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Quality Assurance Specialist

Job in Riyadh, Riyadh Region, Saudi Arabia
Listing for: Sudair Pharmaceutical Company
Full Time position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 150000 - 200000 SAR Yearly SAR 150000.00 200000.00 YEAR
Job Description & How to Apply Below

Sudair Pharmaceutical Company (SPC) was established in 2014 as a Saudi-based company focused on advancing pharmaceutical manufacturing to address chronic and life-threatening diseases. Located in Sudair Industrial City, about 100 km north of Riyadh, SPC oversees a 77,000-square-meter manufacturing complex. The first phase includes an oncology medicine plant, aiming to support regional pharmaceutical innovation. SPC collaborates with international partners and builds specialized local professional teams to ensure world-class healthcare provision.

Role Description

This is a full-time, on-site role for a Quality Assurance Specialist based in Riyadh, Saudi Arabia. The Quality Assurance Specialist will monitor, implement, and ensure compliance with quality management systems and Good Manufacturing Practices (GMP). Day-to-day tasks include conducting quality audits, evaluating quality control processes, identifying areas for improvement, and collaborating with production teams to maintain standards. The role also involves generating, reviewing, and maintaining compliance documentation in alignment with regulatory guidelines.

Responsibilities
  • Monitor, implement, and ensure compliance with quality management systems and GMP.
  • Conduct quality audits and evaluate quality control processes.
  • Identify areas for improvement and collaborate with production teams to maintain standards.
  • Generate, review, and maintain compliance documentation in alignment with regulatory guidelines.
Qualifications
  • Strong skills in Quality Assurance, focusing on implementing and maintaining quality systems
  • Experience in Quality Control processes to ensure products meet established standards
  • Knowledge of GMP to ensure compliance and operational excellence
  • Expertise in Quality Management and Quality Auditing to oversee and assess production processes
  • Exceptional attention to detail and problem-solving skills
  • Familiarity with pharmaceutical and manufacturing regulatory standards
  • Bachelor’s degree in Pharmacy, Life Sciences, or a related field; advanced certifications in quality management are a plus
Seniority level

Entry level

Employment type

Full-time

Job function
  • Quality Assurance
Industries
  • Pharmaceutical Manufacturing
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