Hybrid GMP QA Scientist — Documentation & Compliance

Kymos Group; Barcelona; Híbrido; EUR 42.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible Working Hours

Hybrid work model

23 vacation days + 24th and 31st of de

Canteen and rooftop space

Headquarters near Barcelona

Descripción de la vacante

Kymos Group invites a Quality Assurance Scientist to join our GMP area within the QA Department, located near Barcelona, Spain.

The role focuses on reviewing and approving analytical documentation, auditing processes for cGMP compliance, supporting self-inspections, evaluating deviations and CAPA, and assisting regulatory inspections. You will collaborate with cross-functional teams in a hybrid work setting.

Formación

• Bachelor's degree or higher in chemistry, pharmacy, biosciences or related field.
• At least 1 year of experience in QA, QC or manufacturing in the pharmaceutical industry.
• Knowledge of Pharmaceutical Analysis, Quality Control and Quality Assurance per cGMP.
• High level of English (written and spoken).

Responsabilidades

• Review and approve analytical documentation (CoA, protocols, reports, SOPs, product specifications).
• Audit analytical documentation to ensure compliance with cGMP standards.
• Participate in the QA Annual Program of self-inspections.
• Verify conformity of quality controls in company processes.
• Evaluate deviations, OOS/OOT, complaints, CAPA and Change Controls.
• Review Quality/Technical Agreements with subcontractors, esp. batch certification activities.
• Collaborate in audits by clients or subcontracted manufacturers and support regulatory inspections.
• Participate in implementation and improvement of quality across the company and subcontractors.

Conocimientos

Quality Assurance

Quality Control

GMP knowledge

English proficiency

Educación

Degree in Chemistry

Degree in Pharmacy

Degree in Biosciences

Descripción del empleo

Kymos Group invites a Quality Assurance Scientist to join our GMP area within the QA Department, located near Barcelona, Spain.

The role focuses on reviewing and approving analytical documentation, auditing processes for cGMP compliance, supporting self-inspections, evaluating deviations and CAPA, and assisting regulatory inspections. You will collaborate with cross-functional teams in a hybrid work setting.