Quality Assurance Specialist
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Key skills for this role
About the Role
California Greens Corporation Factory is hiring a QA Specialist to manage In-Process Quality Assurance activities in compliance with GMP and SFDA regulations. Candidates need a Bachelor's in Chemistry or Pharmaceutical Sciences and up to 2 years of experience in the pharmaceutical industry.
Key Skills for This Role
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 closure of deviations, CAPAs, and change controls
- Verify calibration and qualification status of IPC equipment
- Develop and maintain standardized BMR templates
- Archive completed Batch Manufacturing Records
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
- Good observation skills
- Self motivated
- Ability to work effectively within a team
- Excellent knowledge of Microsoft Word, Excel, and PowerPoint
- High level of English proficiency (written and spoken)
Full Job Posting
About the Company
- California Greens Corporation Factory is a leading pharmaceutical manufacturing company committed to high quality products in compliance with SFDA regulations, GMP, and international quality standards.
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, approved specifications, SOPs, BMR/BPR, and regulatory requirements.
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.
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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