QC Validation Specialist (Equipment Qualification/ Pharma/ Contract)

QC Validation Specialist (Equipment Qualification/ Pharma/ Contract) Duration: 6 months Location: Tuas    Salary : Up to $10,000 depending on experience Our client is a US healthcare and a leading global biopharmaceutical company. They have more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission Responsibilities • Perform/review system qualification, requalification, relocation, decommissioning and retirement for laboratory equipment in accordance with approved procedures and standard lead time. • Assume role of Subject-Matter-Expert of laboratory system lifecycle, collaborates closely with cross-functional teams and above-site functions. This includes initiating alignments proactively, sharing expertise, and providing input to ensure alignment and consistency across the organization. • Author/review Quality Notifications and Test Exception Reports, lead root cause analysis and ensure effective implementation of related actions within the agreed timeframe.  • Conduct troubleshooting of laboratory system lifecycle, identifying and resolving any issues that may impact the business/work efficiency and compliance. • Identify opportunities and propose solutions to improve efficiency and compliance in processes, standards, and best practices within the team. • Provide leadership, expert guidance and support to team members, acting as a go-to resource for problem-solving and decision-making.    • Provide skills training to other team members, ensuring they have the necessary knowledge and competencies to perform their duties effectively. • Any other duties as assigned by reporting manager. Requirements: • Diploma or bachelor’s degree in chemical engineering or any other relevant engineering field • At least 5 years of experience in qualification, requalification, relocation, decommissioning and retirement of Good Manufacturing Practice (GMP) Lab equipment (not limited to Ultraviolet–Visible (UV-Vis) Spectrometer, Total Organic Carbon (TOC) Analyzer, Microplate Reader, Liquid Particle Counter, Capillary Electrophoresis (CE), High-Performance Liquid Chromatography (HPLC), Analytical Balances, Incubators, Particle Counters) • Experience in GMP environment within the pharmaceutical/chemical manufacturing. Lim Pey Chyi – Apple.lim@manpower.com.sg Recruitment Consultant (R2090579) Manpower Staffing Services (S) Pte Ltd EA Licence: 02C3423