Manual Tester – Medical Device Testing

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,...

For RARR Technologies Pvt Ltd - 3 - 7 Years- Full Time- FARIDABAD**Job Skills**: SQL QA TESTER REST SOAP DASHBOARD & PERFORMANCE ANALYTICS **Job description** RARR Technologies Pvt. Ltd. is a Tech Product and IT Consulting Company based out of Sector 19, Near Badkal Metro Station, Faridabad. We are recognised startup by Startup India and incubated at...

Job Title: Biomedical Engineer – Device IntegrationLocation: Medanta, GurgaonReports To: CIO & Head - Bio MedicalJob Summary:We are seeking a skilled Biomedical Engineer to lead the integration of biomedical devices with our Hospital Information System (HIS) and Electronic Medical Records (EMR). The ideal candidate will have expertise in bio medical...

Job Title: Biomedical Engineer – Device IntegrationLocation: Medanta, GurgaonReports To: CIO & Head - Bio MedicalJob Summary:We are seeking a skilled Biomedical Engineer to lead the integration of biomedical devices with our Hospital Information System (HIS) and Electronic Medical Records (EMR). The ideal candidate will have expertise in bio medical...

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...

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...

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...