Sr. Project Manager

Title: Project ManagerLocation: Andover, MA (4 days onsite/ 1 day remote)Duration: 12+ Months Job ID: 98711102024Client: EmbectaPay Rate: $61.81/hr on W2Description:The Sr. Project Manager is responsible for leading cross-functional teams, in introducing of injection products that help people with diabetes live healthier lives. Scope includes R&D specific workstreams supporting major initiatives or major product development programs.Responsibilities:This position offers a unique opportunity to lead and manage a portfolio of projects that are critical to the continued viability of the business.Lead a cross-functional team comprised of R&D Change Managers and Engineers for coordinating projects which impact compliance, form/fit/function, cost savings, line extensions and other business opportunities across all plants, quality, and marketing. The program manager works at the interface of multiple stakeholders and will serve as a liaison between business leadership, functional management, and individual project leaders.Duties involve consolidating, prioritizing, resourcing, and monitoring progress of cross-functional projects.Drive project prioritization utilizing appropriate model / methodology and get consensus across functions to focus on projects that create value for the Business.Reports on the progress of the program with an agreed frequency on quality, status, time, and costs to senior management.Work with managers from different functions to ensure allocation of resources and discretionary spending is sufficient to achieve target completion dates. Work with individual project team members to ensure appropriate planning and rigor is maintained to ensure success of these projects. Additionally, help to implement and lead the use of a global portfolio management tool for cross-functional management.EXPERIENCE & EDUCATION: Must have a bachelor’s degree in a technical field, preferably in an engineering or scientific discipline, with at least five (5) years’ experience in engineering project management of Class II or III medical device projects.Experience with life cycle management of products designed for high volume manufacturingStrong demonstrated organizational leadership skills, interpersonal, influence, and conflict management skills. Solid technical and project management judgment, strong communication skills. Demonstrated experience in project planning, management, and budgeting with an orientation towards building and leading effective teams. Experience in managing multiple work streams and competing priorities. Experience in creating and monitoring metrics and reporting dashboards.Experience with, and thorough understanding of disciplined product development processes, regulatory, and quality requirements. Demonstrated ability to communicate concepts, ideas and knowledge effectively and clearly to other individuals and teams Experience with ISO requirements and GMP guidelines, FDA regulations, medical device design control, and manufacturing scale up processes KNOWLEDGE, SKILLS, AND ABILITIES: Technical Skills: Proficiency in tools, such as MS Project, Celoxis, Monday.comSoft Skills: Strong problem-solving skills, excellent communication abilities, and the ability to work effectively in a team environment.Certifications: Relevant certifications - PMP