RQM+ is The MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better.
We don’t make MedTech. We make MedTech happen.
Our experienced teams are cohesive, collaborative, and proactive, constantly seeking to improve and evolve while remaining laser-focused on customer success. RQM+ elevates the MedTech experience through best-in-class service and clear, concise communication. We serve as an extension of our customers establishing and maintaining excellent client and site relationships and providing direct access to our technology platforms for real-time data and study transparency
Remote | Temporary Position, 40 hours/week for 3+ months
We are seeking a detail-oriented and motivated RA/QA professional to support key regulatory and quality activities within our client's medical device operations. This individual will assist with CAPA management, vendor oversight, documentation control, and other compliance-related tasks. While experience with Software as a Medical Device (SaMD) is a plus, it is not required