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Validation Engineer
Responsibilities:
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Support equipment/system qualification and cleaning validation
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Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion
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Manage qualification/validation execution and lead the validation deviation investigations encountered during qualification/validation
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Collaborate with multi functions to arrange, plan and ensure smooth running of the qualification/validation activities
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Participate in site Validation Maintenance Program
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Support Change Implementation on site
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Any other tasks as and when assigned by supervisor
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Support other technical changes and duties as required
About You:
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Engineering/Science Degree or higher from recognised institution
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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.
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Good knowledge and experience of the practical and theoretical requirement of validation program in GMP facility
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Good oral and written communication skills.
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Meticulous and Systematic
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Team player, with strong focus on safety, quality and timeline
Submit your resume to recruitment@nusaprime.com.
Only shortlisted candidates will be contacted.
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