IT Supervisor

Tabuk Pharmaceuticals; Tabuk; On-site; SAR 200,000 - 300,000; Full time

Job summary

A leading pharmaceutical firm in Tabuk is seeking an IT Computer and Software Validation Specialist to ensure quality and compliance of systems. The ideal candidate should have 3-5 years of experience in Computerized System Validation, particularly with SAP qualification and electronic Quality Management Systems. Key responsibilities include participating in validation projects, developing test protocols, and maintaining documentation for compliance with regulatory standards. Competitive remuneration is offered.

Qualifications

• 3-5 years of hands-on experience in Computerized System Validation.
• Experience with SAP systems and electronic Quality Management Systems.
• Ability to perform testing and documentation for compliance.

Responsibilities

• Participate in the full lifecycle of computer and software validation projects.
• Develop and execute validation protocols and test scripts.
• Maintain validation documentation and ensure compliance.

Skills

Computerized System Validation (CSV)

SAP qualification

eQMS experience

Cross-functional collaboration

Tools

Sparta Systems (TrackWise)

LIMS

MES

Track and Trace systems

Job description

We are seeking a highly motivated and detail‑oriented IT Computer and Software Validation Specialist to join our team. This role is crucial in ensuring the quality, reliability, and compliance of our computer systems and software applications, particularly within our regulated pharmaceutical or manufacturing environment. The ideal candidate will have 3‑5 years of hands‑on experience in Computerized System Validation (CSV) across various platforms and applications, including SAP qualification and experience with electronic Quality Management Systems (eQMS).

Responsibilities

• Participate in the full lifecycle of computer and software validation projects, including planning, requirements gathering, risk assessment, design qualification (DQ), installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), and report generation.
• Develop and execute validation protocols, test scripts, and traceability matrices in accordance with relevant regulatory guidelines (e.g., GAMP 5, 21 CFR Part 11).
• Perform thorough testing of computer systems and software applications, documenting any deviations and working with relevant teams to resolve issues.
• Maintain and update validation documentation throughout the system lifecycle, ensuring compliance with internal procedures and regulatory requirements.
• Provide expertise in the validation of SAP systems, including configuration, master data, and interfaces.
• Contribute to the validation and administration of our preferred eQMS, ideally Sparta Systems (TrackWise), as well as experience with EMS (Environmental Monitoring System), LIMS (Laboratory Information Management System), and MES (Manufacturing Execution System).
• Participate in the validation of IT infrastructure components relevant to regulated systems.
• Contribute to the validation efforts for Salesforce implementations and integrations.
• Experience with Track and Trace systems, with a preference for Jekson, is highly desirable.
• Collaborate effectively with cross‑functional teams, including IT, Quality Assurance, Manufacturing, and Laboratory personnel.
• Assist in the development and maintenance of IT validation policies, procedures, and work instructions.
• Participate in internal and external audits related to computer and software validation.
• Stay current with industry best practices and regulatory changes related to CSV.