QA Officer – GMP Packaging & Compliance (3-shift)

SIRE LIFE SCIENCES; Breda; On-site; EUR 48,000 - 60,000; Full time

Job summary

SIRE LIFE SCIENCES in the Netherlands is seeking a proactive Quality Assurance Officer to join the GMP manufacturing team. You will ensure packaging, labeling, and production processes meet quality and regulatory standards in a fast-paced environment.

The role involves reviewing batch records, handling deviations, stopping production when needed, and guiding staff on GMP procedures, with a focus on accuracy, compliance, and cross‑department collaboration.

Qualifications

• Understanding of GMP, GDP, and GCP regulations and able to apply them.
• Strong attention to detail and a methodical approach to quality tasks.
• Fluency in English and effective communication with cross-functional teams.

Responsibilities

• Conduct final quality verification for packaging and labeling orders before release.
• Review batch records and documentation for accuracy, compliance and completeness.
• Manage and resolve deviations or quality issues during production.
• Investigate, document, and follow up on deviations or non-compliance issues.
• Collaborate with Production, Maintenance, QA and other departments to ensure smooth operations.
• Exercise escalation authority by stopping production if quality or compliance concerns arise.
• Provide guidance and support to production staff on GMP standards and procedures.
• Review and approve batch production records and deviation reports.

Skills

GMP knowledge

Attention to detail

Communication skills

Team player

English fluency

Education

MBO or BSc in Pharmaceutical Sciences or Life Sciences

Job description

SIRE LIFE SCIENCES in the Netherlands is seeking a proactive Quality Assurance Officer to join the GMP manufacturing team. You will ensure packaging, labeling, and production processes meet quality and regulatory standards in a fast-paced environment.

The role involves reviewing batch records, handling deviations, stopping production when needed, and guiding staff on GMP procedures, with a focus on accuracy, compliance, and cross‑department collaboration.