1307 Medical Devices Jobs - Page 19

The Senior Validation & Verification Engineer will be responsible for planning, executing, and overseeing the validation and verification processes for products. This role ensures that all products meet industry standards, regulatory requirements, and customer expectations. Key Responsibilities: Validation & Verification Activities: Develop and implement V&V plans, test protocols, and test cases for new and existing products. Execute functional, performance, environmental, and reliability testing on instruments. Analyze test results, identify deviations, and collaborate with design teams to resolve issues. Document test reports and ensure traceability of requirements to test cases. Work on software and hardware validation as per industry standards. Compliance & Quality Assurance: Ensure compliance with ISO 9001, ISO 17025, IEC 61010, IEC 61508 (Safety), or other relevant regulatory standards. Support risk analysis (FMEA, DFMEA, PFMEA) to identify potential failures and mitigation strategies. Ensure that all validation processes adhere to FDA, CE, and other regulatory requirements, if applicable. Process Improvement & Documentation: Participate in design reviews to provide early-stage feedback on product verification strategies. Work closely with R&D, Manufacturing, and Quality teams to enhance validation processes. Develop and maintain Standard Operating Procedures (SOPs) related to V&V. Automation & Tools: Implement automated test scripts and frameworks for V&V where applicable. Utilize test management tools (e.g., Modscan, Modbus Poll, LabVIEW, VB, etc.) to enhance efficiency. Qualifications & Experience: Bachelor s/Master s degree in Electrical, Electronics, Instrumentation, or related fields. 5+ years of experience in V&V within an instrumentation, medical devices, or industrial automation Hands-on experience in hardware, firmware, and software testing of industrial instruments. Familiarity with sensor-based technologies, HMI, PLC/DCS systems, and IoT-enabled devices is a plus. Experience with regulatory audits and certification processes is preferred. Key Skills: Strong knowledge of testing methodologies and defect tracking systems. Expertise in using testing tools such as embedded test frameworks, Modscan. Knowledge of reliability testing methods (HALT, HASS, MTBF analysis). Excellent analytical and problem-solving skills. Strong documentation and communication skills. Preferred Certifications (if applicable): Certified Test Engineer (ISTQB or equivalent). Six Sigma Green Belt (for process improvement).

Position Summary: We are looking for a Clinical Evaluation Expert who is responsible for clinical evaluation and PMCF activities; collaboration with CLM owners/Risk manager/PMS manager. Qualification: MBBS or equivalent Medical degree; specialization in Radiology is preferred. Knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The expected experience is 3-4 years with a minimum of 1 - 2 years of CER writing experience is essential. A minimum of 1 - 2 years of medical writing/reviewing experience is needed. Knowledge on Medical devices regulations The experience is expected to be current or recent (preferably within the past two years), to provide confidence in their experience considering the rapid nature of updates/changes in the regulatory landscape, the device, its functionalities, and the therapy area. Preferred Experience: 1. Significant experience writing scientific, medical/clinical, and technical content. 2. Knowledge in the therapeutic area - specifically in the field of diagnostic radiology, interventional radiology and radiation oncology 3. Familiarity with various country specific standards and regulations for medical devices to be able to assess and provide device appropriate clinical evaluation data for registrations. Duties and Responsibilities 1. Collaborate with the project/program stakeholders for product knowledge and information to develop quality content for the CER s and within the required timelines. 2. Able to work in cross functional teams with strong communication, presentation & interpersonal skills 3. Analytical thinking skills with strong demonstration of scientific writing and verbal communication. 4. Manages projects in the context with full responsibility for the results and drives the development of clinical evaluation report, Pre-CER, CLP and/or services that are on time and meets the quality, regulatory and customer requirements . 5. Mentoring and coaching the team on technical topics 6. Responsible to implement process changes as per the new/updated regulatory requirements 7. Defining clinical development activities/ PMCF activities 8. participating in the assessment of clinical benefit-risk profile of the clinically relevant risks identified in the risk management upon request of the risk manager 9. assessing and aligning the device s clinical benefit-risk profile between the clinical evaluation and risk management jointly with the risk manager 10. supporting post-market surveillance manager on the PSUR/PMS reporting by providing summary of the relevant clinical evaluation report contents, and in planning/coordinating device s PMS activities with the device s clinical evaluation and PMCF.

