Delhi, India
Not disclosed
On-site
Full Time
Job Title: Clinical Support Specialist (Surgical Operations) Company: SS Innovations Pvt. Ltd. Location: India (Multiple locations possible – based on project and hospital site requirements) Job Summary: As a Clinical Support Specialist (Surgical Operations) , you will play a vital role in supporting the clinical use of SS Innovation’s advanced surgical robotic systems across hospitals and surgical centers. You will act as a technical expert during robotic procedures, assist surgeons and clinical teams with system setup, troubleshooting, and training, and ensure optimal performance of the system during surgeries. This is a customer-facing, hands-on technical role that combines biomedical engineering with clinical operations. Key Responsibilities: Provide on-site clinical and technical support during robotic surgeries. Assist surgeons and operating room staff with system setup, calibration, troubleshooting, and operation. Ensure proper maintenance, functionality, and hygiene of surgical robotic systems pre- and post-procedure. Conduct product demonstrations and assist in training programs for surgeons, clinical staff, and hospital administrators. Serve as a technical liaison between the company and hospitals, ensuring customer satisfaction and timely resolution of issues. Provide feedback to R&D and product teams based on real-world clinical usage and system performance. Maintain detailed logs, reports, and documentation for procedures and technical issues. Stay updated with surgical techniques, robotic system updates, and company protocols. Ensure compliance with regulatory standards, hospital guidelines, and company policies. Required Qualifications: Bachelor’s degree in Biomedical Engineering, Electronics, Mechanical Engineering, or a related technical field. 1–3 years of experience in clinical engineering, operating room support, or medical device industry (Freshers with strong internship/project experience may also be considered). Strong understanding of human anatomy, surgical procedures, and medical terminologies. Excellent troubleshooting and problem-solving skills. Strong interpersonal and communication skills; ability to work effectively in high-pressure clinical environments. Willingness to travel frequently and work flexible hours based on surgical schedules. Preferred Qualifications: Experience with surgical robots, minimally invasive surgery (MIS), or medical imaging equipment. Previous work in a hospital, operating room, or with a medical device company. Certification or training in OR protocols or biomedical equipment handling is a plus. Why Join SS Innovations? SS Innovations is a pioneering Indian company at the forefront of robotic surgery, bringing affordable and advanced technology to the healthcare sector. Be part of a passionate team driving the future of surgery through innovation, precision, and patient-first thinking. Show more Show less
Gurugram, Haryana, India
Not disclosed
On-site
Full Time
Responsibilities : Defining design requirements and hardware specification based on user requirement. Working Knowledge of Power management, power converters (AC/DC, DC/DC converters) and battery technology. Working Knowledge of Analog and Digital circuits. Working Knowledge safety regulation standards e.g., IEC 60601, IEC 61010, UL, ANSI and ASTM. Hands-on embedded programming (Embedded C, C, C++) for microcontrollers. Knowledge of industrial and embedded communication protocols (EtherCAT, CANOpen, Ethernet, UART, SPI, I2C, etc.). Defines requirements for test jigs to evaluate system performance. Knowledge of integrating electrical design with mechanical and software modules of the system. Develops, modifies, and approves electrical design documentation, specifications and drawings. Mentor the layout of circuit assemblies to meet emissions and immunity performance requirements and design for manufacturability guidelines. (Knowledge of EMI/EMC). Implements data acquisition and analysis techniques to characterize design performance. Knowledge of Battery modules will be Plus. Executes protocols and testing required to validate the system safety. Good experience in troubleshooting issues related to electrical and electronic devices. Qualifications : Bachelor’s Degree in Electrical / Electrical & Electronics / Electronic & Communications Engineering with 8-10 years of experience. Master’s degree in Electrical Engineering (preferably Power Electronics) with 6-7 years of experience. Required Skills : Excellent understanding of Hardware / Firmware development tools, processes, and technologies. Good working knowledge of Hardware development in Motion Control. Good working knowledge of Real Time Safety Critical Embedded Systems. Good working knowledge of software development in embedded C or comparable language. Experience in all aspects of a product life cycle Requirements, Design, Development, HW/SW integration and test. Functions well in a team environment and has the ability to adapt quickly. Preferred Skills : Expertise: Design and Development of Medical /Automotive/Robotics Products. Relevant Experience: 8-10 years. Pay range and compensation package : Salary: As per current Industry standard. Show more Show less
