Computer Systems Validation Engineer

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective...

**As a computer systems validation specialist you will work as part of a multidiscipline team, supporting the design, construction, commissioning and qualification of new and modified pharmaceutical and life science facilities, equipment and processes.** **Responsibilities**: - Primary focused on Emerson DeltaV, Siemens PLC, MES, LIMS and Data Historian...

Job Title: CSV (Computer System Validation) Engineer - QualityLocation: Tuas, SingaporeIndustry: Life Sciences / Pharmaceutical ManufacturingRole Overview:We are looking for a Computer System Validation (CSV) Engineer with hands-on experience in validation documentation, test execution, and QA oversight support for regulated GxP systems. The ideal candidate...

**Responsibilities** - Develop and implement strategies for the validation of computer systems in compliance with domestic and international regulations. - Prepare and maintain all necessary validation documents, including validation master plans, validation plans, and risk assessments. - Execute validation protocols and prepare validation summary reports. -...

Job Title: CSV (Computer System Validation) Engineer - QualityLocation: Tuas, SingaporeIndustry: Life Sciences / Pharmaceutical ManufacturingRole Overview:We are looking for a Computer System Validation (CSV) Engineer with hands-on experience in validation documentation, test execution, and QA oversight support for regulated GxP systems. The ideal candidate...

**Responsibilities**: - Create and refine validation protocols for GxP critical reports, focusing on Computerized Equipment Validation within the QC lab. - Configure static Master Data for validated/GMP-compliant LabWare LIMS (version 6), specifically emphasizing Computerized Equipment. - Actively participate in executing, reviewing, and approving...

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

We are currently expanding our team within our Life Sciences Division team and are looking for a **CSV Engineer**to support projects on site with a client. The following are key responsibilities: - Design, develop, and execute of CSV strategies for DeltaV systems, ensuring alignment with regulatory requirements and project timelines. - Collaborate with...

**Roles & Responsibilities** The Senior Computer System Validation (CSV) Engineer will be based in one of clients who is among the top tier pharmaceutical giants. The engineer will provide a wide range of support for GMP Computerized System and Data Integrity Activities at site. **Responsibilities** - Coordinate/manage multiple small and large CSV/Data...