Quality Assurance – Documentation and Training Specialist (all genders).

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détails du poste

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détails du poste
For our client Merck in Aubonne, we are looking for a Quality Assurance – Documentation and Training Specialist (all genders) for a period of 12 months.

Your role : 

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)

 Your profile:
  • Bachelor in scientific education.
  • Digital mindset and knowledge.
  • Ability to work in teams.
  • Promote continuous improvement.
  • 2 years in pharmaceutical industry.
  • Experience in training, documentation management and archiving process.
  • Experience in Quality Assurance.
  • Fluent in French, basics in English
For our client Merck in Aubonne, we are looking for a Quality Assurance – Documentation and Training Specialist (all genders) for a period of 12 months.

Your role : 

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)

 Your profile:
  • Bachelor in scientific education.
  • Digital mindset and knowledge.
  • Ability to work in teams.
  • Promote continuous improvement.
  • 2 years in pharmaceutical industry.
  • Experience in training, documentation management and archiving process.
  • Experience in Quality Assurance.
  • Fluent in French, basics in English

informations de contact.

nous sommes à ta disposition pour toute question.

KK

Kata Kulcsár

  • Lausanne Professionals Life Sciences

procédure de candidature.

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