Spécialiste SAP

QP Group; Madrid; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading European CDMO is seeking a QC Specialist – Stability to join their Quality Control team in Girona. The ideal candidate will have strong experience in biologics and a passion for GMP-compliant work. Responsibilities include leading stability studies and collaboration with various teams. Candidates must possess strong analytical skills, fluent Spanish, and the ability to work onsite 3-4 days a week. This is a unique opportunity to be part of a growing organization focused on quality and development.

Servicios

Opportunities for development

Collaborative environment

Formación

• Hands-on experience with HPLC, ELISA, qPCR, and protein-based analytics.
• Background in QC, analytical development, or biologics testing.
• Ability to work onsite in Girona 3-4 days per week.

Responsabilidades

• Lead and execute stability studies for biologic products.
• Collaborate with QC, QA, and manufacturing teams.
• Maintain compliance with GMP and internal quality standards.

Conocimientos

Fluent Spanish

Analytical method troubleshooting

Strong documentation skills

Herramientas

HPLC

ELISA

qPCR

Descripción del empleo

A leading European CDMO is seeking a QC Specialist – Stability to join their growing Quality Control team in Girona. This role is ideal for an analytical scientist with strong experience in biologics and a passion for high-quality, GMP‑compliant work.

Key Responsibilities

• Lead and execute stability studies for biologic products.
• Perform and troubleshoot analytical methods including HPLC, ELISA, qPCR, and protein characterization.
• Support method qualification, validation, and GMP documentation.
• Collaborate with QC, QA, and manufacturing teams to ensure robust stability programs.
• Maintain compliance with GMP and internal quality standards.

Requirements

• Fluent Spanish (written & spoken).
• Hands‑on experience with HPLC, ELISA, qPCR, and protein-based analytics.
• Background in QC, analytical development, or biologics testing (vaccines/proteins preferred).
• Ability to work onsite in Girona 3‑4 days per week.
• Strong documentation skills in GMP settings.

Why Join?

• Be part of a growing CDMO expanding its biologics capabilities.
• Work in a collaborative, science‑driven environment.
• Opportunities for development within a fast‑growing quality organization.