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 Bachelor s Degree in Engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality. . What You Will Do Qualified to assess patient safety risks via one of the following: Medical Doctor with related device experience Engineer who has achieved IBHRE or NASPE Exam certification At least 5 years of clinical field experience in the past 15 years. The relevant field experience could include the following: o Nurse o Field Personnel such as: Clinical Specialist, Technical Field Educator, Field o Clinical Engineer o Technical Services (cardiac products) Personnel with at least 5 years of previous clinical experience related to cardiac therapy products. What You Need Advanced degree in Engineering or Science Proven understanding of reliability engineering principles Strong understanding of and experience in the application of statistics, including experience with Minitab Experience in a highly regulated industry, preferably implantable medical devices Experience with 21 CFR Part 820 (Quality System Regulation), ISO 13485, etc. Experience in the application of Risk Management (ISO 14971) and hazard analysis and risk analysis techniques (e.g., PHA, HA, FTA, DFMEA) Ability to independently lead investigations to identify system/product failures, hazards, hazardous situations, and harms CRE Certified 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 You hold a Bachelor s or Master s degree in Computer Science, Engineering, or a related technical field. Demonstrate strong problem-solving abilities and a deep understanding of backend system design and architecture. You re passionate about clean code , continuous learning, and sharing knowledge with teammates. 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 ! Please be aware that HARMAN recruiters will always communicate with you from an @harman.com email address. We will never ask for payments, banking, credit card, personal financial information or access to your LinkedIn/email account during the screening, interview, or recruitment process. If you are asked for .

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Job Function: Finance Job Sub Function: Accounting Job Category: Professional All Job Posting Locations: Bangalore, Karnataka, India Job Description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where sophisticated diseases are prevented, treated, and cured, where treatments are more inquisitive and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at /. Caring for the world, one person at a time has encouraged and united the people of Johnson & Johnson for over 125 years. We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. With more than $82 billion in 2019 sales, Johnson & Johnson is the worlds most comprehensive and broadly-based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets. There are more than 265 Johnson & Johnson operating companies employing approximately 132,200 people and with products touching the lives of over a billion people every day, throughout the world. If you have the talent and desire to touch the world, Johnson & Johnson has the career opportunities to help make it happen. Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer. Person will be responsible for Monthly & Quarterly closing of management books of accounts as per USGAAP along with closure of accounts as per Ind AS from Statutory perspective. Working on various Ad-Hoc Activities, Reporting and managing Internal, HCC, Compliance Audit requirements. Coordinate and fulfill Statutory audit requirements. Update Process SOPs and compliance with RCM/ SOX requirements. Preparation of P&L & Balance sheet with Commentaries Quarterly. Preparation of closing related journal entries & MIS on monthly / quarterly basis. Supervision of activities and journal entries prepared by 3rd party service provider. Review of Quarterly reports, Journal Logs, Balance sheet reconciliations. Ensure timely closure of books. Qualifications A) CA, CMA, MBA, M.Com or any other professional accounting qualification with 4-6 years of proven experience. B) Accounting Concepts should be strong. Basic knowledge of GST is required. C) Ability to work independently with minimum supervision. Should be self-driven. D) Knowledge of SAP & Excel is must. Alteryx and Tableau knowledge will be beneficial however it is not a mandatory requirement. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Thank you for considering Dexcom and the desire to join our mission to empower people to take control of their health! As Dexcom continues to grow globally, our India team will play a vital role in driving innovation and delivering impactful solutions. Whether youre an experienced professional or just starting your career, we re excited about the possibility of working with you. Our Talent Acquisition team is always seeking passionate individuals who want to make a difference. The best way to stay connected is by joining our Dexcom Career Network this ensures youre among the first to hear about new and exciting opportunities as we grow the team. Hardware Engineering Firmware Development: Create embedded software that powers our medical devices. Firmware Testing: Ensure firmware stability and performance through rigorous validation.

Hiring an experienced professional for New Vendor Development, Vendor Management, and ERP-based Procurement, including RFQ floating and analysis in a dynamic trading environment. Interested can Contact on Whatsapp-9910970479 Required Candidate profile Vendor Development Packaging material Experience is Preferred Strong command over ERP platforms. Sharp negotiation skills with a results-driven approach.

