Job Description

Serve as a highly credible and technically sound regulatory affairs expert with billable project contributions across assigned client portfolios. Meet personal utilization targets while helping colleagues achieve theirs through resource collaboration, mentoring, and ideation. Provide expert guidance on global regulatory strategies, submission pathways, reimbursement approaches, and related client deliverables. Support the operationalization of RQM+’s long-term vision to cover emerging regulatory needs (e.g., combination products, cybersecurity, AI/ML, EU MDR, etc.). Assist in building frameworks for process improvement and profitability tracking across consulting projects. Lead or co-lead initiatives to identify knowledge gaps, propose training opportunities, and build repeatable consulting infrastructure. Contribute to marketing campaigns, co-author thought leadership content and represent RQM+ externally at conferences and events. Serve as a strategic partner to Business Development and Resourcing teams to align new project opportunities with internal capabilities. Take on direct reports as needed, providing mentorship, development support, and performance coaching. Provide timely feedback on consulting and project operations to vertical leadership and contribute to continuous process improvements.

About RQM+

RQM+ is The MedTech CRO, accelerating innovation to patient impact with tailored solutions delivering regulatory and quality expertise.

Apply for This Position