Manufacturing Quality Systems Specialist

Medivant Healthcare; Chandler (AZ); On-site; USD 65,000 - 90,000; Full time

Job summary

Medivant Healthcare in Chandler, AZ is seeking a Manufacturing QMS Associate to support quality management system activities, including change controls, deviations, CAPAs, and documentation.

You will collaborate with cross-functional teams, contribute to investigations, SOP development, and training on cleanroom practices, ensuring regulatory compliance.

This on-site role focuses on continuous improvement of processes and sustained quality across manufacturing operations.

Qualifications

• Bachelor's degree in Pharmacy, Life Sciences, Biotechnology, or a related field.
• 2–4 years of experience in Quality Systems, Manufacturing, or GMP-regulated environments.
• Experience with Change Control, CAPA, Deviations, and SOP documentation.

Responsibilities

• Initiate and review Change Controls, Deviations, and CAPAs.
• Draft investigations, including OOS and deviation reports.
• Prepare and maintain Standard Operating Procedures (SOPs).
• Coordinate with cross-functional teams for timely QMS activities.
• Collaborate with the Quality team for document review and approval.
• Provide training on cleanroom requirements and manufacturing practices.
• Support process improvement initiatives as needed.

Skills

Quality Systems

Change Control

CAPA & Deviations

Investigation Writing

SOP Development

GMP Compliance

Documentation Management

Process Improvement

Cross-Functional Collaboration

Attention to Detail

Education

Bachelor's degree in Pharmacy, Life Sciences, Biotechnology, or related field

Tools

MasterControl

Job description

Medivant Healthcare in Chandler, AZ is seeking a Manufacturing QMS Associate to support quality management system activities, including change controls, deviations, CAPAs, and documentation.

You will collaborate with cross-functional teams, contribute to investigations, SOP development, and training on cleanroom practices, ensuring regulatory compliance.

This on-site role focuses on continuous improvement of processes and sustained quality across manufacturing operations.