QA Laboratory Manager - Remote Options & Compliance

Grifols Sa; Málaga; Híbrido; EUR 65.000 - 95.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Occasional remote work

Equal opportunity employer

Descripción de la vacante

Grifols seeks a qualified QA leader to review and ensure that all procedures align with cGMP in Plasma Testing Laboratories. The role will supervise quality systems, drive investigations and root cause analyses, and support regulatory inspections and audits.

You will manage quality projects, coordinate Change Controls, and monitor CAPA and QRM activities across the labs, with a strong emphasis on compliance and process improvement.

Formación

• Bachelor’s Degree in Life Sciences (Biology, Pharmacy, Biotechnology or related fields).
• 3–5 years of experience in a related field.
• Advanced level of Spanish and English.
• Significant travel and on-site presence in Egypt, with approximately 50% of the role based in Egypt.

Responsabilidades

• Review all procedures to ensure they are in accordance with cGMP.
• Supervise quality system and quality culture in the Laboratories.
• Ensure investigations for incidents are initiated and root causes analyzed.
• Support internal and external regulatory inspections and audits.
• Manage Plasma Testing Laboratories Quality projects and Change Controls.
• Coordinate tasks across company areas and review new procedures under Change Controls.
• Monitor corrective and preventive actions and quality system indicators.
• Coordinate Quality Risk Management (QRM) studies and mitigation tasks.

Conocimientos

Quality systems

Regulatory compliance

Change Controls

QRM

Root cause analysis

SOP enforcement

Communication skills

Educación

Bachelor’s Degree in Life Sciences

Descripción del empleo

Grifols seeks a qualified QA leader to review and ensure that all procedures align with cGMP in Plasma Testing Laboratories. The role will supervise quality systems, drive investigations and root cause analyses, and support regulatory inspections and audits.

You will manage quality projects, coordinate Change Controls, and monitor CAPA and QRM activities across the labs, with a strong emphasis on compliance and process improvement.