Overview
Quality Assurance Specialist Jobs in Riyadh, Riyadh, Saudi Arabia at California Greens
Title: Quality Assurance Specialist
Company: California Greens
Location: Riyadh, Riyadh, Saudi Arabia
Job Vacancy
About the Company
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.
About the Position
· 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.
· Advertisement Start Date: 25/06/2026
· Application Closing Date: 25/07/2026
Job Purpose
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.
Key Responsibilities
· 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.
Qualifications
· Bachelor’s Degree in Chemistry or Pharmaceutical Sciences.
Experience
· Maximum of 2 years of experience as a QA Specialist in the Pharmaceutical Industry.
· Knowledge of GMP requirements.
· Good observation skills.
· Self-motivated.
· Ability to work effectively within a team.
Skills
· Excellent knowledge of Microsoft Word, Excel, and PowerPoint.
· Good internet and computer skills.
· High level of English proficiency (written and spoken).