Chandler, AZ · On-site
$45K - $50K/yr
Position Summary The Validation Engineer and CQV Associate supports validation documentation, data ... Candidates will be solely responsible for managing and maintaining their own visa sponsorship ...
Chandler, AZ · On-site
$45K - $50K/yr
Position Summary The Validation Engineer and CQV Associate supports validation documentation, data ... Candidates will be solely responsible for managing and maintaining their own visa sponsorship ...
Tucson, AZ · On-site
Strong ability to document execution in real time, manage discrepancies, and support protocol package closeout. Include Must Have: * Hands-on validation engineering or CQV experience. * Strong OQ/PQ ...
Tucson, AZ · On-site
Strong ability to document execution in real time, manage discrepancies, and support protocol package closeout. Include Must Have: * Hands-on validation engineering or CQV experience. * Strong OQ/PQ ...
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$45K - $50K/yr
Full-time
Re-posted 20 days 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 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
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.
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.