Key Accountabilities:

• Design standard operating procedures of the quality assurance department in the sterile area and non-sterile area in accordance with the approved guidelines.
• Review and approve standard operating procedures for the sterile area in accordance with the approved guidelines.
• Final approval of batch records before submitting them to the archiving department.
• Ensure that all verification and validation work in the sterile area is carried out and approve the relevant reports.
• Apply the appropriate procedures when any deviations occur during the manufacturing process after consulting with the head of the department.
• Ensure the compliance of the calibration status of all equipment inside the sterile, whether internal or external.
• Train new staff in the quality assurance department.
• Provide continuous training for all production staff in the sterile area on current good manufacturing practices.
• Organize work among department employees, whether on morning or evening shifts.
• Carry out all supervisory duties for the quality assurance department in the sterile area.
• Monitor all quality work in the sterile area and report any deviations to the department section head.

Qualification Requirements:

• Bachelor of science, department Chemistry / Physics
• Computer literate / Fluent in English
• Experience :  5-7 years
• Problems solving and team work attitude
• Proficient English
• Leadership skills
• skill (high accuracy – alertness – precision in working with described
  tools-methods system )