Description
The Project Manager will lead cross-functional technical dossier audit and regulatory readiness projects for in-market clinical diagnostic products. The role coordinates reviews of design and regulatory documentation, identifies compliance gaps, develops remediation plans, manages project risks and deliverables, and communicates status to stakeholders in a matrix organization. It is a 12-month, on-site position in San Diego, California, with a pay rate of $45 and requires a bachelor's degree in a relevant discipline and 3–5 years of regulated-industry project management experience.
