5 - 8 years
3 - 6 Lacs
Posted:19 hours ago|
Platform:
Work from Office
Full Time
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.
Candidate outside aforesaid mentioned location willing to reallocate can only apply.
Pride Drugs and Pharma Pvt. Ltd
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Instantly access job listings, apply easily, and track applications.
kalol, mehsana, ahmedabad
3.5 - 6.0 Lacs P.A.
gurugram
Experience: Not specified
3.0 - 3.5 Lacs P.A.
3.0 - 4.5 Lacs P.A.
12.0 - 15.0 Lacs P.A.
ahmedabad
5.0 - 6.5 Lacs P.A.
ahmedabad
2.16 - 3.0 Lacs P.A.
8.0 - 18.0 Lacs P.A.
2.0 - 5.5 Lacs P.A.
4.0 - 8.0 Lacs P.A.
greater noida
19.0 - 30.0 Lacs P.A.
