 Design including schematics and layout for electronic medical devices that include analog front ends, optics, microcontrollers and various communication interfaces  Complete board bring-up and troubleshooting to meet all specifications  Design product integration and verification strategies that ensure complete coverage of critical medical device functionality and performance according to ISO 13485, FDA and CE guidelines and IEC 60601-1.  Ensure that all the documents needed for manufacturing and testing are complete, confidential and properly stored.  Validate prototypes of solutions in patient care to assess value  Diagnose and root cause hardware and system failures  Review, maintain and enter defects in defect management database.  Maintains good communication within the team and with other groups involved in the project. Job Type: Full-time Pay: ₹900,000.00 - ₹1,100,000.00 per year Benefits: Flexible schedule Health insurance Leave encashment Life insurance Paid sick time Provident Fund Ability to commute/relocate: Ahmedabad - 380015, Gujarat: Reliably commute or planning to relocate before starting work (Required) Experience: medical device hardware: 2 years (Preferred) total work: 5 years (Required)

Responsible for supplier audit planning, scheduling, and conduct supplier audits. • Responsible for vendor/ supplier quality and management issues. • Responsible for implementation of ISO 13485 requirements • Responsible for formulating, document, and maintain quality standards and ongoing quality objectives. • -Analysis of raw material, In-process samples, and finished product. • -Auditing OEM and verify the process control and quality, suggest changes if required to improve quality. • -Responsible to escalate technical issues to the design team and Providing product feedback and customer suggestions to the R&D and Product Management team, also tracking the continuous improvement of the products. • -Responsible to visit critical suppliers to verify and improve quality. • -Interacting with OEM, testing labs, external accreditation bodies. • -Preparing Work instructions, FMEA, RCA, CAPA, PDCA cycle, etc. • Ensure that the processes needed for the Quality Management system are documented, established, implemented and maintained. • Report to the top management comprising of the CEO, Directors of various disciplines and any other person(s) appointed by the CEO for this purpose, the effectiveness of the quality management system and any need for improvement. • Ensure the promotion of awareness of applicable regulatory requirements, quality management system requirements and customer requirements (where applicable) throughout the manufacturing organization. • represent the management and participate in routine meetings with various external agencies for the audit, regulatory and compliance requirements and will obtain regular inputs from the management for the same and provide the feedback. Job Types: Full-time, Permanent Pay: ₹100,000.00 - ₹125,000.00 per month Benefits: Flexible schedule Health insurance Leave encashment Life insurance Paid sick time Paid time off Provident Fund Application Question(s): Do you have experience of preparing Quality document as per regulatory requirement ? Experience: total work: 10 years (Required) medical device: 5 years (Required) Work Location: In person

Develop and maintain web applications using Angular 10+ versions. Must have knowledge of Rxjs library. Apply best practices in HTML, CSS, Javascript, and Typescript to create clean and maintainable code. Develop responsive web designs. Experience consuming REST APIs. Understanding and extensive experience with version control tools like SVN or Git. Knowledge of the Primeng library is an additional benefit. Job Types: Full-time, Permanent Pay: ₹500,000.00 - ₹600,000.00 per year Benefits: Flexible schedule Health insurance Leave encashment Paid sick time Paid time off Provident Fund Experience: total work: 2 years (Preferred) Work Location: In person