KMC Systems, Inc.

Sr Program Manager – Medical Device Development REF2229J

KMC Systems, Inc. Merrimack, NH
No longer accepting applications

Job Description

The Program Manager II will focus specifically on R&D activities. This Program Manager will manage ongoing development efforts for new product design, focused on innovative solutions that complement KMC Systems core technologies. This encompasses direction of a disciplined engineering team, monitoring all aspects of program performance and authority to make decisions to assure the success of the project from inception to completion. This position involves the application of complex electronics, optics, mechanisms and software to advanced medical instruments. Oversees a team and interacts with quality, manufacturing, materials, marketing, and finance departments. Acts as a point contact with internal customers. Assures customer satisfaction on project schedules, instrument technical performance and program cost.

  • Manage the planning and execution of engineering projects, focused on innovative solutions that complement KMC Systems core technologies.
  • Interface regularly with Product Marketing, R&D Continuation Engineering, Supply Chain, and Procurement Engineering functional areas
  • Create and maintain product portfolio roadmap detailing the sustaining efforts required over the lifecycle of each product.
  • Provide leadership to engineering staff regarding project prioritization and execution.
  • Provide project management for sustaining projects.
  • Implement and manage resource planning and project management tools.
  • Coordinate, select and schedule project engineers for Operations projects.
  • Support continuing production, process development and new product introductions.
  • Participate in cross-functional teams.
  • Prepare technical reports, analysis, recommendations and presentations reflecting the status and results of projects in progress on a regular basis.
  • Drive continuous improvement of engineering technical capabilities.
  • Monitor and evaluate project and department progress and results.
  • Ensure a safe work environment consistent with OSHA requirements
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Job function

    Project Management and Information Technology
  • Industries

    Medical Equipment Manufacturing

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