ECY-810 - Quality Control Technician

AL Solutions; Barcelona; Presencial; EUR 25.000 - 35.000; Jornada completa

Descripción de la vacante

Una empresa líder en CDMO busca un Técnico de Control de Calidad para garantizar que los productos farmacéuticos cumplan con los estándares de calidad y regulaciones. El candidato ideal tendrá un grado en Química, Farmacia o Biotecnología, con 1-3 años de experiencia en un entorno GMP. Las responsabilidades incluyen realizar pruebas de laboratorio, documentar resultados y colaborar con equipos multifuncionales para mejorar los procesos de calidad.

Formación

• 1-3 años de experiencia en un laboratorio QC regulado por GMP.
• Experiencia práctica con instrumentos analíticos (HPLC, GC).
• Conocimiento de normas GMP y regulaciones (EMA, ICH, EU GMP).

Responsabilidades

• Realizar análisis rutinarios y no rutinarios de materias primas y productos terminados.
• Asegurar que todas las pruebas se realicen de acuerdo con las GMP y los SOPs.
• Calibrar, mantener y solucionar problemas del equipo de laboratorio.

Conocimientos

HPLC

GC

Trabajo en equipo

Organización

Documentación precisa

Proficiencia en inglés

Educación

Grado en Química

Grado en Farmacia

Grado en Biotecnología

Herramientas

LIMS

Descripción del empleo

I am working with a leading CDMO (Contract Development and Manufacturing Organization) located in Spain, offering end-to-end services in the development and manufacturing of pharmaceutical and biopharmaceutical products. Our mission is to deliver high-quality, compliant, and innovative solutions to our clients across the globe.
Position Summary:
As a QC Technician, you will play a critical role in ensuring that raw materials, intermediates, and finished pharmaceutical products meet established quality standards and regulatory requirements. You will conduct laboratory analyses, maintain accurate documentation, and support continuous improvement in QC processes.
Key Responsibilities:




Perform routine and non-routine analysis of raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, and wet chemistry.
Conduct microbiological testing (if applicable) including bioburden, endotoxin, and environmental monitoring.
Prepare reagents, solutions, and mobile phases as per SOPs.
Ensure all testing is conducted in compliance with GMP, SOPs, and regulatory requirements.
Accurately document all laboratory activities in logbooks, LIMS, and batch records.
Participate in out-of-specification (OOS) investigations and support root cause analysis.
Calibrate, maintain, and troubleshoot laboratory equipment.
Support method transfers and validations as required.
Assist in the review and revision of SOPs and QC documentation.
Collaborate with cross-functional teams including QA, Production, and R&D.;
Maintain a clean and safe laboratory environment.
Qualifications:
Degree in Chemistry, Pharmacy, Biotechnology, or related scientific discipline.
1–3 years of experience in a GMP-regulated QC laboratory, preferably within a CDMO or pharmaceutical environment.




Hands-on experience with analytical instrumentation (e.g., HPLC, GC).
Working knowledge of GMP and regulatory guidelines (EMA, ICH, EU GMP).
Strong organizational and documentation skills.
Basic English proficiency (reading/writing technical documentation); fluent Spanish required.
Preferred Qualifications:
Experience in microbiological testing or biologics QC is a plus.
Familiarity with LIMS and electronic laboratory systems.
Knowledge of method validation and ICH guidelines.

El anuncio original lo puedes encontrar en Kit Empleo:
https://www.kitempleo.es/empleo/201628192/ecy-810-quality-control-technician-barcelona/?utm_source=html