Notice: _load_textdomain_just_in_time تمّ استدعائه بشكل غير صحيح. Translation loading for the astra domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init action or later. من فضلك اطلع على تنقيح الأخطاء في ووردبريس لمزيد من المعلومات. (هذه الرسالة تمّت إضافتها في النسخة 6.7.0.) in /home/vacappqp/public_html/wp-includes/functions.php on line 6114
Senior QA Supervisor At Hikma Pharmaceuticals Company - vacanciesblog 2024
QC Analyst At Hikma Pharmaceutical Company

Senior QA Supervisor At Hikma Pharmaceuticals Company

  Senior QA Supervisor At Hikma Pharmaceuticals Company

 

 Job Summary

Responsible for supervising the work of a number of teams. Job holders have the technical expertise in their area and knowledge of quality section policies and procedures to be able to provide advice and guidance on their particular specialization. They also supervise and give practical and ongoing guidance to junior colleagues.

 

Duties & Responsibilities:

  • Follows all relevant Quality instructions so that work is carried out in a controlled and consistent manner.
  • Follows the day-to-day operations related to own jobs in the function to ensure continuity of work.
  • Supervises the day-to-day operations of quality departments related to one providing some guidance in facilitating related professional work processes in order to achieve high performance standards.
  • Conducts quality compliance audits and inspections in order to identify areas of non-compliance with policies, procedures and legislative requirements relating to quality, and prepares reports recommending remedial actions.
  • Participates in more complex periodic maintenance, testing, operation, etc. of quality checks in order to ensure optimum operational status.
  • Coordinates and conducts orientation and follows-up training programs to ensure a high level of quality awareness amongst employees and contractors.
  • Works on problems of a more complex scope, where the analysis of situations or data requires a review of a variety of factors, in order to identify trends and recommend remedial actions.
  • Provides guidance and support to junior staff and is a point of expertise and reference within own specialisation.
  • Follow-up of shipping plans with external department to ensure achievement.
  • Prepare, update and review standard operating procedure (SOPs) for quality processes to confirm compliance with GMP’s guidelines.

 

Job Qualifications:

  • 7 – 10 year of successful experience (Sterile Area).
  • BSc. Pharmacy or Science (Chemistry)
  • Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqiyah, and 10th of Ramadan) residents

Location:  Egypt

 

Apply Here

اترك تعليقاً

لن يتم نشر عنوان بريدك الإلكتروني. الحقول الإلزامية مشار إليها بـ *

error: Content is protected !!