Validation Engineer and CQV

Medivant Healthcare; Phoenix (AZ); On-site; USD 60,000 - 90,000; Full time

Job summary

Medivant Healthcare is seeking an entry‑level Validation Engineer and CQV Associate for our sterile injectable facility in Arizona. You will support validation documentation, data collection, and QMS activities, gaining hands‑on cGMP experience.

The role emphasizes preparation and execution of IQ/OQ/PQ protocols, environmental monitoring, and CAPA tracking, with training provided. Candidates should have a life sciences degree and 2–3 years of relevant experience.

Qualifications

• Bachelor’s degree or higher in a life sciences field or pharmacy.
• 2–3 years of relevant experience required.
• Understanding of aseptic and sterile processing.
• Strong documentation and communication skills.

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.

Skills

Documentation skills

cGMP knowledge

Aseptic processing

Data collection

Education

Bachelor’s degree in Pharmacy, Biotechnology, Microbiology, Life Sciences, or related field

Tools

QMS systems

Validation protocols

Job description

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

• 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.