Descrizione del lavoro:
Description de l'offre
Reporting to the QA Manager you will collaborate in the management of tasks related to Quality Assurance.
Your main responsibilities would be:
* Review and archiving of documents with GMP value such as log books, standard operating procedures and operating instructions
* Drafting of Process/cleaning validation protocols
* Management of deviations
* Management of Change Control process
* Management of CAPAs and deviations
* Management of Complaint and Recall
* Review of Batch Records
* Participation in GMP training of departments
* Involvement in internal and external audits
Qualifications
* Degree in Chemistry and Pharmaceutical Technologies, Pharmacy or Chemistry
* At least 2 year of experience in the same role
* Knowledge of Office tools (Word, Excel, Powerpoint)