Location
singapore
Job Type
Full-time
Posted
June 10, 2026
Job Description
Position Overview
We are seeking a
Computer System Validation (CSV) Engineer
that is able to join our pharmaceutical operations team
Mid May 2026
. The successful candidate will be responsible for ensuring compliance of computerized systems with regulatory requirements, focusing on the
qualification of standalone systems
used in GMP manufacturing and laboratory environments.
Key Responsibilities Manage the full CSV lifecycle
(planning, design, testing, execution, reporting, and closure) for standalone systems such as LIMS, chromatography data systems, environmental monitoring software, and equipment control systems. Develop and execute validation documentation
including User Requirement Specifications (URS), Functional Specifications (FS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Perform risk assessments
to determine validation scope and ensure compliance with
GAMP...
We are seeking a
Computer System Validation (CSV) Engineer
that is able to join our pharmaceutical operations team
Mid May 2026
. The successful candidate will be responsible for ensuring compliance of computerized systems with regulatory requirements, focusing on the
qualification of standalone systems
used in GMP manufacturing and laboratory environments.
Key Responsibilities Manage the full CSV lifecycle
(planning, design, testing, execution, reporting, and closure) for standalone systems such as LIMS, chromatography data systems, environmental monitoring software, and equipment control systems. Develop and execute validation documentation
including User Requirement Specifications (URS), Functional Specifications (FS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Perform risk assessments
to determine validation scope and ensure compliance with
GAMP...
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