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.
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