Sr. Project Manager, Med Device (Irvine, CA - 5 Days/Wk)

Sr. Project Manager, Med Device (Irvine, CA - 5 Days/Wk)

22 Mar 2024
California, Irvine, 92602 Irvine USA

Sr. Project Manager, Med Device (Irvine, CA - 5 Days/Wk)

Job DescriptionA medical device company is seeking a Senior Project Manager to join their team at their Irvine, CA headquarters five days per week onsite. This PM will initiate, plan, execute, control, and manage all aspects of their projects to ensure ultimate project success. Responsibilities include but are not limited to: · Responsible for all areas of project management, focusing heavily on schedule management, performance metrics, resource management, risk management, communications management, technical involvement, process development, and process improvement. · Develops a high-level milestone plan for the program and manages program change in accordance with the change management plan to control scope, quality, schedule and cost. · Executes project plans (quality, risk, communication, staffing, etc.) and communicates program status and data to maintain accurate and current program information for the use of stakeholders. · Understands complex problems and drives the team to effective resolution when problems arise. · Leads core team meetings and other necessary meetings to drive best in class program execution; Continually improves quality and effectiveness of how meetings are run, decisions are made, and how work gets done. · Serves as a project and program management subject matter expert, including guiding and mentoring peers. · Lead any and all problem solving activity in association with project challenges or problems · Responsible for coordinating with, presenting to, and establishing rapport with all levels of project stakeholders including mid-level and executive functional and business unit leadership and corporate counterparts. · May serve as a representative of the Project Management Office (PMO) in working directly with client. · Establishes and maintains program stakeholder relationships, expectations, and communications, both internal and external to the organization.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com .   To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .Skills and Requirements· 2+ years of complex, hands-on experience Project Management in the Medical Device Field   o Experience managing not only existing products, but also new product development and (NPD) and new product innovation (NPI)   o Expert experience in creating and managing project schedules/budgets and prioritizing needs of different departments. Able to determine the critical path and account for all activities to complete a task/deliverable with the appropriate resources accounted for while utilizing good work breakdown structure. · 5+ years of hands on, complex engineering experience   o Experience through phases and gates of the design control process and functions including R&D, Quality, Manufacturing, Regulatory, Supply Chain, and customers. · Strong background in working within regulated industries · Strong collaboration documentation skills. This includes, but is not limited to; schedules, budgets, risk analyses, FMEAs, product requirements/inputs, design outputs, specifications, and test protocols/reports in support of Verification and Validation activities.Bachelor's Degree of Science in Biomedical/Mechanical/Electrical Engineering or in a related field nullWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HR@insightglobal.com.

Related jobs

Job Details

Jocancy Online Job Portal by jobSearchi.