القائمة الرئيسية

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Senior Validation Officer At Hikma Pharmaceutical

 Senior Validation Officer At Hikma Pharmaceutical 

Senior Validation Officer At Hikma Pharmaceutical






Description: 

Job Summary:


Responsible for performing basic tasks and some standardized routine testing and maintaining a high level of quality sections services by monitoring and recommending solutions to quality related issues. Job holders also train lower level jobs to ensure continuity of work and compliance to set standards.


 


Job Description:


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.

Participates as a team member, under close supervision, and receives and carries out detailed instructions in order to grow professional capability.

Applies standard quality techniques to provide solutions to problems involving a limited number of variables.

Applies technical knowledge, following established procedures and/or standard practices, to perform basic analyses.

Preparation and reviewing of the validation documents, systems, SOPs, protocols & reports preparation.

Preparation and reviewing of the qualification documents, systems, SOPs, protocols & reports preparation.

Preparation and reviewing of the documents related to pharmaceutical premises, utilities, equipment’s & software validation & qualification.

Preparation and reviewing of the documents related to pharmaceutical premises, utilities, equipment’s calibration and the related documents, systems, SOPs, protocols & reports preparation & implementation as per the latest requirements.

Preparation and reviewing of the pharmaceutical laboratories equipment’s validation, qualification, calibration and the related documents, systems, SOPs, protocols & reports preparation & implementation.

Preparation and reviewing of the thermal mapping and internet of things implementation and reporting.

Preparation and reviewing of the pharmaceuticals process validation documents, systems, SOPs, protocols & reports preparation & implementation as per the latest requirements.

Preparation and reviewing of the pharmaceuticals cleaning validation documents, systems, SOPs, protocols & reports preparation & implementation as per the latest requirements.

 


Job Qualifications:


3- 5 year of successful experience (Sterile Area).

B.Sc. degree in Pharmacy, Science or Engineering.

Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqiyah, and 10th of Ramadan) residents


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