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Senior Manager, Audit Intelligence Coordinator

Bristol Myers Squibb
Full-time
Remote friendly (Princeton, NJ)
United States
Operations

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Role Summary

Senior Manager, Audit Intelligence Coordinator, reports to the Senior Director, Operations & Performance. Responsible for planning audits in support of the BMS Competitive Compliance Audit Program, coordinating audits for internal sites, global suppliers, and entities such as CMOs, APIs, raw materials, and external labs. Plans, organizes, and schedules audit assignments in accordance with the global audit plan; supports clinical and commercial business developments through due diligence audits; communicates changes in the global audit plan to stakeholders and audit outsourcing partners. Uses data-driven insights to enhance audit planning and execution, ensure the audit program's health and performance, and integrate with internal processes such as Quality Risk Management and Quality Council.

Responsibilities

  • Develop and implement an annual audit plan using risk-based principles and data-driven decision-making.
  • Plan, organize, and schedule audit assignments in collaboration with Audit Operations, and in accordance with the defined audit program and audit plan.
  • Work with key stakeholders to maintain and update the annual audit plan for both planned and unplanned changes including routine, due diligence audits, pre-approval Inspection readiness, directed or for cause audits, acquisitions, regulatory/agent distributors, labeling and inspection readiness.
  • Enhance efficiency and simplify the management of the audit planning process by leveraging digital solutions such as automation and AI to advance strategic initiatives and focus on high-impact areas.
  • Communicate with stakeholders, Audit Operations, lead auditors and audit outsourcing partners regarding global audit plan changes in a timely manner.
  • Periodically review and update the audit plan using current compliance, quality, data intelligence, and risk-based principles.
  • Ensure exceptions to the global audit plan are documented, justified, and approved.
  • Stay abreast of current and updated regulations affecting the Audit program and modify the plan, policies, and directives to maintain appropriate compliance with regulatory requirements.
  • Maintain and continuously improve governing procedures and processes.
  • Develop and utilize robust metrics and analysis to monitor the health and performance of the Audit program, enhance audit planning, maximize effectiveness, and measure audit outcomes/impacts.
  • Elevate and refine the audit program through vigilant monitoring and data-driven insights in partnership with Competitive Compliance.
  • Utilize internal processes such as Quality Risk Management and Quality Council to communicate signals and trends, mitigate risks, and drive continuous improvement.
  • Obtain business support to manage supplier audit scheduling issues, including audit refusals and audit fees.

Qualifications

  • Required: A minimum of five (5) years' experience in the biopharmaceutical industry in a Manufacturing, Quality, Technical, or Regulatory position or with a regulatory health authority. High level understanding of auditing, metrics, analysis and Business Analytics.
  • Required: Proven ability to understand complex processes/problems and propose alternate solutions.
  • Required: Demonstrates innovation, flexibility, open-mindedness, and adaptability to meet objectives in a rapidly changing environment with shifting priorities.
  • Required: Strong communication, collaboration, negotiation, problem solving and interpersonal skills.
  • Required: Demonstrated ability to work in a matrixed organization with a range of technically, culturally, and geographically diverse teams and to influence areas not under direct control to achieve objectives and effectively communicate challenging goals and objectives.
  • Required: Able to complete multiple, simultaneous projects with minimal supervision and prioritize incoming work appropriately.
  • Required: In-depth knowledge of Global Health Authority regulations, quality systems principles and applications to the pharmaceutical industry.
  • Required: Has a proven track record of working across the network to find common solutions and drive positive impact and benefits for patients.
  • Required: Strong understanding of performance/health program monitoring and data quality assurance principles.
  • Required: Ability to communicate and collaborate with employees and management at all levels and through various formats (e.g. presentations, written proposals, reports, correspondence, lead meetings, face-to-face dialogue).
  • Required: Proficiency in data analytics and advanced analytics tools.

Education

  • Required: Bachelor's degree in pharmaceutical sciences, engineering, biology, or related disciplines.

Additional Requirements

  • Travel: Ability to travel to visit customers, patients or business partners and to attend meetings as directed (essential for field-based and remote-by-design roles).