Job description

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 We are conducting recruitment on an ongoing basis and will close the process as soon as the right candidate is found. If you meet the qualifications and are interested in this opportunity, we encourage you to apply as soon as possible following the link above. 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 Divisione EPD Established Pharma Sede di lavoro Netherlands > Olst : OAA/OAB Sedi di lavoro ulteriori Turni Standard Viaggiare Not specified Controllo medico Not Applicable Attività lavorative significative Not Applicable

Computerized System Validation Specialist

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