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 & QMS 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.