Job Description

Our client, a reputable MNC and leading pharmaceutical company, is inviting applicants with relevant experience to join their dynamic team. Location: Tuas Up to $5,000 Basic + Travel Allowance + Bonus + Staff Benefits Salary will commensurate with Experience & Qualifications 5 Days Week with Flexi Work Arrangement OptionResponsibilities: Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements. Perform / review and document equipment verification and calibration in accordance to procedures. Highlight any abnormalities detected during testing / review and raise laboratory investigations as required. Support laboratory investigations and perform equipment troubleshooting where required. Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed. Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports). Set up and maintain QC processes (e.g. reference standards and retention sample management), perform investigations as required for any associated deviations. Conduct training for fellow colleagues from QC and other departments (e.g. Production). Collaborate with cross-functional teams to drive flawless execution.Requirements: Diploma / Degree in Science (preferably Chemistry) or equivalent Comprehensive knowledge of cGMPs and ALCOA principlesEA License No: 14C7092EA Registration No: R22105950 (Valmond Tham)
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