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Deputy QC Head

APEX Pharma
Badr City, Cairo
Posted 4 years ago
59Applicants for1 open position
  • 5Viewed
  • 0In Consideration
  • 1Not Selected
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Job Details

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Job Description

Job Function: To ensure that the staff, equipment, services and all other relevant resources are available and capable of functioning in accordance with defined standards to ensure that the product can be supplied to the market in an adequate quality

  • Ensure that all inspections are performed in accordance with good control laboratory practice.
  • Ensuring that on job Training are done for all staff under his/ her command.
  • Ensuring that all equipment in his/ her area are calibrated and validated according to a planned maintenance schedules.
  •  Delegate responsibilities to those reporting to him/ her as necessary and appropriately.
  •  Ensure that the implementation of Health & Safety and other legal requirements.
  •  Take part in staff recruitment and oversee the career development of his/ her staff
  •   Approve or reject starting raw and packaging materials, as well as intermediate, bulk and finished product samples.
  • Setting up and revision of Standard Operating Procedures to ensure that the current practices are in accordance with the written procedures which should reflect the current good laboratory practice.
  • Ensure the qualification and maintenance of his/her department, premises and equipment.
  • Approve specifications, sampling instructions, test methods and other quality control procedures.
  • Shares responsibility with the head of QA and production in The monitoring and control of the manufacturing environment Process validation, cleaning validation.
  • Evaluating all staff in the Quality Control department.
  • Authorized to organize work in the Quality Control department.

Job Requirements

  • Bachelor degree of pharmacy.
  • 15+ years of experience in QC in Pharmaceutical field.
  • SAP User.(is a must)
  • Excellent management skills.
  • Result- oriented.
  • Problem solving & Decision making skills.
  • Excellent understanding of the rules and guidance of cGMP.(EC/FDA).
  • Excellent know-how of validation, documentation, internal auditing and training.

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