QC Analyst
CV-LibraryAlmere, FlevolandpermanentPosted: 17 June 2026
Apply NowAre you a detail‑driven laboratory professional with a passion for maintaining high standards in a regulated scientific environment?
Smart4 Sciences are working with a well‑established and innovative organisation within the life sciences sector to recruit a QC Analyst to join their quality control team.
The Role
This is a hands‑on opportunity to support analytical activities within a GMP‑regulated laboratory environment. You will play a key role in the sampling, testing, and reporting of raw materials, intermediates, and finished products, ensuring compliance with GMP and ALCOA+ data integrity principles.
Key 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.
Essential:
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.You'll be joining a quality‑focused organisation that values compliance, teamwork, and continuous improvement, offering an excellent opportunity to further develop your career within a professional laboratory environment
Smart4 Sciences are working with a well‑established and innovative organisation within the life sciences sector to recruit a QC Analyst to join their quality control team.
The Role
This is a hands‑on opportunity to support analytical activities within a GMP‑regulated laboratory environment. You will play a key role in the sampling, testing, and reporting of raw materials, intermediates, and finished products, ensuring compliance with GMP and ALCOA+ data integrity principles.
Key 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.
Essential:
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.You'll be joining a quality‑focused organisation that values compliance, teamwork, and continuous improvement, offering an excellent opportunity to further develop your career within a professional laboratory environment