Quality Validation Consutlant

Quality Validation & Documentation Consultant

Location: Singapore (Onsite)

Contract Length: 12 Months

Start Date: Immediate

Our client is seeking an experienced Quality Validation & Documentation Consultant for a 12-month onsite contract in Singapore. This hands-on role will support validation and GMP quality activities within a regulated manufacturing environment, requiring someone who can work independently and drive validation and documentation deliverables through to completion.

Key Responsibilities:

• Support site validation activities within a GMP-regulated environment.
• Author, review, revise and execute validation documentation, including protocols and reports.
• Prepare, maintain and improve quality documentation.
• Work with site personnel to identify documentation needs and deliver project milestones.
• Review validation and quality records for compliance, accuracy and completeness.
• Identify and help resolve validation and documentation gaps.

Requirements:

• Experience supporting quality activities within pharmaceutical, biotechnology, medical device, or life sciences manufacturing environments.
• Strong hands-on validation experience across equipment, process, cleaning, utilities, or CQV activities.
• Experience preparing, reviewing and maintaining validation and quality documentation.
• Solid understanding of GMP regulations and quality systems.
• Strong technical writing, documentation and communication skills.