Senior Program Manager - Regulated Medical Devices

Integer Holdings; Plymouth (MN); On-site; USD 137,000 - 202,000; Full time

Job summary

Integer Holdings is seeking an experienced Project/Program Manager to lead complex, regulated product development and engineering initiatives. You will drive end-to-end project execution, coordinate with cross-functional teams, and ensure milestones, budgets, and quality requirements are met.

The role requires strong leadership, communication, and problem‑solving skills, with travel as needed to support customers and sites. Applicants with FDA/ISO regulatory exposure are preferred.

Qualifications

• Bachelor's degree in Engineering or related technical field preferred.
• 7+ years of experience, at least 4 in a regulated product environment like medical devices, pharmaceuticals, automotive, and aerospace in addition to 3 in a project management capacity having led multiple projects and project teams.
• Certification in Project/Program Management from an accredited institution preferred.

Responsibilities

• Manage end-to-end projects from inception through successful implementation and hand off.
• Set up and regularly update projects in the Oracle ERP system.
• Forecast projects and ensure adherence to budgets, milestones, and customer agreements.
• Coordinate across functions (marketing, quality, regulatory, design assurance, manufacturing) to deliver initiatives.
• Prepare status reports for management, customers, and suppliers as needed.
• Provide mentoring and training to associates within cross-functional teams.
• May manage 2–3 direct reports and support personal and professional development.

Skills

Team leadership

Coaching

Critical thinking

Communication

Organizational skills

Cross-functional collaboration

Conflict resolution

Education

Bachelor's degree in Engineering

Master's degree in business or technical field

PM certification

Tools

Oracle ERP

Job description

Integer Holdings is seeking an experienced Project/Program Manager to lead complex, regulated product development and engineering initiatives. You will drive end-to-end project execution, coordinate with cross-functional teams, and ensure milestones, budgets, and quality requirements are met.

The role requires strong leadership, communication, and problem‑solving skills, with travel as needed to support customers and sites. Applicants with FDA/ISO regulatory exposure are preferred.