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Job Description
- Checking the QA related documents & Printed Packaging Material in production area during the manufacturing process.
- Checking the QA related Personnel Behavior in production area during the manufacturing process.
- Creating sample "via Oracle" to QC department "Quality Assessing".
- Reviewing "via Oracle" Bill of materials for bulk and package before release to WIP.
- Transferring quality "via Oracle" samples from HWIP inventory to stability inventory.
- Contacting production department to set SOPs, Batch Records & Product improvements.
- Withdrawing of samples from different process steps & finished products samples.Recording inspection check for finished products "Check List of Finished Goods".
- Supervising the dispensing process of raw and packaging materials.
- Reviewing batch records before product release to ensure that batch dossiers are correctly filled and complying.
- Identifying report process changes, incidents & non conformists or any deviations "GMP compliance".
- Monitoring the environmental conditions (Temp. %RH, ΔP) "GMP Compliance".
- Performing "In process" tests to ensure product compliance with established specifications during different production steps.
- Ensuring that all line clearance check is performed Well.
- Monitoring and inspecting the rework of batches "Quality of Products".
- Overseeing the calibration and verification of monitoring and measuring devices.
- Reviewing all raw materials before dispensing to be released from assigned department.
Job Requirements
- General: University graduate, B.Sc. Pharmaceutical Sciences
- Technical: Experience of 2-4 years in The same field.
- excellent communication and interpersonal skills.
- Good Command of English language.