Gurugram, Haryana, India
Not disclosed
On-site
Full Time
Job Title: Senior Manager – Regulatory Affairs Department: Regulatory Affairs Location: Gurugram, India Reporting to: Head – Quality & Regulatory Affairs Company: SS Innovations Pvt. Ltd. Job Summary: SS Innovations Pvt. Ltd., a pioneering medical device company focused on innovative surgical robotics, is seeking an experienced and highly motivated Senior Manager – Regulatory Affairs . The ideal candidate will have strong expertise in global regulatory frameworks including US FDA , EU MDR/CE , and other major international standards (e.g., TGA, Health Canada, CDSCO). This role involves overseeing regulatory strategies, managing submissions, ensuring compliance, and facilitating approvals for new and existing medical devices. Key Responsibilities: Regulatory Strategy & Compliance: Develop and implement regulatory strategies for global markets (US, EU, India, etc.) to ensure timely product approvals and market entry. Monitor regulatory changes and communicate impact to internal stakeholders. Product Submissions & Approvals: Lead the preparation, submission, and management of regulatory dossiers including 510(k) , PMA , Technical Documentation for CE marking , and Indian CDSCO approvals . Coordinate with notified bodies, regulatory agencies, and consultants as needed. Quality System Support: Support Quality Management System (QMS) compliance as per ISO 13485 , 21 CFR Part 820 , and MDSAP requirements. Participate in internal and external audits, including FDA inspections and CE audits. Cross-Functional Collaboration: Work closely with R&D, Clinical, Manufacturing, and Marketing teams during product development to ensure regulatory requirements are integrated early. Provide regulatory guidance on labeling, promotional materials, and product changes. Regulatory Intelligence & Risk Management: Maintain a robust understanding of international regulatory landscapes. Identify regulatory risks and develop mitigation strategies. Team Leadership & Development: Lead and mentor the regulatory affairs team. Develop team capabilities in line with evolving regulatory requirements. Desired Profile: Education: Bachelor’s or Master’s degree in Life Sciences, Biomedical Engineering, Pharmacy, or related discipline. Experience: Minimum 10–12 years of regulatory affairs experience in the medical device industry , with proven exposure to US FDA , CE (EU MDR) , and global regulatory markets . Certifications: RAC (Regulatory Affairs Certification) preferred. Skills: In-depth knowledge of international regulatory requirements and submission processes. Strong project management and leadership abilities. Excellent communication and interpersonal skills. Ability to work in a dynamic, fast-paced environment with cross-functional teams. Why Join SS Innovations? Work with cutting-edge technology in surgical robotics. Be part of a growing global medtech innovator. Collaborate with a passionate and multidisciplinary team. Opportunities for global exposure and career advancement. Show more Show less
Gurugram, Haryana, India
Not disclosed
On-site
Full Time
Job Title: Team Leader – Clinical Support Data Analysis Department: Clinical Affairs / Clinical Support Location: Gurugram, India Reporting To: Head – Clinical Support / Director – Medical Affairs Job Summary: The Team Leader – Clinical Support Data Analysis will be responsible for overseeing and managing a team of clinical data analysts who support clinical operations by analyzing, interpreting, and presenting clinical and procedural data related to the use of surgical robotic systems. This role ensures that data-driven insights support clinical decision-making, product improvements, training effectiveness, and regulatory compliance. Key Responsibilities: Lead a team of data analysts in collecting, curating, cleaning, and analyzing clinical and procedural data from robotic surgical cases. Oversee the development and maintenance of clinical dashboards, performance metrics, and reporting tools for internal stakeholders. Collaborate with surgeons, clinical engineers, product managers, and R&D teams to translate clinical data into actionable insights. Ensure accuracy, consistency, and