees at all levels on a daily basis.