Director Global Regualtory Affairs

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PURPOSE AND SCOPE:

Responsible for leading the strategic direction and execution of regulatory strategies for our global pharmaceutical portfolio.

This position plays a critical role in influencing regulatory decisions, managing complex global submissions, and ensuring successful product development, approval, and market access for FME’s product portfolio.

The Global Strategy Leader will work closely with internal and external stakeholders to align regulatory strategies with business objectives and drive the timely delivery of high-quality pharmaceutical products.

 

PRINCIPAL DUTIES AND RESPONSIBILITIES:


* Regulatory Strategy Leadership:
+ Lead the development of global regulatory strategies for the company’s pharmaceutical portfolio, including IND/CTAs, NDAs, NDSs, MAAs, etc..and other key regulatory submissions.
+ Collaborate with senior leadership in medical/clinical development, commercial, and other functional areas to align regulatory strategy with overall product development and business objectives.
+ Provide expert guidance on regulatory requirements, market access strategies, and potential risks to inform decision-making across the organization.


* Global Regulatory Submissions:
+ Oversee the planning, preparation, and execution of global regulatory submissions to ensure timely approval and market access across key regions (e.g., FDA, EMA, Health Canada, etc.).
o Including global chemistry, manufacturing, and controls writers and authorship
+ Ensure the integration of regulatory considerations into all stages of product development, including preclinical, clinical/medical, CMC, and post-market phases.
+ Monitor regulatory trends, updates, and guidance from global agencies, ensuring the company’s strategies remain aligned with changing regulatory requirements.


* Cross-Functional Collaboration & Stakeholder Management:
+ Serve as a regulatory contact for cross-functional teams, ensuring alignment on regulatory strategy and execution across global markets.
+ Work closely with commercial, clinical/medical, and manufacturing teams to ensure timely and successful regulatory approval of products, addressing any regulatory challenges that arise.
+ Lead interactions with regulatory agencies and stakeholders worldwide to advocate for regulatory positions, influence decisions, and expedite approvals.


* Regulatory Risk Management & Compliance:
+ Identify and manage regulatory risks associated with the global development and commercialization of pharmaceutical products.
+ Ensure compliance with local and global regulatory standards, including FDA, EMA, ICH, and other regulatory bodies, to maintain market access and product integrity.
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