GMP QC Analyst: Precision Testing & Compliance

Science Solutions Recruitment Ltd; Netherlands; On-site; EUR 42,000 - 54,000; Full time

Job summary

Smart4 Sciences is seeking a detail‑driven QC Analyst to join a GMP‑regulated laboratory team. You will perform sampling, testing, and reporting of raw materials, intermediates, and finished products, ensuring GMP and ALCOA+ data integrity.

The role involves handling non‑conformances, deviations, and data reporting, with a strong emphasis on documentation, safety, and continuous improvement in a quality‑conscious setting.

Qualifications

• Experience in analytical testing within a regulated environment (e.g. pharmaceuticals, medical devices, or food manufacturing).
• Strong understanding of GMP and data integrity principles (ALCOA+).
• Experience managing or investigating non‑conformances and deviations.
• Excellent attention to detail and organisational skills.
• A degree in a relevant scientific discipline.

Responsibilities

• Perform sampling, testing, and reporting of raw materials, intermediates, and finished products.
• Ensure all testing is conducted in accordance with GMP and ALCOA+ standards.
• Utilise a range of analytical techniques to support quality control activities.
• Accurately record and report data in line with regulatory requirements.
• Investigate and manage non‑conformances, deviations, and out‑of‑specification results.
• Maintain high standards of laboratory compliance, safety, and documentation.
• Support continuous improvement within the laboratory function.
• Ensure adherence to all health, safety, environmental, and quality guidelines.

Skills

Attention to detail

Organisational skills

Education

Degree in a relevant scientific discipline

Job description

Smart4 Sciences is seeking a detail‑driven QC Analyst to join a GMP‑regulated laboratory team. You will perform sampling, testing, and reporting of raw materials, intermediates, and finished products, ensuring GMP and ALCOA+ data integrity.

The role involves handling non‑conformances, deviations, and data reporting, with a strong emphasis on documentation, safety, and continuous improvement in a quality‑conscious setting.