Top Tech Jobs & Startup Jobs

Lead CAPA lifecycle management, process harmonization across manufacturing sites, and compliance with FDA regulations. Drive continuous improvement and ensure effective CAPA documentation and training.

This role involves supporting regulatory and quality activities for medical devices, including CAPA management, vendor oversight, and documentation control.

The Senior Regulatory Affairs Contractor supports FDA PMA device activities, manages regulatory submissions, and evaluates changes while ensuring compliance with regulations.

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

Drive sales growth for integrated services in MedTech, develop account plans, manage client relationships, and meet sales targets.

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