The Randstad companies are responsible for finding talent to provide services for Philips. If you are selected to provide services to Philips, you will be employed by Randstad and will not be an employee of Philips.

Philips

Senior Quality Program Manager

Posted Mar 17, 2026
Project ID: PHIAJP00003623
Location
Latham
Hours/week
40 hrs/week
Timeline
6 months
Starts: Feb 19, 2026
Ends: Sep 1, 2026
Payrate range
85 - 95 $/hr

Job Title Senior Quality Program Manager

Job Responsibilities

  • Program Management: Manages multi-site or medium/high complex programs over 2–3 years or financial impact of ? €10M. Innovates and elevates program and portfolio capabilities.

  • Strategic Leadership: Provides strategy and direction for major functional areas through assessment of intangible variables and identification of fundamental issues.

  • Risk Management: Encourages balanced risk-taking and mitigates risks to maintain program health. Familiarity with risk management standards such as ISO 14971.

  • Quality Compliance: Utilizes quality principles (QMS, CAPA, Nonconformance, Calibration, PM, Process and Production Controls, Warehousing, etc.) within project management.

  • Stakeholder Engagement: Interacts internally and externally with senior-level management; negotiates extremely critical matters including influencing policymaking.

  • Methodology & Coaching: Expertise in applying PM standards (PMI, PMBoK, SAFe) and coaching others in project/program management processes.

  • Operational Execution: Uses detailed knowledge of company operations to promote innovative concepts and develop resolutions to critical issues. On-site presence required.


Requirements

  • Education: Bachelor’s or Master’s degree in life sciences, business administration, or engineering.

  • Experience: 5–10 years of relevant working experience, including all aspects of project development and execution. 5+ years of program management experience with a demonstrated record of success.

  • Certification: Philips Project Management Practitioner/Expert/Master or equivalent (PMI, PMBoK, SAFe).

  • Compliance Knowledge: Knowledge of ISO 13485 and FDA 21 CFR Part 820 for medical devices; comprehensive training in Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).

Preferred Skills

  • Project/Program Management (PMI, PMBoK, SAFe)

  • Quality Management Systems (QMS)

  • CAPA Processes

  • ISO 13485 & FDA 21 CFR Part 820

  • ISO 14971 Risk Management

  • Strategic Planning & Policy Influencing

  • Negotiation & Senior Stakeholder Management

  • Innovative Problem Solving

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