Conducting regular investigations to guarantee that workers’ follow safety procedures as required
Conducting quality audits as required to ensure compliance with GMP, Quality standards, and sterility regulations throughout the field
Handling the pharmaceutical tailing waste according to the set rules and procedures in this regard
Carrying out material sampling as needed to conduct QA audits, checking samples’ conformity and taking decisions (Batch Release) of samples’ acceptance
Performing pre and post-production quality checks and providing related reports accordingly
Carrying out the issuance and weighing process of raw materials to guarantee the conformity of specifications to quality standards, approving the release of materials to production, as well as ensuring compliance of raw material storage with regulatory guidelines
Ensuring compliance of plant conditions (Humidity, Temperature,…etc) with set guidelines
Checking machine conformity to standards as well as ensuring periodic maintenance implementation
Performing other duties related to the job as assigned by the direct supervisor
Job Requirements
Bachelor’s degree of Pharmacy or Science.
From 1 to 3 years of experience as IPC Officer.
Good Problem-Solving Skills.
Good understanding in the QA processes and the Agile development process
Knowledge of quality assurance terminology, methods, and tools
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