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...

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 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...

Job Title Assistant Project Manager - QA QC Summary This role is responsible for the implementation and maintenance of the quality management system About the Role Preparation and implementation of QA QC policies and procedures Carry out audits for ISO 9001 14001 and OHSAS 18001 and recommend the necessary corrective actions and measures Monitor policies and...

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...

Job Title: Manual Tester – Medical Device TestingLocation: GurugramExperience: 3 to 7 YearsEmployment Type: Full-TimeJob Description:We are seeking a skilled and detail-oriented Manual Tester with experience in Medical Device Testing to join our team in Gurugram. The ideal candidate will have a strong background in manual testing methodologies, regulatory...

Company Description Altos Engineers Pvt Ltd. is a leading manufacturer and exporter in India, known for delivering high-quality products backed by a dedicated professional team and robust infrastructure. The company prioritizes maintaining excellence in product standards, placing it among the top-ranking organizations in the field. Altos Engineers is...

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...

Description Medical Sales Representative (Dental Segment)# Position Executive/Manager Medical Sales Representative - Equipment / Dental Products Location: Faridabad Experience: 3-5 years (preferably in Dental / Medical device sales) Key Responsibilities: - Promote and sell dental equipment and dental consumable products to dentists, dental clinics,...