Validation & QMS Associate at Tailstorm Health Inc – Phoenix, Arizona

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.