R&D Engineer

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

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R&D Engineer

About MedTech

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

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

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

We are searching for the best talent for R&D Engineer to be in Groningen.

Purpose: Driving activities related to the design and development of innovative intraocular lenses (IOLs) for the Research & Development team. Apply advanced skills of the field to construct industry leading products. Contribute to scientific projects and processes under general direction.

You will be responsible for:

• Analyze product and process requirements (materials, quality, EHS) and perform risk and root cause analysis.

• Develop and improve product designs, processes, equipment, test methods, and procedures; define technical requirements.

• Plan and execute validation and verification studies, including test plans, protocols, data analysis, and issue resolution.

• Implement new or modified products and processes, author SOPs, protocols, risk assessments, and train employees.

• Participate in project planning, design reviews, and gate reviews; report progress and close projects per effectiveness checks

• Maintain compliance with cGMP, ISO standards; update procedures, support audits, and resolve CAPAs/NCRs.

• Collaborate with Operations, QA, and Manufacturing Engineering to support implementation and design transfer.

Qualifications / Requirements:

• Bachelor’s degree in Engineering or related field; Master’s preferred.

• Minimum 2–4 years in product and process development within a regulated industry (medical device or pharma).

• Hands-on experience with validation, verification, and compliance activities (cGMP, ISO).

• Strong analytical and problem-solving skills; familiarity with risk analysis and root cause methodologies.

• Proficient in the use of Microsoft Office (Word, Excel) and Microsoft Teams.

• Proficient in applying of statistical methodologies and analysis using Minitab.

• Verbal and written proficiency (at least at B2 level) in English.

Preferred specific knowledge and skills:

• Analysis of datasets using Python or MatLab

• Designing 3D models using SolidWorks

• Experience in rapid prototyping techniques using 3D printing

• Proficient in the use of Microsoft Project

• Verbal and written proficiency in Dutch

  Six Sigma Certified Green Belt / Black Belt

• Knowledge in high precision machining (lathing and milling)

• Knowledge in high precision injection molding

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