QA Coordinator

The Company
Our client is a leading global player in the chemical industry, producing high-quality chemical solutions used in healthcare, industrial, and cleaning sectors. With a strong commitment to GMP and ISO standards, the company ensures the highest levels of quality and safety.
Role Description
As a QA Coordinator, you will be responsible for operational quality assurance activities within a GMP-regulated environment. You will ensure timely product release, maintain GMP documentation systems, and support operators and managers in adhering to strict quality standards. In addition, you will serve as a backup for the QA Manager in specific product release activities. This is a hands-on role that combines documentation, compliance, and training responsibilities with daily interaction across production teams.

Responsibilities

• Release batches, raw materials, labels, and packaging for GMP production
• Review and archive batch records, investigate deviations, and define corrective actions
• Perform visual inspections of final products
• Provide daily support and GMP training to operators and shift leaders
• Write, review, and maintain GMP-related documentation (procedures, forms, instructions)
• Contribute to audits, KPI reporting, and Product Quality Reviews (PQR)
• Act as backup for the QA Manager in releasing PH-grade products
• Communicate effectively with production and management to ensure product quality and timely deliveries

Requirements

• Bachelor’s degree (HBO/HLO) in Chemistry, Life Sciences, or related field
• Experience in Quality Assurance within chemicals, pharmaceuticals, or GMP-regulated production
• Strong knowledge of GMP and ISO systems (ISO 9001, ISO 22000, ISO 13485)
• Detail-oriented with excellent documentation and reporting skills
• Proactive and able to collaborate across departments (operators, managers, QC)
• Strong communication skills in English (Dutch is an advantage)
• Hands-on, structured, and problem-solving mindset

Other Information
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