Senior CQV Engineer: GMP Validation
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PharmEng Technology in Singapore seeks an experienced Commissioning, Qualification and Validation (CQV) Engineer to lead qualification activities for GMP pharmaceutical projects. You will draft and execute CQV documentation, work with QC SMEs on equipment qualification, and coordinate vendor IOQs to ensure timelines and quality.
Responsibilities include managing deviations, risk assessments, CAPA, and ensuring data integrity and regulatory compliance while collaborating with stakeholders across