$45 - $49 per hour (W2) We are seeking a "Project Engineer" to join one of our leading healthcare clients. Job Description Lead the planning, execution, and implementation of sustaining engineering, supplier change, design change, and continuous improvement projects in accordance with client project management methodologies. Independently manage project scope, schedules, milestones, risks, action items, and deliverables to ensure projects are completed on time and aligned with business objectives. Lead cross-functional project teams including R&D, Operations, Manufacturing, Quality, Regulatory Affairs, Supply Chain, Packaging, Labeling, Technical Publications, and other functional stakeholders. Facilitate project team meetings, drive accountability for project deliverables, and ensure alignment across functional groups. Identify project risks, issues, and dependencies; develop mitigation strategies and coordinate resolution activities. Partner with functional team members and managers to support project resource planning, priority setting, and issue resolution. Develop and maintain project plans, schedules, risk registers, action-item logs, and project documentation. Communicate project status, risks, key decisions, and recommendations to project stakeholders and management. Support project governance activities through development of project metrics, dashboards, status reports, and leadership communications. Lead assigned workstreams within larger strategic initiatives while ensuring alignment with overall project objectives and timelines. Execute project support activities including ownership of Change Orders (COs), procurement coordination, project reporting, and maintenance of project tracking systems. Utilize Windchill, SAP, Planview, Ariba, and other business systems to support project execution, reporting, portfolio visibility, and procurement activities. Partner with suppliers and external stakeholders to support project implementation activities and issue resolution. Ensure project activities comply with FDA regulations, applicable quality system requirements, Company policies, and Business Unit operating procedures. Required Qualifications Bachelor's degree in engineering or related field Minimum 5 years of medical device experience in R&D, Manufacturing and/or Quality Engineering Excellent verbal and written communication skills, with the ability to communicate to all levels of the organization as well as suppliers and consultants Experience collaborating with cross-functional team members in a geographically diverse, matrixed organization Demonstrated experience leading cross-functional projects or project workstreams Ability to initiate, prioritize, and coordinate multiple tasks simultaneously Proficient in MS Word, Excel, PowerPoint, and Project Preferred Qualifications Master's degree in a technical or business field PMP, CAPM, or other project management certification Familiarity with Windchill (Product Lifecycle Management System), SAP (Enterprise Resource Management software), Planview (Project and Portfolio Management software), and Ariba (Purchasing system) Experience leading sustaining engineering, supplier change, or operations projects within a regulated industry Experience supporting product lifecycle management activities, including Change Orders (COs), documentation updates, supplier changes, and design transfer activities Experience developing project metrics, dashboards, and leadership communications Experience working in a regulated industry such as medical devices, pharmaceuticals, aerospace, or manufacturing Knowledge of continuous improvement methodologies such as Lean, Six Sigma, or Kaizen We are looking for the candidate who are eligible to work with any employers without sponsorship . If you're interested, please click "Apply" button.
