The opportunity
Teva’s Global Regulatory Affairs Policy and Intelligence (GRAPI) team is at the forefront of regulatory policy and intelligence, transforming complex regulatory landscape updates into actionable insights to inform regulatory strategy and cross-functional strategic decision-making. This role will support GRAPI team in positioning as the definitive source of regulatory intelligence empowering Teva cross-functional teams to navigate regulatory complexity with confidence and foresight.
We are seeking an exceptional expert in Global Regulatory Intelligence to help drive innovation in regulatory intelligence practices. This pivotal role will be responsible for orchestrating a world-class regulatory intelligence practice that anticipates, interprets, and contextualizes regulatory changes globally across key markets, develops global policy positions on key topics with cross-functional input, and services internal regulatory intelligence queries. The role will also provide regulatory policy support for key international markets in collaboration with International Markets (IM) Regulatory Affairs (RA) regional leads. Lastly, the role will serve as a point of contact for Global Regulatory Affairs (GRA) for regulatory due diligence requests from Business Development (BD), providing help with coordination and tracking all due diligence requests from BD for GRA.
This position requires a high level of expertise in regulatory frameworks, industry drivers, regulatory intelligence tools and information sources, and practices. The ideal candidate will take pride in delivering high-quality work and apply extensive knowledge of regulatory frameworks to develop innovative approaches and provide actionable insights to internal stakeholders. The primary challenge in this role will be optimizing productivity amidst a diverse and broad remit, requiring flexibility and autonomy. Reporting to the Global Head of GRAPI, the role will have regular formal and informal interactions. Supervisory guidance will be available to support all efforts, while allowing for autonomous work.
How you’ll spend your day
This pivotal role will be responsible for orchestrating a world-class regulatory intelligence and research function that goes beyond reporting to provide forward-looking strategic foresight.
Willingness to travel as required for cross-functional customer meetings, industry events, and other business engagements.
Willingness to work across time zones and flexibility with working hours. The role is part of a global team with members based in USA and Europe.
Support the high-performance GRAPI team with deep regulatory expertise and innovative thinking by proactively anticipating, identifying, interpreting, analyzing, synthesizing, and contextualizing emerging regulatory changes and trends across multiple jurisdictions and key markets globally (including but not limited to US, EU, China, Japan, Canada).
Engages with GRAPI colleagues and IM RA teams and IM regulatory health authorities, industry, and professional association leaders at the policy level; leverages understanding of regulatory health authorities, industry trade associations, and other relevant organizations, to advance Teva’s position related to regulatory policy in key IMs.
Cultivates internal cross-functional partnerships and provides partners (including, e.g., US and EU GRAPI partners, GRA, Government Affairs, R&D, Medical, Safety, Legal) with a strategic regulatory policy and intelligence perspective.
Create frameworks for transforming complex regulatory data into high-value, actionable intelligence to inform strategic decision-making.
Build adaptive research capabilities that can rapidly respond to dynamic regulatory environments.
Cultivate a culture of continuous learning, intellectual curiosity, and regulatory intelligence.
Coach and develop cross-functional colleagues working on developing regulatory strategy for Teva development programs to become world-class experts in regulatory interpretation and analysis.
