Overview
Quality Systems Auditor Jobs in United States at GForce Life Sciences
Title: Quality Systems Auditor
Company: GForce Life Sciences
Location: United States
Summary
Our client,a revolutionizing software prescription medical device company, is seeking a highly skilled Quality Systems Auditor with expertise in regulatory compliance for medical devices, specifically software as a medical device. This role will focus on auditing quality management systems to ensure compliance with global medical device regulations and standards.
Requirements
ISO 13485 and MDSAP regulatory requirements and audit processes
21 CFR Part 820 compliance and the transition to QMSR
Software as a Medical Device (SaMD) and general software-related regulations
Nice to Have
Cybersecurity standards and best practices (nice to have)
Terms & Start
Remote
1-week audit
