Quality Assurance Specialist

California Greens Corporation Factory is a leading pharmaceutical manufacturing company committed to delivering high-quality products in compliance with SFDA regulations ,
Good Manufacturing Practices (GMP) , and international quality standards. We believe that our employees are our greatest asset and strive to provide a professional work environment that supports continuous learning, innovation, and career growth.

• Position: QA Specialist (Quality Assurance)
• Department: Quality Assurance
• Work Location: Kingdom of Saudi Arabia
• Employment Type: Full Time
• Nature of Work: Managing and overseeing In-Process Quality Assurance (IPQA) activities to ensure compliance with GMP requirements, approved specifications, SOPs, Batch Manufacturing Records (BMR/BPR), and applicable regulatory requirements.
• Benefits: Professional and motivating work environment, career development opportunities, competitive salary and benefits package based on qualifications and experience.

Managing and overseeing all activities related to In-Process Quality Assurance (IPQA) to ensure compliance with GMP requirements, approved specifications, SOPs, batch manufacturing records, and regulatory standards.

• Perform routine In-Process Control (IPC) checks during manufacturing.
• Monitor critical process parameters and quality attributes.
• Verify line clearance, equipment readiness, and proper material usage.
• Conduct IPC sampling, testing, and documentation according to GxP procedures.
• Ensure compliance with GMP, internal quality standards, and regulatory requirements.
• Review Batch Manufacturing Records (BMR/BPR) for completeness and accuracy.
• Report deviations, complaints, and change controls to QA Management.
• Support the closure of deviations, CAPAs, and change controls.
• Verify calibration and qualification status of IPC equipment.
• Ensure IPC instruments are maintained and functioning properly.
• Develop and maintain standardized BMR templates.
• Archive completed Batch Manufacturing Records.
• Ensure BMR documentation complies with GMP and SFDA requirements.

• Bachelor’s Degree in Chemistry or Pharmaceutical Sciences.

• Maximum of 2 years of experience as a QA Specialist in the Pharmaceutical Industry.
• Knowledge of GMP requirements.
• Self-motivated.
• Ability to work effectively within a team.

• Excellent knowledge of Microsoft Word, Excel, and PowerPoint.
• Good internet and computer skills.
• High level of English proficiency (written and spoken).