1307 Medical Devices Jobs - Page 8

General Manager Commercial (Medical Devices IVF Domain) Location: Mumbai, India Lead and manage overall commercial operations including Sales, Marketing, and Key Account Management for the IVF product portfolio Drive strategic planning and execution of product launches and new product development (NPD) initiatives Build and maintain strong relationships with KOLs, fertility clinics, hospitals, and IVF specialists Act as the primary liaison between Indian operations and global headquarters, ensuring seamless communication Oversee national business performance, forecasting, budgeting, and commercial strategy implementation Monitor competitor activities and market trends to ensure proactive business positioning Lead cross-functional teams and ensure operational excellence across supply chain, logistics, and customer service Ensure compliance with regulatory, quality, and ethical standards relevant to medical devices in India Report directly to top management, providing timely updates on all commercial and operational KPIs Inspire, mentor, and develop high-performing teams to drive sustainable business growth across India

We are looking for a highly skilled and experienced Biomedical Engineer to join our team at Raigad Hospital and Research Centre. Roles and Responsibility Design, develop, and test biomedical devices and systems. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and implement testing protocols for biomedical devices. Analyze data and troubleshoot issues with biomedical devices. Ensure compliance with regulatory standards and guidelines. Participate in the development of technical documentation and reports. Job Requirements Bachelor's degree in Biomedical Engineering or related field. Proven experience in designing and developing biomedical devices and systems. Strong understanding of medical devices and regulations. Excellent problem-solving and analytical skills. Ability to work effectively in a team environment. Strong communication and interpersonal skills.

Function:PMSRole:Post Market SurveillanceDesired Skills:PMS, complaint handlingCreate PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis Risk management Risk assessment. Required Candidate profile Propose strategies and solutions to data issues or challenges that occur during the PSUR writing and conclusion process.

A Day in the Life We are seeking an Engineering Manager focused on Product Security to lead a dynamic team responsible for developing, implementing, and monitoring security solutions for Medtronic s cardiac medical devices and infrastructure. This role requires a strategic thinker with strong leadership skills to drive product security initiatives, ensure compliance with regulatory standards, and foster collaboration across various teams. Responsibilities may include the following and other duties may be assigned. Lead and manage a team of engineers and cybersecurity professionals dedicated to product security for cardiac medical devices. Execute a comprehensive Product Security strategy aligned with Medtronic s cardiac business objectives and regulatory requirements. Collaborate with cross-functional global teams (R&D, quality assurance, and regulatory affairs) to integrate security practices throughout the product lifecycle. Oversee the identification and remediation of vulnerabilities, ensuring timely and effective incident response. Establish and maintain security standards, frameworks, and best practices for product development and deployment. Monitor industry trends and emerging technologies to inform security strategies and practices. Communicate complex security concepts clearly to diverse stakeholders, including executive leadership, customers, and regulatory bodies. Foster a culture of security awareness and continuous improvement within the team and across the organization. Manage project timelines, budgets, and resources to ensure successful delivery of product security initiatives. Drive best-in-class Product Security design for new cardiac product development, and released products, ensuring scalable and risk-mitigated designs. Execute risk-based security assessment processes and implement them across product efforts. Build and sustain a product security team capable of assessing and testing new and released cardiac products that transcend technology (ex. embedded, mobile, web application ) Required Knowledge and Experience: Bachelor s degree in engineering, Computer Science, or a related field; advanced degree preferred. Minimum of 15+ years of experience in engineering or cybersecurity roles. Proven expertise in product security, particularly in medical device or other highly regulated industries. Strong understanding of cybersecurity principles, risk management processes, and regulatory requirements for medical devices. Demonstrated ability to lead and develop high-performing teams, fostering collaboration and innovation. Excellent communication and interpersonal skills to build relationships with internal and external stakeholders. Desirable Qualifications: CISSP, OSCP or similar cybersecurity certifications. Experience with IoT devices, embedded, mobile, cloud security, and data protection architectures. Familiarity with security incident management and operations center (SOC) practices. Knowledge of national and international laws related to medical device cybersecurity. Experience in healthcare or other heavily regulated industries. Understanding compliance with FDA, GDPR, EUMDR, and other international regulations. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission to alleviate pain, restore health, and extend life unites a global team of 95, 000+ passionate people. We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here

