Senior QA Manager, Sterile Injectable Pharma

RXinsider LTD.; Chandler (AZ); On-site; USD 120,000 - 165,000; Full time

Job summary

Medivant Healthcare, a provider of sterile injectable medications, seeks a Manager QA– MQA in Chandler, AZ to oversee documentation control, batch record review, sampling, and regulatory compliance. The role ensures cGMP adherence across production and packaging and supports daily quality operations on site.

The ideal candidate has 7–10 years in pharmaceutical QA/manufacturing quality assurance, with strong attention to detail, MasterControl experience, and familiarity with MBR/BMR processes.

Qualifications

• 7–10 years in pharmaceutical QA or manufacturing quality assurance.
• Strong knowledge of cGMP, documentation practices, sampling procedures, and material release processes.
• Strong attention to detail and organizational skills.

Responsibilities

• Upload documents into the Document Management System (DMS – Master Control or equivalent).
• File and archive documents with tracking records for retrieval and archival.
• Review and release incoming materials per Approved Vendor List and COA 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.
• Prepare MBMRs and review executed 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.

Skills

cGMP knowledge

Documentation control

Batch record review

AQL inspections

Line clearances

Material release

Education

Bachelor’s degree in Pharmacy

Tools

MasterControl

Electronic document system

Job description

Medivant Healthcare, a provider of sterile injectable medications, seeks a Manager QA– MQA in Chandler, AZ to oversee documentation control, batch record review, sampling, and regulatory compliance. The role ensures cGMP adherence across production and packaging and supports daily quality operations on site.

The ideal candidate has 7–10 years in pharmaceutical QA/manufacturing quality assurance, with strong attention to detail, MasterControl experience, and familiarity with MBR/BMR processes.