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Validation Engineering Tech

Description

We are seeking a Validation Engineering Tech to join our team! In this role, you will have the opportunity to assist Validation Engineers, Quality Engineers, and other teams in the completion of validation projects at various Phillips-Medisize sites. We are seeking a highly motivated individual with a strong ability to think outside the box, who is able bring forward ideas for continuous improvement and process facilitation and has strong project management skills.

 If you are looking for a great opportunity to join a dynamic team and grow your career, this is the right role for you! 

What You Will Do In Your Role

  • Lead low-complexity validation projects. Manage multiple projects and/or challenging projects.
  • Learn and deploy IQMS and SAP related tools and deliverables associated with validation deviations, customer approvals, and document approval workflows.
  • Suggest creative validation process improvement opportunities.
  • Provide qualification and validation support to sites and Validation Engineers.
  • Assist with creating, updating and training on WI, SOP, and other necessary documents needed to perform validation work.
  • Support global rollout of Global Validation requirements and on-site or desk audits of Phillips-Medisize sites to ensure compliance to the global standards.
  • Set up and manage SharePoint as a global point of contact containing validation best practices information and examples of executed validations. Develop content for the site as needed.
  • Occasional travel to other Phillips-Medisize and vendor sites.
  • Safety/Environmental: where applicable, individual is pre-planning safety into work activities to improve performance, proactively identifies safety concerns, complies with Environmental Management System Program SOP’s/WI, Policy & Program elements and encourages responsible use of resources

 

The Experience You Will Bring

  • The organizational skills to manage document workloads for multiple validation projects.
  • Learn and deploy document control related tools and deliverables associated with validation deviations, customer approvals, and document approval workflows.
  • Suggest creative validation process improvement opportunities.
  • Assist with creating, updating and training on WI, SOP, and other necessary documents needed to perform validation work.
  • Support global rollout of Global Validation requirements through engagement in engineering council initiatives.
  • Set up and manage SharePoint as a global point of contact containing validation best practices information and examples of executed validations. Develop content for the site as needed.
  • Safety/Environmental: where applicable, individual is pre-planning safety into work activities to improve performance, proactively identifies safety concerns, complies with Environmental Management System Program SOP’s/WI, Policy & Program elements and encourages responsible use of resources

 

Requirements:

  • Associate's Degree
  • Experience using Microsoft Office (Outlook, Word, Excel, PowerPoint)
  • Willing and able to travel to other Phillips-Medisize and vendor sites
  • This position is not eligible for visa sponsorship



What Will Put You Ahead:

  • Bachelor’s Degree
  • Medical manufacturing experience or working in a regulated manufacturing environment
  • Quality technician or engineering experience


Salary and Benefits Commensurate with Experience
Equal Opportunity Employer
Except where prohibited by state law, all offers of employment are conditioned upon successfully passing a drug test

This employer uses E-Verify. Please visit the following website for additional information: www.kochcareers.com/doc/Everify.pdf

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