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    "requisitionDescription": "<div><div><div><div><p data-pasted=\"true\"><strong>About Medivant Healthcare</strong></p><p>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.</p><p><strong>Position Summary</strong></p><p>The <span style=\"color: black;font-size:16px;font-family: Aptos, Aptos_EmbeddedFont, Aptos_MSFontService, Calibri, Helvetica, sans-serif;\" data-pasted=\"true\">Validation Engineer and CQV</span> Associate supports validation documentation, data collection, and quality system activities in Medivant&rsquo;s sterile injectable facility. This entry-level role is ideal for recent graduates seeking hands-on cGMP and aseptic processing experience.</p><p><strong>Key Responsibilities</strong></p><p>&bull; Assist in execution of media fill studies and documentation.</p><p>&bull; Support area qualification and environmental monitoring tasks.</p><p>&bull; Help draft IQ/OQ/PQ protocols and assist execution.</p><p>&bull; Collect data for HVAC, WFI, and compressed air validation.</p><p>&bull; Assist in cleaning validation logs and sample documentation.</p><p>&bull; Participate in process validation protocol preparation.</p><p>&bull; Support change control documentation.</p><p>&bull; Assist in deviation data collection and preliminary reports.</p><p>&bull; Track CAPA activities and closure evidence.</p><p>&bull; Ensure cGMP compliance in all assigned tasks.</p><p><strong>Qualifications</strong></p><p>Required:</p><p>&bull; Bachelor&rsquo;s degree in Pharmacy, Biotechnology, Microbiology, Life Sciences, or related field.</p><p>&bull; 2-3 years of relevant experience is required</p><p>&bull; Understanding of aseptic and sterile processing.</p><p>&bull; Strong documentation and communication skills.</p><p>Preferred:</p><p>&bull; Experience in sterile manufacturing or validation support.</p><p>&bull; Knowledge of QMS processes and cGMP environments.</p><p><strong>Employment Details</strong></p><p>&bull; Full-time onsite role at Medivant Healthcare facilities.</p><p>&bull; Standard work schedule: Monday&ndash;Friday.</p><p>&bull; Training provided for all validation and QMS procedures.</p><p><br></p><p><span data-teams=\"true\" data-pasted=\"true\"><strong>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.</strong></span></p><p><br></p></div></div></div></div>\n",
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