Johnson & Johnson
Senior Project Manager
Johnson & Johnson, Danvers, Massachusetts, us, 01923
Description:
Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Sr. Project Manager located in Danvers, MA.Principal Duties and Responsibilities:Manage complex design and development projects focusing on novel hemodynamic support consoles.Establish design goals and specifications based on requirements and user needs.Transform clinical observations into new device concepts or approaches.Bring solutions to market by collaborating with an exceptional cross-functional team.Work with internal and external partners to ensure robust designs within an aggressive timeline.Develop and set interim goals and milestones to ensure overall project success.Address technical and programmatic risks, ensuring effective risk identification, assessment, and mitigation.Prepare and present design reviews to ensure the technical integrity of the product design.Prepare and present management reviews to effectively communicate cross-functionality the project issues, risks, and timing of the product.Work with engineering teams to ensure timely and complete design control deliverables.Suggest and contribute to initiatives that improve the Engineering Department’s operations and procedures.Qualifications:BS in Electrical, Biomedical Engineering or directly related scientific discipline.7+ years’ relevant experience leading and executing the coordination of programs/projects and the delivery of products in engineering/R&D teams. Exceptional project coordination skills while being able to multi-task and meet multiple project schedules on time.Successful completion of a medical device development project from concept to launch. Expert in understanding design controls and deliverables.Strong verbal and written communication, analytical/problem solving, negotiation, and interpersonal skills.Ability to understand and apply applicable FDA regulations and company operating procedures, processes, policies, and rules.Familiarity presenting on and explaining projects at all levels of the organization.Team oriented. Proven teamwork skills in a cross-functional engineering environment, ability to motivate and empower team members, set and manage expectations.Committed to being patients first and responsive to unmet needs.Experience and ability interacting with FDA and other regulatory agencies.Proficiency with project budgeting and forecasting, MS PowerPoint, Project Management software, MS Excel.10% Travel (project dependent).
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Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Sr. Project Manager located in Danvers, MA.Principal Duties and Responsibilities:Manage complex design and development projects focusing on novel hemodynamic support consoles.Establish design goals and specifications based on requirements and user needs.Transform clinical observations into new device concepts or approaches.Bring solutions to market by collaborating with an exceptional cross-functional team.Work with internal and external partners to ensure robust designs within an aggressive timeline.Develop and set interim goals and milestones to ensure overall project success.Address technical and programmatic risks, ensuring effective risk identification, assessment, and mitigation.Prepare and present design reviews to ensure the technical integrity of the product design.Prepare and present management reviews to effectively communicate cross-functionality the project issues, risks, and timing of the product.Work with engineering teams to ensure timely and complete design control deliverables.Suggest and contribute to initiatives that improve the Engineering Department’s operations and procedures.Qualifications:BS in Electrical, Biomedical Engineering or directly related scientific discipline.7+ years’ relevant experience leading and executing the coordination of programs/projects and the delivery of products in engineering/R&D teams. Exceptional project coordination skills while being able to multi-task and meet multiple project schedules on time.Successful completion of a medical device development project from concept to launch. Expert in understanding design controls and deliverables.Strong verbal and written communication, analytical/problem solving, negotiation, and interpersonal skills.Ability to understand and apply applicable FDA regulations and company operating procedures, processes, policies, and rules.Familiarity presenting on and explaining projects at all levels of the organization.Team oriented. Proven teamwork skills in a cross-functional engineering environment, ability to motivate and empower team members, set and manage expectations.Committed to being patients first and responsive to unmet needs.Experience and ability interacting with FDA and other regulatory agencies.Proficiency with project budgeting and forecasting, MS PowerPoint, Project Management software, MS Excel.10% Travel (project dependent).
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