We are Hiring Medical Sales Representative for the Surgical disposables / Endo Surgery Products for renowned Surgical Devices Company Vacant Head Quarters: CALICUT, BANGALORE, JAIPUR, HYDERABAD, CHENNAI, MYSURU, MUMBAI, MANGALORE, CHANDIGARH, HUBLI, KOTA, SHIMOGA, DURGAPUR, SURAT, Qualification : Any Graduation JOB DESCRIPTION 1. Meeting doctors and OT staff, promotion and demand generation for the requisite product portfolio. 2. To ensure complete coverage of doctors as per the specifications and classifications given by the Company. 3. To implement the sales strategies in the respective territory of the Company. 4. To collect the various relevant market information & submit it to the ABM. 5. To respect and work within the systems and the values of the company. Prior working Experience of Surgicals is NOT MANDATORY Thanks & regards HR APLE PHARMA Aastha Mishra 7015693171, 8950062647 Share your CV at resume@aplepharma.com Required Candidate profile Should be confident, good in communication skills, Should have working experience in Sales of Pharma/ Surgical Note: You can also share references of Medical representatives interested in Surgical segment.

We are hiring Biomedical engineer who will be based out of Bailey Road, Patna Qualification - B. E - Biomedical Engineering Experience - 3 - 5 years of experience in managing medical equipment's of hospital. Candidate will manage/travel Pan India Clinics as an when required. Role & responsibilities 1.0. As equipments/instruments are integral part for diagnosis/treatment for ailment of patients hence keeping these always in working condition is must & to make it happen, this role /job is must for the organization & therefore this job fits into the organization 1.1. Ensuring timely delivery of equipment/ instruments at the center. 1.2. Coordinating with operation team/vendors/center head/maintenance team/project vendors for smooth installation. 1.3. Ensuring correct documentation from vendors for equipment/ instruments. 1.4. Coordinating with operation team & govt dept for registration of machines. 1.5. Maintaining records of all documents pertaining to machines & booking them into books as FAR through accounts department. 1.6. Keeping track records of AMC/CMC & timely renewal. 1.7. Guiding concerned Dr/staff about application /settings & knobology of machines. 1.8. Ensuring that breakdown of machines is repaired in shortest time. 1.9. Finalization of lay out of all centers as per statutory requirements. 1.10. Coordinating with pathology partner for smooth functioning of lab. Interested candidates may email their resumes along with below details to sakshi.pawar@matcarewellness.co.in Total Experience - Current CTC - Expected CTC - Notice Period - Candidate with only experience from Distributor or sales should not apply.

Develop & maintain strong, long-lasting relationships with key account, including hospitals, clinics, healthcare provider. Main point contact ensuring customer needs met and issues resolved promptly. Negotiate contracts, pricing, terms of agreements.

Taking initiative for Sales growth in the assigned territory. Drive execution of sales plans in own territory to grow sales. Strengthen relation with channel partners. Territory Coverage - Assam, West Bengal & some part of Jharkhand.

Design Engineer - Mechanical Department: Engineering R&D, Industry: Medical Devices / Healthcare Technology Employment Type: Full Time, Permanent Key Responsibilities: Design and develop over 100 plastic molded products with 3D Cad modelling and 2D drawing with 99% accuracy Follow industry best practices and implement in the design process Excellent knowledge of plastic manufacturing processes Superior experience in manufacturing unit plastic engineering work Perform and qualify the parts with T0, T1 trails Test and analyze the properties of different plastic materials Exceptional knowledge of extrusion processing and plastic material Sound skills in report writing and document processing Good ability to meet deadlines for multiple simultaneous projects Create and implement quality control measures for plastic manufacturing Collaborate with other engineers and professionals to solve technical problems related to plastic materials and products Qualifications: GTTC (DTDM-Diploma in Tool &Die Making) 4-5 year of experience in Product development, Engineering design. Medical equipment manufacturing industry experience preferred Job Types: Full-time, Permanent

Regulatory compliance, dossier preparation, CER, risk management (ISO 14971), audit support, CDSCO/FDA licensing, SOP drafting, validation reports, NPD change control, ,ensuring product certification in domestic ,international medical device markets Required Candidate profile B.Pharm, M.Pharm, Biomedical Engineering, Life Sciences, Regulatory Affairs Certification. Perks and benefits Food, PF, Medical Insurance

Required Education - Diploma / Degree in biomedical engineering Experience- 2-5 yr for Degree and 5 - 8 years of experience for diploma holder in minimum 250+ Bedded Hospital ; Knowledge and Specific Skills knowledge of maintenance of medical equipments. Location: Gurugram For inquiries, kindly reach out to Mr. Uma Shankar Mohanta via email uma.mohanta@fortishealthcare.com Job Profile - To maintain records of all the maintenance activities carried out in the respective area. To carry out maintenance activities according to the schedule drawn. To maintain assets register. To maintain a list of spares for all the equipments maintained by him. To make immediate action in reducing the breakdown time of the equipment in their area. To consult with Biomedical Engineering HOD for procurement of new equipments. To Coordinate the Installation / Upgradation of equipment with Vendors To co-operate with Biomedical Engineer in giving training for the trainee. To perform any other work assigned by the HOD

