The Project Manager will lead cross-functional initiatives focused on technical dossier audits and regulatory readiness activities for in-market clinical diagnostic products
- Bachelor's degree in a scientific, engineering, regulatory, or related discipline.
- Minimum of 3-5 years of experience in project management within a regulated industry.
- Experience working in medical devices, in vitro diagnostics (IVD), biotechnology, life sciences, or related regulated environments.
- Demonstrated experience leading cross-functional initiatives involving multiple stakeholders and competing priorities.
- Working knowledge of product development documentation, design controls, quality systems, and regulatory submission processes.
- Experience coordinating complex projects involving documentation review, compliance assessments, or remediation activities preferred.
- Familiarity with global regulatory frameworks applicable to medical devices and IVD products is preferred.
- Experience supporting regulatory submissions, product registrations, or compliance programs is a plus.
- Project Management Professional (PMP) certification is a plus but not required.
Project Manager in San Diego at Indotronix Avani Group
This position is listed as full time and onsite. It was posted 2 days ago.