Lead Internal Service Programs & PMO

Philips Iberica SAU; Plymouth (MN); On-site; USD 123,000 - 195,000; Full time

Benefits offered by this job

PTO

Total Rewards benefits

401k match

Job summary

Philips is seeking a Service Internal Project Manager to lead critical service programs and projects, partnering with stakeholders to standardize processes and address IGTD needs. You will mentor junior project managers and service engineers while driving process improvements and PMO development.

We emphasize in-person collaboration with onsite presence three days per week. The role requires extensive experience in project/program management, preferably in a medical device regulated environment,

Qualifications

• 8+ years of experience with Bachelor's or 5+ years with Master's in Project Management, Program Management, Agile Methodology or equivalent.
• Medical Device (regulated environment) preferred.
• Office-based role with in-person collaboration for this position.

Responsibilities

• Lead high-impact service programs and projects, managing scope, budget, resources, timelines, risks, and quality.
• Lead cross-functional teams through ERP/CRM implementation and integration across multiple projects.
• Build relationships across functions and business units using communication and stakeholder management to drive alignment.
• Identify risks and opportunities for process improvement and deliver practical solutions.
• Drive best practices in program and project management within a complex enterprise.

Skills

Stakeholder management

Cross-functional leadership

PMO development

Process improvement

Analytics

Education

Bachelor's degree in a related field

Master's degree in Project Management or related field

Tools

ERP systems

CRM systems

Job description

Philips is seeking a Service Internal Project Manager to lead critical service programs and projects, partnering with stakeholders to standardize processes and address IGTD needs. You will mentor junior project managers and service engineers while driving process improvements and PMO development.

We emphasize in-person collaboration with onsite presence three days per week. The role requires extensive experience in project/program management, preferably in a medical device regulated environment,