A Day in the Life Be a part of the Medtronic Engineering and Innovation center (MEIC) by applying your skills to the growth and development & sustaining efforts of Medical Devices products at MEIC. As a member of the MEIC team, you will collaborate with the broader Medical Devices engineering team, clinical and commercial teams globally. You will enable design & development of medical devices/products and the associated infrastructure & capability building elements in close conjunction with the Global teams. Responsibilities may include the following and other duties may be assigned Experience in distributed product development, team building skills, talent management, conflict resolution, budget management and global stake holder management are critical to the role. Manage a cross functional (SW, FW, HW, Systems) engineering technical team size of 20 or more. Provide a blend of people management and technical savviness. Should have worked on development of products and on successful delivery of solutions. Deep understanding in product development processes & regulations (IEC 60601, IEC 62304, ISO 13485, ISO 14971) Design controls for medical device development in order to coach and guide the technical leads is expected. Identify the needs and prepare capabilities in the cross functional areas, SW development and verification and validation areas to foster full turnkey solution to the business. Provide a deep understanding of the embedded and application SW development processes (Agile, waterfall methodology) and help establish SW metrics & recommended the processes for the team. Research and maintain solution architecture, technical design, tools and technology stack and related system and drive proof of concept efforts in MEIC. Must be able to support the global team in organic, blended, inorganic product development projects. Support the technology road map of Medical Devices by proactively pitching for technology development and turnkey projects. Support Regional Growth plans and product requirements to boost tailored product for the regions Establish and remain educated on the relevant technology standards (DICOM, HL7, 62304, ISO 11073 etc. ) Develop junior members by coaching, empowering, reviewing results, both in technical areas and in soft skills. Identify solution knowledge gaps within MEIC in Medical Devices solutions and prepare plans to address them ( strategic alliances and self-managed teams ) The incumbent would work with the project management office at MEIC to ensure that resource forecasts, project metrics are correctly captured and presented to the leadership Frequent interaction with team members from other disciplines, cross functional teams, to understand project requirements and to adhere to project schedules. Possible interaction with clinicians, third-party vendors, manufacturers, and subcontractors. Required Knowledge and Experience Good hands on experience in Linux-based development environments with strong proficiency in C, C++, or Rust. Skilled in contributing to end-to-end software solutions. Knowledgeable in design controls for medical devices (related to CFR 820. 30) 510K, IEC 62304 & other relevant standards. Product development experience for local markets ( in country for country) would certainly be a plus. Strong proven capability & track record in developing product applications and strong knowledge in device communication & diagnostics, database systems and latest communication protocols. Hands-on application development (right from requirement analysis to deployment) and management of sizeable teams in FW, HW, & SW application development & verification activities. Strong Leadership expectations traits for mid-level leaders (internal candidates only) Bachelor s or Master s degree either in Computer Science, Computer Engineering or Electronics & communication Engineering. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission to alleviate pain, restore health, and extend life unites a global team of 95, 000+ passionate people. We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here

Sets up and operates haemodialysis machine to provide dialysis treatment for patients with kidney failure Attach dialyzer and tubing to machine and prime the extracorporeal circuits with 0.9% normal saline to prepare machine for use. Label dialyser blood lines with patient name ID prior to the first use (excluded single use). Preparing dialysis solutions and mixing bicarbonate according to formula Explains dialysis procedure and operation of haemodialysis machine to patient before treatment to allay anxieties. Connects haemodialysis machine to patient s access site to initiate dialysis. Monitor haemodialysis machine for malfunction. Maintain all the log books, forms registers. Fresenius Medical Care is a global leader in providing high-quality healthcare solutions and services. We are committed to fostering an inclusive and diverse work environment where all employees are treated with respect and fairness, regardless of race, gender, caste, ethnicity, religion, disability, or any other characteristic. We believe in equal opportunities for all and celebrate diversity as a key driver of innovation and success. Our commitment to equality ensures that every individual has the opportunity to thrive

