Project Manager R&D New Product Introduction – Intraocular Lenses (IOL)

Johnson & Johnson Vision Groningen is specialized in the development, improvement, and manufacturing of state-of-the-art surgical ophthalmic products, mainly intraocular lenses. The facility consists of small and integrated Research, Development and Manufacturing teams that have strong track records.

We are searching for the best talent for Project Manager R&D New Product Introduction – Intraocular Lenses (IOL).

Purpose: The Project Manager R&D New Product Introduction – Intraocular Lenses (IOL) will be responsible for the end-to-end management of new intraocular lens development projects, from early concept and feasibility through design, industrialization, regulatory approval, and market introduction.

This role provides leadership to virtual, cross-functional project teams operating, with frequent collaboration with stakeholders in a.o. the United States. The Project Manager acts as the central integrator between R&D, Regulatory Affairs, Quality, Operations, Clinical, Marketing, and external partners to ensure successful delivery of complex medical device programs.

About Vision

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

You will be responsible for:

• Own and drive end-to-end NPI projects for intraocular lenses (project plans, schedules, budgets, and resource needs).
• Lead virtual cross-functional teams across different time zones.
• Ensure full compliance with Design Control, Risk Management, and Change Management requirements.
• Oversee creation, maintenance, and approval of project documentation throughout the development lifecycle.
• Ensure adherence to GMP, QSR, ISO 13485, and applicable internal procedures.
• Support regulatory submission activities in close collaboration with Regulatory Affairs and Quality.
• Maintain clear and consistent communication with global stakeholders, including regular interaction with EU, US and APAC based teams.
• Facilitate effective governance, escalation, and decision-making within a matrix organization.

Qualifications / Requirements:

• Bachelor’s or master’s degree in engineering, Life Sciences, Physics, Optics, or a related technical discipline.
• 5–8 years of relevant project management experience in a regulated, technology-driven environment.
• Demonstrated experience managing medical device NPI projects, preferably involving implantable or ophthalmic products.
• Proven ability to lead global, virtual project teams across multiple time zones.
• Strong knowledge of Project Management, Design Control, and Risk Management.
• Working knowledge of GMP, QSR, ISO 13485, and medical device development processes.
• High proficiency in MS Project & MS Office (Excel, PowerPoint, Word) for project planning, reporting, and stakeholder communication.
• Experience with project management tools and structured reporting methodologies.
• Fluent in English; Dutch is an advantage.
• Availability to work 100% on site job, in Groningen (The Netherlands) with occasional international travels.

Required Skills:

Business Process Management (BPM), Communication, Critical Thinking, Cross-Functional Collaboration, Problem Solving

Preferred Skills:

Agility Jumps, Business Alignment, Coaching, Collaborating, Continuous Improvement, Operational Excellence, Performance Measurement, Process Control, Process Improvements, Project Management Methodology (PMM), Project Management Office (PMO), Project Reporting, Project Schedule, Quality Control (QC), Research and Development, Tactical Planning, Technical Credibility

Location: Groningen, NL