QA/QC Manager-Medical Devices

Role Overview:Responsible for implementing and maintaining the Quality Management System (QMS) in compliance with ISO 13485 and regulatory standards. Ensures product quality, process integrity, and audit readiness across all manufacturing operations.Key Responsibilities:Oversee incoming, in-process, and final product inspections.Ensure compliance with ISO...

Role Overview:Responsible for implementing and maintaining the Quality Management System (QMS) in compliance with ISO 13485 and regulatory standards. Ensures product quality, process integrity, and audit readiness across all manufacturing operations.Key Responsibilities:Oversee incoming, in-process, and final product inspections.Ensure compliance with ISO...

Role Overview: Responsible for implementing and maintaining the Quality Management System (QMS) in compliance with ISO 13485 and regulatory standards. Ensures product quality, process integrity, and audit readiness across all manufacturing operations. Key Responsibilities: - Oversee incoming, in-process, and final product inspections. - Ensure compliance...

Role Overview:Responsible for implementing and maintaining the Quality Management System (QMS) in compliance with ISO 13485 and regulatory standards. Ensures product quality, process integrity, and audit readiness across all manufacturing operations.Key Responsibilities:- Oversee incoming, in-process, and final product inspections.- Ensure compliance with...

QA/QC Civil EngineerLocation: Faridabad, HaryanaCompany: JPG Engineers Pvt. Ltd.Experience: 3–8 years (preferred in civil construction projects)Employment Type: Full-timeJob Description:We are looking for a QA/QC Civil Engineer to oversee quality control and assurance activities for our ongoing civil construction projects in Faridabad. The role involves...

Role Overview: Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements. Key Responsibilities: - Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.). - Ensure compliance with ISO 13485, EU...

Role Overview: Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements. Key Responsibilities: Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.). Ensure compliance with ISO 13485, EU MDR...

Role Overview:Responsible for preparing, reviewing, and maintaining regulatory submissions and product registrations to ensure compliance with CDSCO, US FDA, and EU MDR requirements.Key Responsibilities:- Prepare and compile regulatory submissions (e.g., Device Master File, Technical File, 510(k), CE marking, etc.).- Ensure compliance with ISO 13485, EU MDR...

QA/QC Civil EngineerLocation: Faridabad, HaryanaCompany: JPG Engineers Pvt. Ltd.Experience: 3–8 years (preferred in civil construction projects)Employment Type: Full-timeJob Description:We are looking for a QA/QC Civil Engineer to oversee quality control and assurance activities for our ongoing civil construction projects in Faridabad. The role involves...

Quality Assurance Administration training and auditing of Quality System Tools Customer Complaints CAPA Training Control Documents Standards Ensure compliance of quality procedures and work instructions with applicable standards Conduct audits training preventive and corrective actions to maintain the QA system Maintain training qualification and...