Assistant Manager-Validation & QMS

Medivant Healthcare • Full-time • Chandler, AZ, US • $62,000 - $65,000 / year • 23h ago

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 Assistant Manager – Validation & QMS supports Medivant’s sterile injectable manufacturing operations by coordinating validation activities, quality system processes, and compliance initiatives. This role ensures all validation work meets cGMP, FDA requirements, and internal SOPs.

Key Responsibilities

Execute and support media fill studies; review results and recommend corrective actions.
Lead area qualifications for classified areas (Grade A–D) and support environmental monitoring.
Prepare and execute IQ/OQ/PQ protocols and review qualification documentation.
Coordinate utility validation (HVAC, WFI, compressed air).
Develop and review cleaning validation procedures and reports.
Lead process validation protocol creation, execution, and reporting.
Initiate and review change controls and assess impacts.
Perform deviation investigations and root-cause analysis.
Lead CAPA implementation and verify timely closure.
Support OOS/OOT investigations and regulatory documentation.
Assist during internal/external audits.

Qualifications

Required:

Bachelor’s or Master’s in Pharmacy, Biotechnology, Microbiology, or related field.
2–5 years of validation/QMS or sterile manufacturing experience.
Knowledge of cGMP, FDA regulations, and aseptic practices.
Strong analytical, documentation, and communication skills.

Preferred