Global Quality Programs Director, Medical Devices

Philips; Linwood (PA); On-site; USD 170,000 - 270,000; Full time

Benefits offered by this job

Total Rewards benefits

Job summary

Philips is seeking a Director, Quality Programs (PMO)‑Ambulatory Monitoring & Diagnostics to lead global quality programs aligned with FDA and international standards. The role requires strategic guidance, regulatory submission oversight, and cross‑functional collaboration across product development and manufacturing sites.

You will drive continuous improvement, manage budgets and risk, and ensure timely execution of quality initiatives with senior stakeholders.

Qualifications

• Minimum 10+ years’ experience leading full‑cycle, global Quality Programs in FDA regulated medical device environments.

Responsibilities

• Provide strategic guidance to managers on quality improvement and fostering a culture of quality excellence.
• Tackle complex issues by analyzing situations to drive effective solutions and align with organizational objectives.
• Oversee regulatory submission processes and harmonize guidelines across products and operations.
• Lead management reviews and ensure routine reporting on regulatory compliance activities.
• Assist succession planning, talent management and career development aligned with goals.

Skills

Quality leadership

Global PMO experience

Regulatory knowledge

Data analytics

Stakeholder management

Budgeting

Education

Bachelor's degree in Engineering/Quality/Life Sciences

Job description

Philips is seeking a Director, Quality Programs (PMO)‑Ambulatory Monitoring & Diagnostics to lead global quality programs aligned with FDA and international standards. The role requires strategic guidance, regulatory submission oversight, and cross‑functional collaboration across product development and manufacturing sites.

You will drive continuous improvement, manage budgets and risk, and ensure timely execution of quality initiatives with senior stakeholders.