Quality Assurance

QA responsibilities:

1.������ Maintaining the compliance of the Pharmaceutical Quality System (PQS) to the cGMP and applicable regulations
2.������ Monitoring and promoting improvements of the PQS
3.������ Managing Self audits
4.������ Managing Deviations/Investigations and implementing CAPA system
5.������ SOP management
6.������ Management of the master manufacturing document
7.������ Participate and supervises the activities concerned with the validation of manufacturing processes, equipment, analytical methods and computerized systems
8.������ Approval of the reference documents for analytical methods
9.������ Handling quality complaints and investigation
7.������ GMP Training
8.������ Review of the batch records
9.������ Annual Product Quality Review (AQR)
10. ��� Change Control system
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Valpharma S.p.A. - Via Ranco, 112 - 47899 - Serravalle - Tel. +378 0549 900936 - E-mail: valpharma@valpharma.com- Privacy Policy - C.o.E. SM02686