Regulatory Affairs Program Director

August 27

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Manufacturer of Contact Lenses • Women's Health Devices • IVF • Medical Device • Vision Correction

10,000+

💰 Post-IPO Equity on 2021-12

Description

• As an integral part of the Regulatory Affairs (RA) team, the RA Program Director translates regulatory strategies and objectives into executable programs. • Develop program and/or project structure and governance. • Ensure the integration of project management methodology to prioritize and deliver transformational regulatory projects globally.

Requirements

• Bachelor's degree or higher required • RAC and/or PMP certification preferred • Medical Device Regulatory Affairs experience conveying a working knowledge of global medical device regulations • Demonstrated leadership skills: a proven leader who can lead others through influence • Ability to manage & balance multiple priorities • Strong learning agility • Excellent written and verbal communication skills; must be fluent in written and spoken English • Advanced skills in Microsoft PowerPoint, Excel, Word and Project Management tools (e.g., Microsoft Project, Smartsheet, etc.)

Benefits

• Competitive pay • Comprehensive benefits • Focus on wellness