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From Bristol Myers Squibb’s original posting
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. · Take the responsibility for implementing and delivering regulatory submission and approval and maintenance for products / projects within agreed timeline. Ensure regulatory compliance with government policy and company required SOPs · Establish and maintain close relationship with NMPA/ CDE/ NIFDC and other appropriate regulatory agencies and under manager’s guidance have a close/ effective communication with relevant regulatory agencies to consult regulatory strategy, determine status and facilitate the approvals of applications submitted to NMPA. · Conduct scientific discussion with relevant external and internal scientific functions…
Open full posting on Bristol Myers Squibb’s site