Description Requirements Introduction: A Career at HARMAN Digital Transformation Solutions (DTS) We re a global, multi-disciplinary team that s putting the innovative power of technology to work and transforming tomorrow. At HARMAN DTS, you solve challenges by creating innovative solutions. Combine the physical and digital, making technology a more dynamic force to solve challenges and serve humanity s needs Work at the convergence of cross channel UX, cloud, insightful data, IoT and mobility Empower companies to create new digital business models, enter new markets, and improve customer experiences About the Role Medtronic is a world leader in providing health care products that benefit individuals well-being. Our organization contributes directly to this mission. Principal Engineer I is responsible for supporting the Design Controls, Medical Device Regulations Gap Assessment and Remediation activities. Principal Engineer I is expected to have the appropriate Knowledge/Experience on product development and cross-functional aspects. It is expected that the RD Principal Engineer I is capable of learning the product and process quickly. Exchange information of facts, statuses, ideas and issues to achieve objective, and influence decision-making. . What You Need Exposure to or experience working in or with Design, Quality, Regulatory, Clinical and/or Manufacturing Experience in the design, maintenance, or continuation engineering of released software or software systems, including mobile applications Knowledge of Design for Reliability (DfR), Design for Reliability and Manufacturability (DRM), Design for Six Sigma (DFSS), Design for Lean Sigma (DFLS), and/or robust design practices What Makes You Eligible Bachelor s Degree in Mechanical Engineering / Bio-Medical / Bio-Tech with 8 to 12 Years of professional experience. Good knowledge on medical device regulations like IEC-60086, ISO-22442, FDA Guidance etc. Theoritical Knowledge on Medical Devices. Knowledge of Creo or any modeling Software and Manufacturing Operations. Excellent Communication - Written and Oral. What We Offer Access to employee discounts on world class HARMAN/Samsung products (JBL, Harman Kardon, AKG etc.) Professional development opportunities through HARMAN University s business and leadership academies. Flexible work schedule with a culture encouraging work life integration and collaboration in a global environment. An inclusive and diverse work environment that fosters and encourages professional and personal development. Tuition reimbursement. Be Brilliant employee recognition and rewards program. You Belong Here HARMAN is committed to making every employee feel welcomed, valued, and empowered. No matter what role you play, we encourage you to share your ideas, voice your distinct perspective, and bring your whole self with you all within a support-minded culture that celebrates what makes each of us unique. We also recognize that learning is a lifelong pursuit and want you to flourish. We proudly offer added opportunities for training, development, and continuing education, further empowering you to live the career you want. About HARMAN: Where Innovation Unleashes Next-Level Technology Ever since the 1920s, we ve been amplifying the sense of sound. Today, that legacy endures, with integrated technology platforms that make the world smarter, safer, and more connected. Across automotive, lifestyle, and digital transformation solutions, we create innovative technologies that turn ordinary moments into extraordinary experiences. Our renowned automotive and lifestyle solutions can be found everywhere, from the music we play in our cars and homes to venues that feature today s most sought-after performers, while our digital transformation solutions serve humanity by addressing the world s ever-evolving needs and demands. Marketing our award-winning portfolio under 16 iconic brands, such as JBL, Mark Levinson, and Revel, we set ourselves apart by exceeding the highest engineering and design standards for our customers, our partners and each other. If you re ready to innovate and do work that makes a lasting impact, join our talent community today! HARMAN is proud to be an Equal Opportunity employer. HARMAN strives to hire the best qualified candidates and is committed to building a workforce representative of the diverse marketplaces and communities of our global colleagues and customers. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.HARMAN attracts, hires, and develops employees based on merit, qualifications and job-related performance.( www.harman.com )

Job Title: Product Sales Manager - BiPAP and CPAP Job Summary: We are seeking an experienced Product Sales Manager to lead the sales and marketing efforts for our BiPAP and CPAP products in Chennai. The successful candidate will have a strong background in sales and marketing, excellent communication skills, and experience in managing sales teams. Key Responsibilities: 1. Sales Strategy and Planning: - Develop and execute sales strategies to achieve business objectives for BiPAP and CPAP products. - Identify and pursue new business opportunities in the sleep therapy market. - Collaborate with cross-functional teams to drive business growth. 2. Team Management: - Lead and manage a team of sales professionals to meet sales targets. - Coach and mentor team members to improve sales performance and achieve business objectives. - Conduct regular performance evaluations and provide feedback. 3. Customer Relationship Management: - Build and maintain strong relationships with key customers, including hospitals, clinics, and medical professionals. - Identify and address customer needs and concerns. - Develop and implement customer retention strategies. 4. Market Analysis: - Stay up-to-date with market trends, competitor activity, and regulatory changes. - Analyze market data to inform sales strategies and business decisions. Requirements: 1. Experience: 7+ years of experience in sales and marketing, preferably in the medical device industry. 2. Education: Bachelor's degree in Business Administration, Marketing, or a related field. MBA or other advanced degrees preferred. 3. Skills: - Strong sales and marketing skills, with experience in managing sales teams. - Excellent communication, negotiation, and interpersonal skills. - Ability to analyze market data and make informed business decisions. - Strong customer relationship management skills. 4. Product Knowledge: Familiarity with BiPAP and CPAP products and sleep therapy market is desirable. Location: - Chennai - Hyderabad - Bangalore

Responsibilities: * Manage sales team performance and development. * Lead medical equipment sales strategy. * Collaborate with marketing on healthcare campaigns. * Build strong customer relationships. Health insurance Provident fund

