Senior Regulatory Professional developing regulatory strategies and leading execution via cross - functional teams for Novo Nordisk, focusing on Obesity and Diabetes portfolio.
PP
Hybrid Senior Director, Regulatory Affairs – CMC, Regulatory Operations, Lifecycle Management
Posted 3 months ago
About the role
- Senior Director overseeing global regulatory strategies for Perrigo's diverse product portfolio. Driving compliance and innovation in Chemistry, Manufacturing & Control (CMC) and regulatory operations.
Responsibilities
- Serve as the visionary leader shaping Perrigo’s global regulatory future
- Champion the development and execution of cutting-edge Chemistry, Manufacturing & Control (CMC) strategies
- Drive the creation of robust quality dossiers and seamless navigation of regulatory landscapes
- Orchestrate timely submissions and proactively identify risks and mitigation plans
- Inspire and empower a high-performing regulatory team
- Oversee lifecycle maintenance, safeguarding ongoing compliance and success of all Perrigo products
- Build a resilient framework that streamlines processes and advances organizational excellence
Requirements
- Advanced degree in Life Sciences (PhD, PharmD, MSc preferred)
- 15+ years of progressive experience in regulatory affairs, with leadership roles in CMC, Regulatory Operations, and Lifecycle Management
- Proven track record of successful global submissions and approvals across diverse product categories
- Strong strategic, financial, and operational acumen
- Exceptional leadership, collaboration, and stakeholder engagement skills
- Experience with global regulatory systems and digital platforms
Benefits
- Competitive compensation
- Benefits tailored to supporting you and your family
- Career development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
Regulatory Affairs Specialist responsible for leading regulatory strategies for Novo Nordisk’s Obesity and Diabetes portfolio. Collaborate with cross - functional teams and health authorities for submissions and documentation.
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