Senior Specialist, APMC Data Management

We are seeking a Senior Specialist, APMC Data Management to join our team. This role will involve executing daily operations within regulatory systems, collaborating with cross-functional teams, and ensuring compliance with GMP standards and BMS policies and procedures.

Requirements

• Demonstrated understanding of Biologics, Pharmaceutical, and/or Cell Therapy operations and processes
• Operates under routine supervision from a direct manager
• Minimum 3 years of experience in a technical, quality, and/or regulatory role within the biopharmaceutical industry
• Strong ability to assess data accuracy and consistency between manufacturing and regulatory information
• Solid working knowledge of Bills of Materials as they relate to the pharmaceutical supply chain

Benefits

• Competitive benefits, services, and programs
• Flexible work environment
• Opportunities for growth and development
• Collaborative and supportive culture