Sr. Associate - Quality Assurance; MQA

Join to apply for the Sr. Associate - Quality Assurance (MQA) role at Medivant Healthcare
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This range is provided by Medivant Healthcare. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$50,000.00/yr - $55,000.00/yr

Medivant Healthcare manufactures high‑quality sterile injectable medications at its FDA‑inspected facilities. The company is committed to strong quality systems, regulatory compliance, and delivering safe and effective products.

The Associate / Senior Associate – MQA supports documentation control, batch record review, sampling activities, material releases, investigations, and manufacturing quality oversight. This role ensures compliance with cGMP requirements and supports daily quality operations across production and packaging.

• Upload documents into the Document Management System (DMS – Master Control or equivalent).
• File and archive documents while maintaining tracking records for timely retrieval and archival.
• Review and release incoming materials in accordance with the Approved Vendor List and Certificate of Analysis requirements.
• Issue controlled documents and logbooks to all departments.
• Perform AQL inspections as required.
• Conduct line clearances, in‑process sampling, and finished‑product sampling for manufacturing and packaging operations.
• Prepare Master Batch Manufacturing Records (MBMRs) and review executed Batch Manufacturing Records (BMRs).
• Pull, label, and store product samples after manufacturing.
• Support product and material destruction processes.
• Participate in failure investigations and support documentation.
• Review label printing activities for accuracy and compliance.
• Perform any additional duties assigned by the Department Head or designee.

• Bachelor’s degree in Pharmacy, Biotechnology, Chemistry, or related scientific discipline.
• 2-3 years of experience in pharmaceutical QA or manufacturing quality assurance roles.
• Knowledge of cGMP, documentation practices, sampling procedures, and material release processes.
• Strong attention to detail, documentation accuracy, and organizational skills.

• Experience in sterile manufacturing or injectable facilities.
• Experience with Master Control or similar electronic documentation systems.
• Familiarity with batch record review and AQL inspection processes.

• Full‑time onsite role requiring presence in production and packaging areas.
• May require extended standing, gowning, and movement between controlled environments.