Sr Process Improvement Engineer

Join VitalPath as a Sr Process Improvement Engineer! About VitalPath VitalPath is a trusted partner in the catheter design and manufacturing of custom medical devices that save lives and restore patient health and vital function.

We’re excited about this important work and bring vital energy to our customer partnerships. In our growing organization it’s important that we continue to offer a small-company, family-oriented environment with competitive pay and benefits.

If you want to make a difference in people’s lives and be a part of a friendly, fun place to work with people that value diversity, come join our team! About the Position The Sr.

Process Improvement Engineer / Lean Expert will be responsible for CI Programs across all facilities, implementing a Lean culture with emphasis for basic Lean principles and tools and develop a culture of Continuous improvement within the organization.

Perform work in adherence to the VitalPath Quality Management System (QMS), and Policies and Procedures in place. Also, lead or participate in special projects across the organization as assigned.

Responsibilities Manage CI program across the organization i n order to reduce the cost and improve yields in the production area.

Develop a priority list of CI projects based on savings, timelines and resources needed and execute Lean events. Management of Special projects needed across the organization, projects related to Operations, QA and RD as required Provide basic Lean training to different teams participating in Lean events.

Work in a cross-functional environment partnering with RD, Operations and Quality departments in order to deliver the CI projects.

Help to develop and order tooling and fixtures to improve the manufacturing processes and ease the operator’s job in the assembly area.

Working knowledge of manufacturing processes related to catheter manufacturing. Actively participate as a Coach in all Lean manufacturing events and initiatives taking place on manufacturing floor.

Support all VitalPath initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

Able to drive and work between all facilities. As this position is predicted to grow there is a possibility that direct reports will be added and / or a specific department will be created.

Other duties as assigned. Requirements Bachelor’s Degree in plastics, chemical, biomedical or mechanical engineering 3-5 years of experience implementing Lean Principles Understanding of Lean principles and basic Lean Tools, Green or Black belt certification preferred 1 to 3 years in a catheter manufacturing environment, with exposure to manufacturing or development A working knowledge of catheter assembly manufacturing processes Demonstrated excellent written and oral communication skills Experience with design controls, FDA regulation, GMP practices, and QSR requirements Willingness to travel to different VitalPath manufacturing sites as required Benefits Comprehensive, Low Cost Health and Dental Insurance Plans Available Vision Insurance Health Savings Account with company contribution Short and Long Term Disability Supplemental insurances (short term disability, AD&D, life insurance, and more) Paid Time Off Sick Time Off Paid Holidays 401K with company match Competitive compensation Opportunities for career growth and advancement VitalPath is an Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, work related mental or physical disability, veteran status, sexual orientation, gender identity, or genetic information.

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