Job description Location : Baner,Pune Description: At least 4-6 years of professional experience in innovative product development, preferably including medical devices and -imaging. Experience in translating customer needs into technical requirements Proficient in 3D CAD, preferably Creo (Pro-Engineer) , SolidWorks, Onshape. Proficient in Windchill. Knowledge of Arena PLM is a plus. Special emphasis on profound understanding of mechanical design principles and analytical skills. Broad technical knowledge and experience with bringing medical products to the market, including knowledge of regulatory design- and safety standards, such as IEC-60601, ISO13485, FDA. Robust knowledge of design controls and risk management standards. Good understanding of design for quality aspects, testing critical to quality and regulatory requirements. Design for Six Sigma and GreenBelt certification (or equivalent) is a plus Utilizes in-depth knowledge of Geometric Dimensioning and Tolerancing (GD&T) and precise datuming techniques to create and interpret complex engineering drawings, ensuring accurate dimensioning, tolerancing, and tolerancing stack-ups. Interested Candidates can share their updated CV on k.minakshi@randstad.in and juhi.srivastava@randstad.in

UNITY DERMA are looking for hardworking Sales persons in Ahmedabad /Delhi location 1. The base location for the hired individual would be Ahmedabad /Delhi (any one ) of cosmetology, dermatology segment as Aesthetics Devices & Products 2.Only Medical Device ,Pharma and Aesthetics device related field interested person should be apply for this position Roles and Responsibilities meeting ,follow up and closing high cost Devices with doctors ,purchase and Medispa owners Develop good relationship with the customers and partners. Conduct and participate in various brand promotion activities Viz; CMEs, medical Conferences and workshops Direct meeting with doctors ,purchasers and able to achieve sales target Business Development on Aesthetics Lasers and professional cosmeceutical products Fresher is also welcome Desired Candidate Profile Should be self-driven by 2 wheeler and willing to travel other cities depend work Should have good networking skills Must be a team player Prior experience in this field of cosmetology in Aesthetics Devices OR medical device will be added advantage Perks and Benefits Good Salary ,incentive and Travelling allowance

Job Description: Compare and evaluate offers from Suppliers Negotiate contract terms of agreement and pricing Track orders and ensure timely delivery Review of quality of purchased products Enter order details ( e.g. vendors, quantities, prices) into internal database Maintain updated records of purchased products, delivery information and invoices Prepare reports on purchases, including cost analyses Monitor stock levels and place orders as needed Desired Candidate Profile: Proven work experience as a purchasing executive Good knowledge of vendor sourcing practices (researching, evaluating and liaising with vendors) Understanding of supply chain procedures Negotiation Skills

WZ-1, Phool Bagh, Rampura, Near Ashok Park Main Metro Station, Delhi 110035. Qualification: Bachelor s degree in a related field preferred. Job Description: Fluent English in Speaking and Writing is mandatory. Candidate should have minimum 02-year experience in Export Marketing. A candidate from Medical Device Industry will be preferred. Key Responsibilities : Direct Communication with Overseas clients via phone/ WhatsApp /email/ video conferencing. Follow up for Orders with Clients and Communication for . Our HR team will call you for the interview if your resume is selected.

