Validation Engineer
Job in
Phoenix, Maricopa County, Arizona, 85003, USA
Listed on 2026-06-26
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
- 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
- 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
- Hybrid in Greater Phoenix; 3 days onsite
- 6+ month contract
- Start ASAP
- Benefits included (Medical, Dental, Vision, 401k options)
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