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Senior Quality Assurance ( Quality systems
Job in
Tabuk, Saudi Arabia
Listed on 2026-05-07
Listing for:
Tabuk Pharmaceuticals
Full Time
position Listed on 2026-05-07
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst, QA Specialist / Manager
Job Description & How to Apply Below
Responsibilities
- SAP & Master Data Governance:
Managing and overseeing Quality-related modules in the SAP system, (e.g., material masters, inspection plans, and quality info records) to ensure accuracy of master data & data integrity and compliance. - Investigation & CAPA Management:
Lead the review of non-conformances and market complaints, ensuring all investigations are exhaustive, root causes are identified, and Corrective and Preventive Actions (CAPA) are implemented and verified for effectiveness. - OOS & Manufacturing Investigations:
Oversee the review of Out-of-Specification (OOS) results, ensuring rigorous manufacturing investigations and technical evaluations are conducted in compliance with regulatory standards. - Quality Risk Management (QRM):
Evaluate and approve quality risk management records, ensuring that mitigation strategies are robust, CAPAs are aligned, and residual risks are maintained within acceptable limits. - Audit Coordination:
Facilitate external and regulatory audits, managing requirements, identifying necessary systemic improvements (CAPA), and ensuring timely closure of audit findings. - Documentation Control:
Manage the issuance and lifecycle of Logbooks, SOP controlled copies, and technical documents, ensuring strict adherence to documentation protocols across all departments. - DMS & Technical Support:
Provide high-level support for QA documentation activities, including the review and synchronization of DCRs, SOPs, and Master Lists within the Document Management System (DMS). - Product Quality Review (PQR):
Preparing & uploading of product quality review reports (PQR) for Tabuk & Multinational products according to SOP, current GMP and corresponding quality agreements. - Leadership Support:
Act as the designated backup for the QA Supervisor, ensuring continuity of quality operations and decision-making processes. - Operational Agility:
Contribute to cross-functional QA activities as assigned, including IPC oversight during peak periods or personnel transitions to maintain seamless quality coverage.
- Required Educational Level and Certificates:
Bachelor Degree in Pharmacy, Science, Medicine or Chemistry. - Required Experience: 5-7 years of experience in a similar position.
Position Requirements
10+ Years
work experience
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