ISO 13485 Lead Auditor
RQM+United States
Posted October 16, 2025
Contract / Temporary
About the Company
RQM+ is The MedTech CRO, accelerating medical technology from innovation to patient impact. With expertise in regulatory compliance, quality systems, clinical trials, and reimbursement strategies, RQM+ partners with manufacturers to bring life-changing technologies to market faster and safer. Their tailored solutions ensure seamless product development and post-market support across various device types and therapeutic areas.
Job Description
RQM+ is seeking a motivated ISO 13485 Lead Auditor to support their global audit practice. This client-facing role involves auditing, training development, and client meetings, requiring strong communication, integrity, and problem-solving skills. The position offers a supportive environment focused on employee growth and success within a fast-paced regulatory industry.
Requirements
- MDSAP auditing experience
- FDA 21 CFR Part 820 experience
- Robust auditing experience
- High level of integrity
- Laser focused on customer success
- Strong communication skills
- Cohesive and proactive team player
Benefits
- Competitive compensation package
- Work life balance focus
- Learning and development opportunities