QC Associate - System Support (Equipment Qualification/ Validation/Pharma)

QC Associate - System Support (Equipment Qualification/ Validation/Pharma) 6 Months Contract Location : Gul Circle Salary Up to $6,800 depending on experience Completion Bonus 1 Month Our client delivers vital healthcare solutions worldwide, powered by the precision and dedication of its Manufacturing & Supply teams. With your talent, they can expand their impact—protecting more people and offering hope to patients and their families. Responsibilities: • Updating the site validation master plan and procedures related to ALCM and CPV of GXP lab equipment. • Support periodic analytical method control trend review/ investigation and data evaluation on method performance, recommend method improvements where appropriate. • Support the life cycle management of the QC lab equipment i.e qualification of QC equipment and periodic review are maintained for their intended use. • Decommissioning of QC equipment and maintaining up to date the lab equipment inventory. • Participate in proper documentation issuance and review of qualification and maintenance deliverables, such as risk assessments, traceability matrices, protocols, reports, deviations, and summary reports. • Support laboratory qualification Investigation and resolving any quality control events, issues or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs. • Providing support during regulatory inspections and audits. • Prepare metrics and monitoring data for the qualification and validation activities, to identify trends and issues, during life cycle management of QC laboratory equipment. • Support initiatives for continuous improvement in QC support processes related to lab equipment management in coordination with QC excellence team. • Support invalid assay trending program in the QC laboratory. • Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements. • Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasks. Requirements • Minimum of two (2) years of experience in quality control within the pharmaceutical industry , including good knowledge of Good Manufacturing Practices (GMP) and regulatory requirements, with hands-on exposure and theoretical requirement of QC laboratory instruments and ALCM management. • Bachelor’s Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology • Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements. • Proficiency in identifying issues and implementing effective solutions to resolve quality control problems. • Good understanding of good laboratory practices, good documentation practice and data integrity requirements. • Experienced in analytical method continuous monitoring requirements. • Strong interpersonal relationships to establish the partnerships necessary for the development of the Quality culture. Lim Pey Chyi - Apple.lim@manpower.com.sg Recruitment Consultant (R2090579) Manpower Staffing Services (S) Pte Ltd EA Licence: 02C3423