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QA IPC Section Head

Rameda
6th of October, Giza
Posted 3 years ago
65Applicants for1 open position
  • 6Viewed
  • 0In Consideration
  • 13Not Selected
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Job Details

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Job Description

  • In coordination with QA Manager, he/she should assist all aspects of IPC Section in order to assure that RAMEDA Quality Management System complies with internal requirements (e.g. quality policy, company manual, SOPs, specifications, and other quality documents) and external national and international requirements (e.g. guidelines, standards, regulations, and laws).
  • Assess implementation, effectiveness, efficiency, maintenance, and continual improvement of the Quality Management System.
  • Supervision, planning and implementation of all quality operations activities in order to optimize production within safety, legislative, environmental and company requirements.
  • Establish work schedules and prioritize activities to meet company requirements.
  • Ensure adequate training for all Direct Reports on quality procedures and all activities associated with their role.
  • Ensure Investigations are conducted and adequately resolved in a timely manner, with appropriate CAPAs in place to prevent reoccurrence of issues.
  • Ensure compliance with cGMP and Safety standards at all times.
  • Focus on efficiency within the Quality operations & compliance Department
  • Assure accurate and timely completion of all tasks relating to the day to day activities (sampling, testing and inspection (as AQL)) for all Rameda and Toll Products.
  • Responsible for ensuring that batches released for commercial fully meet regulatory requirements
  • Ensure all manufacturing batch documents related to finished products produced at the site are properly maintained and controlled.
  • Works closely with the operations team to ensure that the quality management system and quality plan supports current quality management strategy themes, corporate objectives and industry requirements.
  • Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001, ISO 14001, OHSAS 18001).

Job Requirements

  • Exp from 8-10 years 
  • Bachelor degree in science or pharmacy
  • Males only

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