Pride Drugs and Pharma Pvt. Ltd

Role & responsibilities 1 Preparation of standard operating procedure. 2 Preparation of quality documents. 3 Initiate / review of change control system. 4 Initiate / review of deviation. 5 Initiate / review of CAPA. 6 To control, issue, retrieve, retention and disposal of GMP documents as per standard procedure. 7 Review of MFR/BMR/BPR/ECR. 8 Review of validation protocols and report. 9 To participate in investigation of OOS for RM/intermediate/FP. 10 To participate in market complaint handling. 11 Review of vendor qualification documents. 12 Review of executed manufacturing and analytical records. 13 Preparation of annual product quality review. 14 To take plant round and ensure compliance of SOPs and cGMP. 15 To give line clearance. 16 Preparation of risk assessment protocol and report. 17 To ensure dispatch of finished goods as per standard practices. 18 Any other responsibility as and when delegated by HOD/Management. Preferred candidate profile Male/ Female Candidate from kadi, Kalol and Mehsana / Ahmedabad meeting above criteria may apply at hr@pridedrugs.co.in or WhatsApp on 7043639390 Candidate outside aforesaid mentioned location willing to reallocate can only apply.