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
3-6 month project | Temporary Position | Candidates must be local to Wayne, IN
We are seeking a highly skilled CAPA Leader to support a critical quality and compliance initiative for one of our clients. This role will be based onsite in Wayne, NJ, and will focus on harmonizing processes across three manufacturing sites operating under two separate Quality Management Systems (QMSs). The ideal candidate brings deep CAPA expertise, strong cross-functional leadership skills, and proven experience navigating FDA regulatory actions, including 483 observations and Consent Decree–related remediation activities.