Validation Engineer

Barry Wehmiller Design Group

Fat sat iq oq documentation development
Fda compliance protocols for pharmaceutical equipment
3 years project experience in validation
You will join the Regulatory Compliance Practice to deliver high-quality solutions to clients in the pharmaceutical industry

Job Summary

  • You will join the Regulatory Compliance Practice to deliver high-quality solutions to clients in the pharmaceutical industry.
  • The role involves developing and executing validation documents including FAT, SAT, IQ, and OQ for automated systems.
  • Candidates must possess a B.S. in a related engineering field and have at least three years of relevant project experience.

Matching Summary

You will join the Regulatory Compliance Practice to deliver high-quality solutions to clients in the pharmaceutical industry.

Skills & Requirements

Must-have

  • FAT SAT IQ OQ documentation development
  • FDA compliance protocols for pharmaceutical equipment
  • 3 years project experience in validation
  • Experience in pharmaceutical or medical device environments
  • B.S. in Bioengineering Biomedical Chemical Engineering

Nice-to-have

  • Strong technical writing and oral communications
  • Ability to interact with all levels of management
  • Willingness to travel for project installation
  • Experience authoring CAPAs deviations SOPs

Key Requirements

  • Minimum 3 years project experience with validation
  • Minimum 3 years in pharmaceutical or medical device environments
  • B.S. degree in Bioengineering Biomedical Chemical Engineering or related field
  • Strong computer skills including Microsoft Office Project and AutoCAD

Work Rights

Not specified

Tailored Resume

Cover Letter