VP Manufacturing

Benefits

Additional Information

We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Job Description The VP Manufacturing will lead two strategically critical BD manufacturing sites-El Paso, TX and selected operations in Sandy, UT-ensuring consistent, compliant, and high-performing operations aligned with BD's quality and operational standards. This role is accountable for delivering strong performance across safety, quality, delivery, and cost, while strengthening manufacturing processes, systems, and capabilities to support long-term business objectives. This leader ensures the sites operate with high levels of discipline, accountability, and operational rigor, while building a sustainable foundation for future performance and growth. Success in the role requires the ability to stabilize and continuously improve operations, embed robust manufacturing and quality practices, and develop strong leadership teams capable of sustaining results over time. Key Accountabilities 1. Manufacturing Leadership & Site Accountability Lead operations for El Paso and defined Sandy scope Own site performance across safety, quality, delivery, and cost (SQDC) Ensure safe, reliable, and compliant manufacturing operations Provide strong, visible leadership presence across both sites 2. Remediation Execution & CGMP Compliance Ensure all manufacturing processes, practices, and controls are fully compliant with CGMP (21 CFR 210/211). Drive disciplined and timely implementation of corrective actions, ensuring sustainable adherence to approved quality systems. Maintain continuous inspection readiness across both sites. 3. Manufacturing Excellence & Process Capability Stabilize and improve manufacturing performance, with focus on: Process capability and consistency Yield and defect reduction Reduction of variability and recurring deviations Implement robust, data-driven performance management, including: Trend analysis of defects, complaints and out-of-specification results End-to-end process monitoring and continuous improvement Ensure manufacturing processes are robust, repeatable, and compliant by design 4. Facility, Equipment & Capex Transformation Lead planning and execution of capital investments and facility upgrades required to meet pharmaceutical manufacturing standards Ensure manufacturing infrastructure, equipment, and environments are fit for compliant and reliable operations Partner with Engineering to establish strong equipment lifecycle and maintenance practices 5. Manufacturing-Engineering Integration Ensure strong integration between Manufacturing and Engineering to deliver: Robust process design Equipment reliability and uptime Sustainable compliance and performance Drive alignment on technical solutions that address root causes, not symptoms 6. Quality Culture & Operational Discipline Build and embed a "quality-first, right-first-time" culture across operations. Ensure that quality is fully integrated into daily manufacturing practices Reinforce strong execution discipline, documentation practices, and adherence to procedures at all levels of the organization. 7. Organization & Talent Leadership Assess and strengthen the capability of site leadership teams, particularly in: Root cause analysis and investigation rigor CGMP compliance and operational discipline Foster accountability, engagement, and performance in a demanding transformation context. Build a strong leadership bench capable of building a sustainable foundation for future performance and growth. 8. Stakeholder Management & Governance Ensure consistent standards, processes, and behaviors across both sites Partner with ISC, Quality, Engineering, and Supply Chain leadership to ensure alignment on priorities and resource allocation. Support regulatory interactions as appropriate in coordination with the Quality organization. Profile & Experience Required Experience 15+ years of manufacturing leadership experience in pharmaceutical, sterile, or highly regulated environments Demonstrated experience in FDA remediation / warning letter response Deep understanding of CGMP requirements and Manufacturing Process Control Proven track record of leading operational turnarounds or complex site transformations Leadership Capabilities A transformation-focused manufacturing leader who combines deep operational expertise with strong quality and compliance discipline, capable of stabilizing complex sites while building a sustainable, pharma-grade operating system. A leader who moves the organization from reactive firefighting to disciplined, sustainable performance, while bridging site execution