Transitioning from FDA to Industry – Strategies for Success
Gain clarity, confidence, and connections to accelerate your next career move.
As FDA professionals face organizational changes, transitioning into the medical device and pharmaceutical industries can seem overwhelming. We understand your challenges and are here to help you explore new opportunities. Join us for an engaging panel discussion where seasoned industry experts will share insights, strategies, and actionable steps to help FDA professionals successfully navigate the shift into industry or consulting.
Key Discussion Topics:
- Understand Your Unique Value in Industry: Learn how your FDA background translates into high-demand roles in regulatory affairs, quality assurance, clinical strategy, and consulting.
- Explore Diverse Career Options: Get an insider’s look at various industry roles (Regulatory Affairs, CMC, Quality, Medical Writing, Compliance, etc.), consulting opportunities, and alternative career paths.
- Optimize Your Professional Profile: Tips on tailoring your resume and LinkedIn profile to highlight regulatory expertise, risk-based decision-making, and cross-functional collaboration.
- Build & Leverage Your Network: Learn strategies for effective networking, leverage professional organizations like RAPS, DIA, and ISPE, and connect with recruiters and hiring managers.
- The Consulting Pathway: Understand the steps to establish yourself as a consultant, market your expertise, and transition into independent or firm-based consulting.
- Ace Your Interviews: Learn proven strategies to position yourself confidently, answer industry-specific questions, and clearly showcase your impact.
Who Should Attend:
FDA professionals impacted by layoffs, those considering a career transition, and anyone looking to understand industry opportunities and consulting pathways.
Panelists:
Our panel features industry leaders from diverse backgrounds who’ve made the jump from the FDA into roles in industry, consulting, and law firms. They’re here to share their personal experiences and insights on navigating this career shift, including what it takes to successfully hire former FDA professionals.
- Neelu Gibson, former Worldwide Vice President, Regulatory Affairs MDS, BD (currently, Retired)
- Lee Evans, former Head of Global Regulatory Affairs, Philips (currently Executive Advisor, Network Partners Group)
- Phil Desjardin, former FDA Associate Director of Policy (currently Partner, Arnold & Porter)
- Kim Quaintance-Lunn, former Associate Director of Regulatory Affairs at FDA (currently VP Head of Regulatory Science and Execution @ Alexion Pharmaceuticals)
- Deb Autor, former Deputy Commissioner at FDA, former Director of the Office of Compliance at FDA CDER (currently CEO @ Healthcare Innovation Catalysts)
- Ritu Dhami, President Regulatory Practice, Network Partners Group
