Stability Lab Specialist - Pharma Quality & Compliance

Galenicum; Esplugues de Llobregat; Presencial; EUR 28.000 - 38.000; Jornada completa

Descripción de la vacante

Galenicum is seeking a Stability Technician to join our Laboratory Team in Spain. You will revise stability reports for R&D projects, manage stability studies with CMOs, and ensure timely analysis and documentation.

The role requires GLP/GMP analytical development experience and coordination across departments. Educational background in life sciences (Pharmacy preferred) and fluent English and Spanish are required.

Formación

• Minimum 1–2 years in analytical development in GLP/GMP environments.
• Experience in validating and developing methods (HPLC/UPLC/LC-MS).
• Knowledge of regulatory guidelines (EMEA/FDA/ICH/ISO) is valuable.
• Experience organizing and revising stability reports and protocols.

Responsabilidades

• Revise stability reports from R&D and external labs/CMOs.
• Organize and revise stability results across studies and transfers.
• Monitor ongoing stability studies and review trends and deviations.
• Approve stability protocols and ensure timely follow-up actions.
• Maintain up-to-date results on shared platforms for departments.
• Create and maintain SOPs; train staff accordingly.

Conocimientos

Analytical development

HPLC

UPLC

LC-MS

GMP/GLP

Dissolution testing

Data analysis

MS Office

Educación

Life sciences degree (Pharmacy preferred)

Herramientas

MS Office

Descripción del empleo

Galenicum is seeking a Stability Technician to join our Laboratory Team in Spain. You will revise stability reports for R&D projects, manage stability studies with CMOs, and ensure timely analysis and documentation.

The role requires GLP/GMP analytical development experience and coordination across departments. Educational background in life sciences (Pharmacy preferred) and fluent English and Spanish are required.