Sr. Manager, Regulatory Affairs
Aliso Viejo, CA
Hybrid work schedule
Full Time / Direct Hire
In this key leadership role, you will drive and support the execution of global regulatory strategies for innovative drug/device combination products and prescription pharmaceuticals. You will lead the preparation of high-quality regulatory submissions, ensure cross-functional alignment, and help shape product development, regulatory approvals, and long-term compliance. Your work will help bring pioneering treatments to patients globally.
At the company, we’re a community of innovators focused on transforming the standard of care for chronic eye diseases. With a pioneering spirit and patient-first mindset, we are advancing bold new treatments that improve lives. Join our client as they lead the way in sight-saving innovation.
What Will You Do?
Drive Regulatory Strategy and Execution:
Prepare and Submit Regulatory Documentation:
Engage with Global Regulatory Authorities:
Collaborate and Lead Across Projects:
Stay Informed and Elevate Best Practices:
How Will You Get Here?
Education:
Experience:
Knowledge, Skills, and Competencies:
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