Responsible for auditing planning, executing audits, issuing reports, client training, and maintaining knowledge of regulations. This role requires client interaction and effective communication.

The Lead Auditor is responsible for project management, audit planning, execution, and client relationship management in the Medical Device industry, along with supporting training development and maintaining compliance with regulations.

The ISO 13485 Lead Auditor will manage and execute audits, provide mentorship, develop training modules, and maintain regulatory compliance for medical devices and client-facing roles.

The Business Development Professional will drive sales growth by managing client relationships, developing strategic sales plans, and promoting RQM's integrated solutions in MedTech.

RQM+ seeks individuals interested in MedTech consulting, emphasizing regulatory and quality expertise to enhance client relationships and support product lifecycle management.

RQM+ seeks personnel with expertise in Regulatory Affairs, Quality Assurance, Clinical Trials, Auditing, Medical Writing, and Laboratory services to enhance MedTech innovation and client engagement.