Abbott Laboratories
R&D Project Manager
Abbott Laboratories, Alameda, California, United States, 94501
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.The OpportunityWe are searching for an R&D Project Manager to join our dynamic team. We are helping people with Diabetes lead healthier, happier lives. As a global leader in diabetes care, Abbott is constantly working to deliver the highest quality products and unwavering support to our customers.This position manages programs of small to medium scope, or a significant subsection of a large program. As an R&D Project Manager, you will be expected to lead cross-functional teams to develop and execute strategies for new product development and successful commercialization. In this role you will manage matrixed resources to ensure programs meet their agreed upon milestones and deliverables, represent the program to the organization and report core team progress, program recommendations, risks, and resolutions of issues to senior leadership.This is an
onsite opportunity
in Alameda, CA or Milpitas, CA.What you’ll work on:Lead cross-functional teams through project planning exercises to develop detailed schedules and integrated project plans.Utilize project scheduling software to plan and track tasks using tools such as MS Project and JIRA. Work with appropriate staff to understand tasks necessary to complete project.Communicate with all levels of the organization to represent the objectives, risks, and needs for the program.Lead activities across numerous functions to meet the objectives of a given program including scope and schedule.Establish and maintain the program and product Design History File in partnership with the Program Director and fellow core team members.Direct project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans.Develop plans with core members to eliminate and/or mitigate risk. If risks cannot be mitigated within the core team, determine appropriate means to communicate and elevate issues to appropriate individuals within the organization.In partnership with the Director, identify opportunities for improving overall performance of the program.Work closely with functional core team leaders and mentor when necessary.Assure project quality by using standard development methodologies and by working with the quality engineering team to develop and execute project quality plans.Resolve project issues by working with team members, project customers, and others as appropriate.Establish priorities of individual or project assignments. Select methods and techniques to lead a project to completion.Maintain a safe and professional work environment.Comply with worldwide medical device regulations including U.S. FDA, company policies and Good Manufacturing Practices.Required Qualifications:Bachelor’s Degree in Engineering or Science equivalent.5+ years of progressively responsible experience in engineering or related technical discipline.Demonstrated expertise in Project Management tools and processes.Successfully led several high complexity projects from beginning to end.Preferred Qualifications:PMP (Project Management Professional) qualification preferred.Experience in Project Management tools such as MS Project, Smartsheet, or JIRA.Requires strong leadership, influencing, and negotiation skills.Experience with software development of complex systems, including experience with web applications or App development projects or programs.Experience with Agile project management techniques.General knowledge of regulations and standards related to medical devices (e.g. FDA, ISO, QSR design controls) is ideal.Ability to travel approximately 10% of the time.The base pay for this position is $95,500.00 – $190,900.00. In specific locations, the pay range may vary from the range posted.
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onsite opportunity
in Alameda, CA or Milpitas, CA.What you’ll work on:Lead cross-functional teams through project planning exercises to develop detailed schedules and integrated project plans.Utilize project scheduling software to plan and track tasks using tools such as MS Project and JIRA. Work with appropriate staff to understand tasks necessary to complete project.Communicate with all levels of the organization to represent the objectives, risks, and needs for the program.Lead activities across numerous functions to meet the objectives of a given program including scope and schedule.Establish and maintain the program and product Design History File in partnership with the Program Director and fellow core team members.Direct project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans.Develop plans with core members to eliminate and/or mitigate risk. If risks cannot be mitigated within the core team, determine appropriate means to communicate and elevate issues to appropriate individuals within the organization.In partnership with the Director, identify opportunities for improving overall performance of the program.Work closely with functional core team leaders and mentor when necessary.Assure project quality by using standard development methodologies and by working with the quality engineering team to develop and execute project quality plans.Resolve project issues by working with team members, project customers, and others as appropriate.Establish priorities of individual or project assignments. Select methods and techniques to lead a project to completion.Maintain a safe and professional work environment.Comply with worldwide medical device regulations including U.S. FDA, company policies and Good Manufacturing Practices.Required Qualifications:Bachelor’s Degree in Engineering or Science equivalent.5+ years of progressively responsible experience in engineering or related technical discipline.Demonstrated expertise in Project Management tools and processes.Successfully led several high complexity projects from beginning to end.Preferred Qualifications:PMP (Project Management Professional) qualification preferred.Experience in Project Management tools such as MS Project, Smartsheet, or JIRA.Requires strong leadership, influencing, and negotiation skills.Experience with software development of complex systems, including experience with web applications or App development projects or programs.Experience with Agile project management techniques.General knowledge of regulations and standards related to medical devices (e.g. FDA, ISO, QSR design controls) is ideal.Ability to travel approximately 10% of the time.The base pay for this position is $95,500.00 – $190,900.00. In specific locations, the pay range may vary from the range posted.
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