Quality Assurance Coordinator

SIRE LIFE SCIENCES; Boxmeer; On-site; EUR 42,000 - 62,000; Full time

Job summary

SIRE LIFE SCIENCES in the Netherlands is seeking a detail-oriented Quality Assurance Coordinator to support GMP-compliant quality management systems and regulatory compliance across documentation, batch records, audits, and supplier quality interfaces.

The role emphasizes implementing regulatory changes within quality systems such as SAP, LIMS, and Microsoft Office; ensuring updates meet GMP and GDocP standards; collaborating with Qualified Persons (QPs) and cross-functional teams; and

Qualifications

• Bachelor’s degree in Biochemistry, Microbiology or a related field.
• At least 1 year of relevant work experience in QA.
• Experience with SAP and quality systems.
• Solid understanding of GMP and GDocP practices.

Responsibilities

• Implement regulatory changes accurately within quality systems.
• Ensure updates and documentation meet GMP and GDocP standards.
• Collaborate with Qualified Persons (QPs) and cross-functional teams.
• Maintain accurate records and documentation in compliance with regulations.
• Contribute to continuous improvement initiatives within the quality department.

Skills

Quality assurance

Regulatory knowledge

Attention to detail

Quality systems knowledge

Education

Bachelor’s degree HBO in Biochemistry or Microbiology

Tools

SAP

LIMS

Microsoft Office

Job description

Company

A leading multinational, dedicated to advancing healthcare through innovative pharmaceutical solutions. The organization prides itself on maintaining the highest standards of quality and compliance in its operations, ensuring the delivery of safe and effective products.

Role Description

We are seeking a detail-oriented Quality Assurance Coordinator to join a dynamic team in a vital role supporting the company's quality management systems. The successful candidate will play an essential part in ensuring regulatory compliance and maintaining GMP standards across various systems and documentation processes.

Responsibilities

• Implement regulatory changes accurately and efficiently within quality systems such as SAP, LIMS, and Microsoft Office.
• Ensure all updates and documentation meet GMP and GDocP standards.
• Collaborate closely with Qualified Persons (QPs) and integrated process teams to uphold quality compliance.
• Maintain accurate records and documentation aligned with regulatory requirements.
• Contribute to continuous improvement initiatives within the quality department.

Requirements

• Minimum of 1 year relevant work experience.
• Fluent in Dutch and proficient in English.
• Bachelor’s degree (HBO) in Biochemistry, Microbiology, or a comparable field.
• Experience working with SAP.
• Solid understanding of GMP and GDocP practices.