Validation Engineer

Design Group

3 years project experience in validation
Fat sat iq oq documentation development
Experience with fda compliance protocols
You will join a committed team of over 1500 professionals within the Regulatory Compliance Practice to deliver high-quality solutions

Job Summary

  • You will join a committed team of over 1500 professionals within the Regulatory Compliance Practice to deliver high-quality solutions.
  • The role involves developing and executing validation documents for pharmaceutical equipment including FAT, SAT, IQ, and OQ protocols.
  • Candidates must possess at least 3 years of project experience in validation within pharmaceutical or medical device environments.

Matching Summary

You will join a committed team of over 1500 professionals within the Regulatory Compliance Practice to deliver high-quality solutions.

Skills & Requirements

Must-have

  • 3 years project experience in validation
  • FAT SAT IQ OQ documentation development
  • Experience with FDA compliance protocols
  • Knowledge of CFR 21 Part 211 and 820
  • B.S. in Bioengineering or related technical degree

Nice-to-have

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

Key Requirements

  • Minimum 3 years project experience with validation
  • Minimum 3 years experience in pharmaceutical or medical device environments
  • B.S. in Bioengineering Biomedical Engineering Chemical Engineering or related field

Work Rights

Not specified

Tailored Resume

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