Requisition #: 16926 Our Mission: Powering Innovation That Drives Human Advancement When visionary companies need to know how their world-changing ideas will perform, they close the gap between design and reality with Ansys simulation. For more than 50 years, Ansys software has enabled innovators across industries to push boundaries by using the predictive power of simulation. From sustainable transportation to advanced semiconductors, from satellite systems to life-saving medical devices, the next great leaps in human advancement will be powered by Ansys. Innovate With Ansys, Power Your Career. Summary / Role Purpose Join the Ansys Customer Excellence team to support our customers on all the aspects of their real-world engineering simulation projects and integration of Ansys software in their design workflows and grow Ansys business. You will use engineering knowledge to provide technical post-sales support, find solutions to a wide variety of technical challenges and channel customer feedback to improve Ansys products. You will be a part of our positive, dynamic team of enthusiastic and passionate engineers striving to deliver the highest quality solutions to our customers, advancing your knowledge, experience, and your impact on the success of our customers and Ansys. Key Duties and Responsibilities Deploy and exploit the full Ansys Technical Support Toolset to complement your own engineering expertise and knowledge of simulation to assist customers in solving their engineering problems and enabling their usage of Ansys products. The Ansys Technical Support Toolset includes Ansys Innovation Space, AnsysGPT and other Ansys AI-based platforms introduced to assist with identifying and delivering the most relevant answers to customers problems Ensure customers ability to get accurate timely answers resulting in high Ansys customers satisfaction. Ensure high Customer Satisfaction and Customer Success that enable customers usage/deployment/adoption of Ansys software Develop subject matter expertise and specialization on Ansys simulation products and applications. Share your extensive knowledge and experience by creating & updating content for your Primary Focus Area to ensure the most relevant help and information is available for customers and internal colleagues. Create and execute repeatable workflows for data capture, processing, and deployment for support through the Ansys Technical Support Toolset. Minimum Education/Certification Requirements and Experience Required education and degree type: BS or MS in Electronics and Communication Engineering or related field Required minimum years of professional experience in an engineering software environment: MS+0 ; BS+2 Demonstrated use of relevant Ansys software or knowledge of other commercial CAE, CAD, EDA, PLM software packages Logical problem-solving, strong interpersonal and communication skills, fluent in writing and speaking English Strong organizational and time management skills, possesses a sense of urgency Preferred Qualifications and Skills Preferred education and years of professional experience in an engineering software environment: MS+3, PhD+0 Preferred engineering degree in electronics and/or electromagnetics Ability to travel domestically up to 10% of time At Ansys, we know that changing the world takes vision, skill, and each other. We fuel new ideas, build relationships, and help each other realize our greatest potential. We are ONE Ansys. We operate on three key components: our commitments to stakeholders, our values that guide how we work together, and our actions to deliver results. As ONE Ansys, we are powering innovation that drives human advancement Our Commitments: Amaze with innovative products and solutions Make our customers incredibly successful Act with integrity Ensure employees thrive and shareholders prosper Our Values: Adaptability: Be open, welcome what s next Courage: Be courageous, move forward passionately Generosity: Be generous, share, listen, serve Authenticity: Be you, make us stronger Our Actions: We commit to audacious goals We work seamlessly as a team We demonstrate mastery We deliver outstanding results VALUES IN ACTION Ansys is committed to powering the people who power human advancement. We believe in creating and nurturing a workplace that supports and welcomes people of all backgrounds; encouraging them to bring their talents and experience to a workplace where they are valued and can thrive. Our culture is grounded in our four core values of adaptability, courage, generosity, and authenticity. Through our behaviors and actions, these values foster higher team performance and greater innovation for our customers. We re proud to offer programs, available to all employees, to further impact innovation and business outcomes, such as employee networks and learning communities that inform solutions for our globally minded customer base. WELCOME WHAT S NEXT IN YOUR CAREER AT ANSYS At Ansys, you will find yourself among the sharpest minds and most visionary leaders across the globe. Collectively, we strive to change the world with innovative technology and transformational solutions. With a prestigious reputation in working with well-known, world-class companies, standards at Ansys are high met by those willing to rise to the occasion and meet those challenges head on. Our team is passionate about pushing the limits of world-class simulation technology, empowering our customers to turn their design concepts into successful, innovative products faster and at a lower cost. Ready to feel inspired? Check out some of our recent customer stories, here and here . At Ansys, it s about the learning, the discovery, and the collaboration. It s about the what s next as much as the mission accomplished. And it s about the melding of disciplined intellect with strategic direction and results that have, can, and do impact real people in real ways. All this is forged within a working environment built on respect, autonomy, and ethics. CREATING A PLACE WE RE PROUD TO BE Ansys is an S&P 500 company and a member of the NASDAQ-100. We are proud to have been recognized for the following more recent awards, although our list goes on: Newsweek s Most Loved Workplace globally and in the U.S., Gold Stevie Award Winner, America s Most Responsible Companies, Fast Company World Changing Ideas, Great Place to Work Certified (China, Greece, France, India, Japan, Korea, Spain, Sweden, Taiwan, and U.K.). For more information, please visit us at www.ansys.com Ansys is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other protected characteristics. Ansys does not accept unsolicited referrals for vacancies, and any unsolicited referral will become the property of Ansys. Upon hire, no fee will be owed to the agency, person, or entity.

