Senior Validation Engineer

Chicago, IL

Posted: 06/20/2019 Industry: Healthcare Job Number: 2023 Pay Rate: $90K-$105K

Senior Validation Engineer, Northwest Chicagoland

Our client is a leading global provider of medical technologies. Not only is their business booming, but they have been recognized as a “Best Place to Work” in 2018! This is attributed to their winning products and innovation as well as their positive culture and strong leadership collaboration. If you are a Validation Engineer looking to advance your career to an exciting organization on the rise, this is the opportunity for you!

This role supports a team that is responsible for engineering & manufacturing. You will provide processing support for products, assemblies, Blow Fill Seal processes, packaging processes, and supporting utilities. In addition to performing engineering duties to set up engineering tests, studies, and validations, you will assist engineers with evaluations and recommend improvements to manufacturing procedures.

What you will do:

  • Evaluate the processes and equipment utilized to manufacture products
  • Provide technical expertise to the manufacturing floor in the areas of root cause analysis, troubleshooting, process problem solving, risk analysis, statistical analysis, and process improvements
  • Develops product specifications, process steps, diagrams, protocols, procedures, forms, Engineering Orders, drawings, and documents related to manufacturing processes
  • Prepare/collect data to ensure BOM accuracy
  • Provide sample documentation, review results, and issue specifications
  • Ensures products are produced to specifications; writes operating procedure changes to improve the production process as necessary

What you need:

  • GMP and related requirements for sterile blow, fill, seal operation and assembly of critical medical components and devices
  • Working knowledge of sterile processing equipment operation
  • Knowledgeable of FDA, USP, ISO, EU, OSHA, EPA regulations
  • Bachelor’s degree and/or Associate Degree in Engineering, Science, Quality Systems, and/or Industrial Manufacturing Technology.
  • Understanding of the principles and practices of processing equipment

Interested?

If you want to join a team that is passionate in making a difference in people’s lives while being part of an outstanding culture that focuses on core values, don’t hesitate and contact Andrew at andrew@worldbridgepartners / 847-550-1300 ext 42.

What you need:

  • GMP and related requirements for sterile blow, fill, seal operation and assembly of critical medical components and devices
  • Working knowledge of sterile processing equipment operation
  • Knowledgeable of FDA, USP, ISO, EU, OSHA, EPA regulations
  • Bachelor’s degree and/or Associate Degree in Engineering, Science, Quality Systems, and/or Industrial Manufacturing Technology.
  • Understanding of the principles and practices of processing equipment

Interested?

Lauren Kondic
Recruiting Specialist

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