Global Medical Devices Program Leader

Sterling-Industries-4; Texas Charter Township (MI); On-site; USD 75,000 - 115,000; Full time

Job summary

Sterling-Industries-4 seeks a seasoned Program Manager Lead to oversee a portfolio of programs and projects in the medical devices sector. You will guide program managers, drive execution, and ensure alignment with strategic goals while managing scope, schedule, and budget.

The role demands deep knowledge of program and project management methodologies, design controls, risk management, and regulatory requirements (FDA/ISO 13485).

Qualifications

• Bachelor’s degree in business administration, Engineering, or related field.
• 10+ years in program and project management, with at least 3 years in a leadership role in medical devices.
• Strong leadership, communication, and interpersonal skills.
• Experience from concept to commercialization in medical devices; FDA/ISO knowledge.

Responsibilities

• Lead and manage a portfolio of programs and projects, overseeing program managers and project teams.
• Develop and implement comprehensive program plans, monitor performance, risks, and budgets.
• Establish and enforce program management procedures for consistency and efficiency.
• Mentor and develop team members, set goals, and conduct regular performance evaluations.

Skills

Leadership

Project management

Regulatory knowledge

Design controls

Risk management

Validation processes

Communication

Multitasking

MS Project

Data-driven decisions

Stakeholder management

Education

Bachelor’s degree in business administration, Engineering, or related field

Tools

MS Project

Job description

Sterling-Industries-4 seeks a seasoned Program Manager Lead to oversee a portfolio of programs and projects in the medical devices sector. You will guide program managers, drive execution, and ensure alignment with strategic goals while managing scope, schedule, and budget.

The role demands deep knowledge of program and project management methodologies, design controls, risk management, and regulatory requirements (FDA/ISO 13485).