QA Compliance Specialist

QA Compliance Specialist

Alternate/Related Job Titles:

Quality Systems Compliance Specialist

Regulatory Compliance Analyst

Quality Assurance Auditor

Location: Columbus, OH

On-site Flexibility: On-site

Contract Details:

Position Type: Contract

Contract Duration: 12 months

Start: As Soon As Possible

Pay Rate: $53.45/hr

Job Summary:

The QA Compliance Specialist supports the execution of quality and regulatory functions to maintain compliance with applicable regulations, standards, and corporate policies. This role ensures that the organization’s quality systems remain audit-ready, fully documented, and aligned with both corporate and industry requirements. The specialist will support audits, CAPA activities, documentation maintenance, metrics reporting, and continuous improvement initiatives across the quality system.

Key Responsibilities:

Support external audit activities, including FDA, FDB, and ISO registrar audits.

Audit areas of the Vascular Quality System for compliance with established standards.

Support the administration of Quality System processes such as CAPAs and Internal Audits.

Generate and distribute periodic open CAPA and Internal Audit Corrective Action (IACA) reports.

Track, trend, and report compliance activities, including CAPA and IACA metrics.

Provide timely feedback to stakeholders on open corrective actions.

Participate in cross-divisional activities to integrate and improve Quality System information.

Review and update Quality System procedures as needed.

Assist in developing and conducting Quality System training.

File and organize Quality Records such as audit reports, IACAs, and CAPAs.

Ensure all responsibilities are carried out in full compliance with governing regulations and standards.

Required Experience:

Bachelor’s Degree or equivalent.

4+ years of relevant QA, compliance, or quality systems experience.

Hands-on experience with CAPA processes, audits, and regulatory compliance.

Nice-to-Have Experience:

Experience in medical device, pharmaceutical, diagnostics, or healthcare product environments.

Experience with ISO, FDA, or global regulatory audits.

Knowledge of cross-functional quality integration practices.

Required Skills:

Quality System auditing

CAPA management

Regulatory compliance knowledge

Preferred Skills:

Procedure writing and document control

Quality metrics development and reporting

Training development and delivery

Cross-functional communication

Additional Skills:

Internal Audit Corrective Action (IACA) support

Quality record management

Trending and analysis of compliance data

Collaboration across divisions

Benefits:

Medical, Vision, and Dental Insurance Plans

401k Retirement Fund

About the Client:

A global healthcare innovator offering medical devices, diagnostics, nutrition products, and branded generics. The organization focuses on improving lives worldwide through groundbreaking technologies, high-quality products, and a commitment to global health advancement.

About GTT:

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. As a Native American-owned, economically disadvantaged corporation, we highly value diverse and inclusive workplaces. Our clients are Fortune 500 banking, insurance, financial services, and technology companies, along with some of the nation’s largest life sciences, biotech, utility, and retail companies across the US and Canada. We look forward to helping you land your next great career opportunity!

Job Number:

25-28445 #gttjobs #LI-Onsite #LI-GTT