Key Responsibilities : • Define and document software requirements to meet UI/GUI system, application, human factor, and clinical needs. • Interface with firmware engineers to define system requirements and specifications. • Develop scalable software architecture at the device and system level. • Take complete ownership of software systems from concept to production. • Lead and mentor a team of embedded software engineers, fostering technical excellence. • Optimize framework software for performance, reliability, and code efficiency. • Conduct thorough code reviews to ensure compliance with industry standards and best practices. • Develop and execute integration testing and validation plans for embedded firmware and software. • Stay updated on advancements in embedded systems and incorporate relevant technologies. • Document software design, development processes, and test reports with clarity and accuracy. • Ensure compliance with medical device regulations, providing necessary support to the software team. • Coordinate cross-functional demands efficiently during product development and maintenance. • Embedded Systems Expertise: Understanding microcontrollers, microprocessors, and real-time operating systems. • HMI Design & Development: Experience with graphical user interfaces (GUI) and human-machine interaction principles. • Programming Languages: Proficiency in C, C++, Python, and/or embedded-specific languages like C / C++ for free RTOS and Linux, embedded systems concepts, and hardware-software integration • Designs and implements embedded software to log medical device performance and therapy session data • Hardware Integration: Familiarity with display technologies such as LCD, OLED, and touch interfaces. • Medical Device Standards: Compliance with regulations like IEC 62304 for software development in medical devices. • Hands-on experience in at least one complete SDLC for medical devices, from concept development to design release. • Proficiency with integrated development environments (IDEs) such as Eclipse, Visual Studio, etc. • Experience with communication protocols including Ethernet, BLE, USB, HDMI, and DVI. • Solid background in algorithm development for Class II/III and Class B/C medical devices. • Proficient in simulation-based software testing at unit, integration, and system levels. • Strong understanding of image processing (ISP), V4L2 or MIPI CSI drivers, and HDMI/DVI interfaces. • Design and develop software applications using the QT framework with QML • Familiarity with UI development using QT/GTK libraries. • Knowledge of regulatory standards and documentation requirements (SDLC IEC 62304, ISO 13485, ISO 14971). • Experience in software risk management, code reliability, and hazardous software assessment. • Exposure to product and operational data security standards (NIST/HIPAA). • Excellent presentation, written, and verbal communication skills. • Strong ownership mentality, collaborative mindset, and ability to work independently. • Experience in embedded firmware development for medical devices, preferably in endoscopy, urology lasers, and diagnostic imaging devices. • Prior involvement in at least one full SDLC for medical devices, from concept development to design release and production. • Knowledge of modern software development methodologies (Agile, Scrum). • Familiarity with version control systems such as Git and SVN.

Hardware Design Engineer Job description: Location : (Kattankulathur) Chennai Experience : 2 to 6 Years Role & responsibilities 1. Responsible for all electronic related issues/concerns as regards to design & development, integration, quality, reliability, and EMI/EMC issues. 2. Experience in Microcontroller based Product design with High speed board bring up design. 3. Experience in IOT, Digital, Mixed signal design; with automotive/industrial experience. 4. Experience in Power electronics, Switch mode power supply, analog digital circuit design and BLDC Motor control drive. 5. Responsible for new hardware design(Digital, Analog, Low voltage Power supplies), Coordinating within departments and vendors for arranging the Components, PCBs(Bare and assembled), etc. 6. Responsible for completing CE certification of the products. Addressing technical and nontechnical requirements for certification. 7. Responsible for generating and maintaining electronics design documents (Concept/Block diagrams, Power requirements, Schematic, Gerber, BOM, Test plans, Verification and Validation reports. 8. Ensuring that the product development cycle is followed through all the critical steps by continuous monitoring and control. Supporting the Product development team in developing and testing the prototype to achieve the functional and performance requirements. 9. Ensuring war footing response for closure of critical complaints, obsolence requirements. Address queries and improvements raised during manufacturing process. 10. Responsible to create detail designs from the concept/s, to ensure robustness of the respective system by meeting component level and system level design validation requirements. 11. Identifying and achieving the potential cost saving areas of electronic systems without compromising functionality and reliability. 12. Creating value enhancement opportunities for existing and new products by virtue of conceptualizing and developing new features. 13. Maintaining existing hardware systems, providing support and executing changes. 14. Team-up with SW team on Hardware bring up and development. Work with other functional teams to find root-causes and solutions. Work with operations team on manufacturing developed designs and give support for existing developed designs. * In addition to the above you may be given additional responsibilities as per business requirement and your JD can be altered at the discretion of your superiors. Requirement profile : Experience in a design role with exposure to production methodology. ashok.panneerselvam@srmtech.com

