QA Validation Specialist 1 (1-Year Contract)

About This Role

GSK seeks a QA Validation Specialist for a 1-year contract in Tuas, Singapore. This role provides oversight and leads validation activities for major projects, ensuring compliance with quality systems.

Responsibilities

• Provide QA oversight for validation projects (equipment/CS).
• Lead cleaning validation strategy and execution.
• Author, review, and approve validation documents (plans, protocols, reports).
• Assess validation impact for changes, deviations, and investigations.
• Act as QA approver for critical quality documents (deviations, CAPAs).
• Provide SME on validation strategy to cross-functional teams.

Requirements

• Bachelor’s degree in science, engineering, or related field.
• Minimum 5 years' experience in pharma QA/validation roles.
• Practical knowledge of cGMP and regulatory requirements.
• Experience authoring/approving validation documents and SOPs.
• Proven experience assessing impact of changes/deviations on validation status.
• Strong cross-functional communication skills.