Auditor in the Quality Assurance Unit (QAU)

JR Spain; Barcelona; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

Una empresa de crecimiento en Barcelona busca un Auditor en la Unidad de Aseguramiento de Calidad para realizar auditorías internas y gestionar acciones correctivas. Se requiere grado en ciencias de la vida y experiencia en regulaciones GLP y GCP. Se valora el dominio del inglés y conocimientos de herramientas bioanalíticas. Se ofrece un entorno internacional y oportunidades de crecimiento profesional.

Servicios

Oportunidades de crecimiento profesional

Ambiente internacional y multicultural

Formación

• Se valorará experiencia bajo regulaciones GLP y GCP.
• Inglés escrito y hablado fluido.
• Conocimientos de técnicas bioanalíticas (LBA, LC-MS/MS) también serán valorados.

Responsabilidades

• Realizar auditorías internas y coordinar inspecciones por auditores externos.
• Gestionar y ejecutar acciones correctivas y preventivas.
• Preparar y organizar la documentación del Sistema de Calidad.

Conocimientos

Organización

Atención al detalle

Autonomía

Trabajo en equipo

Motivación

Educación

BSc o MSc en ciencias de la vida

Herramientas

MS-Office

Descripción del empleo

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Auditor in the Quality Assurance Unit (QAU), barcelona

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Client:

Anapharm Bioanalytics

Location:

barcelona, Spain

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

514148100187199897632460

Job Views:

1

Posted:

23.07.2025

Expiry Date:

06.09.2025

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Job Description:

MAIN DUTIES & RESPONSIBILITIES

• Conduct internal audits (both study specific and Quality System related) and coordinate inspections by external auditors, according to GCP and GLP regulations.
• Manage and execute corrective and preventive actions (CAPA).
• Prepare and organize documentation of Quality System (SOPs, forms, training records, etc.).
• Participate in the validation of computerized systems.
• Actively support QAU Director in evaluating and implementing new department and Company processes.

REQUIRED PROFILE & QUALIFICATIONS

• BSc or MSc in life sciences.
• Experience working under GLP and GCP regulations will be greatly valued.
• Fluent written and spoken English.
• Proficiency in MS-Office, especially Word and Excel.
• Knowledge of bioanalytical techniques (LBA, LC-MS/MS) will also be valued.

OTHER REQUIRED SKILLS

• Good organizational skills and high attention to detail, with the ability to handle multiple tasks effectively and efficiently.
• Ability to work both autonomously and as part of a team, as required.
• High level of motivation.

WHAT IS OFFERED

• Opportunity to work and contribute to the success of an expanding CRO and a growing team.
• Solid scientific and QA teams with career growth opportunities.
• International and multicultural environment in company based in Barcelona.
• Diligent, professional organization, with a human touch.