Csv engineer jobs in Singapore

A CSV engineer consultant position at Antaes Asia clients contributing to Life Science projects. · Work with cross-functional teams providing quality oversight in computerized system life cycle procedure ensuring compliance to GXP standards. · ...

+Job summary · +Develop and review validation plans, protocols (IQ, OQ, PQ), and reports for computerized systems. Ensure compliance with regulatory guidelines such as FDA 21 CFR Part 11, EU Annex 11, and GAMP 5.Bachelor's degree in Pharmacy, Life Sciences, Engineering, Computer ...

Contribute to Life Science projects for Antaes Asia clients. · ...

Develop 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. · ...

Develop 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 ...

The candidate is responsible for the validation of automated equipment and/or control systems. · Manage Computer System Validation Lifecycle from design to execution phases; Including relevant CSV documentations such as Configuration specification, design review, commissioning do ...

Our client is looking for a Senior CSV Engineer who can operate independently to take full ownership of end-to-end CSV activities for automation and computerized systems. · ...

We are seeking Computer System Validation (CSV) Engineers with strong hands-on experience in Emerson DeltaV systems. · Competitive remuneration. · ...

Lead end-to-end Computer System Validation (CSV) activities for DeltaV automation systems ensuring full compliance with GMP requirements. · Review and approve DeltaV Functional Specification (FS) and Design Specification (DS) · ...

About No deviation · No deviation is dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, ...

About No deviation is looking for a CSV Validation Engineer to support the validation lifecycle of automation systems in a regulated pharmaceutical manufacturing environment. The role involves creating and reviewing documentation such as URS and qualification protocols. · Develop ...

· About No deviation · At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory ...

Key Responsibilities: · Deliver consulting projects to support implementation of computerized systems (e.g., DCS, PLC, MES) in the Life Sciences clients with compliance of GxP and other relevant regulatory standards. · Deliver consulting projects to support OS (e.g., Windows OS) ...

You will manage Computer System Validation activities and system lifecycle from design requirement analysis to retirement for drug substance and drug product manufacturing. · ...

We are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. · As a dynamic expert in engineering consultancy, · Commissioning Qualification Validation (CQV), and Quality, Compliance, · and Regulatory services, · we are looking for ind ...

This is a job summary for the Quality Control Specialist position at Amaris Consulting.The successful candidate will be responsible for leading analytical equipment qualification and ensuring timely implementation of projects while maintaining full compliance with corporate and r ...

A leader in life science manufacturing technology solutions seeks a top talent to drive business growth as a CSV Consultant with 3–6 years of experience in GxP-compliant DeltaV systems within pharmaceutical manufacturing environments. · ...

We are seeking a CSV Consultant with 3–6 years of experience to support GxP-compliant DeltaV systems within pharmaceutical manufacturing environments. · ...

We are seeking a Senior CSV / C&Q Lead with deep expertise in GxP Computer System Validation and Commissioning & Qualification across pharmaceutical manufacturing environments. · Lead and execute end-to-end CSV and C&Q activities across the full lifecycle: · URS Risk Assessment I ...

We are seeking a Senior CSV / C&Q Lead with deep expertise in GxP Computer System Validation and Commissioning & Qualification across pharmaceutical manufacturing environments. · The role requires strong hands-on experience across the full CSV and C&Q lifecycle. · ...