CQV & Validation Specialist – Hybrid, Singapore

NO DEVIATION PTE. LTD.; Singapore; Hybride; SGD 90 000 - 140 000; Plein temps

Résumé du poste

NO DEVIATION PTE. LTD. in Singapore seeks a CQV, Validation & Quality Consultant with a hybrid profile to support end-to-end commissioning, qualification, validation and quality assurance across pharma, biotech and medical device projects.

You will lead CQV activities, develop validation protocols, prepare QA documents, support regulatory compliance and collaborate with engineering, QA and digital teams to deliver compliant solutions.

Qualifications

• Bachelor's or master's degree in Engineering, Life Sciences or Pharmacy
• Minimum 3 years' CQV/validation/quality experience in pharma/biotech/medical devices
• Strong GMP knowledge and validation protocol experience
• Hands-on equipment/utilities qualification and CSV
• Excellent documentation and English communication
• Singapore/APAC experience is a plus

Responsabilités

• Lead and execute CQV for equipment, utilities, facilities and CSV
• Develop, review and execute DQ/IQ/OQ/PQ and cleaning/process validation
• Prepare and optimize QA documents (SOPs, reports, risk assessments)
• Support GMP/FDA/EMA/PIC/S or HSA Singapore regulatory compliance
• Manage client audits, inspections and remediation actions
• Collaborate with engineering, QA and digital teams for project delivery
• Advise on data integrity and participate in digital validation projects
• Provide technical expertise and training to client teams

Connaissances

CQV

Validation

Quality Assurance

Documentation

English Communication

Project Management

Formation

Engineering/Life Sciences/Pharmacy degree

Outils

GxP Systems

CSV & Qualification Docs

Description du poste

NO DEVIATION PTE. LTD. in Singapore seeks a CQV, Validation & Quality Consultant with a hybrid profile to support end-to-end commissioning, qualification, validation and quality assurance across pharma, biotech and medical device projects.

You will lead CQV activities, develop validation protocols, prepare QA documents, support regulatory compliance and collaborate with engineering, QA and digital teams to deliver compliant solutions.