Quality Validation Engineer

Job Title: Senior / Quality Validation EngineerLocation: Tuas, Singapore | 1-year contractEligibility: Singapore Citizens or Permanent Residents onlyOverview:We are looking for a motivated Senior / Quality Validation Engineer to drive validation activities across manufacturing systems, equipment, processes, and computerized systems. The role ensures compliance with GMP, regulatory requirements, and internal quality standards. You will play a key part in reviewing validation documentation, leading validation activities, managing change controls, and supporting investigations to maintain validated status across the site.Key Responsibilities:Validation Governance & DocumentationDraft, review, and update validation policies, SOPs, protocols, and reports.Ensure documentation complies with cGMP and regulatory guidelines.Approve qualification deliverables (IQ/OQ/PQ) before progressing to the next phase.Change Control & ComplianceAssess changes affecting equipment, systems, or processes.Approve change controls and validate impact assessments.Support audits by providing validation documentation and evidence of compliance.Investigations & CAPA SupportParticipate in investigations to determine root causes and assess validation impact.Recommend corrective and preventive actions related to validation compliance.Ensure investigation records are complete, accurate, and timely.Project & Validation CoordinationAct as Validation Coordinator for projects with quality or regulatory impact.Lead validation-related discussions and ensure milestones are met.Support commissioning, qualification, FAT/SAT, and other validation lifecycle activities.Ongoing Validation MaintenanceConduct periodic validation reviews to ensure continued compliance.Recommend and plan re-validation based on review outcomes.Review and approve Continued Process Verification (CPV) documentation.Qualifications:Bachelor’s degree in Science, Engineering, or related field.1–5 years of experience in the pharmaceutical or biotech industry.Strong knowledge of GMP, validation lifecycle, and Computer System Validation (CSV).Hands-on experience with validation documentation, change control, and investigations.Excellent attention to detail, analytical skills, and ability to manage multiple validation tasks.Strong collaboration and communication skills.#SingaporeJobs #GMP #ValidationEngineer #PharmaCareers #QualityAssurance #CSV #LifeSciences #TuasJobs #EngineeringRoles