13 May 2026

R&D Engineer

Johnson & Johnson

Groningen

13 May 2026

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R&D Engineer

Johnson & Johnson MedTech seeks an R&D Engineer for a 2-year contract in Groningen to design and develop innovative intraocular lenses. The role involves analyzing requirements, developing designs, validating processes, and collaborating with cross-functional teams. Requires a Bachelor's in Engineering, 2-4 years of regulated industry experience, and proficiency in English.

On-siteFull-timeMid LevelMicrosoft OfficeMicrosoft Teams

R&D Engineer

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On-siteFull-timeMid LevelMicrosoft Office

Salary

Not specified

Work Location

Groningen, Groningen, Netherlands, NL

Work Model

On-site

Experience Required

4 years

Employment Type

Full-time

Experience Level

2-4 years in product and process development

Contract Length

24 months

Core Qualifications

Technical (Must-have)

Microsoft OfficeMicrosoft TeamsMinitabcGMPISO standardsrisk analysisroot cause analysisvalidationverification

Soft Skills

CollaboratingCritical ThinkingCross-Functional CollaborationAnalytical ReasoningExecution FocusTeamworkTechnologically Savvy

Tools (Must-have)

Microsoft OfficeMicrosoft TeamsMinitab

Preferred Qualifications

Technical (Nice-to-have)

PythonMatLabSolidWorks3D printingMicrosoft ProjectSix Sigma Green BeltSix Sigma Black Belthigh precision machininghigh precision injection molding

Tools (Nice-to-have)

Microsoft ProjectSAP Product Lifecycle Management

Key Responsibilities

•Analyze product and process requirements 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.

R&D EngineerMedical DevicesIntraocular LensesProduct DevelopmentValidationcGMPISOGroningenFull-timeContract

Core Qualifications

Technical (Must-have)

Microsoft OfficeMicrosoft TeamsMinitabcGMPISO standardsrisk analysisroot cause analysisvalidationverification

Soft Skills

CollaboratingCritical ThinkingCross-Functional CollaborationAnalytical ReasoningExecution FocusTeamworkTechnologically Savvy

Tools (Must-have)

Microsoft OfficeMicrosoft TeamsMinitab

Key Responsibilities

•Analyze product and process requirements 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.