Pharma QA Associate: GMP, Audits & Documentation

SGS; Muntinlupa; On-site; PHP 360,000 - 900,000; Full time

Job summary

SGS Philippines is seeking an experienced QA professional to support Change Control, document control, and quality systems in a GMP setting. You will ensure timely closure of CCRs and act as site representative for training and document control programs.

You will maintain client test methods and databases, coordinate Quality Agreements, and support internal and regulatory audits, including responses to findings. A 3-month onsite start with potential hybrid work is noted.

Qualifications

• Bachelor's in a scientific field is required.
• Minimum 3 years QA in Pharma.
• Knowledge of GMP regulations required; USP preferred.
• Proficiency with MS Office applications (Outlook, Word, Excel).
• Excellent written and strong verbal communication skills in English.

Responsibilities

• Review and approve CCRs and ensure timely closure with owners.
• Be site representative for Training and Document Control systems.
• Maintain client test methods and specification databases; coordinate Quality Agreement approvals.
• Coordinate and support audits; prepare responses to audit findings.
• Provide QA backup, including release of Certificates of Analysis and vendor evaluations.

Skills

Quality Assurance

GMP Knowledge

English Proficiency

Education

Bachelor’s degree in a scientific field

Tools

MS Office

Job description

SGS Philippines is seeking an experienced QA professional to support Change Control, document control, and quality systems in a GMP setting. You will ensure timely closure of CCRs and act as site representative for training and document control programs.

You will maintain client test methods and databases, coordinate Quality Agreements, and support internal and regulatory audits, including responses to findings. A 3-month onsite start with potential hybrid work is noted.