Pharma Csv Engineer

**Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and CSV system) - Responsible for overseeing execution of but not limited to IQ, OQ, PQ and ERES Test Scripts of QC laboratory equipment (lab...

**About the Role**: We are hiring a CSV Engineer to support pharmaceutical manufacturing projects in Singapore. The role focuses on validating GxP computerised systems to ensure compliance with relevant regulatory and data integrity standards across the project lifecycle. **Key Responsibilities**: - Author and review validation documentation (URS, FS, RTM,...

**Job description**: **Responsibilities**: - POC and coordinator for data integrity projects, ensure company’s quality requirements and agencies’ requirements are met. - Quality oversight for automation qualifications (Delta V and BAS) and GMP equipment qualifications - Review and approve of qualifications - related documentations (protocols and...

**Responsibilities**: - Manage Computer System Validation Lifecycle from design to execution phases; Including relevant CSV documentations such as Configuration specification, design review, commissioning documents, and protocols. - Responsible for preparation of CSV documents and protocols, perform execution for automated equipment and/or control systems,...

Position Description: - The CSV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site. - Position Requirements: - BS in a Computer Science or Engineering field or equivalent...

This role is responsible for supporting Identity and Access Management systems and other projects to qualify some IT systems. **Responsibilities**: - Manage Computer System Validation Lifecycle from design to execution phases, Including relevant CSV documentations such as Configuration specification, design review, commissioning documents, and protocols. -...

**Responsibilities**: - Manage Computer System Validation Lifecycle from design to execution phases; Including relevant CSV documentations such as Configuration specification, design review, commissioning documents, and protocols. - Responsible for preparation of CSV documents and protocols, perform execution for automated equipment and/or control systems,...

Boon Lay Way, Singapore | Posted on 09/18/2025Develop and review validation plans, protocols (IQ, OQ, PQ), and reports for computerized systems. Perform risk assessments and impact analysis related to system validation. Ensure compliance with regulatory guidelines such as FDA 21 CFR Part 11, EU Annex 11, and GAMP 5. Collaborate with IT, Quality Assurance,...

This position is responsible for the validation of automated equipment and/or control systems. Familiarity in DCS (Distributed Control System), PLC/SCADA and OSI PI is a plus and also have thermal mapping experience. In this role, the engineer has to work in accordance with the company’s policies and procedures to ensure validation is performed in...

This position is responsible for the validation of automated equipment and/or control systems. Familiarity in DCS (Distributed Control System), PLC/SCADA and OSI PI is a plus and also have thermal mapping experience. In this role, the engineer has to work in accordance with the company’s policies and procedures to ensure validation is performed in...