compliance of clinical data with regulatory and ethical guidelines. Review and validate data analytics reports for training outcomes, procedure efficiency, and patient safety. Support clinical studies, registries, and post-market surveillance with relevant data analysis and interpretation. Drive continuous improvement in data collection methodologies and analytical tools. Mentor, train, and evaluate team members to ensure high performance and knowledge enhancement. Present key findings to leadership, medical teams, and external partners as needed. Coordinate with IT/Data teams to maintain secure and reliable data infrastructure. Qualifications and Experience: Bachelor’s or Master’s degree in Life Sciences, Biomedical Engineering, Health Informatics, or related field. 5–8 years of experience in clinical data analysis, preferably in a MedTech or medical device environment. Minimum 2–3 years of team leadership or managerial experience in a clinical support or data analytics function. Required Skills: Strong expertise in clinical data management, statistics, and healthcare analytics. Proficiency in tools like Excel, SQL, Python/R, Power BI/Tableau, and statistical software. Familiarity with clinical workflows, surgical robotics, or medical device environments. Strong understanding of data privacy, security, and regulatory frameworks (e.g., HIPAA, GCP). Excellent leadership, communication, and problem-solving skills. Ability to work cross-functionally in a dynamic and evolving clinical setting. Preferred Attributes: Experience with surgical robotics or operating room clinical data. Exposure to AI-based clinical insights, predictive analytics, or machine learning models. Certification in clinical data management or health informatics (optional but preferred). SS Innovations Pvt. Ltd. is an equal opportunity employer, and this role offers an exciting opportunity to lead data-driven clinical support functions in one of the most innovative medical technology environments in India. Show more Show less
Gurugram, Haryana, India
Not disclosed
On-site
Full Time
Job Title: Statistics Specialist – Clinical Support Department: Clinical Affairs / Data Analytics Location: SS Innovations Pvt. Ltd., Gurugram, India Experience Required: 3–5 Years Reporting To: Team Leader – Clinical Support Data Analysis / Clinical Affairs Manager Job Summary: The Statistics Specialist – Clinical Support is responsible for managing and analyzing clinical and operational data related to surgical robotic systems. The role requires strong statistical acumen to support clinical trials, post-market surveillance, research studies, and evidence generation initiatives. This position plays a key role in transforming complex data into meaningful insights to aid clinical decision-making and regulatory submissions. Key Responsibilities: Perform statistical analysis of clinical study data, observational studies, and retrospective reviews related to SS Innovations’ surgical robotic systems. Provide statistical input for clinical study design, sample size calculations, and protocol development. Support data management activities including cleaning, validation, and review of clinical data for accuracy and consistency. Prepare statistical analysis plans (SAP), summary tables, figures, listings, and final study reports. Collaborate with clinical, R&D, and regulatory teams to generate data-driven evidence to support safety, efficacy, and usability claims. Work with biostatistical software such as SAS, R, or SPSS to conduct exploratory and confirmatory data analysis. Contribute to scientific publications, abstracts, posters, and conference materials. Assist in preparation of data for regulatory submissions (e.g., US FDA, CE Marking, CDSCO, etc.). Monitor data trends to identify early signals, adverse events, or areas requiring further investigation. Ensure compliance with ICH-GCP, ISO 14155, and other applicable statistical and clinical research standards. Requirements: Master’s degree in Statistics, Biostatistics, Mathematics, Epidemiology, or a related field. 3–5 years of experience in a clinical or medical device/statistics role. Strong knowledge of clinical trial methodology, design, and statistical principles. Proficiency in statistical software (SAS, R, SPSS, or equivalent). Experience working with large datasets and clinical databases (EDC, CRFs, etc.). Excellent analytical, problem-solving, and documentation skills. Strong communication skills and ability to work in a cross-functional, fast-paced environment. Familiarity with global regulatory requirements and standards for medical devices is preferred. Preferred Skills: Prior experience in a MedTech or surgical robotics company. Exposure to clinical study submissions to US FDA, CE, or other regulatory bodies. Understanding of AI-assisted data models and predictive analytics in healthcare. Show more Show less
