Industrial Engineer II

Penumbra, Inc.; Roseville (CA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) with match

Parental leave

Equity program

Job summary

Penumbra, Inc. seeks an Industrial Engineer II to drive lean improvements in manufacturing, reduce waste, and boost productivity and quality through optimized use of people, machines, and space.

You will work with cross-functional teams, perform time studies, support lean programs, train staff, and ensure safety and compliance while advancing the IE group.

Qualifications

• Bachelor's degree in Industrial, Manufacturing, or Mechanical Engineering or related field.
• 2+ years of experience in medical device or related industry.
• Creativity, critical thinking, problem solving, and analytical skills.
• Excellent written and verbal communication; ability to present findings.

Responsibilities

• Review schedules, specs, and processes to understand methods used in manufacturing.
• Analyze systems to maximize efficiency and quality with minimal supervision.
• Identify opportunities with cross-functional teams for equipment and layout improvements.
• Conduct Time Study Analysis and present improvement plans to stakeholders.
• Develop processes and train staff on Lean Manufacturing concepts and tools.
• Ensure safety, quality, and regulatory compliance across the facility.

Skills

Lean Principles

Process Improvement

Analytical Thinking

Cross-functional Collaboration

Documentation

Education

BS in Industrial, Manufacturing, or Mechanical Eng

Tools

MS Office

Job description

The Industrial Engineer II is focused on eliminating wastefulness in production processes, and in developing ways to improve productivity, quality, and efficiency through the effective use of workers, machines, materials, and space information.

The Industrial Engineer II will leverage a strong understanding of Lean Programs and drive continuous improvements working with cross-functional teams.

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.

Annual Base Salary Range: $90,000 to $120,000

We offer a competitive compensation package plus a benefits and equity program, when applicable.

Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.

What We Offer

• A collaborative teamwork environment where learning is constant, and performance is rewarded.
• The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
• A generous benefits package for eligible employees that includes 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, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).

Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc.

Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, military or veteran status, or any other characteristic protected by federal, state, or local laws.

If you reside in the State of California, please also refer to Penumbra's Privacy Notice for California Residents.

For additional information on Penumbra's commitment to being an equal opportunity employer, please see Penumbra's AAP Policy Statement.