Tegra Medical

Engineering Project Manager

Tegra Medical Massachusetts, United States

Job Summary

The project manager is principally responsible for ensuring communication between the customer and the ME group to implement quality and productivity improvements in order to provide continuous improvement and enhanced customer experience. The ideal candidate will be accountable for overall project implementation by coordinating with cross functional teams to deliver manufacturing solutions for medical device production.

Role And Responsibilities

  • Lead cross-functional teams to ensure successful project execution with stakeholders including customers and internal teams to produce desired results and meet project milestones.
  • Effectively liaisons with Tegra customers, Engineering, Quality, Operations, and Materials teams to produce desired results and meet project milestones.
  • Drives supplier change requests externally and internally to support quality, production efficiency, and capacity improvements.
  • Successful planning, execution and delivery of continuous improvement and cost reduction projects after handover to serial production in a timely and cost-efficient manner.
  • Develops project plan and timeline, and holds team accountable to meeting established deliverables and deadlines.
  • Establishes regular project meetings involving Engineering, Quality, Operations and Customer Service
  • Principal point of contact between customer and production team.
  • Prepare project reports and presentations
  • Drive and maintain multiple project schedules and report status of projects on a regular basis, including schedule updates, resource allocation, and cost tracking.
  • Troubleshoot problems with production and take corrective action. Provide technical solutions as needed.
  • Identify and manage project risks
  • Ensure customer satisfaction throughout the project

Skill/Education/Experience

  • A Bachelor’s degree in Engineering and at least 2+ years engineering experience in a medical device manufacturing environment is required.
  • Must have experience with Class II & Class III finished medical devices.
  • Should have experience in managing product and process developments as well as the ability to lead programs that involve the design and manufacture of medical components and devices.
  • Must be a self-motivated individual possessing a proactive attitude with a strong sense of urgency and passion for the products.
  • Must have the ability to react quickly to changing requirements and priorities as well as have a keen interest in quickly learning and applying new skills.
  • Experience with Microsoft Project preferred.
  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Job function

    Project Management and Information Technology
  • Industries

    Medical Equipment Manufacturing

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