GLP QA Scientist — Hybrid, Flexible Hours & Growth

Kymos Group; Barcelona; Híbrido; EUR 42.000 - 62.000; Jornada completa

Descripción de la vacante

Kymos Group is seeking a Quality Assurance Scientist for its GLP area in the QA Department. The role focuses on reviewing and auditing analytical documentation, supporting self-inspections, and ensuring GLP/GCP compliance in all processes.

The ideal candidate holds a degree in chemistry, pharmacy, or biosciences with at least 1 year of QA or clinical/preclinical trial experience in the pharmaceutical industry. Strong English and Spanish are required.

Formación

• Degree in chemistry, pharmacy, biosciences or related field.
• At least 1 year of experience in Quality Assurance or in Clinical and Preclinical trials in the Pharmaceutical Industry.
• Knowledge of Good Laboratory Practices (GLP) is required.

Responsabilidades

• Review and approve documentation involved in the analytical activity (protocols, reports, SOPs, raw data).
• Audit analytical documentation to ensure compliance with GLP/GCP standards.
• Participate in the QA Annual Program of self-inspections.
• Verify conformity of quality controls in company processes.
• Manage deviations, incidents, CAPA and Change Controls affecting compliance.
• Collaborate in client audits and inspections by regulatory authorities.
• Support implementation and improvement of quality across the company and subcontractors.

Conocimientos

Quality Assurance

GLP compliance

Analytical skills

English proficiency

Spanish proficiency

Educación

Degree in chemistry, pharmacy, biosciences

Herramientas

GxP knowledge

Descripción del empleo

Kymos Group is seeking a Quality Assurance Scientist for its GLP area in the QA Department. The role focuses on reviewing and auditing analytical documentation, supporting self-inspections, and ensuring GLP/GCP compliance in all processes.

The ideal candidate holds a degree in chemistry, pharmacy, or biosciences with at least 1 year of QA or clinical/preclinical trial experience in the pharmaceutical industry. Strong English and Spanish are required.