PRINCIPAL ENGINEER/ SENIOR TECHNICAL ARCHITECT Job Requirements We are seeking an experienced Embedded Software Architect to lead and oversee the design and development of embedded software systems. The ideal candidate will have over 15 years of experience in the field, with a strong background in C/C++ programming, real-time operating systems, and hardware-software integration. This role involves collaborating with cross-functional teams to deliver innovative and high-quality embedded solutions. Responsibilities include - Design and architect embedded software systems from concept to production. - Lead and mentor a team of embedded software engineers. - Develop and maintain embedded software architectures and design patterns. - Optimize software for performance, reliability, and power consumption. - Conduct code reviews and ensure compliance with industry standards and best practices. - Interface with hardware engineers to define system requirements and specifications. - Develop and execute testing and validation plans for embedded software. - Stay updated with the latest advancements in embedded systems and incorporate relevant technologies. - Document software design and development processes. - Guide and provide necessary support for embedded software development according to medical device compliance and regulations. - Adaptive to managing and co-ordinate cross functional demand during product development and maintenance. Work Experience Required Skills: Bachelor's or masters degree in computer science, Software Engineering, Electronics Engineering, or a related field. - Embedded architect experience specifically in hemodialysis machine and Renal care device generally. - Medical devices experience who can write SRS and run the entire product design process. - Over 15 years of experience in embedded software development and architecture. - Proficiency in C, C++, and assembly languages. - Extensive experience with real-time operating systems (RTOS) and embedded Linux. - Strong knowledge of microcontroller/microprocessor architectures. - Experience with communication protocols such as I2C, SPI, UART, USB , etc. - Excellent problem-solving and debugging skills. - Proven track record of leading and managing engineering teams. - Strong communication and documentation skills. - Professional certifications in embedded systems or software architecture are a plus. Preferred Skills: - Experience with hardware design and schematic review. - Knowledge of modern software development methodologies (Agile, Scrum). - Familiarity with version control systems such as Git. - Understanding of safety-critical systems and compliance standards.

Responsibilities: * Manage international healthcare sales * Report on global market trends * Identify new business opportunities * Develop strategic partnerships * Drive revenue growth through medical device solutions Provident fund Annual bonus Health insurance

Opening - Area Sales Manager - Brief Job Role: Creating new leads for sales of medical products Contacting prospective customers Doing regular follow-ups with new and existing customers for these sales Assisting the product management team Creating Weekly reports & MIS Co-ordinating for events like conferences. symposiums, learning based lectures, etc. Attending conferences This is an Individual contributor role Candidates with exp in IVF / Hormones /Gynec - Mandatory Job involves extensive traveling ( atleast 12-15 days in a month ) and visiting hospitals and clinics (IVF/IUI/ Ob/Gyne) Currently looking for Multiple locations (will be handling respective state and nearby regions) ASM - Kolkata, WB (Regional Branch Office) ASM - Punjab (based in Chandigarh - Resident Position) ASM - Cochin, Kerela (Regional Branch Office) ASM - Coimbatore (TN full South - Resident Position) Required Experience, Skills and Qualifications Qualification - Graduate - B Sc / B Pharma / BE Bio Medical Experience - 4 yr to 10 yrs in Gyne / Hormones / IVF Please apply on mail - Contact HR Office - 022-42385230/33 mail cv on - hr@intermedics.in

The Project Manager Embedded Systems will be responsible for leading the end-to-end development of embedded hardware and firmware for advanced medical diagnostic devices. You will manage design activities, coordinate with internal and external teams, and ensure timely delivery of projects aligned with business objectives. Key Responsibilities: - Lead analog and embedded hardware design for new product development - Oversee embedded firmware and algorithm development (STM32, HAL, RTOS) - Coordinate with development partners and manage project execution - Ensure comprehensive documentation aligned with relevant industry standards - Supervise prototyping, design verification, and product lifecycle management - Support manufacturing and deployment of products - Collaborate with stakeholders to ensure alignment of product development with strategic goals Required Qualifications and Experience: - Bachelor's or Masters degree in Electronics or related field - Minimum 6 years of experience in embedded systems development - At least 4 years in firmware development and 4 years in analog hardware design - Experience with communication peripherals such as BLE, NFC, USB, OLED, LCD - Minimum 2 years of experience in project and delivery management - Experience with rechargeable battery-operated IoT and medical devices - Proficiency in C++, Embedded C, and Python - Familiarity with agile, waterfall, and product lifecycle methodologies Desirable Attributes: - Strong leadership and people management skills - Excellent analytical, communication, and coordination abilities - Prior experience in R&D or engineering roles within medical, IoT, or electronics manufacturing industries - Exposure to OEM/ODM collaboration and supply chain management,

