Cadila Pharma

"•	To inform all department for periodic review of Specification and STP index monthly basis and prepare master list of Spec and STP six monthly.
•	Issuance, Retrieval and Archival of Master documents, logbooks, training and control copies of Biotech.
•	Destruction and disposal of documents after their shelflife.
•	To maintain final scan copy of current MMD, MFC, Protocols, reports and SOPs.
•	To prepare Editable ROAs.
•	To revise Master Equipment list of Cadila biotech and CPLB facilities.  
•	To prepare Standard Operating Procedures pertaining to QA department. 
•	To review SOPs, Quality analysis documents. 
•	Timely prepare Purchase Indent for QA stationary and general requirements of QA and take Follow ups for same.    
•	To participate in cross functional activities as defined by Immediate supervisor from time to time.
•	Any other job assigned by immediate superior/HOD/Designee from time to time."
•       To prepare BQA monthly report and BQA monthly planner.


"•	Handling of QMS documents (Deviation, Incident, OOS, Market complaints, shutdown related to VLP, botulinum, BQA, EPO, STR, IMM, BQC, BMN, GCF facilities and CPLB R&D as required. 
•	To be part of the Investigation, Root cause analysis and impact assessment done at site.
•	Handling of Change management system and Risk Assessment related to VLP, botulinum, BQA, EPO, STR, IMM, BQC, BMN, GCF facilities and CPLB R&D as required. 
•	Monitoring the improvement timely for on time closure of CAPA and its effectiveness of 
•	To maintain all QMS Logbooks and their excel file for better tracking. 
•	Cross function co-ordination for any QA related activities.
•	To prepare the process validation protocol, Cleaning validation, Hold time study protocol, execution of the protocols and finally preparation of the process validation report as per requirement.
•	Cross function co-ordination for any QA related activities.
•	To prepare protocol and reports related to additional Process validation and Cleaning validation.
•	Review Stability data of Drug Product and Drug Substance and its maintenance in document cell. 
•	To Update QMS logbooks and prepare QMS trends as require.

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