Senior QA Validation Lead - Pharma Manufacturing

Kingsforce Management Services Pte Ltd; Singapore; On-site; SGD 120,000 - 160,000; Full time

Job summary

Kingsforce Management Services Pte Ltd is seeking a senior QA/Validation professional for a project-based assignment in Tuas, Singapore. You will support commissioning, qualification and validation across facilities for clinical and commercial manufacturing, working with Manufacturing, Engineering, QC, MS&T and IT teams.

The candidate should have 10+ years' validation experience in regulated pharma, solid cGMP knowledge, and provide QA oversight on deliverables, investigations, audits and risk

Qualifications

• 10+ years validation experience in a sizeable QA function within regulated pharma environments.
• Strong understanding of cGMP requirements and Pharmaceutical Quality Systems.
• Experience providing quality oversight within manufacturing/QC, validation, and related operations.
• Excellent verbal and written communication with stakeholder management.

Responsibilities

• Provide QA oversight during commissioning, qualification and validation of manufacturing equipment, utilities, QC instruments, and facilities.
• Review and approve qualification/validation deliverables and change controls.
• Guide on GxP expectations and participate in audits, inspections, and health authority interactions.
• Identify and communicate quality risks and ensure mitigations are implemented.
• Deliver quality training and mentor junior team members.

Skills

cGMP knowledge

QA oversight

Validation leadership

Risk management

Regulatory interpretation

Cross-functional collaboration

Audits & inspections

Investigations & CAPAs

Education

Bachelor's or Master's in Science/Engineering

Tools

Pharma systems

Data analytics tools

Job description

Kingsforce Management Services Pte Ltd is seeking a senior QA/Validation professional for a project-based assignment in Tuas, Singapore. You will support commissioning, qualification and validation across facilities for clinical and commercial manufacturing, working with Manufacturing, Engineering, QC, MS&T and IT teams.

The candidate should have 10+ years' validation experience in regulated pharma, solid cGMP knowledge, and provide QA oversight on deliverables, investigations, audits and risk