QA Specialist

Pfizer · Tuas, Singapore

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QualityFull-timeCompany career page

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Role summary

Pfizer seeks a QA Specialist in Singapore to review and approve pharmaceutical manufacturing records, ensure regulatory compliance, and support GMP operations. The role involves batch record evaluation, deviation management, and inspection readiness for intermediates and active pharmaceutical ingredients.

What they're looking for

Diploma with 4+ years relevant experience, or bachelor's degree with 1+ year experience
Pharmaceutical industry experience with quality-administered systems
Strong knowledge of current Good Manufacturing Practices (GxP)
Effective written and oral communication skills
Ability to collaborate within team and interdepartmental environments
Batch record review and deviation management experience (preferred)
Familiarity with enterprise resource planning systems and root cause analysis (preferred)

What you'll be doing

Review and approve master batch records and completed batch records for manufacturing compliance
Review and approve cleaning instructions and GMP documents including SOPs and change controls
Manage deviations, investigation reports, and corrective/preventive actions with subject matter experts
Maintain quality tracking systems and identify trends to support continuous improvement
Support regulatory submissions, inspections, and GMP system validation activities

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