QR
Posted:
June 17, 2026
Location:
Cidra, Cidra, Puerto Rico
Job Description
We are seeking a Quality Management System (QMS) Consultant to support a QMS Remediation Plan for critical quality system improvement initiatives within a regulated medical device environment. This role is key to identifying compliance gaps, driving remediation activities, and strengthening the organization’s QMS to meet global regulatory standards.
Key Responsibilities
- Lead and support quality system remediation projects, including gap assessments and corrective action plans
- Review, update, and enhance QMS documentation (procedures, work instructions, templates)
- Ensure compliance with regulatory standards such as:
- FDA (21 CFR Part 820)
- ISO 13485:2016
- FDA (21 CFR Part 820)
Apply for this Job
Submit your application for the QMS Consultant position at QRC Group, LLC.
Apply Now Save for LaterJob Overview
Job Type:
Full-time
Location:
Cidra, Puerto Rico
Posted:
June 17, 2026
Deadline:
July 27, 2026