GMP Compliance & Quality Audit Specialist

Blaine Corporation; Carmona; On-site; PHP 320,000 - 460,000; Full time

Job summary

Blaine Corporation seeks a QA Compliance Specialist to monitor and maintain GMP documentation and ensure site-wide compliance. You will assist in audits and supplier accreditation, supporting CAPA and continual improvement initiatives.

The role requires 2–3 years in related fields with deep experience in document review, regulations, and change management across veterinary, cosmetics, or pharmaceutical sectors.

Qualifications

• 2-3 years working experience in related field.
• 3 years working experience in document review, audits, regulations, standards, supplier accreditation, document and change management.

Responsibilities

• Monitor and maintain completeness of GMP process documentation.
• Maintain site-wide compliance by keeping activities and docs current and in-use.
• Assist with internal and external audits and third-party audit prep.
• Support supplier accreditation/qualification and regulatory compliance.
• Manage documentation for Quality Management System processes.

Skills

Documentation review

Audit preparation

Regulatory compliance

CAPA implementation

Quality mgmt systems

Continuous improvement

Education

BSc in Food Technology / Chemistry / Pharmacy

Tools

Document control systems

Job description

Blaine Corporation seeks a QA Compliance Specialist to monitor and maintain GMP documentation and ensure site-wide compliance. You will assist in audits and supplier accreditation, supporting CAPA and continual improvement initiatives.

The role requires 2–3 years in related fields with deep experience in document review, regulations, and change management across veterinary, cosmetics, or pharmaceutical sectors.