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Role Summary
Responsible for end-to-end implementation of labelling activitiesu2014from requirement definition to production releaseu2014by collaborating with Project Managers, interpreting standards, and driving execution through cross-functional teams.
Key Responsibilities
Own end-to-end labelling lifecycle including requirement definition, design, verification/validation, and release to production
Collaborate with Project Managers to gather inputs and convert them into clear, structured, and compliant labelling requirements/design inputs
Interpret international standards and regulatory requirements and translate them into actionable label specifications
Plan and manage project timelines, deliverables, and resource execution, ensuring timely and high-quality output
Lead and coordinate cross-functional teams to drive label development (device, packaging, localization) and ensure consistency across all touchpoints (IFU, packaging, systems, symbol glossary)
Ensure all label requirements are complete, non-conflicting, testable, and compliant, and support verification/validation and market-specific needs
Manage design and regulatory changes, and drive continuous improvement by identifying better processes, tools, and implementation strategies
Key Requirements
Experience: 8u201310 years in labelling (preferably in medical devices or regulated industry)
Strong experience in:
End-to-end label lifecycle and requirement engineering
Working with Project Managers and cross-functional teams
Planning and managing project deliverables
Good understanding of:
International standards and regulatory requirements
Design control processes (Design Input u2192 Output u2192 Verification/Validation)
Proven ability to:
Lead teams and drive execution
Handle ambiguity and deliver solutions effectively
Behavioral Expectations
Ownership-driven and proactive mindset
Strong communication and stakeholder management skills
Open to new challenges and continuous improvement
Ability to drive process and strategy enhancements
Success Criteria
Seamless end-to-end execution with minimal rework
Accurate translation of standards into implementable requirements
On-time delivery aligned with project milestones
Continuous improvement in labelling quality and efficiency
Additional skills:
Labelling testing knowledge (Durability, Legibility and Environmental conditioning test)
Handling Zebra printers and LVS micro scanners
Creating barcodes compliant with GS1 standards
How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the companyu2019s facilities.
Field roles are most effectively done outside of the companyu2019s main facilities, generally at the customersu2019 or suppliersu2019 locations.
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About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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If youu2019re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .
#EOS
Job ID: 149913499
Skills:
Design control processes, Zebra printers, Requirement engineering, LVS micro scanners, End-to-end label lifecycle, International standards and regulatory requirements, Labelling testing knowledge
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