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Validation Engineer


  • Support equipment/system qualification and cleaning validation

  • Develop validation lifecycle document and protocols/reports in accordance with relevanpolicies, standards, procedures and guidelines, and completed in a timely fashion

  • Manage qualification/validation execution and lead the validation deviation investigationencountered during qualification/validation

  • Collaborate with multi functions to arrange, plan and ensure smooth running of the qualification/validation activities

  • Participate in site Validation Maintenance Program

  • Support Change Implementation on site

  • Any other tasks as and when assigned by supervisor

  • Support other technical changes and duties as required

About You:

  • Engineering/Science Degree or higher from recognised institution

  • At least 5 years of experience in Equipment Qualification in the pharmaceutical/biotech industry. Experience in Critical Utilities, Cleaning validation and temperature mapping is preferred.

  • Good knowledge and experience of the practical and theoretical requirement of validation program in GMP facility

  • Good oral and written communication skills.

  • Meticulous and Systematic

  • Team player, with strong focus on safety, quality and timeline

Submit your resume to
Only shortlisted candidates will be contacted. 
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