CSV Engineer

Job Description  We are looking for a CSV Engineer to support validation and qualification activities within a pharmaceutical environment. The role focuses on ensuring compliance of computerized systems with regulatory standards while supporting manufacturing and digital system initiatives.
Responsibilities   Prepare, review, and approve validation documentation.
Maintain accurate and compliant validation records.
Support validation and qualification activities for computerized systems.
Ensure systems are used in line with GxP regulations and internal protocols.
Train end users on proper system usage and compliance requirements.
Collaborate with cross-functional teams to support system integration and improvements.
Profile / Requirements   Bachelor's degree in IT, Business, or related field (or equivalent experience).
Experience working in a GxP-regulated environment.
Understanding of computerized system validation (CSV) processes.
Ability to work independently with moderate supervision.
Strong adaptability and problem-solving mindset.
Excellent written communication skills in English.
Nice to Have   Knowledge of automation systems (ISA-95 level 2/3).

Experience with SDLC (Systems Development Lifecycle).
Exposure to manufacturing systems or pharma environments.
AO3934

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