What are the responsibilities and job description for the Validation & QMS Associate position at Medivant Healthcare?
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
Required:
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.
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.
- Experience in sterile manufacturing or validation support.
- Knowledge of QMS processes and cGMP environments.
- Full-time onsite role at Medivant Healthcare facilities.
- Standard work schedule: Monday–Friday.
- Training provided for all validation and QMS procedures.
Salary : $50,000 - $60,000