QC Validation Specialist

Job Description: QC Validation Specialist

Work Schedule: Monday - Friday, 8:00 AM - 5:00 PM

Project Overview

We are seeking dedicated QC Validation Specialists to support a biotech plant project in Tuas. The project is a high-impact opportunity for professionals who thrive in fast-paced, milestone-driven environments.

The Role

Reporting to the Associate Director of Quality Control, you will ensure that all equipment qualification and retirement activities are executed in strict accordance with global GMP standards.

This role focuses on the end-to-end lifecycle management of lab systems during a site transition.

Core Responsibilities

• Execute the qualification, requalification, and relocation of laboratory equipment.

• Manage the decommissioning and retirement protocols for a wide range of GMP systems.

• Ensure all documentation meets the compliance standards of a world-class pharmaceutical manufacturing site.

• Collaborate with cross-functional teams

Requirements

Education & Experience

• Academic: Diploma or Bachelor's Degree in any Engineering field, Chemical, Biotechnology, Pharmaceutical Sciences or Mechanical.

• Industry Background: Must have direct experience within a GMP Pharmaceutical or Biopharma environment.

Technical Headcount :

• Senior Specialist : . Minimum 5 years of experience in the qualification and decommissioning of complex GMP lab equipment.

• Junior Specialist : . Minimum 2 years of experience focused on simpler GMP equipment.

Why Apply

• Hiring Process: Streamlined interview process (1-round in-person interview).
• Stable Hours: Standard office hours with no routine overtime required.
• Transport Allowance is provided.