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Quality Assurance Supervisor (IPC)

Orchidia Pharmaceutical Industries
Obour City, Cairo
Posted 4 years ago
102Applicants for1 open position
  • 83Viewed
  • 9In Consideration
  • 75Not Selected
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Job Details

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Job Description

  • Follow up GMP  regulations and procedures for quality management system
  • Ensure timely completion of QA procedures, manufacturing, and packaging and in- process sampling.
  • Report non-conformance  that are identified during  routine operations and in process
  • Monitoring all phases of manufacturing , packaging of products in compliance with relevant standard operating procedures and manufacturing practices
  • Review procedures and processes for accuracy and completion.
  • Audit suppliers and vendors to assure their compliance  with GMP  and GSP regulation  and customer quality requirements
  • Follow up on preventive maintenance plan and completion of maintenance tasks
  • Approval of batch record & release of finished products for marketing
  • Record GMP deviation reports and follow CAPA system
  • Check and investigate customers complaints up to corrective and preventive actions
  • Design internal auditing plan, conduct the plan and  follow up CAPA system
  • Product description & specification
  • Applied standard lists issue. 
  • Communication with notified body in registration purposes and audit notification, CAR follow up
  • Supervise , support the quality  assurance personnel
  • Formulate technical training programs  and schedules based on   knowledge of identified training needs , company production processes, business systems , or changes in products  , procedures or services Follow up GMP  regulations and procedures for quality management system
  • Ensure timely completion of QA procedures, manufacturing, and packaging and in- process sampling.
  • Report non-conformance  that are identified during  routine operations and in process
  • Monitoring all phases of manufacturing , packaging of products in compliance with relevant standard operating procedures and manufacturing practices
  • Review procedures and processes for accuracy and completion.
  • Audit suppliers and vendors to assure their compliance  with GMP  and GSP regulation  and customer quality requirements
  • Follow up on preventive maintenance plan and completion of maintenance tasks
  • Approval of batch record & release of finished products for marketing
  • Record GMP deviation reports and follow CAPA system
  • Check and investigate customers complaints up to corrective and preventive actions
  • Design internal auditing plan, conduct the plan and  follow up CAPA system
  • Product description & specification
  • Applied standard lists issue. 
  • Communication with notified body in registration purposes and audit notification, CAR follow up

Job Requirements

  • Bachelor in pharmacy or science.
  • Five  years’ experience in pharmaceutical operations , including three years in overseeing QA compliance
  • Understanding of methodologies and best QA practices
  • Knowledge of documentation reviews and requirements analysis.
  • Ability to troubleshooting and resolving complex issues effectively.
  • Excellent English, verbal / written communication
  • Ability to work well through others
  • Excellent computer skills

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