Engineering Project Manager — Med Device Manufacturing

Tegra Medical; Franklin (MA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

On-the-job training

Competitive benefits

Paid time off

Tuition reimbursement

Job summary

Tega Medical seeks a Project Manager – Engineering to lead cross-functional engineering and manufacturing projects from initiation to closure in Franklin, MA. You will manage schedules, milestones, actions and risks while coordinating with Engineering, Quality, Operations and suppliers.

The role emphasizes root-cause analysis, corrective actions and continuous-improvement initiatives, with exposure to validation and production-transfer activities within a regulated medical-device setting.

Qualifications

• Bachelor's degree in engineering or related technical discipline required.
• 3–5 years engineering experience in manufacturing.
• Medical-device or regulated environment preferred.
• Strong project planning and organization skills.
• Experience leading cross-functional teams without direct authority.

Responsibilities

• Lead assigned projects from authorization through implementation and closure.
• Develop and maintain project schedules with milestones and due dates.
• Track actions, decisions, deliverables and open issues to completion.
• Coordinate cross-functional resources and supplier activities.
• Provide status reports and manage risks and changes.
• Support validation, qualification planning and production readiness.

Skills

Project management

Cross-functional leadership

Communication

Root-cause analysis

Manufacturing knowledge

MS Project

Excel

Lean/Six Sigma

Problem solving

Education

Bachelor's degree in engineering or related technical discipline

Tools

Microsoft Project

Excel

PowerPoint

Job description

Tega Medical seeks a Project Manager – Engineering to lead cross-functional engineering and manufacturing projects from initiation to closure in Franklin, MA. You will manage schedules, milestones, actions and risks while coordinating with Engineering, Quality, Operations and suppliers.

The role emphasizes root-cause analysis, corrective actions and continuous-improvement initiatives, with exposure to validation and production-transfer activities within a regulated medical-device setting.