Validation Engineer and CQV
About The Position
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. 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.
Requirements
- Bachelor’s degree in Pharmacy, Biotechnology, Microbiology, Life Sciences, or related field.
- 2-3 years of relevant experience is required
- Understanding of aseptic and sterile processing.
- Strong documentation and communication skills.
Nice To Haves
- Experience in sterile manufacturing or validation support.
- Knowledge of QMS processes and cGMP environments.
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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
