Senior QA Associate - cGMP & Batch Records (Onsite)

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

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.