We provide program and project manager consultant service to drive program and projects internally for your business needs. Specializing in highly regulated and quality driven medical device manufacturing environments, we can successfully engage and drive team delivery from corporate initiative level all the way to plant level implementations.

Providing effective and best practice execution tools utilizing portfolio, program, and project methodologies, activities, and planning. RPM LLC provides a subject matter expertise customized to the specific needs of medical device manufacturing regulatory compliance initiatives.

Providing the execution arm for regulatory driven updates to EU MDR technical documentation which includes Research & Development, Bio Compatibility, Sterilization, Risk Management, Labeling, Product Management, Manufacturing Processes, Medical Operations, Medical Affairs updates to internal medical device manufacturing documentation for EU MDR compliance.

Providing labeling conformance expertise in UDI driven labeling requirements involving serialization, manufacturing process updates, quality system revisions, vision system and scanning technology, validation & verification, as well as aggregation tracking systems implementation.

RPM LLC provides project management and SME analyst candidates experienced in medical device manufacturing areas. Candidates will typically have experience in regulatory, quality, and IT functional areas - but will be tailored to the level of experience and budget required to ensure a proper fit for the role needing to be filled.