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Job Description
- Check machine/line for clearance as per written approved procedures before the start of batch manufacturing/packaging.
- Periodically inspect the manufacturing and/or Packaging Areas for appropriate cGMP compliance.
- Ensuring that all steps of operation on department are done as its requirement.
- Give start up or release for machine/line so as to start manufacturing/packaging after making sure that all procedures have been properly followed and that there are no deviation(s) from cGMP rules and/or written procedures.
- Collect samples from batch being manufactured/packaged as per written sampling procedures and test, examine or analyze samples as per written approved methods and procedures.
- Follow up & Performing IPC activities and testing for the different operations in the production areas (solid, liquid and packaging) in the plant.
- Check and report about methods and procedures being followed during process he/she is supervising and insure proper timely documentation.
- Document his/her own work (analysis, inspection or check) and include with batch record prior to delivery with relevant samples to DCC.
- Implementation of deviation system and recording it to follow up
- Participating in deviation investigations.
- Checking and signing every step in the process batch record.
- Responsible for compliance with quality integrated system for quality, environment, health and safety in relation with his job and duties.
- In Process Control for Manufacturing & Packaging of various dosage forms.
- On Job Training Team Member.
- Responsible for follow up the environmental monitoring.
- Implementation of GMP in production.
- Plus any additional work that is requested by his/her boss.
Job Requirements
- BSC in pharmacy, Science or any related field.
- (1-2) Years of experience.
- (Menoufya or Gharbia) resident.
- Good command of English.
