What is your current job title and, in a few words, please tell us what it is that you do? Dr. Jessica Nwabuoku is a United States Regulatory Lead (USRL) at Amgen supporting Obstructive Sleep Apnea and other Obesity Related Conditions. She oversees regulatory submissions (e.g., INDs, NDAs, BLAs) and prepares materials for FDA (and other agency) interactions. She also crafts and directs regulatory strategies for obesity treatments—from early development through approval and post-market support.
I earned my double bachelors degree in Biology and Psychology from the University of Bridgeport and my PharmD degree from Howard University College of Pharmacy. I then completed a two year post doctoral fellowship at Amgen in partnership with Howard University.
I am grateful to be retained at Amgen, one of the world’s leading biotechnology companies. Amgen is dedicated to discovering, developing, and delivering innovative human therapeutics, with a strong focus on serious illnesses in areas like oncology, cardiovascular disease, inflammation, and obesity. The company uses advanced science and cutting-edge biotechnology to serve patients by addressing unmet medical needs and improving health outcomes globally.
I was first introduced to Amgen during the fellowship application process, and I immediately felt aligned with the company’s mission. Amgen’s commitment to “compete to win” truly resonated with me, as I’ve always held myself to a high standard of excellence. Throughout my four years in pharmacy school, I was recognized with 19 awards which is an achievement that reflects my drive, discipline, and commitment to going above and beyond in everything I do.
The company’s ability to stay at the forefront of biotechnology while maintaining a strong ethical foundation really stands out to me. I’m especially inspired by Amgen’s culture of excellence, collaboration, and its commitment to diversity and inclusion. It’s a place where overachievers are challenged, supported, and given opportunities to make a meaningful impact and that’s the kind of environment where I thrive.
Strong communication, strategic thinking, and regulatory knowledge are key to my success as a U.S. Regulatory Lead. I’m skilled at asking the right questions, interpreting complex data, and aligning scientific goals with regulatory requirements. I chose this field because it blends my love for science with my natural ability to advocate and analyze. I was often told I should be a lawyer because I always had a point to prove—regulatory affairs gives me that same challenge, with a purpose rooted in public health.
I attribute my success to my proactive mindset—consistently taking initiative, asking to assist with key regulatory milestones, and stepping up in moments that matter most. I actively seek out opportunities to lead, collaborate cross-functionally to solve complex challenges, and remain committed to continuous learning.
The most fulfilling aspect of my job is knowing that I’m contributing to a highly impactful and rapidly evolving therapeutic area like obesity—bringing breakthrough medications to patients and making a difference in a space where innovation and competition are at the forefront of healthcare.
Be persistent and trust the process—every experience, whether big or small, builds skills that will serve you in your next phase. Stay curious, always be a learner, and don’t be afraid to ask questions or seek mentorship. Growth often happens outside of your comfort zone, so take opportunities that stretch you. Most importantly, believe in your value and be intentional about aligning your path with your purpose. The right opportunity will meet you when preparation and passion align.
The last book I read was poor dad rich dad by Robert T. Kiyosaki