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VALIDATION ENGINEER

YOUR ASSIGNMENT

  • Preparation of validation plans, protocols, reports and procedures of critical process and equipment;
  • Managing validation projects;
  • Execution in cooperation with involved departments of equipment and process validation;
  • Filling in validation protocols;
  • Collecting information from involved departments to prepare validation documents;
  • Review and integration in company system protocols and reports from suppliers;
  • Preparation of plans, protocols, reports and procedures of computer system validation;
  • Supporting the coordinator in preparation and updating Validation Master Plan;
  • Performing statistical data analysis;
  • Collaboration with project leaders to prepare and manage project documentation;
  • Supporting involved departments in risk analysis of manufacturing processes.

YOUR PROFILE

  • Scientific University Degree, preferably biomedical engineering;
  • Minimum 2 years in process validation in biomedical or pharmaceutic industry;
  • Biomedical standards
  • ISO standards
  • FDA standards;
  • Very good It skills (word, excel, power point, access, minitab)

 

Degrees of interest: Scientific University Degree, preferably biomedical engineering.

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