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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.

The Director of Regulatory Affairs will lead regulatory strategies, mentor team members, contribute to client relationships, and improve operational efficiency in MedTech projects.

The Staff Toxicologist conducts risk assessments for medical devices, guides regulatory submissions, mentors junior staff, and collaborates with stakeholders to ensure product safety and compliance.