Preparation & implementation of SOPs related to the concerned department & Specificatio
The conducts regular internal audits of the manufacturing facility to ensure that the facility meets the required quality standards.
handles the Regulatory and Customer audit and its compliance
Responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.
Responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA).
Responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations
Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their
Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.
Implementation & verification, in-process checks, online entries in BPR
Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing
Monitoring and ensuring the good laboratory practice (GLP) by laboratory personal during the routine analysis and instrument operation ensure adherence to procedure
Preparation & review of Quality Risk
Employement Category:
Employement Type: Full timeIndustry: Pharma / BiotechRole Category: Quality (QA-QC)Functional Area: Not SpecifiedRole/Responsibilies: Head Quality Assurance