Associate Director, MQSA Regulatory Intelligence and Standards

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.

Execute the enterprise regulatory intelligence and surveillance program; monitor, analyze, and interpret evolving global regulations, guidance documents, and Health Authority expectations related to aseptic processing, contamination control, and microbial quality (FDA 21 CFR Parts 210/211/600, EU GMP Annex 1 and Part IV, ICH Q9/Q10, USP //, PIC/S). Owns updates to global procedures based on the assessments.

Conduct systematic regulatory change impact assessments and draft change notification packages; elevate significant compliance gaps or emerging regulatory risks for strategic assessment and enterprise response.

Maintain the regulatory intelligence deliverables library, including gap assessments, applicability matrices, regulatory horizon scanning summaries, and compliance position papers to ensure enterprise-wide readiness.

Support regulatory engagement strategy with Health Authorities and industry bodies; serve as a primary operational contact during site inspections, agency inquiries, and regulatory filings related to CCS/SA matters.

Translate regulatory intelligence findings into actionable recommendations, briefing documents, and compliance alignment proposals.

Own and maintain commercial CCS/SA governance documentation, including global procedural documents (GPOs), policies, and standards — ensuring alignment with the overarching enterprise governance framework.

Execute compliance gap assessments and applicability matrices across aseptic processes, microbial control, and sterility assurance for all relevant manufacturing environments (sterile, aseptic, non-sterile).

Drive the practical adoption and operationalization of enterprise standards at site level, working closely with site quality teams to ensure scalable and sustainable implementation.

Establish and maintain governance documents, white papers, storyboards and inspection-ready deliverables supporting the enterprise CCS/SA framework.

Support the organizational transition from current-state to a single, unified enterprise CCS/SA function with clear decision rights, including workforce transition planning and role definition activities.

Lead day-to-day inspection readiness activities across the commercial manufacturing network related to CCS/SA; serve as the primary operational subject matter expert resource during Health Authority inspections and agency engagements related to CCS/SA.

Develop and maintain inspection-ready documentation packages, site-level compliance assessments, and regulatory response materials for CCS/SA-related matters.

Provide technical compliance support related to regulatory interpretation, microbiological data integrity, critical investigations, and inspection readiness activities; elevate complex or high-risk matters to the Senior Director as the enterprise escalation point.

Coordinate with site quality teams and cross-functional partners to ensure consistent, defensible, science-based responses during regulatory inspections and agency interactions.

Contribute to the development of the…