QA Validation Officer

About the Company

Our client is a leading provider of pharmaceutical packaging solutions, specializing in advanced and innovative services to meet the needs of the pharmaceutical industry. Committed to delivering the highest quality standards, they support clients globally with a range of services, from packaging design to serialisation and clinical trial solutions. With a focus on precision, safety, and compliance, they are trusted worldwide to ensure the utmost quality in each step of the packaging process.

Position Overview

To strengthen their team in Limburg Region, we are seeking a QA Validation Officer. As QA Validation Officer, you will be responsible for ensuring that systems, processes, installations and equipment are validated and maintained in compliance with GMP and international regulatory standards. You will act as a key quality partner for internal stakeholders and, where applicable, for clients.

Key Responsibilities

• Lead and coordinate validation activities for systems, processes, utilities and equipment.
• Define validation strategies in line with regulatory requirements and client expectations.
• Set up, implement and maintain validation studies in close collaboration with Operations, Supply Chain, Technical Services and QA.
• Prepare, review and approve validation documentation and reports.
• Assess validation impact related to changes (change control).
• Ensure timely execution of validation activities and sustained validated status.
• Participate in internal, customer and external audits, and support audit readiness.
• Contribute to continuous improvement of quality processes, systems and procedures.
• Draft and update SOPs related to validation activities.

Profile

• Bachelor's or Master's degree in Industrial Sciences or a related scientific discipline.
• First experience within a pharmaceutical or GMP-regulated production environment is a strong asset.
• Solid knowledge of GMP guidelines, pharmaceutical regulations, validation principles, and basic understanding of microbiology and hygiene.
• Experience with quality systems, procedures and documentation.
• Comfortable working with MS Office.
• Good command of English, both written and spoken.
• Strong analytical mindset, structured and detail-oriented.
• Able to work autonomously while collaborating effectively within cross-functional teams.
• Demonstrates ownership, reliability and a proactive attitude.

Why Join Us

This role offers the opportunity to play a key part in a high-quality pharmaceutical environment where precision, responsibility and continuous improvement are central.

How to Apply

Apply by visiting our website at https://www.key4nova.com/ or by sending your CV to: [email protected]