QA Operations Specialist — GMP & Validation

NUSANTARA PRIME CONSULTING PTE LTD (Nusaprime); Singapore; On-site; SGD 65,000 - 120,000; Full time

Job summary

NUSANTARA PRIME CONSULTING PTE LTD (Nusaprime) is seeking a QA professional to oversee manufacturing, testing and validation activities in a GMP-driven Biopharma environment.

You will ensure compliance with internal procedures and regulatory requirements, manage deviations, CAPA, change controls, and data integrity across documentation and systems. The role supports a 12-month contract with opportunities to contribute to site readiness and client audits while working with cross-functional teams.

Qualifications

• Bachelor''s degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields.
• 1-3 years QA experience in Biopharma for junior role; 3-5 years for senior role.
• Familiar with FDA, EMEA, and GMP requirements.

Responsibilities

• Oversee routine quality control for on-site GMP production and testing.
• Contribute to establishing an effective quality system across GMP functions.
• Provide QA oversight for validation and re-qualification activities.
• QA Review of Qualification and Validation protocols and reports, including computer system validation.
• Ensure data integrity of documentation and electronic data per regulations and SOPs.
• Participate in site readiness programs, self-inspection, and data integrity surveillance for audits.
• Manage quality events: deviations, change controls, CAPA, and lab investigations.
• Carry out additional tasks as assigned by leadership.

Skills

Quality Assurance

GMP Knowledge

Data Integrity

Cross-functional Communication

Education

Bachelor''s degree or higher in Biologics/Pharma

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

NUSANTARA PRIME CONSULTING PTE LTD (Nusaprime) is seeking a QA professional to oversee manufacturing, testing and validation activities in a GMP-driven Biopharma environment.

You will ensure compliance with internal procedures and regulatory requirements, manage deviations, CAPA, change controls, and data integrity across documentation and systems. The role supports a 12-month contract with opportunities to contribute to site readiness and client audits while working with cross-functional teams.