You are invited to join Cyrix Healthcare Pvt Ltd as a Sales Engineer in Bengaluru. We are seeking proactive individuals to promote and sell biomedical equipment and devices. Your main responsibilities will include achieving sales targets, establishing lasting client relationships, and ensuring utmost customer satisfaction within the biomedical sector. Your duties will involve promoting and selling biomedical equipment/devices, identifying new business opportunities, generating leads through various means, and nurturing relationships with key stakeholders. You will be expected to negotiate sales deals, maintain detailed records of client interactions, and stay informed about product developments and industry trends. To excel in this role, you should possess a solid understanding of biomedical equipment/devices, demonstrate proven sales skills (particularly in healthcare or medical devices), and exhibit excellent communication, negotiation, and presentation abilities. Whether you are a fresher or have up to 2 years of experience, we welcome enthusiastic candidates with a BE/BTECH/Diploma in Biomedical. A valid Two Wheeler license is mandatory, as this role requires extensive travel within the designated region. If you are ready to take on this challenging yet rewarding opportunity, please send your CV to tacyrix@gmail.com. This is a full-time, permanent position offering benefits such as health insurance and Provident Fund. The work schedule is during day shifts, and proficiency in English is preferred. The work location will be in person. We look forward to welcoming you to our team at Cyrix Healthcare Pvt Ltd!,

Greetings from Ababil Healthcare Pvt Ltd!! We are currently looking for a Preventive Maintenance Service Engineer to join our team in Chitradurga. The ideal candidate will have a Diploma or BE in Biomedical with 0 to 3 years of experience. As a Preventive Maintenance Service Engineer, your responsibilities will include system installations, troubleshooting, service, and repair. You will be in charge of performing preventative maintenance and managing regional schedules. Additionally, you will be responsible for completing service calls, managing customer accounts, providing onsite training, managing expenses and spare parts inventory, and ensuring zero breakdowns in the respective region. To excel in this role, you should possess strong communication and networking skills, good planning and organizational abilities, self-motivation, drive, and initiative. The role also requires flexibility to adapt to changes in products and healthcare systems, along with documentation skills, training management, equipment calibration, sterilization, conceptual skills, and business acumen. If you are passionate about the healthcare industry and have the necessary skills and qualifications, we would love to hear from you. Please contact our HR Department at 7824848607 or email us at hr.chennai@ababilhealthcare.com to apply. Thank you for considering a career with Ababil Healthcare Pvt Ltd.,

Hi, We at CIPLA Limited are hiring for Hospital Business Manager role for Diagnostics Business to be based in Hyderabad Please find below job details : Position : Hospital Business Manager Role : Hospital Business / Key Accounts Management Location : Hyderabad Roles & Responsibilities: Select Potential Hospitals / Laboratories / Doctors and Customers Target customers like KOL/KBL Drs, Pathologists, Technicians, PROs, Purchase officers, CEOs of institution for better hold over the business Ensure availability of key products at such institutions Develop the secondary customers. Develop brand image & leverage for the diagnostics product basket. Visit KOL/KBL customers to engage them and generating business. Ensure the price & brand matrix accountability. Ensure brand matrix productivity through effective business planning & market updates. Control the Sales return and expiry Manage the profitability of business through priority products as directed by HO. Preferred Qualification and criteria Science graduates Should have minimum 3 yrs. sales experience in diagnostics / surgical / medical devices Should be ready to handle larger geography Individual Contributor Role Interested candidates are requested to apply on the job posting. Regards HR Team CIPLA Limited

Job Summary: Responsible for managing day-to-day operations of the calibration lab, maintaining documentation, ensuring compliance with ISO/IEC 17025 and regulatory requirements, and overseeing calibration activities for thermal and biomedical devices. Acts as the coordinator equipment traceability, and calibration data management. Key Responsibilities: Maintain and control all calibration-related documents such as SOPs, calibration procedures, master equipment records, and logbooks. Review calibration results and ensure correctness before issuing certificates. Monitor the validity and performance of master equipment and arrange for their periodic calibration. Maintain equipment history cards and calibration status labelling Ensure compliance with ISO/IEC 17025, ISO 13485, and NABL documentation requirements. Manage environmental monitoring records (temperature, humidity) for thermal calibration setups. Qualifications and Skills: Experience in NABL Lab [Calibration discipline- Medical devices, Thermal etc, QA Testing]. Understanding ISO/IEC 17025. Preferably a person with thermal training certificate. Minimum 2-3 years of experience in calibration lab with exposure to medical and thermal disciplines. Document Control & Record Keeping, Verifying the calibration & QA report, Excel techniques etc. No. of positions: 1

