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International Quality Assurance Specialist

Tecnimede Group · Sintra

Mid 🇬🇧 English
GMP GDP ISO standards Quality Management Systems Quality Control

Descrição do cargo

About the role

We are seeking an International Quality Assurance Specialist to support and monitor quality and technical activities at our Atlas Pharm manufacturing unit in Morocco, ensuring alignment with headquarters procedures and compliance with GMP standards. The role is based at our HQ in Abrunheira/Sintra, Portugal, with frequent travel to Casablanca.

Key responsibilities

  • Prepare and review Quality Assurance documentation.
  • Review technical area documentation and ensure consistency with HQ standards.
  • Support and monitor production, quality control and other technical departments.
  • Implement process improvements and optimisation initiatives.
  • Ensure compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
  • Align and harmonise local procedures with headquarters standards.

Required profile

  • Degree in Pharmaceutical Sciences, Engineering or a related field.
  • Minimum 3 years experience in an industrial GMP environment.
  • Knowledge of production and/or quality control processes.
  • Familiarity with quality management systems (GMP, GDP, ISO standards).
  • Fluent in written and spoken English; French is a strong plus.
  • Willingness to travel regularly to Morocco.

Required skills

  • GMP
  • GDP
  • ISO standards
  • Quality Management Systems
  • Production processes
  • Quality Control techniques

What we offer

  • Opportunity to work in a multinational pharmaceutical group.
  • Exposure to international quality standards and continuous improvement projects.
  • Professional development within a dynamic, innovation‑focused environment.

Questions fréquentes

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Tecnimede Group

Sintra