Responsibilities: The Regulatory Affairs Manager is responsible for the development and execution of global regulatory strategy and tactical planning for assigned microbiology on market products or those products in development. ssures that defined regulatory strategies defined are effectively implemented and maintained in line with changing regulatory and business needs This individual identifies and gathers data needed to support filings, responses to inquiries, and registration maintenance to enable commercialization of products that are developed, manufactured, or distributed to meet relevant global regulatory requirements. You will be a part of the QRC team and report. Sr Director QRC responsible for microbiology quality, regulatory, and clinical. If you thrive in an amazing, multifunctional, leadership, fast paced, supporting role and want to work to build a world-class Regulatory Affairs organization-read on. Responsible for a product(s) with multiple driver indications within a Therapeutic Area. Sr Manager Clinical Affairs in the development & execution of the regulatory strategy. ssigned matters may have a moderate impact on business activities and operations. Serves as regulatory affairs liaison and interfaces with FDA for meetings, teleconferences and coordinates preparation and completion of FDA meeting briefing packages and responses. dvise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial. Key contributor responsible for the preparation and review of regulatory submissions consistent within global regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review. Recommends and implements changes to difficult projects based on knowledge and expertise, accurate interpretation of US and Canada government regulations, guidance, as well as corporate policies and management-related considerations. Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program.
(QDP) Requirenents: Bachelor's degree (pharmacy, biology, chemistry, microbiology) or industry-related with 9+ years of experience or, master's degree with 7+ years of experience, or PHD with 5+ years of experience. Demonstrates excellent negotiation skills, problem-solving skills and builds consensus Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization. Able to deliver challenging messages effectively without compromising important business relationships. Proven skill at implementing successful global regulatory strategies regulatory strategies. Experience working in a complex matrix environment.