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-Take samples of intermediates and finished products for each batch to obtain
representative samples.
- Perform checking samples of intermediates and finished products for each batch to obtain
representative samples.
- Observe conditions on line and in-process area for compliance with the process method,
for correct operation of procedures and for cleanliness and clearance of other
components.
- Report data to prepare a batch report on the key components used and their status,
clearance and cleanliness in-process checks and general comments on conditions of the
area and flow of process.
- Review the executed manufacturing batch records for completeness, correctness,
compliance of in-process control results with specification and reporting of “unusual
incidents.”
- Ensure production materials meet defined quality standards prior to disposition.
-Responsible for tracking and trending results, failure investigation, nonconformance,
deviations, change controls, and complaints.
Qualifications
* Bachelor’s degree in pharmaceutical sciences
* From 5-7 years’ experience in the same field
* Six Sigma and TQM Certificates is a plus
* Excellent knowledge of Microsoft office Professional (word, Excel, Power Point, MS Outlook).
* Fluency in English is a must.
*Strong verbal and written communication skills
*Strong project and time management skills with a proven ability to focus on priorities, solve problems and meet deadlines.
-Giza Or 6th Of October residents are preferred
Job Details
Preferred Candidate
About This Company
