Pharma Documentation QA Specialist – Digital Records & GxP

Manpower Staffing Services (Singapore) Pte Ltd; Singapore; On-site; SGD 81,000 - 97,000; Full time

Job summary

Manpower Staffing Services Singapore Pte Ltd in Tuas is hiring a Documentation QA Specialist (Pharma GMP/GxP/Compliance) on a 12-month contract to maintain document management processes meeting global quality standards and regulatory expectations.

Responsibilities include GMP governance, archival and scanning, lifecycle management, and cross-department collaboration to ensure content accuracy and regulatory compliance on site.

Qualifications

• Minimum 2 years experience in Manufacturing, Validation, Quality in pharma/biotech industry.

Responsibilities

• Maintain Document Management Processes to meet quality standards and regulatory expectations.
• Support implementation of digital documentation solutions like electronic logbooks and forms on site.
• Perform archival and scanning of documents for electronic archival.
• Manage the GxP documentation lifecycle (creation, revision, obsolescence).
• Collaborate with other departments to ensure content addresses business needs and regulatory requirements.

Skills

Documentation

GxP

Regulatory knowledge

Tools

Electronic logbooks

Digital forms

Job description

Manpower Staffing Services Singapore Pte Ltd in Tuas is hiring a Documentation QA Specialist (Pharma GMP/GxP/Compliance) on a 12-month contract to maintain document management processes meeting global quality standards and regulatory expectations.

Responsibilities include GMP governance, archival and scanning, lifecycle management, and cross-department collaboration to ensure content accuracy and regulatory compliance on site.