Senior Validation Officer At Hikma Pharmaceutical
Job Summary:
Responsible for performing basic tasks and some standardized routine testing and maintaining a high level of quality section 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 & software validation & qualification.
Preparation and reviewing of the documents related to pharmaceutical premises, utilities, equipment 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.
Qualification:
Minimum years of experience 3:5 years
Prefer having experience in both oral & sterile dosage form