Global QA & GMP Compliance Specialist

Tecnimede Group; Sintra; Presencial; EUR 45 000 - 65 000; Tempo integral

Resumo da oferta

Tecnimede Group seeks an International Quality Control Specialist to support QA and technical activities at Atlas Pharm, a Tecnimede Group unit in Morocco, ensuring alignment with HQ procedures and GMP standards.

Based in Abrunheira/Sintra (HQ) with frequent travel to Casablanca, you will review documentation, monitor Quality Control, and drive process improvements while upholding regulatory compliance and high-quality manufacturing practices.

Qualificações

• Degree in Pharmaceutical Sciences, Engineering or similar.
• Minimum of 3 years experience in an industrial GMP environment.
• Knowledge of Production and/or Quality Control.
• Knowledge of Quality Management systems (GMPs/ GDPs/ ISO Standards).
• Fluency in written and spoken English is mandatory; French is a strong plus.

Responsabilidades

• Preparation and review of Quality Assurance documentation;
• Review of Technical Areas documentation;
• Support and monitoring of Quality Control and other technical areas;
• Implementation of process improvements and optimisation initiatives;
• Ensuring compliance with Good Manufacturing and Laboratory Practices;
• Alignment and harmonisation of local procedures with HQ standards.

Conhecimentos

Quality Assurance

Quality Control

GMP

Documentation

Formação académica

Degree in Pharmaceutical Sciences or Engineering

Descrição da oferta de emprego

Tecnimede Group seeks an International Quality Control Specialist to support QA and technical activities at Atlas Pharm, a Tecnimede Group unit in Morocco, ensuring alignment with HQ procedures and GMP standards.

Based in Abrunheira/Sintra (HQ) with frequent travel to Casablanca, you will review documentation, monitor Quality Control, and drive process improvements while upholding regulatory compliance and high-quality manufacturing practices.