Jobs in the Netherlands, in English.

Senior Validation/Qualification Engineer

On-site in the Netherlands·Full-time·Added 2 months ago (last checked 8 Oct)

MSD

66 open roles

Overview

Contract
Full-time
Languages
Dutch

This job advert was originally written in Dutch.

Requirements

What we're looking for

  • HBO degree in a technical field and 5-7 years of experience in the pharmaceutical industry.

  • Demonstrable knowledge of GMP and experience with validation and calibration processes.

  • Strong in analyzing technical documents and writing clear reports.

  • Communicatively skilled in Dutch and English.

  • Analytically strong, with a customer-oriented and service-oriented attitude.

  • Flexible, proactive, and able to work both independently and in a team.

Nice to have

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Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Pay & benefits

What you'll get

  • A competitive salary.

  • 35.5 vacation days.

  • 8% holiday allowance and 3% year-end bonus.

  • Bonus scheme.

  • An excellent pension.

  • Various training modules and career growth opportunities.

The role

Job Description

Do you want to apply your technical expertise at one of the largest industrial players in the Netherlands? Do you like working in a high-tech environment where you make an impact with products that truly matter? Then we are looking for you!

For our department, we are looking for a Senior Validation/Qualification Engineer.

What you'll do

Welcome to our team
You will be part of the validation and calibration team of the technical service, which is responsible for coordinating, performing, and reporting on validations, qualifications, and calibrations for our various locations. We work closely with various departments, such as the integrated process teams, centers of expertise, and the Research & Development department.

As a Senior Validation/Qualification Engineer, you are the expert in the field of validation, qualification, and calibration. You develop and manage validation and qualification protocols and actively contribute to improving our processes. You analyze data, identify opportunities for improvement, and support these with clear improvement proposals. With this, you increase not only productivity but also safety and quality within our organization.

About the role
In the first year, you are expected to show affinity with the industry and relevant areas of knowledge. This forms the basis for effective collaboration within the team. You contribute to preventing backlogs and ensuring quality.

The goal is to be fully trained after one year and to be able to contribute independently, whereby the workload of the team is noticeably reduced. Success is assessed on independence and impact on the team.

  • Drafting, checking, and managing validation, qualification, and calibration protocols, including reports and annual plans.

  • Performing data analyses and registrations in the CMMS system, with a focus on continuous improvement of processes.

  • Assessing technical documentation such as qualification and 'as built' reports, and providing support during audits.

  • Acting as a Subject Matter Expert (SME) in the field of qualification and calibration within projects and regarding compliance issues.

  • Securing knowledge and supporting departments with technical expertise and training.

  • Ensuring compliance with safety, health, and environmental policies and relevant laws and regulations.

Distribution of duties

  • Review of reports (25%)

  • User Requirements Specification input/evaluations (20%)

  • Technical consultation with stakeholders (25%)

  • Improving and ensuring procedures (20%)

  • Technical input for deviation management (10%)

Stakeholders: suppliers, process owners, direct colleagues, and engineering teams.

Your profile

What we offer
Working at our organization means working together for health in an international working environment with dedicated colleagues. You will get all the space to develop yourself and show who you are. Furthermore, you can count on attractive employment conditions, such as:

Required Skills

Calibration of Equipment, Computerized Maintenance Management Systems (CMMS), Process Instrumentation, Protective Security, R&D Engineering

Employee Status

Regular

Flexible Work Arrangements

Not Applicable

Job Posting End Date

10/22/2026

About MSD

Industry
Pharma
Founded
1891
Employees
50,000–100,000
Headquarters
Rahway, USA
Website
msd.es

In their own words

Additional information

Do you have questions about this vacancy?
Send your question, including the vacancy number and the vacancy title, to the following email address: RecruitmentNL@MSD.com. Applying is only possible via the website.

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