QA/QC Executive

As a QA/QC Executive, you will play a crucial role in managing and maintaining documentation essential for quality assurance processes. Your attention to detail and organizational skills will ensure that all records, SOPs, and quality-related documents are up-to-date and compliant with regulatory standards. By supporting the QA team in organizing documents, tracking changes, and ensuring data accuracy and consistency, you will contribute to the smooth operation of the Quality Management System (QMS) and help maintain compliance with industry regulations. Key Responsibilities: - Maintain and update QA/QC documentation, SOPs, and regulatory records. - Ensure compliance with industry standards and regulatory requirements. - Organize and track document changes, ensuring accuracy and consistency. - Assist in quality audits and inspections by providing necessary documentation. - Collaborate with the QA team to improve documentation processes. - Ensure that quality-related data is properly recorded and maintained. - Support cross-functional teams in maintaining compliance with quality standards. - Identify documentation gaps and suggest improvements. Qualifications Required: - Post-Graduate in Biotech, Microbiology, B.Pharm, or M.Pharm. - Strong communication and technical skills. - Attention to detail and ability to manage documentation effectively. - Basic knowledge of quality assurance processes and compliance standards. - Ability to work in a fast-paced environment and manage multiple tasks. - Proficiency in Microsoft Office (Word, Excel, PowerPoint). - Strong organizational and time-management skills. (Note: No additional details of the company were provided in the job description) As a QA/QC Executive, you will play a crucial role in managing and maintaining documentation essential for quality assurance processes. Your attention to detail and organizational skills will ensure that all records, SOPs, and quality-related documents are up-to-date and compliant with regulatory standards. By supporting the QA team in organizing documents, tracking changes, and ensuring data accuracy and consistency, you will contribute to the smooth operation of the Quality Management System (QMS) and help maintain compliance with industry regulations. Key Responsibilities: - Maintain and update QA/QC documentation, SOPs, and regulatory records. - Ensure compliance with industry standards and regulatory requirements. - Organize and track document changes, ensuring accuracy and consistency. - Assist in quality audits and inspections by providing necessary documentation. - Collaborate with the QA team to improve documentation processes. - Ensure that quality-related data is properly recorded and maintained. - Support cross-functional teams in maintaining compliance with quality standards. - Identify documentation gaps and suggest improvements. Qualifications Required: - Post-Graduate in Biotech, Microbiology, B.Pharm, or M.Pharm. - Strong communication and technical skills. - Attention to detail and ability to manage documentation effectively. - Basic knowledge of quality assurance processes and compliance standards. - Ability to work in a fast-paced environment and manage multiple tasks. - Proficiency in Microsoft Office (Word, Excel, PowerPoint). - Strong organizational and time-management skills. (Note: No additional details of the company were provided in the job description)