Quality Systems Specialist: Docs, Change Control & Audits

Elos Medtech; Memphis (TN); On-site; USD 70,000 - 100,000; Full time

Job summary

Elos Medtech in Memphis, TN is seeking a Quality System Specialist I to support the QMS through document control, change management, and supplier quality activities. The role ensures regulatory compliance and audit readiness across quality processes.

You will work with cross-functional teams to maintain controlled documents, track changes, and support internal and supplier audits, contributing to continual improvement and data integrity.

Qualifications

• Bachelor's degree in a related field or equivalent experience.
• ASQ certification preferred.
• Experience in a regulated QA environment and with QA processes.

Responsibilities

• Coordinate document control and change management activities.
• Maintain accurate, audit-ready documentation within the QMS.
• Support supplier quality records and documentation.
• Assist in supplier audits and change control processes.
• Administer document routing, revision, and approval workflows.
• Collaborate across Manufacturing, Engineering, and Supply Chain.

Skills

Organizational skills

Attention to detail

Cross-functional

Communication

Education

Bachelor's degree or equivalent experience

ASQ certification preferred

Tools

ETQ

eQMS

Job description

Elos Medtech in Memphis, TN is seeking a Quality System Specialist I to support the QMS through document control, change management, and supplier quality activities. The role ensures regulatory compliance and audit readiness across quality processes.

You will work with cross-functional teams to maintain controlled documents, track changes, and support internal and supplier audits, contributing to continual improvement and data integrity.