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Director, Industrial Launch Leader Careflux

Fresenius Medical Care

Ogden, UTOnsitePosted 31 days ago
Full TimeDirector & AboveManufacturing & CMCHealthcare Provider
Original posting ↗

Summary

The Director, Careflux Industrial Launch Leader will lead the end-to-end NPI product development cycle from concept, design freeze through manufacturing transfer, qualification, ramp up and ensure reliable, high-yield commercial production. Together with the Product development and Manufacturing and Supply Chain representatives (MSC). The Director owns Design Transfer and industrial Ramp-Up phase, ensuring qualified machinery, supply chain capacity, and trained personnel required to meet volume targets.

Job description

Principal Duties and Responsibilities

The Director will lead the program to make it a successful launch to market from Industry readiness prospective by working with multiple workstreams as mentioned below.

  • Responsible for Design Verification & Validation, and Design Transfer preparation
  • Ensure entire product portfolio and all its variants are verified, validated for all dialysis platforms and ecosystems for commercial launch.
  • Secure product quality and long-term robustness early by ensuring they are thoroughly verified during formal verification testing phases.
  • Drive early, proactive alignment between the Vertical, Manufacturing Supply Chain (MSC), and Supplier Quality Readiness (SQR) to ensure manufacturing requirements and design for manufacturability/assembly considerations are incorporated early enough in product development to minimize industrialization risk prior to the MR2 milestone and confirm product manufacturability prior to the MR3 milestone.
  • Establish clear roles and responsibilities across engineering and operations teams throughout the entire design verification and transfer.
  • Ensure product quality performance by mitigating manufacturing variability during the production ramp-up phase.
  • Ensure rigorous production process validations (IQ/OQ/PQ) on time, scaling them precisely for each planned capacity step.
  • Ensure seamless transfer of validated production processes, technical product knowledge, and manufacturing risk mitigations across different manufacturing facilities and global production sites.
  • Evaluate supplier selection and technical capability with a view to implementing strategic single- or dual-sourcing risk mitigations.
  • Ensure part qualification and secure formal approval from FME teams to supply parts via a signed Part Submission Warrant (PSW).
  • Ensure supplier target cpk, scrap rates, and production yield are achieved.
  • Validate that suppliers have the installed equipment and scheduled shifts required to hit capacity targets, proving readiness through successful Overall Equipment Effectiveness (OEE) trial runs
  • Confirms the entire product portfolio and all its variants have appropriate regulatory clearances for commercial release and launch.
  • Drive end-to-end demand, capacity, and inventory planning across the complete value chain, connecting Sales, the Manufacturing Supply Chain (MSC), and external Suppliers to prevent shortages or excess inventory.

Experience and Required Skills

  • Minimum bachelor’s degree in biomedical engineering, Manufacturing Engineering or related engineering field. Advanced Degree preferred
  • 15 years of comparable business experience in program management, project management, and product innovation
  • 10 years in medical device industry leading complex cross-functional programs.
  • Experience in leading product development in multicomponent therapy systems.
  • Experience in leading industrialization of large volume medical device products.
  • Ability to drive program results by taking cross-functional team along and collaboration.
  • Ability to create, alignment, collaboration and accountability by leading global complex cross functional teams
  • Ability to solve complex, extensive, and sometimes contradictory information to solve problems effectively.
  • Have experience with converting complex launch requirements into clear plans, milestones, ownership and measurable outcomes
  • Effectively communicates with the cross-functional team and all levels in the organization
  • Must be creative and use most effective and efficient ways to get tasks done, with a focus on continuous improvement.
  • Must understand product development, manufacturing processes, equipment validation, quality and supply chain dependencies sufficiently to identify and resolve industrialization risks
  • Ability to manage risks quickly.
  • Strong business acumen applies knowledge about the business and market to drive the organization’s objectives.
  • Strong experience using data, risk and business priorities to make timely decisions and escalates critical issues.
  • Ability to build strong customer relationships and deliver customer-oriented solutions.
  • Ability to anticipate future opportunities and translates them into breakthrough strategies.

Requirements

  • Minimum bachelor’s degree in biomedical engineering, Manufacturing Engineering or related engineering field
  • 15 years of comparable business experience in program management, project management, and product innovation
  • 10 years in medical device industry leading complex cross-functional programs
  • Experience in leading product development in multicomponent therapy systems
  • Experience in leading industrialization of large volume medical device products
  • Ability to drive program results by taking cross-functional team along and collaboration
  • Ability to create, alignment, collaboration and accountability by leading global complex cross functional teams
  • Ability to solve complex, extensive, and sometimes contradictory information to solve problems effectively
  • Have experience with converting complex launch requirements into clear plans, milestones, ownership and measurable outcomes
  • Effectively communicates with the cross-functional team and all levels in the organization
  • Must be creative and use most effective and efficient ways to get tasks done, with a focus on continuous improvement
  • Must understand product development, manufacturing processes, equipment validation, quality and supply chain dependencies sufficiently to identify and resolve industrialization risks
  • Ability to manage risks quickly
  • Strong business acumen applies knowledge about the business and market to drive the organization’s objectives
  • Strong experience using data, risk and business priorities to make timely decisions and escalates critical issues
  • Ability to build strong customer relationships and deliver customer-oriented solutions
  • Ability to anticipate future opportunities and translates them into breakthrough strategies

Company overview

Fresenius Medical Care AG & Co. KGaA is the world's leading provider of products and services for individuals with renal diseases, serving as a global healthcare company specializing in kidney dialysis treatment. Founded in 1996 and headquartered in Bad Homburg, Germany with North American operations based in Waltham, Massachusetts, the company operates an extensive network of 4,171 outpatient dialysis centers across approximately 50 countries, serving over 345,000 dialysis patients worldwide. As the clear market leader in dialysis services, Fresenius Medical Care holds a dominant 38% market share of the dialysis market in the United States. The company provides comprehensive renal care solutions including hemodialysis machines, dialyzers, peritoneal dialysis solutions, and related medical devices through its 42 production sites globally. With approximately 128,000 employees, Fresenius Medical Care focuses on improving patients' quality of life through innovative technologies and therapies for end-stage renal disease treatment, offering both in-center and home dialysis options while maintaining a strong commitment to value-based care and patient well-being.

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