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).

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Do you have experience with Change Control? *

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