Quality Assurance Manager – Sterile Injectables

Medivant Healthcare; Chandler (AZ); On-site; USD 110,000 - 150,000; Full time

Job summary

Medivant Healthcare is seeking a Manager QA– MQA to oversee documentation control, batch record review, sampling, material releases, investigations, and QA oversight in manufacturing and packaging. The role ensures compliance with cGMP and supports daily quality operations onsite.

The ideal candidate has a Bachelor’s degree in a related science field and 7–10 years of pharmaceutical QA experience, with familiarity in MasterControl or similar systems, AQL inspections, and batch record workflows.

Qualifications

• Bachelor’s degree in a related scientific discipline.
• 7-10 years of pharmaceutical QA or manufacturing QA experience.
• Knowledge of cGMP and documentation practices.
• Experience with electronic documentation systems preferred.

Responsibilities

• Upload documents into a DMS (MasterControl or equivalent).
• Review and release materials per AVL and COA requirements.
• Prepare MBMRs and review BMRs.
• Conduct AQL inspections and line clearances.
• Support investigations and participate in failure analysis.
• Review label printing for accuracy and compliance.

Skills

cGMP knowledge

Documentation management

Batch record review

Quality assurance

Attention to detail

Education

Bachelor’s degree in Pharmacy, Biotechnology, Chemistry, or related scientific discipline

Tools

MasterControl or similar electronic documentation systems

Job description

Medivant Healthcare is seeking a Manager QA– MQA to oversee documentation control, batch record review, sampling, material releases, investigations, and QA oversight in manufacturing and packaging. The role ensures compliance with cGMP and supports daily quality operations onsite.

The ideal candidate has a Bachelor’s degree in a related science field and 7–10 years of pharmaceutical QA experience, with familiarity in MasterControl or similar systems, AQL inspections, and batch record workflows.