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Associate Validation Engineer


  • Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion.

  • Manage qualification execution and lead validation deviation investigation encountered in qualification.

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

  • Participate in site Validation Maintenance Program.

  • Write execution related deviations and change requests.

  • Support change implementation on site.

  • Any other task as assigned by Supervisor/Manager

About You:

  • Diploma / Bachelor Degree in Engineering / Science or related Pharmaceutical courses.

  • Min. 2 years' experience in Equipment Qualification in the pharmaceutical/biotech industry.
    Experience in Critical Utilities, Cleaning validation and temperature mapping is preferred.

  • Fresh Graduates welcome to apply.

  • 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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