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Validation Engineer

Job in Phoenix, Maricopa County, Arizona, 85003, USA
Listing for: GForce Life Sciences
Full Time position
Listed on 2026-06-26
Job specializations:
  • Engineering
    Validation Engineer, Quality Engineering, Medical Device Industry, Biomedical Engineer
Job Description & How to Apply Below

Consultant, Validation Engineer, Medical Devices Summary

Our client, a leader in medical device reprocessing, has engaged GForce Life Sciences to provide a Validation Engineer with strong technical writing experience to support a new manufacturing line being installed in Tempe. This role is open due to continued growth in the client’s business. This engineer will play a key role in supporting a manufacturing transfer and new production line launch, ensuring all equipment and processes are properly validated and documented in accordance with medical device regulatory standards.

Responsibilities
  • Lead validation activities for new manufacturing equipment and processes supporting the new production line
  • Support equipment installation and startup for the new manufacturing line
  • Develop and execute validation strategies including IQ/OQ/PQ
  • Perform product and process validations for reprocessed medical devices
  • Identify equipment requirements and ensure validation readiness for new manufacturing processes
  • Collaborate cross-functionally with engineering, quality, and manufacturing teams
  • Draft validation protocols, reports, and supporting documentation
  • Manage documentation through internal document management systems
  • Ensure validation documentation meets regulatory and quality requirements
  • Maintain clear, compliant documentation throughout the validation lifecycle
Requirements
  • 3+ years of Validation Engineering experience
  • Experience drafting validation protocols, reports, and managing technical documentation
  • Medical device industry experience required
  • Hands-on experience executing IQ/OQ/PQ validations
  • Strong understanding of validation lifecycle and regulatory documentation
  • Ability to work cross-functionally with engineering, manufacturing, and quality teams
Nice to Have
  • Experience using Val Genesis validation lifecycle management software
  • Prior experience with reprocessed medical devices or sustainability-focused healthcare technologies
  • Experience supporting manufacturing transfers or new line installations
Terms & Start
  • Hybrid in Greater Phoenix; 3 days onsite
  • 6+ month contract
  • Start ASAP
  • Benefits included (Medical, Dental, Vision, 401k options)
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