csv

Job Description Contribute to Life Science projects for Antaes Asia clients. Work with cross functional team in providing Quality oversight in computerized system life cycle procedure and ensure compliance to GXP standards and company policies and procedures. Provide guidance and support to establish systems for ensuring Data integrity, compliance to CSV...

We are seeking a CSV Engineer to support manufacturing operations within a leading biopharmaceutical facility. The successful candidate will work closely with cross-functional teams to support a major migration and equipment validation programme within a regulated pharmaceutical environment. Key Responsibilities: Lead and support CSV activities for...

Key Responsibilities: Deliver CSV consulting projects to support implementation of computerized systems (e.g., DeltaV, Siemens PCS7, Rockwell PLCs) in the Life Sciences clients with compliance of GxP and other relevant regulatory standards. Deliver CSV consulting projects to support OS upgrade (e.g., Windows 11 upgrade) for laboratory and manufacturing...

Position Overview We are seeking a CSV Engineer to support the validation of Emerson DeltaV automation systems in a pharmaceutical and biopharmaceutical manufacturing environment. Responsibilities include reviewing URS, functional and design specifications, drafting and executing test scripts for batch recipes, control logic, interlocks, alarms and...

Job Title: CSV Engineer – Pharmaceutical Manufacturing Location: Singapore Employment Type: Full‑time About The Role We are seeking experienced CSV Engineers to join our team in Singapore. The role involves leading computerized system validation activities in GMP‑regulated environments, ensuring compliance with global standards, and supporting...

RoviSys partners with biotech and pharmaceutical manufacturing clients to deliver automation, IT/OT integration, and computer system validation services. The CSV Engineer supports client CSV strategy and validation activities for automation and IT/OT products deployed on client sites, including local software instance qualification for global/core systems...

Job Title: CSV Engineer – Pharmaceutical Manufacturing Location: Singapore Employment Type: Full‑time About The Role We are seeking experienced CSV Engineers to join our team in Singapore. The role involves leading computerized system validation activities in GMP‑regulated environments, ensuring compliance with global standards, and supporting digital...

Position Overview We are seeking a CSV Engineer to support the validation of Emerson DeltaV automation systems in a pharmaceutical and biopharmaceutical manufacturing environment. Responsibilities include reviewing URS, functional and design specifications, drafting and executing test scripts for batch recipes, control logic, interlocks, alarms and...

Position Overview We are seeking a CSV Engineer to support the validation of Emerson DeltaV automation systems in a pharmaceutical and biopharmaceutical manufacturing environment. Responsibilities include reviewing URS, functional and design specifications, drafting and executing test scripts for batch recipes, control logic, interlocks, alarms and...

RoviSys partners with biotech and pharmaceutical manufacturing clients to deliver automation, IT/OT integration, and computer system validation services. The CSV Engineer supports client CSV strategy and validation activities for automation and IT/OT products deployed on client sites, including local software instance qualification for global/core systems...

AMTSOL: A leader in Life Science Manufacturing Technology solutions, we are looking for top talent to be part of the dynamic team and drive the growth of the business. AMTSOL: A leader in Life Science Manufacturing Technology solutions, we are looking for top talent to be part of the dynamic team and drive the growth of the business. Job Titles CSV...

About the Role We are seeking a CSV Engineer to support manufacturing operations within a leading biopharmaceutical facility. The successful candidate will work closely with cross-functional teams to support a major migration and equipment validation programme within a regulated pharmaceutical environment. Key Responsibilities: Lead and support CSV...

Manage end-to-end system administration for all supported applications and infrastructure, including user access management, incident troubleshooting, issue resolution, and root cause analysis (RCA). Support and progressively take ownership of digital project execution, including functional testing, User Acceptance Testing (UAT), system implementation,...

Primary Objective / Purpose To execute rigorous analytical testing to guarantee vaccine quality, safety, and efficacy during validation and commercial production. Key Responsibilities Execute in-process testing, raw material testing, and stability testing. Perform batch release testing for PPQ batches. Conduct analytical method validation and equipment...

ORKA LIFESCIENCE PARTNERS PTE. LTD. is seeking a CSV Consultant to support validation activities for computerized systems in regulated Life Sciences environments in Singapore. You will ensure GxP compliance and oversee documentation across URS, FDS, Risk Assessments, and validation plans. The role requires 2–4 years in CSV or related quality roles, with...

ANTAES Asia Pte. Ltd. is seeking a CSV/GxP specialist to contribute to life science projects in Singapore. You will oversee the computerized system lifecycle and ensure adherence to GXP standards and company policies. The role involves guiding data integrity, CSV planning, and 21 CFR Part 11 compliance. You will act as a key focal point for CSV topics such...

Manpower Staffing Services (Singapore) Pte Ltd seeks a Pharma Life Cycle Management Engineer (CSV/Automation) for a 12-month contract at Tuas, Singapore. The role involves end-to-end lifecycle activities for computerized systems, CSV development, and validation planning in a pharmaceutical context. The candidate will generate C&Q protocols, execute...

NOVEXX PTE. LTD. in Tuas, Singapore, seeks a Life Cycle Management Engineer to oversee the full lifecycle of computerized systems within the pharmaceutical sector, from design and installation through qualification and retirement. You will draft C&Q/CSV documentation (IQ/OQ/PQ), maintain validation plans, and ensure compliance with GAMP, cGMP, and industry...

RoviSys in Singapore seeks a CSV Engineer to support client CSV strategy and validation activities for automation and IT/OT products deployed on client sites, including local software instance qualification for global/core systems (e.g., MES). You will collaborate with client IT/OT, Quality, MSAT/Automation, Manufacturing, and Quality Control teams on...

No deviation Pte Ltd. in Singapore seeks a CSV Engineer to validate Emerson DeltaV automation systems in pharma manufacturing. You will draft and execute test scripts for batch recipes, interlocks, alarms, and sequences, review URS/FS/DS, and support FAT, SAT, IQ, and OQ activities. The role emphasizes GMP/GAMP 5 compliance, strong documentation, and...