Associate Director Global Regulatory Affairs Pharma Safety & Efficacy, New developments M/F/D

Job description

We are currently hiring a Associate Director Global Regulatory Affairs to provide comprehensive regulatory input for pharmaceutical safety and efficacy during development. Key responsibilities include preparing regulatory submissions and ensuring compliance with EU and global standards. Ideal candidates will have significant experience in pharma product development and regulatory affairs. Job Description. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with externa... Job Description. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external r... regulatory submissions, pharmaceutical product development, eu regulatory submissions, regulatory

compliance, regulatory filings, regulatory documentation, regulatory filings strategy, regulatory submissions management, fda regulations, regulatory operations, regulatory labeling, strategic thinking, cross-cultural awareness, change management, data management, systems development lifecycle, vendor management, policy implementation, employee training programs, english proficiency, german proficiency