Group Manager R&D LCM

Full Time Manager Level 8+ years

Posted 4 weeks ago

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About This Role

Lead a team of individual contributors to manage product lifecycle management (LCM) activities for the DePuy Synthes Trauma/CMF team, ensuring product compliance and supporting in-market needs. This role involves balancing quality, speed, cost, and resource allocation while collaborating with strategic marketing and cross-functional teams.

Responsibilities

  • Lead a team of individual contributors in the delivery of projects taking product through product life-cycle-management (LCM) after commercialization
  • Provide in-market support, balancing requirements of quality, speed, cost and resource allocation
  • Ensure products are compliant with industry requirements, standards and regulations
  • Collaborate with strategic and commercial marketing on product improvements, harmonizations and/or strategic projects and programs to efficiently manage Trauma/CMF product portfolio
  • Accountable for global Trauma/CMF R&D Business Continuity projects and efforts
  • Serve as Global DRI for timeliness of all Business Continuity related LCM tasks and projects
  • Investigate and suggest improvements in business processes and product manufacturing in areas of quality, service, growth and values
  • Work with value streams, worldwide manufacturing facilities and external partners to analyze investment requirements, development timing, market potential and return on investment related to the defined program
  • Manage a subset of budget for the department including human resources, capital equipment, and general expenses
  • Set business metrics for the team and provide performance feedback to employees
  • Use expertise to improve operational efficiencies and meet compliance requirements
  • Support the development of a global regulatory strategy to ensure compliance in all regions
  • Support regional needs for technical product registration issues in collaboration with RA teams
  • Maintain knowledge of competitive landscape and scientific developments related to their functional area
  • Plan, conduct and direct research, development or engineering assignments
  • Perform other special projects and functions as assigned

Requirements

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or equivalent
  • Minimum of 8 years of relevant experience (or Master's degree with 5 years)
  • Minimum of 5 years of experience as a technical leader and contributor
  • Minimum of 5 years’ experience in R&D and/or product /project management
  • Solid understanding of market planning and development, forecasting, financial analysis/budgeting and general market management
  • Knowledge and experience with product new developments and their introduction processes
  • Experience in medical device industry
  • Knowledge of Design Controls

Qualifications

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or equivalent
  • Minimum of 8 years of relevant experience with a Bachelor's degree, or 5 years with a Master's degree; minimum of 5 years as a technical leader and contributor; minimum of 3 years of supervisory/managerial experience preferred; minimum of 5 years’ experience in R&D and/or product/project management

Nice to Have

  • Master’s degree
  • Minimum of 3 years of supervisory/managerial experience
  • Experience in coaching direct reports
  • Orthopaedics trauma experience (product knowledge and clinical expertise in Trauma and CMF procedures)
  • Proficient in all compliance aspects of medical device management
  • Well versed in US FDA and EU MDD/MDR requirements
  • Thorough knowledge of related disciplines, precision metal machining and manufacturing processes
  • Experience in leading international technical teams (US, EU, India)
  • Excellent communication and interaction skills with the ability to lead across a matrix organization
  • Ability to provide clear communication to a broad leadership team
  • Ability to motivate and build a team
  • Ability to manage interdisciplinary teams with demonstrated delegating skills
  • Ability to break down barriers and remove roadblocks to resolve risks while effectively building consensus across the organization
  • Utilization of Project Management Excellence, Design Excellence, and Process Excellence tools
  • Strong initiative and follow through in executing project responsibilities, overcoming obstacles and balancing multiple priorities effectively through strong technical and/or project leadership experience
  • Ability to review and critically assess patents and other forms of intellectual property

Skills

Process Excellence * Design Controls * R&D Engineering * Project Management Excellence * Design Excellence *

* Required skills

About Johnson & Johnson MedTech

Johnson & Johnson MedTech is revolutionizing healthcare innovation to prevent, treat, and cure complex diseases with smarter, less invasive, and personalized solutions, focusing on cardiovascular health.

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