Global NPI Project Manager – Intraocular Lenses

Johnson & Johnson; Netherlands; On-site; EUR 90,000 - 120,000; Full time

Job summary

360Pharma is seeking a Project Manager for New Product Introduction of intraocular lenses (IOL). You will lead end-to-end NPI programs, coordinating R&D, Regulatory, Quality, and Supply Chain across time zones and with US teams. The role requires strong PM skills, design control, risk management, and GMP/QSR/ISO13485 knowledge.

On-site work in Groningen, NL with occasional international travel is expected. Fluent English is required and Dutch is an advantage.

Qualifications

• Experience leading medical device NPI projects or equivalent regulated environment.
• Strong knowledge of Design Control and Risk Management principles.
• Working knowledge of GMP, QSR, ISO 13485 and device development processes.
• Proven ability to lead cross‑functional teams across multiple time zones.

Responsibilities

• Own end-to-end NPI projects for intraocular lenses, including plans, schedules, budgets and resource planning.
• Lead virtual, cross‑functional teams across multiple time zones.
• Ensure compliance with Design Control, Risk Management, and Change Management requirements.
• Oversee creation, maintenance and approval of project documentation throughout development.
• Support regulatory submission activities in collaboration with Regulatory Affairs and Quality.
• Maintain clear communication with global stakeholders (EU, US, APAC) and enable governance in a matrix organization.

Skills

Project management

Leading global virtual teams

Regulatory knowledge (GMP/QSR/ISO 134,

MS Project / MS Office

Stakeholder communication

Education

Bachelor’s or Master’s degree in Engineering/Life Sciences/Physics/Optics

Tools

MS Project

Microsoft Office

Job description

360Pharma is seeking a Project Manager for New Product Introduction of intraocular lenses (IOL). You will lead end-to-end NPI programs, coordinating R&D, Regulatory, Quality, and Supply Chain across time zones and with US teams. The role requires strong PM skills, design control, risk management, and GMP/QSR/ISO13485 knowledge.

On-site work in Groningen, NL with occasional international travel is expected. Fluent English is required and Dutch is an advantage.