Cqv Engineer – Analytical/QC Laboratory Equipment (Pharmaceutical)

About our client : Our client is a leading global pharmaceutical company. About the role : Responsible for commissioning, qualification, and validation activities for analytical and QC laboratory equipment to ensure compliance with GMP requirements, regulatory standards, and company procedures. Develop and execute qualification protocols including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Perform commissioning and qualification activities for analytical/QC laboratory equipment such as HPLC/UHPLC, Gas Chromatography (GC), UV-Vis Spectrophotometers, TOC Analysers, Dissolution Systems, pH & Conductivity Meters, Balances, Laboratory Incubators, Ovens, and Refrigerators. Prepare and review qualification documents, risk assessments, validation protocols, and summary reports. Support FAT (Factory Acceptance Test), SAT (Site Acceptance Test), calibration, and vendor management activities. Perform temperature mapping activities and support equipment qualification lifecycle activities. Manage deviations, CAPAs, and change controls to ensure timely resolution and compliance. Ensure complete traceability from User Requirement Specifications (URS) through qualification testing and documentation. Support integration and verification of laboratory systems including LIMS, CDS, PCS, MES, and OSI PI Historian. Verify data integrity requirements including audit trails, user account management, security roles, electronic signatures, backup and restore functionality, and time synchronization. Collaborate with QA, QC, Engineering, Automation, IT teams, and vendors to ensure successful execution of qualification activities. About you: Bachelor’s Degree in Engineering, Life Sciences, Pharmaceutical Sciences, Chemistry, or related discipline. Minimum 5 years of experience in Commissioning, Qualification & Validation (CQV) activities for analytical and QC laboratory equipment within pharmaceutical, biotechnology, or GMP-regulated environments. Strong understanding of GMP requirements, Data Integrity principles (ALCOA+), and qualification lifecycle processes. Hands-on experience in executing IQ/OQ/PQ protocols and managing qualification documentation. Experience in risk assessments, deviation management, change controls, and validation reporting. Familiarity with chromatography data systems such as Empower or Chromeleon and knowledge of Computer System Validation (CSV) requirements will be advantageous. Knowledge of regulatory requirements including FDA, EU GMP, and PIC/S guidelines is preferred. Strong technical writing and documentation skills with good analytical and problem-solving abilities. Excellent communication, stakeholder management, and coordination skills. Strong attention to detail with a proactive approach and ability to work independently in a cross-functional environment. Other: Employment Type: Contract Work Schedule: 5 days per week Location: Tuas, Singapore *Please note that only shortlisted candidates will be contacted.* Employment Agency: Kingsforce Management Services Pte. Ltd. Employment Agency Licence No: 94C3545 EA Personnel: Kimberly Wong EA Personnel Reg. No.: R1984508