Stryker Corporation
Sr. Project Manager - Advanced Operations
Stryker Corporation, Jackson, Mississippi, United States,
Sr. Project Manager - Advanced Operations
ApplyLocations:
Gurugram, IndiaTime Type:
Full timePosted On:
Posted 5 Days AgoJob Requisition ID:
R525079Work Flexibility:
HybridResponsibilities:
Management of significant Engineering projects through PMO.Build and update planning, budgets, and workload of projects for which you will be responsible.Lead local steering meetings with the various departments of Design, Quality, Sourcing, and Operations.Represent the site's Advanced Operations team at global project meetings and communicate to the leaders of the different departments the progress and risks of the project.Bring your technical and industrial knowledge to help the project team create the best possible compromise through the application of techniques such as Design For Manufacturing & Inspection (DFM & I).Collaborate with the Advanced Operations teams of other sites (US, EU, etc.) to optimize the chances of success of projects.Participate in the development of the validation and verification plan of the manufacturing processes.Provide Technical leadership from an engineering perspective to the Advanced Operations Engineers.Structured problem solving and continuously improve the performance of the process.Train and mentor Engineers in the team.Interface with Materials Science, Design, and Quality Assurance departments to provide customers with a quality product in a timely manner.Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.Participate in PFMEA, Control Plan, SOP, Make Vs Buy, Design transfer milestones, and PPAP generation associated with product launches.Monitor and control progress of work ensuring sound application of engineering principles and the appropriate use of policies and procedures.All other duties as assigned.Skills Sets:
Proven Project Management skills through the delivery of business-critical projects.Strong communication and influencing skills with both internal and external stakeholders.Capable of working as part of a multi-disciplined team in an aggressive, dynamic, and results-motivated environment.Experience of GD&T, Process mapping, statistical methods, and process/product validations; PMP certification would prove beneficial.Commercially and financially aware.Confident and effective decision maker, with a proven project management ability to negotiate and influence others.High level of PC Skills required (MS Excel, Access, PowerPoint, MS Project, PowerApps, Power BI dashboards).Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams.Excellent attention to detail.Additional Skills:
Excellent analytical skills.Effective interpersonal communications skills.Good knowledge of project management.Education:
B.Tech./M.Tech./MS in Mechanical Engineering or relevant discipline or equivalent technical experience is required.Experience:
10+ years of relevant experience.Experience in an FDA regulated or regulated industry beneficial.Working experience/knowledge of ISO 13485 and other Medical devices regulations.Travel Percentage:
10%
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ApplyLocations:
Gurugram, IndiaTime Type:
Full timePosted On:
Posted 5 Days AgoJob Requisition ID:
R525079Work Flexibility:
HybridResponsibilities:
Management of significant Engineering projects through PMO.Build and update planning, budgets, and workload of projects for which you will be responsible.Lead local steering meetings with the various departments of Design, Quality, Sourcing, and Operations.Represent the site's Advanced Operations team at global project meetings and communicate to the leaders of the different departments the progress and risks of the project.Bring your technical and industrial knowledge to help the project team create the best possible compromise through the application of techniques such as Design For Manufacturing & Inspection (DFM & I).Collaborate with the Advanced Operations teams of other sites (US, EU, etc.) to optimize the chances of success of projects.Participate in the development of the validation and verification plan of the manufacturing processes.Provide Technical leadership from an engineering perspective to the Advanced Operations Engineers.Structured problem solving and continuously improve the performance of the process.Train and mentor Engineers in the team.Interface with Materials Science, Design, and Quality Assurance departments to provide customers with a quality product in a timely manner.Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.Participate in PFMEA, Control Plan, SOP, Make Vs Buy, Design transfer milestones, and PPAP generation associated with product launches.Monitor and control progress of work ensuring sound application of engineering principles and the appropriate use of policies and procedures.All other duties as assigned.Skills Sets:
Proven Project Management skills through the delivery of business-critical projects.Strong communication and influencing skills with both internal and external stakeholders.Capable of working as part of a multi-disciplined team in an aggressive, dynamic, and results-motivated environment.Experience of GD&T, Process mapping, statistical methods, and process/product validations; PMP certification would prove beneficial.Commercially and financially aware.Confident and effective decision maker, with a proven project management ability to negotiate and influence others.High level of PC Skills required (MS Excel, Access, PowerPoint, MS Project, PowerApps, Power BI dashboards).Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams.Excellent attention to detail.Additional Skills:
Excellent analytical skills.Effective interpersonal communications skills.Good knowledge of project management.Education:
B.Tech./M.Tech./MS in Mechanical Engineering or relevant discipline or equivalent technical experience is required.Experience:
10+ years of relevant experience.Experience in an FDA regulated or regulated industry beneficial.Working experience/knowledge of ISO 13485 and other Medical devices regulations.Travel Percentage:
10%
#J-18808-Ljbffr