Validation Engineer and CQV

**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** Required: • 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. Preferred: • Experience in sterile manufacturing or validation support. • Knowledge of QMS processes and cGMP environments. **Employment Details** • Full-time onsite role at Medivant Healthcare facilities. • Standard work schedule: Monday–Friday. • Training provided for all validation and QMS procedures. **Please note that we are not providing H1B visa sponsorship for this role. Candidates will be solely responsible for managing and maintaining their own visa sponsorship status.**