Especialista Administrativo de GMP - Contrato Temporal

Administer and manage quality systems in the production or engineering area to comply with local and corporate procedures, as well as national and international regulations applicable.

Requirements

• Degree in chemical, pharmaceutical, biological, or industrial engineering
• Three years of experience in solid non-sterile pharmaceutical forms and/or liquid manufacturing processes or experience in the area of maintenance and/or projects, quality management systems
• Experience in closing investigations, change controls, CAPAs, and risk analysis on time and form
• Intermediate-advanced level of English