Csv Engineer – Deltav (Pharmaceutical)

About our client : Our client is a leading global pharmaceutical company. About the role : Plan, execute and manage DeltaV Computer System Validation (CSV) lifecycle activities. Prepare, review and execute validation documentation including URS, FS, DS, Risk Assessments, Traceability Matrix, IQ, OQ, PQ protocols and Validation Reports. Perform qualification of DeltaV hardware infrastructure, including Professional Plus, Application & Operator Stations, M-Series/S-Series/PK Controllers, CIOCs, I/O systems, network components and virtual environments. Validate DeltaV software applications, system configurations, security settings and functionality. Review and test Control Modules (CM), Equipment Modules (EM), Unit Modules, Batch Phases, Recipes, Alarms, Interlocks and Graphics. Execute and support IQ, OQ, PQ, FAT, SAT, commissioning and regression testing activities. Support integration activities involving MES and OSI PI Historian systems. Ensure compliance with GMP Data Integrity requirements, audit trails, user access management, security roles, electronic signatures, backup and restore functionality and time synchronization. Support cybersecurity and system hardening activities for validated systems. Manage deviations, discrepancies, change controls and validation deliverables. Participate in design reviews, risk assessments, FAT/SAT activities and change control reviews. Collaborate with Automation, CQV, Quality, IT, Manufacturing teams and external vendors throughout the project lifecycle. About you: Bachelor’s Degree in Engineering, Computer Science, Automation, Instrumentation, Pharmaceutical Technology or a related technical discipline. Minimum 5 years of experience in DeltaV Computer System Validation (CSV) within regulated pharmaceutical, biotechnology or life sciences environments. Proven experience in qualifying DeltaV hardware infrastructure and software modules. Strong knowledge of GAMP 5, FDA 21 CFR Part 11, EU Annex 11 and GMP Data Integrity requirements. Hands-on experience in preparing and executing IQ, OQ and PQ protocols and validation documentation. Experience with FAT, SAT, commissioning and change control processes. Experience with DeltaV integration involving MES and OSI PI Historian will be an advantage. Experience in CSV qualification of PLC/HMI-based systems such as Siemens SIMATIC/WinCC, SCADA systems or Siemens SIMATIC Logon will be desirable. Strong documentation, analytical and communication skills with the ability to work independently and collaborate effectively with cross-functional teams. 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