FIND_THE_RIGHTJOB.
Egypt
Job Purpose
To perform day-to-day and routine validation activities to ensure that all challenges are resolved effectively and in a timely manner, in compliance with SOPs, GMP, and WHO requirements.
Responsibilities
Follow all relevant quality instructions to ensure work is carried out in a controlled and consistent manner.
Carry out the day-to-day operations related to the role to ensure continuity of work.
Adhere to all relevant departmental policies, processes, standard operating procedures, and instructions so that work is performed in a consistent and compliant manner.
Apply technical knowledge by following established procedures and/or standard practices to perform basic analyses.
Prepare and review validation documents, systems, SOPs, protocols, reports, and their implementation.
Prepare and review validation documents for pharmaceutical premises, utilities, and equipment, including systems, SOPs, protocols, reports, and implementation.
Prepare and review validation documents for computerized systems, including systems, SOPs, protocols, reports, and implementation.
Prepare and review process validation documents, including systems, SOPs, protocols, reports, and implementation.
Prepare and review cleaning validation documents, including systems, SOPs, protocols, reports, and implementation.
Prepare and review transportation validation documents, including systems, SOPs, protocols, reports, and implementation, in accordance with the latest requirements.
Qualifications, Experience & Skills
Minimum Qualifications: Bachelor’s degree in Pharmaceutical Sciences or Science.
Minimum Experience: 4 years
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