نوع العمل : عمل جزئى
الخبرة : 0-3 سنة
الراتب : Not Mentioned
المكان : Cairo, EG
الخبرة : 0-3 سنة
الراتب : Not Mentioned
المكان : Cairo, EG
Conduct routine and non-routine analyses of in-process materials, finished goods, or stability samples in a timely manner.
Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release.
Conduct chemical or physical laboratory tests in making qualitative or quantitative analyses
Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms.
Write technical reports or prepare graphs or charts to document experimental results.
Calibrate, validate, or maintain laboratory equipment.
Participate in out-of-specification and failure investigations and recommend corrective actions.
Supply quality control data necessary for regulatory submissions.
Investigate or report questionable test results.
Addition and withdrawal of stability samples from stability chambers
Performance of data entry and trend analysis
Reviewing, filing ,reporting and trending of stability data
Perform the Analytical Method Transfer Exercise (AMTE) for the new test procedures required for manufacturing of new product in our site.
Perform Validation required for the new developed test procedures.
Execute all activities related to process, cleaning and instrument validation.
Preparing and executing the SOPs, calibration and validation documents (IQ, OQ & PQ) related to chemical laboratory tasks.
Implementing the PQS requirements regarding the chemical laboratory
Using, monitoring and controlling Reference standards inventory and expiry
Using, monitoring and controlling of expiry and inventory of laboratory stock items including reagents, glassware, filters, etc.
Perform Data loggers monitoring, downloading and reviewing
Writing and revision of Quality Control SOPs
Working on improving his process by implementing lean and 6σ projects.
Responsibility for implementation of Data integrity program in the relevant work area and Insure following up ALCOA principles all over operations.
Active implementation of Notification to Management procedures.
Responsibility for compliance with Pfizer Quality Standards.
Skills:
Good English written and spoken.
Good Communication Skills
Technical Competency
Ability to Work in Harmony with Co-Workers
Problem-Solving Skills
Decision-making and good time management
Apply for here
Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release.
Conduct chemical or physical laboratory tests in making qualitative or quantitative analyses
Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms.
Write technical reports or prepare graphs or charts to document experimental results.
Calibrate, validate, or maintain laboratory equipment.
Participate in out-of-specification and failure investigations and recommend corrective actions.
Supply quality control data necessary for regulatory submissions.
Investigate or report questionable test results.
Addition and withdrawal of stability samples from stability chambers
Performance of data entry and trend analysis
Reviewing, filing ,reporting and trending of stability data
Perform the Analytical Method Transfer Exercise (AMTE) for the new test procedures required for manufacturing of new product in our site.
Perform Validation required for the new developed test procedures.
Execute all activities related to process, cleaning and instrument validation.
Preparing and executing the SOPs, calibration and validation documents (IQ, OQ & PQ) related to chemical laboratory tasks.
Implementing the PQS requirements regarding the chemical laboratory
Using, monitoring and controlling Reference standards inventory and expiry
Using, monitoring and controlling of expiry and inventory of laboratory stock items including reagents, glassware, filters, etc.
Perform Data loggers monitoring, downloading and reviewing
Writing and revision of Quality Control SOPs
Working on improving his process by implementing lean and 6σ projects.
Responsibility for implementation of Data integrity program in the relevant work area and Insure following up ALCOA principles all over operations.
Active implementation of Notification to Management procedures.
Responsibility for compliance with Pfizer Quality Standards.
Skills:
Good English written and spoken.
Good Communication Skills
Technical Competency
Ability to Work in Harmony with Co-Workers
Problem-Solving Skills
Decision-making and good time management
Apply for here