QA System Specialist - 6 month

As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:

Documentation and archiving:

• Manage the distribution and life cycle of GxP documentation.
• Administration of operational activities.
• Administrate active BCP once it's activated.
• Act as key user for the documentation management system (DMS)
  

Training:

• Administration of operational activities
• Provide trainings for areas under your responsibility
• Act as key user for Learning Management System LMS

Projects:

• Process improvement of areas under your responsibilities
• Automatization of routine tasks (with tools like Power Apps, Power Automate)

• Bachelor in scientific education.
• 2 years in pharmaceutical industry.
• Experience in training, documentation management and archiving process.
• Experience in Quality Assurance.