Regulatory Director， RI&Operation (BB-6C931)
Found in: Neuvoo CN
Description:At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Build and retain effective RI & operation team to streamline working efficiencies to ensure quality and meet global & China regulatory requirements Lead for the capturing, distribution, assessment and advocacy of the regulatory policy/regulation, communicate with stakeholders to assure understanding and exert external influence to shape the regulatory environment Develop and maintain relevant regulatory quality documents & training system to ensure compliance and quality Develop the Chinese label & Artwork for products registration/ launch in China, ensure high standard of regulatory compliance on label to support the company’s business objectives Lead eCTD quality system to meet regulatory requirement and ensure submission and approval Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
calendar_today2 days ago
info Full time
work Bristol-Myers Squibb