Validation Engineer — CQV & GxP Specialist

ESCO ASTER PTE. LTD.; Singapore; Vor Ort; SGD 70.000 - 100.000; Vollzeit

Zusammenfassung

Esco Aster Pte Ltd is seeking a dedicated MSAT CQV professional to lead commissioning, qualification and validation for biopharma equipment, utilities and processes in a GxP setting. You will prepare validation protocols, write reports and coordinate with multiple teams to ensure compliance.

The role requires a degree in engineering or science, strong CQV knowledge, and the ability to travel if required. Singapore site-based position with full-time commitment.

Qualifikationen

• GxP knowledge and regulatory awareness for pharma/biopharma.
• CQV/Validation lifecycle experience (URS, DQ, FAT/SAT, IOQ, CSV).
• Strong technical writing and presentation skills.
• Excellent written and verbal communication; able to coordinate cross-functionally.

Aufgaben

• Perform risk-based CQV activities for equipment, utilities, facilities and processes.
• Develop validation protocols and regulatory-compliant reports.
• Coordinate with internal teams and external vendors to meet CQV objectives.
• Prepare design reviews, URS and qualification documents as needed.
• Investigate deviations and contribute to CAPA and incident reports.

Kenntnisse

GxP knowledge

CQV/Validation

Technical writing

Communication

Ausbildung

Engineering/Science degree

Tools

MS Office

Jobbeschreibung

Esco Aster Pte Ltd is seeking a dedicated MSAT CQV professional to lead commissioning, qualification and validation for biopharma equipment, utilities and processes in a GxP setting. You will prepare validation protocols, write reports and coordinate with multiple teams to ensure compliance.

The role requires a degree in engineering or science, strong CQV knowledge, and the ability to travel if required. Singapore site-based position with full-time commitment.