Gurugram, Haryana, India
Not disclosed
On-site
Full Time
Job Title: Travel Desk Executive Location: Gurugram Haryana Department: Administration / Operations Company: SS Innovations About SS Innovations: SS Innovations is a cutting-edge medical technology company focused on developing advanced surgical systems and devices that improve the quality and accessibility of healthcare. As we continue to grow, we are looking for a proactive and detail-oriented Travel Desk Executive to join our team and manage all corporate travel needs efficiently. Job Summary: The Travel Desk Executive will be responsible for planning, coordinating, and managing travel arrangements for employees and guests of SS Innovations. The role involves handling bookings, ensuring cost-effective travel, maintaining compliance with travel policies, and providing timely support and communication. Key Responsibilities: Manage end-to-end domestic and international travel arrangements (flights, hotels, transport, visas, etc.) Develop service providers and vendors (Hotels/ Transport) all across the country and negotiate the best possible rates for the company Liaise with travel agencies, vendors, and internal teams to secure bookings at the best possible rates Ensure all travel plans comply with company policies and budgetary guidelines Assist employees with travel-related queries, changes, or emergencies during travel Coordinate airport pick-up and drop-off services as required Maintain accurate records of bookings, costs, and invoices for reporting and audits Monitor travel expenses and work closely with the finance team for reimbursements and reconciliation Handle documentation for visa applications and international travel compliance Manage travel itineraries and communicate relevant updates to travelers in a timely manner Provide support during corporate events and conferences or visits that involve travel or accommodation arrangements Requirements: Bachelor’s degree in any discipline (Hospitality or Travel Management preferred) 4+ years of experience in corporate travel management or a similar administrative role Strong knowledge of domestic and international travel procedures, visa processes, and airline regulations Proficiency in using travel management tools and booking platforms Excellent communication and interpersonal skills Strong organizational and time management abilities Attention to detail and ability to handle last-minute changes under pressure Preferred Skills: Experience working in a healthcare or technology organization Familiarity with expense management software (e.g., SAP Concur, Zoho Expense) Multilingual abilities (preferred but not mandatory) To Apply: Please send your resume and a brief cover letter to hr@ssinnovations.org Show more Show less
Gurugram, Haryana, India
Not disclosed
On-site
Full Time
Job Title: Software Quality Engineer (QA/RA) Location: Gurugram Haryana Department: Software R&D Company: SS Innovations About SS Innovations: SS Innovations is a cutting-edge medical technology company focused on developing advanced surgical systems and devices that improve the quality and accessibility of healthcare. As we continue to grow, we are looking for a proactive and detail-oriented Travel Desk Executive to join our team and manage all corporate travel needs efficiently. Job Description - Design, develop, and optimize high-performance SAMD applications using SIMD for real-time. Ensure all software development complies with regulatory standards such as IEC 62304, ISO 13485, FDA 21 CFR Part 820, and EU MDR. Collaborate with cross-functional teams (RA/QA, Software/firmware development, and R&D teams) to ensure the software meets safety and performance requirements. Create and maintain documentation such as SDLC deliverables, Risk management files, Verification and Validation protocols, Usability, and Cybersecurity deliverables. Participate in internal audits, regulatory submissions, and post-market surveillance for software updates. Support validation and verification activities, including unit testing, integration testing, and system testing under regulatory frameworks. Deep understanding of IEC 62304, ISO 14971, ISO 13485, IEC 82304 guidelines, and Usability and FDA (Pre- and Post-market) Cybersecurity Guidelines. Prior experience with FDA 510(k) or PMA/De-Nova submissions and regulatory submissions. Maintaining a complete track record of all the software changes and documents. To Apply: Please send your resume and a brief cover letter to hr@ssinnovations.org Show more Show less
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