Job Summary: To provide clinical application training, technical support, and product demonstrations for Cyrix Healthcares medical devices in Hospitals. The Clinical Application Specialist will ensure customers receive effective training, maximize product utilization, and improve patient outcomes. Key Responsibilities: Clinical & Technical Support Responsibilities Conduct on-site and virtual clinical training sessions for healthcare professionals. Provide application support to customers, ensuring effective usage of Cyrix Healthcare s medical devices. Assist in troubleshooting technical and clinical issues related to product applications. Stay updated on industry best practices and clinical guidelines to enhance training programs. Customer Responsibilities Act as a primary point of contact for hospitals, clinics, and medical professionals regarding product applications. Ensure customer satisfaction by addressing queries and providing continuous education. Develop strong relationships with key stakeholders, including doctors, nurses, and hospital administrators. Sales & Business Development Support Support the sales team by conducting product demonstrations and technical presentations. Collaborate with sales representatives to develop training plans tailored to customer needs. Provide pre-sales and post-sales support to drive customer confidence in Cyrix Healthcare s solutions. Marketing & Research Responsibilities Participate in industry conferences, workshops, and seminars to showcase product capabilities. Gather clinical feedback from users to support product enhancements and innovation. Work closely with the marketing team to create educational materials, case studies, and clinical documentation. Operational & Internal Responsibilities Ensure proper documentation of training sessions, client interactions, and feedback reports. Assist in the development and standardization of training materials and clinical protocols. Collaborate with cross-functional teams to align clinical support activities with company objectives. Learning and Growth Responsibilities Continuously enhance technical and clinical knowledge through training and certifications. Stay updated with the latest advancements in medical technology and industry regulations. Foster a knowledge-sharing culture within the team by mentoring junior specialists. Qualifications and Skills: Minimum 3-5 years in a clinical support or application specialist role Knowledge in Clinical workflow, medical device applications, regulatory compliance Strong communication, problem-solving, training, and presentation skills Relevant scientific or clinical degree, degree in Biomed or hospital registrations No. of positions: 1

Job summary: Seeking a skilled Biomedical Equipment Field Service Engineer with 3 8 years of experience in troubleshooting, calibrating, and maintaining critical medical devices (X Ray, Dialysis, ICU/OT, Lab), who thrives in a collaborative, innovative environment and is ready to support healthcare delivery across diverse locations. Key Responsibilities: Maintain & Troubleshoot: Handle breakdown and preventive maintenance for critical equipment like X-Ray, Dialysis, ICU/OT systems, and lab instruments. User Support: Provide technical assistance and training to healthcare professionals. Vendor Coordination: Liaise with OEMs and vendors for spares and technical support. Multi-Modal Expertise: Manage equipment across ICU, OT, Imaging, and Lab settings. Travel Ready: Willingness to travel extensively within assigned territories. Qualifications and Skills: 3-8 years in biomedical equipment service and maintenance. Proficiency in troubleshooting, calibration, and performance testing. Excellent interpersonal and communication skills. Degree/Diploma in Biomedical, Medical Electronics, or Electronics & Instrumentation. No of positions: 1

Seeking an experienced RPA (Robotic Process Automation) Developer to join our team. As a developer, you will be responsible for in working in a project team in developing, testing and the processes as per client needs. Qualifications and Experience: Skills Required: Design, Develop and test: Development of RPA processes using any of the RPA tools, test the processes and deploy to production. Proven experience of 2+ years as an RPA Developer and implementing RPA solutions. Knowledge or experience in creating frameworks, modifying, and maintaining. In-depth knowledge and experience on RPA tools such as UiPath, Automation Anywhere, or Blue Prism(any 1 tool) Working with Orchestrator and Control Room, configuring machines, bots, and other areas is an added advantage. Experience on QA processes. Excellent problem-solving and analytical skills Strong communication skills Certification in one RPA tool (UiPath, Automation Anywhere, or Blue Prism) is mandatory.

