Job Description

Explore a Career in System Validation

Job Description:


In this role, you will be responsible for ensuring the quality and integrity of computerized systems within Life Sciences organizations. Your primary focus will be on ERP and other system validations, encompassing IQ, OQ, PQ phases. You will prepare and review critical documentation such as VMPs (Validation Master Plans), URSs (User Requirements Specifications), and SOPs.



  • Strong expertise in CSV (Computer System Validation) with experience in preparing and reviewing validation documents.
  • In-depth knowledge of EU GMP Annex 11, FDA 21 CFR Part 11 guidelines.



h4 Other Opportunities:


lili take part in projects to expand your system validation skills.,

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