Hiring for QA Head - Ankleshwar (API Pharma)

Growing CareersBharuch, Gujarat
Adzuna INPosted 9h agoOriginal Listing
manufacturing-jobs

Job Description

Essential Duties and Responsibilities :  Knowledge of all regulated Guideline Pharmacopoeia.  Preparation & implementation of SOPs related to the concerned department & Justification of Specification.  Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing.  collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.  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 ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements  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 closing.  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  Review of Manufacturing Processes.  Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site.  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 Assessment.  Preparation & review of process validation, cleaning validation, equipment qualification  To prepare/review the Validation Master Plan, Site Master File, Drug Master File, Annual Product Quality Review, Plant Layout and other documents related to QA Skills: Quality Assurance Manager Experience: 15.00-22.00 Years

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