Job Description
Job Title: CSV Engineer – Pharmaceutical Manufacturing
Location: SingaporeEmployment Type: Full‑time
About the RoleWe 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 transformation initiatives.
Key Responsibilities- Execute Computerized System Validation (CSV) lifecycle activities for manufacturing systems.
- Author and review deviation reports, change control documentation, and operating plans .
- Develop and maintain validation protocols (IQ/OQ/PQ) and system test scripts.
- Support system validation projects including MES, automation, and IT systems.
- Collaborate with QA, document control, and operations teams to ensure compliance with GMP, FDA 21 CFR Part 11, and GAMP 5. <...
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Submit your application today and join our talented team at Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL).
Submit ApplicationJob Details
- Location singapore, singapore
- Job Type Full-time
- Category Other-General
- Posted Date July 03, 2026
- Application Deadline August 12, 2026