Quality Auditor - II - Administrative (B Support / Professional) - P2, Boxmeer, Noord-Brabant

The Company
This organization is a leading provider in the pharmaceutical and chemical industry, committed to ensuring the highest standards of quality and regulatory compliance across global markets. They focus on delivering safe, effective products while adhering to strict industry regulations and best practices.

Role Description
We are recruiting for a Quality Auditor II to join our client’s quality assurance team. The ideal candidate will carry out audits to verify compliance with GMPs, SOPs, and international regulations, supporting quality assurance processes and ensuring data integrity across manufacturing and laboratory activities.

Responsibilities

- Perform routine audits of data, processes, procedures, equipment, and systems, including computer systems, to confirm adherence to SOPs, GMPs, and worldwide regulatory standards.
- Review and approve production and analytical documentation related to the release of active pharmaceutical ingredients (APIs), safety assessments, or clinical supplies, ensuring compliance with relevant regulations.
- Communicate audit findings, resolve comments, and support areas in implementing corrective actions.
- Conduct inspections of designated areas or systems under supervision or as part of a team to assess compliance with company and regulatory standards.

Requirements

- Proven experience in the pharmaceutical, chemical industry, or a government drug-regulatory agency.
- Strong knowledge of cGMP regulations and quality systems, including deviation and change management, validation, and qualification processes.
- Excellent oral and written communication skills and the ability to work collaboratively.
- Experience in performing audits, inspections, and document reviews.

Other Information
If you are interested and want to apply, please submit your application via the apply button below and contact me.

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