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Becton Dickinson

Global medical devices, lab equipment supplier

Director, MLR Excellence & Digital Enablement

Business OperationsConfirmed live in the last 24 hours
Full-timeFranklin Lakes, NJ, USA

About the Job

Requirements

  • A bachelor's degree is required.
  • At least 10 years of experience in marketing or marketing operations within MedTech, pharmaceutical, biotechnology, or other regulated healthcare environments is required.
  • Direct experience in Medical, Legal, and Regulatory review, regulatory affairs, or compliant marketing operations is required.
  • A proven track record of improving promotional review efficiency, quality, and compliance outcomes is required.
  • Expertise in process mapping, workflow design, root cause analysis, and continuous improvement within compliance-driven processes is required.
  • Experience implementing technology and AI solutions within regulated marketing environments, including organizational change management to drive adoption and sustained impact, is required.
  • Experience designing, building, or deploying AI-enabled workflows, intelligent automations, assistants, or agents that deliver measurable business value, together with sound judgment regarding appropriate and effective AI use cases, is required.
  • A strong analytical mindset and the ability to leverage data to optimize processes, influence decision-making, and present recommendations to senior stakeholders are required.
  • Demonstrated success delivering both compliance and commercial business outcomes is required.

Responsibilities

  • Define and execute the MLR technology and process roadmap, aligning business requirements with regulatory and compliance objectives.
  • Lead implementation and continuous optimization of AI-enabled content review, automation, and workflow management solutions.
  • Establish and govern standardized MLR processes, operating procedures, metrics, and performance dashboards across business units and geographies.
  • Drive process harmonization, simplification, and continuous improvement to reduce cycle times while maintaining compliance and quality standards.
  • Partner with Regulatory, Legal, Medical, IT, and Marketing stakeholders to enhance end-to-end content approval workflows and user experience.
  • Use data analytics and process intelligence tools to identify bottlenecks, monitor performance, and accelerate review effectiveness.
  • Champion generative AI, machine learning, workflow automation, and digital collaboration platforms to modernize the MLR ecosystem.
  • Build organizational capabilities in digital fluency, AI adoption, process excellence, and change management.
  • Own BD’s global end-to-end MLR process standard across content review and approval, localization and translation, and in-region and in-country approval, including the associated operating documentation.
  • Establish autonomous approval in production for low-risk content categories, with rules, thresholds, audit trails, and signature handling agreed with Regulatory Affairs and operating across regions.
  • Achieve a 90% reduction in the overall approval timeline from content creation to in-market approval, measured against a published baseline.
  • Own standard operating procedures, cycle-time and quality metrics, dashboards that make rework visible to business-unit and regional leadership, and root-cause analysis of process time.
  • Drive regional adoption of the central capability instead of local equivalents.
  • Partner across Marketing, Legal, Regulatory, Medical, and Commercial teams as a global center-of-excellence leader, enabling consistent ways of working across businesses and regions.

Desired Qualifications

  • An MBA or advanced degree is preferred.
  • Hands-on expertise in Veeva PromoMats or a comparable promotional review system is preferred.

About the Company

Becton Dickinson

Global medical devices, lab equipment supplier

BD (Becton, Dickinson and Company) is a global medical technology company that designs, manufactures, and sells medical devices, laboratory equipment, and related services for hospitals, labs, clinicians, and biopharma partners. It operates in four segments: Medical Essentials (medication delivery and specimen management devices), Connected Care (medication management and advanced patient monitoring systems), BioPharma Systems (drug delivery systems for pharmaceutical partners), and Interventional (surgical, endovascular, urological, and critical care products). In addition to devices, BD offers connected software, analytics, clinical education, customer portals, and service programs to support its products. The company’s goal is to help healthcare providers improve patient outcomes by enabling safer and more efficient delivery of care through integrated devices, data, and services across the health ecosystem.

Company size
10,001+
Company stage
IPO
Headquarters
Franklin Lakes, NJ
Founded
1961

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