Validation Engineer

Johnson & Johnson | Vision

Groningen

On-site

EUR 41,328 - 68,880

Full time

14 days+

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Benefits offered by this job

Competitive hourly rate

Job summary

A leading healthcare company is seeking a Validation Engineer in Groningen, Netherlands. This contract role requires expertise in equipment validation and GXP/GMP practices. You will work collaboratively to implement new production equipment and improve processes. Ideal candidates will have a relevant Bachelor’s degree, proficiency in English, and experience in regulated environments. Join to help innovate in the healthcare sector.

Qualifications

Minimum 3 years in Manufacturing/Industrial Engineering.
English proficiency at B2 level.
Experience with validation in a regulated sector.

Responsibilities

Lead rollout of new equipment to production.
Develop and improve products and processes.
Organize and execute validation studies.

Skills

GXP knowledge

GMP practices

CSV application

Statistical analysis

Collaboration skills

Education

Bachelor of Science in a relevant field

Advanced degree (MSc. or PhD)

Tools

Minitab

Metrology systems

Job description

Overview

Join to apply for the Validation Engineer role at Johnson & Johnson | Vision.

Location: Groningen, The Netherlands • Duration: 12 months • Hours: Full-time

Imagine your next project. You will play a key part in the thinking, strategy, dynamism, and impact of this iconic global healthcare company as they touch the lives of nearly a billion people every day. This role is your chance to contribute to the next healthcare breakthrough by leading equipment implementation activities with a strong emphasis on validation.

Responsibilities

Leading the rollout of new equipment to production lines.
Developing, improving, and characterizing products, processes, equipment, and test methods.
Organizing and executing engineering, validation, and verification studies, including setting up test plans, protocols, and criteria.
Performing technical writing of protocols and validations in collaboration with Subject Matter Experts (SMEs).
Gathering requirements and specifications to write documents such as URS, TM, FAT, IQ, OQ, and PQ for machines and software.
Analyzing product and process requirements and performing risk and root cause analysis.
Planning and evaluating the implementation of new or modified products and processes, including writing SOPs and training employees.

How to Succeed

You will be a subject matter expert in GXP, GMP, and CSV as they relate to hardware solutions in the medical device sector. You will also bring:

A minimum of a Bachelor of Science in a relevant subject (e.g., Mechanical/Electrical/Engineering).
At least three years of experience in a Manufacturing and/or Industrial Engineering role in medium to high-volume manufacturing.
Verbal and written proficiency in English (at least B2 level).
Demonstrated knowledge in Design for Manufacturing (Lean Manufacturing, Tolerancing, Poka Yoke design, Theory of Constraints).
Proficiency in applying statistical methodologies and analysis using Minitab.
Proven track record as a validation SME within a highly regulated sector (e.g., medtech, pharma).
Hands-on mentality and strong collaboration skills with all teams.

Desired Qualifications

An advanced degree (MSc. or PhD) in a relevant subject.
Verbal and written proficiency in Dutch.
Experience with metrology systems, vision systems, or SCADA system deployment and validation.
Knowledge of high-precision machining or injection molding.

This contract role offers a very competitive hourly rate and will run for 12 months.

Benefits and Inclusion

You Are Welcome Here

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued, and each of our people feels that they belong and can reach their potential. No matter who they are.

About Johnson & Johnson

Caring for the world, one person at a time, has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you'll play a key part in the thinking, strategy, the dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson.

Application Process

We are looking to process the first round of applications within the next two working days. We do not accept applications via email.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity, and inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong.”

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