Work Flexibility: HybridWhat You Will DO:Having strong communication, analytical, & problem-solving skillsShould be Goal oriented with a strong sense of responsibility & ability to work with cross-functional teamsResponsible for managing high performance team of individuals to create world class medical devices.Develop Individual Development plans and conduct staffing reviews.Setting up team’s KRAs and identifying the training needs based on Individual Development plan.Review meetings with the team to monitor progress of projects and provide guidance, develop contingent plans, and arrange resources as needed.Align dedicated and shared resources cross-functionally to optimize to ensure achievement of business results, acquire and develop middle to junior level resources as needed, manage pipeline.Communicating frequently across all project disciplines to ensure project team and senior management are aware of upcoming milestones and risks/issues.Align dedicated and shared resources cross-functionally to optimize to ensure achievement of business results, acquire and develop middle to junior level resources as needed, manage pipeline and contribute to absorption of new technologies, processes and methods by making them part of own team's deliveryPlan and compliant to Quality Management System and Design Controls.Communicating frequently across all project disciplines to ensure project team and senior management are aware of upcoming milestones and risks/issues.Compliance to Quality Management System and Design Controls.What You Will NeedBasic Qualification:Experience: 11-14 years of technical & people management roles3 -5 years of people management experience of team size of 10 preferably.Product development experience in a regulated environment like medical devices, Aerospace etc.Must have led R&D teams for product development & testing. Experience of project and product life cycle is must.Good Experience in project management principles and methodologies.4+ years of experience of managing budgets and justifying resource needs to senior leaders and finance partners.BE/B.Tech/ME/M. Tech in Electronics/ Electrical/Mechanical EngineeringPreferred Qualification:Should have good understanding & knowledge of Mechanical competencyKnowledge & understanding of Mechanical design/ Analysis experience with US FDA quality regulations 21CFR part 820ISO 13485 standardsExperience in working in a government-regulated industryTravel Percentage: 10%
