شركة California Greens تعلن عن وظيفة أخصائي ضمان الجودة في الرياض

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).