Group Manager R&D LCM
Johnson & Johnson MedTech
West Chester, PA
Full Time
Manager Level
8+ years
Posted 4 weeks ago
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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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