Associate Director, Regulatory Information Management & Innovation

Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsAssociate Director, Regulatory Information Management & InnovationWarsaw - PLApply NowFind out how well you match with this jobUpload your resumeJob descriptionLife at BMSWorking with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.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. Read more: careers.bms.com/working-with-us.Position SummaryThe Associate Director, Regulatory Information Management and Innovation will support working with business and IT teams to design future releases and integrations, evolving system functionality to meet new Health Authority / business needs, working with the vendor to evaluate new platform releases.Position ResponsibilitiesMaintains comprehensive knowledge of the assigned Regulatory Capabilities and/or ProcessesIdentify and track progress against key project milestones partnering with business, quality and other enabling functions and any external providers to ensure overall project successActively engage with leadership from business case development through program delivery, broker the delivery of critical programs within the portfolio, ensure organizational alignment on scope, schedule, quality, benefits and implement and monitor appropriate controls to proactively deal with barriers to completionSupport the development, deployment and maintenance of processes, procedures, and training materials in compliance with Global GxP requirements, BMS Global Quality StandardsMaintains global expert level knowledge of the assigned Regulatory Capabilities and/or ProcessesLeads system and/or process implementations and/or system enhancements in collaboration with Information Technology Business Partners and according to validation rulesLead the evaluation, design, and adoption of AI‑enabled capabilities across Regulatory Information Management and submission platforms (e.g., Veeva RIM), driving measurable improvements in data quality, process effectiveness, operational efficiency, and inspection readiness within approved governance and compliance frameworks.Partner with business, IT, Quality, and external vendors to define AI use cases, influence platform roadmaps, and oversee pilot‑to‑production deployment of AI‑assisted solutions (e.g., automation, analytics, content intelligence), ensuring appropriate validation, documentation, risk management, and change adoption.Work with RIM System Business Lead and IT Business Partner to support development, approval, and...