Manager Events QualiZeal is seeking a dynamic and experienced Manager Events to spearhead our event marketing efforts. You will play a pivotal role in shaping and executing our event marketing strategy. You will be responsible for planning, organizing, and executing a wide range of events-- including owned events and participation in industry events to drive brand awareness, engage our target audience, and contribute to our revenue growth. This role requires a strategic thinker with a keen eye for detail, exceptional project management skills, and a passion for creating memorable experiences. Key Responsibilities: 1. Owned Events Management: Plan and execute (host, co-host, or organize) a variety of owned events, including webinars, podcasts, roundtables, meetups, fireside chats, tech talks, hackathons, and user conferences. Collaborate with internal subject matter experts and external stakeholders (experts, influencers, customers, partners) for participation and content curation. Determine the appropriate format and mode (virtual, physical, hybrid, live, recorded) for each event to achieve specific objectives. Oversee end-to-end event logistics, from conceptualization to post-event follow-up. 2. Industry Events Participation: Identify relevant industry conferences, trade shows, and other 3rd-party events for QualiZeal s participation. Manage event sponsorships, including booth setups, speaking opportunities, co-presentations with customers/partners, product/service launches, and private gatherings. 3. Strategy and Planning: Develop a comprehensive events strategy aligned with our business goals and marketing objectives. Create event calendars, budgets, and project plans for timely execution. Track and report on ROI for each event to assess its impact on the company s growth. Create compelling event marketing campaigns to drive attendance and engagement. Work closely with the marketing team to leverage digital marketing, social media, email marketing, and other channels to promote events effectively. 5. Post-Event Analysis: Conduct post-event evaluations to measure the success of each event, gather feedback, and identify areas for improvement. Collaborate with marketing, sales, and demand generation teams for post-event marketing. Qualifications and Experience: Requirements: Bachelor s degree in Marketing, Communications, Business, or a related field. (MBA or Master s degree preferred.) Proven experience (5+ years) in event management, preferably in the technology or software industry. Demonstrated success in planning and executing a variety of events, from webinars and podcasts to large-scale conferences. Strong project management skills with the ability to handle multiple tasks and deadlines simultaneously. Excellent communication and interpersonal skills to liaise with internal teams, external partners, and event participants. Familiarity with event management software and tools.

Senior Test Engineer As a Test Engineer / Senior Test Engineer, you will be responsible for designing, implementing, and maintaining automated systems. Your role will be critical to enhancing and upholding highest standards of efficiency, quality, and reliability of high-impact systems and applications of our industry-leading clients including Fortune 500 enterprises. You will work on various mission-critical automation projects and collaborate with cross-functional teams to integrate automation technologies successfully across the organization. Key Responsibilities: Develop test plans to ensure automated systems meet performance, safety, and functionality standards. Execute automated tests, validate results, and make necessary adjustments to improve the systems. Provide ongoing support and maintenance for automation systems, ensuring minimal downtime. Troubleshoot and resolve issues with automation systems to maintain system reliability. Develop and implement automation scripts for testing across various frameworks and technologies. Deep expertise in Java Selenium / C# Selenium / Python. Understanding of integrations with multiple tools across the testing ecosystem. Collaboration with cross-functional teams for smooth integration of automation technologies. Engage in client interactions to understand requirements and provide updates on testing progress. Qualifications and Experience:

Experience 5+ Years Job Type Full Time Key Responsibilities: Develop and execute a comprehensive Analyst Relations (AR) strategy to enhance QualiZeal s reputation and recognition in the Quality Engineering industry. Build and nurture strong relationships with analysts and key stakeholders at prominent analyst firms, such as Gartner, Forrester, NelsonHall, Everest Group, IDC, etc. Facilitate analyst briefings, inquiries, and presentations to ensure analysts have a deep understanding of QualiZeal s offerings and capabilities. Collaborate with cross-functional teams to ensure analysts have access to relevant information and insights about QualiZeal s products, services, and industry trends. Ensure that QualiZeal is well-positioned and prominently featured in analyst reports, Magic Quadrants, Waves, and other relevant publications. Identify and build relationships with influential Deal Advisory firms like ISG, Zinnov, etc. that help enterprises with their RFP processes, market assessments, and vendor selections in the Quality Engineering space. Work closely with the sales, presales, and business development teams to leverage deal advisory partnerships in sales processes. Regularly analyze and report on the impact of AR and deal advisory activities on the company s growth and revenue. Track and manage the budget allocated for AR and deal advisory initiatives. Stay updated on industry trends, market dynamics, and competitive landscape to identify growth opportunities and potential risks. Skills Required: Bachelor s degree in Business, Marketing, Public Relations, or a related field. (MBA preferred.) Minimum 5+ years of relevant experience in Analyst Relations, Deal Advisory, or related roles within the IT services or technology industry. Excellent communication and interpersonal skills, with the ability to build and maintain relationships with industry analysts, advisors, influencers, and internal stakeholders. Self-driven, proactive, and capable of working independently and collaboratively. Strong project management and organizational skills.