QA Associate

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Full Time Chandler, AZ, US

3 days ago Requisition

Salary Range: $45,000.00 To $45,000.00 Annually

The Quality Assurance Associate – Document Control & Compliance is responsible for supporting document control, customer qualification, regulatory compliance, and record management activities within Medivant Healthcare. This role ensures the accurate maintenance of controlled documentation, customer credential verification, controlled substance order reviews, and compliance record management in accordance with company procedures, regulatory requirements, and quality standards. The ideal candidate is detail-oriented, organized, and capable of managing documentation and compliance activities within a regulated pharmaceutical environment.

• Perform customer qualification and order vetting activities for controlled substance transactions.
• Verify DEA registrations, state licenses, permits, and other customer credentials.
• Support customer onboarding and qualification processes in accordance with regulatory requirements.
• Review regulatory databases and publicly available information to identify potential compliance concerns.
• Verify customer and business information, including legal entity status, addresses, and licensing information.
• Escalate potential compliance risks or discrepancies for further review.

• Manage the issuance, tracking, revision, maintenance, and archival of controlled documents.
• Maintain document control systems and ensure proper version control practices.
• Support the preparation, review, distribution, and retention of controlled quality documents.
• Ensure documentation is complete, accurate, and maintained in accordance with company procedures.
• Assist with document retrieval and record requests during audits and inspections.

• Maintain compliance records and supporting documentation.
• Manage controlled records including Batch Manufacturing Records (BMRs), logbooks, forms, and compliance-related documentation.
• Ensure records are organized, current, and readily accessible for regulatory and internal review.
• Support documentation reviews to ensure compliance with established procedures and quality standards.
Assist in maintaining data integrity and documentation best practices.

• Support Manufacturing, Quality Assurance, Regulatory, and Compliance teams with documentation-related activities.
• Assist with quality system processes and related administrative tasks.
• Participate in compliance reviews and documentation audits as assigned.
• Support continuous improvement initiatives related to document control and compliance programs.
• Assist with preparation and organization of records for internal and external audits.

• Ensure compliance with applicable company procedures, regulatory requirements, and industry standards.
• Identify, document, and communicate compliance concerns when identified.
• Support activities related to controlled substance compliance requirements.
Maintain confidentiality of sensitive business, customer, and compliance information.
• Perform additional duties and special projects as assigned.

• High School Diploma or equivalent required;
  Associate Degree preferred.
• Minimum one (1) year of experience in document control, compliance, quality, manufacturing, healthcare, administration, or another regulated environment.
lStrong attention to detail and organizational skills.
• Proficiency with Microsoft Office…