Sr. Associate - Quality Assurance (MQA)

Medivant Healthcare; Chandler (AZ); On-site; USD 50,000 - 60,000; Full time

Job summary

Medivant Healthcare in Chandler, AZ is seeking a Sr. Associate - Quality Assurance (MQA) to support documentation control, batch record review, sampling activities, material releases, investigations, and manufacturing quality oversight.

This onsite role requires a Bachelor’s degree in a scientific field, 2–3 years in pharmaceutical QA, and knowledge of cGMP and documentation practices. The position emphasizes accuracy, organization, and cross‑functional collaboration.

Qualifications

• 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.
• Preferred: experience in sterile manufacturing or injectable facilities.
• Preferred: experience with MasterControl or similar electronic documentation systems.
• Preferred: familiarity with batch record review and AQL inspection processes.

Responsibilities

• Upload documents into the Document Management System (DMS – MasterControl 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.

Skills

Attention to detail

Documentation accuracy

Organizational skills

Quality mindset

Education

Bachelor's degree in Pharmacy/related

Tools

MasterControl

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Sr. Associate - Quality Assurance (MQA)

Full Time Chandler, AZ, US

2 days ago Requisition ID: 1072

Salary Range: $50,000.00 To $60,000.00 Annually

About Medivant Healthcare

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.

Position Summary

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.

Key Responsibilities

• Upload documents into the Document Management System (DMS – MasterControl 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.

Qualifications

Required:

• 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.

Preferred:

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

Work Environment & Physical Requirements

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

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.