Manufacturing Process Engineer (2nd shift)

Resuscitation, ZOLLMED.com

At ZOLL, we're passionate about improving patient outcomes and helping save lives.

We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions.

The Resuscitation division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service.

At ZOLL, you won’t just have a job. You’ll have a career—and a purpose.

Join our team. It’s a great time to be a part of ZOLL!

Job Summary

Responsible for partnering with the manufacturing, engineering and quality teams in the design, implementation and validation of new processes to manufacture high quality medical devices and associated accessories. Utilizes a variety of tools to continuously improve existing manufacturing while acting as an innovator in the areas of Lean manufacturing processes. Works with in-house personnel to develop test recommendations to ensure that product requirements meet customer expectations and are testable. Works to standardize manufacturing processes and put appropriate controls in place to monitor status. Interacts with product development engineers and is responsible for leading product transfer involving process capability and operator training.

Essential Functions

• Optimize manufacturing processes to provide sustainable gains in gross margin and product performance through capital projects, statistical analysis, designed experiments, procedural changes, simulation and modeling
• Provide on-going technical support to production line for equipment, process, or design related issues
• Monitor process and equipment performance; identify and implement process improvement activities to increase/optimize yield, efficiency or throughput
• Maintain safety, product quality, and manufacturing effectiveness by examining equipment, processes, operations, product components and assembly to determine time or quality revisions and suggests/implements improvements
• Works with suppliers and participates in multi-functional teams to resolve technical/quality issues and develop new products
• Participate in new product design and development reviews; suggest ways to enhance DFM; develop process FMEAs; lead transfer of products from design to production; supports product scale-up activities
• Drive a Lean culture of continuous improvement; lead and participate in Kaizen events; promote 5s activity to standardize work; work with manufacturing manager to establish task time to maximize throughput, reduce cycle time, identify constraints and balance work content; create and update value stream maps
• Specify, evaluate, select, and implement new equipment and fixtures; develop and execute installation, operation, and performance qualification protocols
• Design and implement validation protocols for process improvements and material changes including comprehensive engineering reports providing analysis of results
• Develop efficient, effective systems for capturing critical process metrics for all manufacturing operations; implement automated data collection where possible
  
  

Required/Preferred Education And Experience

• BS in industrial engineering required or
• Other technical degree with equivalent experience required
• Minimum of 2-4-years’ experience in a commercial manufacturing environment driving continuous improvement with demonstrated experience in use of rotary/converting equipment and automation of manufacturing processes. required and
• Medical device manufacturing experience with exposure to FDA requirements required and
• Production of electromechanical assemblies required
  
  

Knowledge, Skills And Abilities

• Experienced in designing and performing process validations
• Works well in dynamic, cross-functional team environment
• Strong analytical skills and common sense with emphasis on a scientific method of problem solving
• Able to model and simulate manufacturing flows
• Able to accept and produce timely results on multiple concurrent projects of significant complexity
• Able to write clear, concise and visual work instructions
• Possess effective verbal and written communication and interpersonal skills to interact with associates at all levels of the organization
• Knowledge of design controls, FDA and MDD requirements; able to work within a medical device quality management system
• Strong project management skills sufficient to take a proposed solution from resource appropriation through project scheduling and execution as well as being able to work as part of a decision-making team to bring about positive change
• Has a fundamental drive for continuous process improvement.
  
  

ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.