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Tier-1 brand but senior, niche medical-device quality requirements moderate applicant density.
High; medical-device QMS, ISO 13485 and FDA regulatory expertise is industry-specific.
Strict due to explicit 15+ years, certifications, and regulatory (ISO, FDA) QMS requirements.
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Owns and directs programs with multiple interdependent projects to deliver intended benefits aligned with Quality Operation’s Strategy.
Develops and manages program plans, schedules, and deliverables with strict compliance to PSQ policies and standards.
Leads cross-functional and multi-site project teams to achieve medium/high complexity programs with financial impact over €10M, ensuring risk mitigation and program health.
Bachelor’s or master’s degree in life sciences, business administration, or engineering.
Minimum 15 years of relevant project/program management experience, including 5+ years in program management roles.
Certifications in Philips Project Management Practitioner/Expert/Master or equivalents like PMI, PMBoK, SAFe.
On-site presence required with full-time presence in the company’s facilities.
Expertise in quality management systems including ISO 13485, FDA 21 CFR Part 820, QMS, CAPA, risk management (ISO 14971), and regulatory frameworks.
Proven success managing complex, multi-site programs (>2-3 years duration or >€10M financial impact) using standardized project management methodologies.
Ability to engage senior management, influence policy, innovate program capabilities, and operate across multiple business functions.