Global Regulatory Submissions Lead

GForce Life Sciences in Des Plaines, Illinois is seeking an experienced candidate for regulatory project management roles. The position involves collaborating with cross-functional teams, monitoring submission deliverables, and ensuring adherence to regulatory processes for global product registrations. The ideal candidate should have approximately 3–5 years of experience, strong organizational skills, and a solid understanding of IVD regulations. This is a pivotal role in maintaining compliant regulatory workflows and supporting efficient project execution.
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