Arthrex, Inc. is a global medical device company leader in new product development and medical education in orthopedics. We are actively searching for an Engineering Project Manager to strategically manage new product development projects and existing product improvement projects within our Packaging team. The ideal candidate will build relationships with key stakeholders and internal departments to drive fast-paced project success by utilizing effective communication, planning and risk management tools. Excellent interpersonal, organizational, and leadership skills, two years or more of post graduate, related project management experience, and a bachelor's degree in Engineering are essential for this position. This position will be located at our Naples, FL campus. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.
Essential Duties and Responsibilities:
Manages subsidiary-based and global projects/programs within the scope of the new product development
Develops project objectives by reviewing project proposals and business plans, conferring with senior management and key stakeholders
Determines project schedule by studying project plan and specifications, calculates time requirements, identifying and sequencing project elements and discreet tasks
Maintains project schedule by monitoring project progress, coordinating activities, and resolving risks or obstacles
Determines project responsibilities by identifying project phases and elements, requesting and allocating resources as necessary
Ensure design history file facilitation for assigned projects, adhering to Arthrex design control procedures.
Ensure project progresses within the boundaries of the approved scope. Manage the scope of the project and guarantee scope changes are properly documented and implemented.
Identify opportunities for improvement within the Project Management Governance and Design Control Process to improve speed to market.
Monitor resource capacity within the New Product Development groups and cross-functional resources and communicate constraints or needs to senior management.
Help facilitate, with interdepartmental managers, the availability, assignment, and accountability of downstream resources and technology
Help facilitate project, program and portfolio status to management and key stakeholders with applicable metrics and project constraints.
Education/Experience:
BS Engineering required. Packaging, BioMedical, or Mechanical preferred
2 years relevant experience
Skills:
Ability to effectively communicate project planning requirements, including task elucidation, duration, and resource requirements.
Strong strategic thinker, excellent collaboration and communication skills, careful attention to detail
Ability to balance business and technical risks while remaining compliant with internal systems.
Awareness of full life cycle development of medical devices, which includes initiation, design, development, execution, and sustaining.
Working knowledge of medical device regulations and associated quality systems, particularly design controls and risk management.
Manufacturing process knowledge preferred.
Awareness orthopedic surgery principles, theories, and products preferred
Knowledgeable of FDA and ISO guidelines for the development of medical devices preferred.
Strong communication skills and accountability to project deliverable timing and budgets required.
Ability to confidently lead complex, cross functional teams independently
Demonstrable bias for action
Strong desire and proven ability to learn quickly
Continuously seeking ways to improve complex systems of people and process, while eliminating waste.
All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.
