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Validation Engineer and CQV
Medivant Healthcare
Phoenix, USA
Full-time
Mid · 2+ years experience
Onsite
USD 50000-60000 yearly / year
Discovered 1 weeks ago
Free
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The Validation Engineer and CQV Associate supports validation documentation, data collection, and quality system activities in Medivant’s sterile injectable facility. This entry-level role is ideal for recent graduates seeking hands-on cGMP and aseptic processing experience.
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About Medivant Healthcare
Medivant Healthcare is a U.S.-based pharmaceutical manufacturer specializing in sterile injectable generics for hospitals, clinics, and healthcare providers nationwide. Our FDA-registered facilities in Chandler and Deer Valley, Arizona, are dedicated to ensuring consistent product quality, regulatory compliance, and affordable medication access.
Position Summary
The Validation Engineer and CQV Associate supports validation documentation, data collection, and quality system activities in Medivant’s sterile injectable facility. This entry-level role is ideal for recent graduates seeking hands-on cGMP and aseptic processing experience.
Key Responsibilities
- Assist in execution of media fill studies and documentation.
- Support area qualification and environmental monitoring tasks.
- Help draft IQ/OQ/PQ protocols and assist execution.
- Collect data for HVAC, WFI, and compressed air validation.
- Assist in cleaning validation logs and sample documentation.
- Participate in process validation protocol preparation.
- Support change control documentation.
- Assist in deviation data collection and preliminary reports.
- Track CAPA activities and closure evidence.
- Ensure cGMP compliance in all assigned tasks.
Qualifications
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