Sr. Computerized System Validation Specialist

Abbott Labs (Malaysia) Sdn. Bhd.

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Netherlands - Olst Until 10/6/2026 3+ years exp H-1B sponsor history First posted July 21, 2026 Last posted August 7, 2026
Job description

     

JOB DESCRIPTION:

Senior CSV Specialist

At Abbott Olst, we work every day on life-saving nutritional and pharmaceutical products. Within Manufacturing Automation, we are looking for a CSV Specialist who ensures reliable and compliant computerized systems.

Location: Olst, The Netherlands. This is an onsite position that requires you to be onsite a minimum of 4 days a week.

About the Department

Manufacturing Automation consists of Application Managers, Automation Engineers and MES Designers and supports production, laboratories, facilities and utilities. The department forms the bridge between technology, compliance and the production departments.

The role

  • You are the SME for CSV, Data Integrity and GMP compliance;

  • You lead complex validation and implementation projects;

  • You develop CSV standards, governance and procedures;

  • You translate new regulations such as NIS2, Annex 11 and CSA into the organization;

  • You coach colleagues and advise management and project owners;

  • You actively contribute to the future CSV strategy for the Olst and Weesp sites (OneNL).

Your Responsibilities

  • Prepare, review and effectively coordinate validation documentation

  • Handle deviations, exceptions and CAPAs

  • Support audits and inspections

  • Ensure continuous availability of up-to-date information, reports and evaluations regarding Computer System Validation

  • Collaborate with QA, Operations, Engineering and IT

  • Ensure compliant lifecycle management of computerized systems

  • Act as the CSV project SME for projects involving automation aspects.

What Do You Bring?

  • Bachelor's or Master's level education, preferably in Process Engineering, Automation or Business IT

  • A minimum of 3-5 years of CSV experience in a GMP environment

  • Demonstrated experience as an SME or lead in validation projects

  • Knowledge of GAMP5, NIS2, GMP Annex 11, Data Integrity and CSA

  • Strong stakeholder management and advisory skills

  • Fluency of both Dutch and English, spoken and written

Why Abbott?

You will have a visible role within a modern pharmaceutical environment where digitalization, compliance and continuous improvement are central. You will work with experts from various disciplines and have ample opportunities for development and impact.

Application

Apply directly with your CV! For questions, please email us at recruitment.netherlands@abbott.com and a member of our Talent Acquisition Team will get back to you shortly.

     

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Operations Quality

     

DIVISION:

EPD Established Pharma

        

LOCATION:

Netherlands > Olst : OAA/OAB

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Not specified

     

MEDICAL SURVEILLANCE:

Not Applicable

     

SIGNIFICANT WORK ACTIVITIES:

Not Applicable

     

     

     

About this role

Summary

Lead validation projects, develop CSV standards, ensure GMP compliance, support audits, and collaborate across departments.

Job title

Sr. Computerized System Validation Specialist

Experience level

3-5 years

Minimum experience

3+ years exp

Industry

pharmaceuticals

Location requirements

Onsite in Netherlands, minimum 4 days/week, remote not allowed

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

CSVData IntegrityGMP Annex 11GAMP5CSA

Preferred skills

None specified

Specializations

CSVData IntegrityGMP compliancevalidation projectsregulatory standards
Locations

Structured locations inferred from the posting.

Netherlands

On-site Country

Olst, Netherlands

On-site City
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