Regulatory Affairs Manager

hace 1 semana


distrito federal, México Eli Lilly and Company A tiempo completo

Join to apply for the Regulatory Affairs Manager role at Eli Lilly and Company . At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life‑changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Role The purpose of the Affiliates Regulatory Affairs (P3) role is to manage all aspects of regulatory affairs for the marketing affiliate, including: Supervise the Regulatory Affairs activities to ensure the success of new product registration, line extensions and new indications in alignment with the affiliate business plan, while maintaining compliance for all products with local regulations and quality system requirements (whichever is more stringent). Foster an environment of operational excellence through regulatory expertise and, if relevant, managing and developing direct reports and collaborating with cross‑functional teams to successfully achieve Affiliate regulatory objectives. Cultivate external relationships with the relevant Government bodies and industry associations. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Seniority level Mid‑Senior level Employment type Full‑time Job function Legal Pharmaceutical Manufacturing #J-18808-Ljbffr



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