QA Validation Specialist, Breda, Noord-Brabant

Location: Breda, Noord-Brabant  |  Sector: Pharmaceuticals  |  Start Date: 11/6/2025  |  Job ref: 56567

The Company
Our client is a global pharmaceutical organization dedicated to improving health outcomes through science and innovation. Their site operates under strict GMP standards, ensuring the highest levels of product quality and compliance.

Role Overview
We’re seeking a Sr. Associate QA (Validation / Packaging / PASX Master Data) to provide quality oversight for equipment validation, packaging qualification, and PASX electronic batch record master data. You’ll ensure all processes comply with corporate, site, and regulatory standards.

Key Responsibilities
- Review and approve validation documentation (equipment, process, automation).
- Provide QA support for validation, testing strategies, and investigations.
- Oversee PASX master data entries and ensure system compliance.
- Review and approve changes to equipment and packaging.
- Act as QA SME for deviations and change control processes.
- Support continuous improvement and compliance initiatives.

Requirements
- MBO/Bachelor’s degree in Life Sciences, Process Technology, or related field.
- 3+ years’ experience in QA or Validation within pharma or medical devices.
- Strong GMP and Annex 11 / Part 11 knowledge.
- Experience with equipment validation and automation systems.
- Fluent in English;
- Experience in change control and deviation handling.
- Good understanding of quality engineering tools and documentation.

Apply Now
If you’re a QA Validation professional ready to make an impact in a GMP-driven environment — apply today or share this opportunity with someone in your network!

56567

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