Senior Site QA Lead – GMP Compliance & Validation

Manpower Singapore; Singapore; On-site; SGD 120,000 - 180,000; Full time

Benefits offered by this job

Medical coverage

Career growth opportunities

Job summary

Manpower Singapore is seeking a Site Quality Manager to lead QA activities across manufacturing, packaging, warehouse and supporting areas to ensure GMP, QMS and regulatory readiness.

You will supervise QA personnel, develop site QA plans, oversee material release and cleaning validation, and lead audits and CAPA processes with a strong focus on data integrity and continuous improvement.

Qualifications

• Bachelor’s degree or above in Pharmacy, Pharmaceutical Science, or a related discipline.
• Minimum 5 years of relevant experience in pharmaceutical QA, GMP, and site quality management.
• At least 2 years of supervisory or teams leadership experience in QA.
• Knowledge of GMP standards (PIC/S, EU, FDA) and data integrity practices.

Responsibilities

• Lead on-site QA activities to ensure GMP, QMS and regulatory compliance.
• Develop site QA work plans and allocate resources for monitoring and material release.
• Supervise QA personnel and provide coaching for effective quality oversight.
• Conduct GMP inspections, audits, and quality risk assessments; drive issue resolution.
• Provide QA oversight during cleaning validation, deviation management and CAPA tracking.

Skills

GMP knowledge

QA leadership

Documentation control

Root cause analysis

Data integrity

Audit coordination

Education

Bachelor’s degree in Pharmacy or related field

Tools

LIMS

SAP

Job description

Manpower Singapore is seeking a Site Quality Manager to lead QA activities across manufacturing, packaging, warehouse and supporting areas to ensure GMP, QMS and regulatory readiness.

You will supervise QA personnel, develop site QA plans, oversee material release and cleaning validation, and lead audits and CAPA processes with a strong focus on data integrity and continuous improvement.