Quality Systems Associate: Manufacturing & Compliance

Tailstorm-Health-Inc; Chandler (AZ); On-site; USD 41,000 - 50,000; Full time

Job summary

Tailstorm-Health-Inc in Chandler, AZ is seeking a Manufacturing QMS Associate to support Quality Management System activities. The role focuses on managing change controls, deviations, CAPAs, investigations, SOP documentation, and ongoing improvement while ensuring compliance with regulatory requirements.

You will initiate and review change controls via Master Control, draft investigations, prepare SOPs, and collaborate with cross-functional teams to train on cleanroom standards and

Qualifications

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

Responsibilities

• Initiate and review Change Controls, Deviations, and CAPAs through Master Control.
• 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.
• Perform additional duties as assigned by the HOD.

Skills

Quality Systems

Change Control

CAPA

Deviations

SOP Documentation

Investigations

Training

Education

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

Tools

MasterControl

QMS Documentation

Job description

Tailstorm-Health-Inc in Chandler, AZ is seeking a Manufacturing QMS Associate to support Quality Management System activities. The role focuses on managing change controls, deviations, CAPAs, investigations, SOP documentation, and ongoing improvement while ensuring compliance with regulatory requirements.

You will initiate and review change controls via Master Control, draft investigations, prepare SOPs, and collaborate with cross-functional teams to train on cleanroom standards and