Job Description - R&D LCM Manager (2406220545W)
R&D LCM Manager - 2406220545W
Description Johnson & Johnson is currently seeking an R&D LCM (Lifecycle Management) Manager to join our team located in Ballybrit, Galway.
As part of the Johnson & Johnson family of companies, our Purpose is 'We blend heart, science and ingenuity to profoundly change the trajectory of health for humanity.'
Job Summary: Johnson & Johnson MedTech Neurovascular is recruiting for an R&D LCM Manager in Galway, Ireland.
The R&D LCM Manager will be responsible for managing design changes and sustaining activities, providing technical leadership and judgment to a team of engineers in the life cycle of a portfolio of devices to treat ischaemic and haemorrhage stroke. The R&D LCM Manager is also responsible for co-ordinating the activities of a multi-disciplinary team to ensure the successful completion of projects within planned timescales.
The responsibilities and the impact YOU will have: Responsible for R&D Lifecycle Management (LCM) activities for the J&J MedTech Neurovascular portfolio of products. R&D LCM team leadership, with responsibility for team structure, team development, and performance management. Identify critical project tasks, define project strategy, and set team priorities. Develop detailed project goals, plans, and budget. Report progress across the organisation. Organizing and prioritizing activities, including escalations, in collaboration with key functions and aligning on deliverables and timing. Manage interfaces between other functions, especially Supply Chain, Quality and Regulatory, to plan and support R&D activities required to support product lifecycle management. Support customer complaint technical investigations and site representative for review meetings. R&D point-person to review complaint trending, alert and action levels. Contribute to the cultural development of the R&D department by identifying opportunities for improvements in ways of working, and proactively implementing ideas for continuous improvement. Qualifications Degree in Mechanical or Biomedical Engineering or equivalent. Significant experience in medical device industry and project leadership with prior product development experience required. Deep understanding of Design Control Systems, CFR 820 and ISO 13485 quality system requirements. Proficiency in statistical techniques. Ability to assess multiple priorities for determination on best next action. Influential communicator with heightened sense on when to deploy constructive challenge tactics. Ability to set goals and motivate team to deliver on project targets. Excellent writing, presentation, and verbal communication skills essential. Location & Travel This role will be an onsite role based in Galway, Ireland with flexible work arrangements from time to time in agreement with management and per the J&J Flexible Work policy. As part of a global company, travel will be required from time to time, up to 15%. This is what awaits YOU: An opportunity to be part of a global market leader. A dynamic and inspiring working environment. Opportunities to work on challenging projects and assignments. Possibilities for further personal and professional development/education. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Primary Location Europe/Middle East/Africa-Ireland-Galway-Galway
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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