Senior Specialist, APMC Data Management

Working with Us, Challenging. 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.

Requirements

• Execute daily operations within regulatory systems such as Veeva Vault RIM, Quality Veeva Systems, and Regulatory Content Repositories
• Execute daily configuration activities within SAP Batch Release Hub
• Execute daily configuration activities within Change Control Restriction Management
• Execute daily operations within Authorized Supply Chain Maps
• Execute daily operations within Document Data Extraction
• Assess data from eCTD and CTD Module 3 documents to ensure accuracy, completeness, and consistency with relevant information from Quality and Supply Chain functions
• Collaborate closely with CMC, Supply Chain, and Quality teams to align priorities, resolve issues, and provide status updates
• Escalate unresolved deficiencies to the appropriate stakeholders
• Escalate risks proactively to support the timely release of products
• Identify and recommend opportunities for process improvement
• Ensure compliance with GMP standards and BMS policies and procedures
• Provide support for issue resolution across additional electronic systems

Benefits

• Competitive benefits
• Services and programs
• Employee resources to pursue goals