QA Associate – Sterile Injectable Manufacturing

RXinsider LTD.; Phoenix (AZ); On-site; USD 60,000 - 75,000; Full time

Job summary

Medivant Healthcare is seeking an Associate / Senior Associate - MQA to support documentation control, batch record review, sampling, and material releases. The role ensures compliance with cGMP and supports daily quality operations across production and packaging.

The candidate will perform document uploads, material release reviews, line clearances, and investigations, contributing to quality oversight in sterile injectable manufacturing environments.

Qualifications

• Bachelor's degree in a relevant scientific discipline.
• 1-2 years in pharmaceutical QA or manufacturing QA roles.
• 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 MasterControl or equivalent).
• File and archive documents with tracking records for retrieval.
• Review and release incoming materials per Approved Vendor List and COA requirements.
• Issue controlled documents and logbooks to departments.
• Perform AQL inspections as required.
• Conduct line clearances, in-process sampling, and finished-product sampling.
• Prepare Master Batch Manufacturing Records and review Batch Manufacturing Records.
• 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

Attention to detail

Documentation

cGMP knowledge

Quality assurance

Lab skills

Education

Bachelor's degree in Pharmacy Biotechnology Chemistry

Tools

MasterControl

Job description

Medivant Healthcare is seeking an Associate / Senior Associate - MQA to support documentation control, batch record review, sampling, and material releases. The role ensures compliance with cGMP and supports daily quality operations across production and packaging.

The candidate will perform document uploads, material release reviews, line clearances, and investigations, contributing to quality oversight in sterile injectable manufacturing environments.