We are looking for a skilled and detail-oriented QA Executive to join our team. The candidate will be responsible for ensuring the quality and regulatory compliance of medical devices in line with EU MDR 2017/745 and Indian Medical Device Rules (IMDR). This role involves preparing, reviewing, and updating key technical and regulatory documentation and supporting post-market surveillance activities. Roles & Responsibilities Preparation, review, and updating of Technical Files as per EU MDR 2017/745 and Device Master Files (DMF) as per IMDR . Maintenance of General Safety and Performance Requirements (GSPR) documentation in compliance with applicable guidelines. Preparation of Risk Management Plans and Reports as per ISO 14971 and other applicable standards. Development and review of Clinical Evaluation Protocols and Reports (CEP/CER) as per MDR/IMDR guidelines. Preparation and maintenance of Post-Market Surveillance (PMS) , Post-Market Clinical Follow-up (PMCF) , and Periodic Safety Update Reports (PSUR) . Documentation of Design and Development activities, ensuring alignment with regulatory and internal design control requirements. Drafting and reviewing Usability Engineering Protocols and Reports in compliance with ISO 62366. Monitoring, tracking, trending, and reporting of all reportable events , including serious/adverse incidents and field safety corrective actions (FSCA) . Keeping up to date with current national and international regulations, standards, and best practices relevant to the medical device industry. Ensure proper handover of responsibilities to designated personnel during absence. Desired Candidate Profile Prior experience in quality assurance or regulatory affairs for medical devices. In-depth understanding of EU MDR 2017/745 , IMDR , and related standards (e.g., ISO 13485, ISO 14971, ISO 62366). Strong documentation and review skills. Attention to detail with good organizational and analytical abilities. Effective communication skills and the ability to work independently as well as in a cross-functional team.

We are currently seeking a talented Senior Verification & Validation Engineer to join our dynamic team. The ideal candidate will have extensive experience in system engineering, requirement management, risk management, verification and validation, navigating the cybersecurity guidance, as well as a deep understanding of the medical device industry. Job Title: Senior Verification & Validation. Experience: 5 - 10 Years Qualification: B.E/B.Tech or equivalent degree in Computer Science / Information Technology. Job Description: Biovantage is looking for a qualified Senior Verification & Validation Engineer to perform end to end software verification and validation for our various Medical Device and Software as a Medical Device product development projects. As a Senior V&V Engineer, you will be actively involved in understanding / authoring the software requirements, developing test protocols, executing test cases, and automating those test cases. You will continuously track software bugs and control the overall quality of the software. Required Skills: Experience in software testing and automation for Embedded Software, Web Applications & Mobile Applications. Excellent aptitude and reasoning with understanding of Software QA methodologies, tools, and processes. Experience in development, execution and review of software verification plan, test methods, test strategies, acceptance criteria, test cases, test reports, and traceability reports. Experience working in an ISO 13485 compliant environment. Strong problem-solving skills to participate in troubleshooting of issues with different teams to drive towards root cause identification and resolution. Good team player with excellent communication skills, to be able to collaborate and work with cross functional teams. Ability to work in a fast-paced, dynamic work environment with a focus on technical excellence, responsiveness to meet timelines. Ability to work on multiple projects in a deadline driven environment. Preferred Skills: Experience in software testing for medical domain products. Experience in building test automation framework. Familiarity with Requirements management tools, configuration management tools and test management tools like Git, TestRail, Jira, Helix/TestTrack, Confluence, etc. Experience with software and system risk analysis (per ISO 14971) including fault tree analysis, software failure mode and effects analysis (FMEA). Experience with FDA Guidance for Cybersecurity in Medical devices including threat modelling techniques and security risk management. Responsibilities: Responsible for the verification and validation of a medical software, including but not limited to development of software verification plan, review of system and subsystem requirements, design test strategies and methods, write and execute test cases, generate traceability reports, generate test execution reports. Identify / build test automation tools and framework, automate test cases. Collaborate with Product development teams to understand the product specification, system interfaces, operational requirements, performance requirements, software requirements, software design, etc. to discuss and review test methods and test strategies. Participate in review meetings with cross functional teams and contribute to writing software requirements, developing software verification protocol, etc. Teach and mentor fellow engineers, and work to foster an environment of development and inclusivity.

Organise sales visit,give demo of critical care equipment to customer Sell by creating customer contact,relations Maintain relationship,support, info,guide Recommend solution to client problems Analyse competition brand Work with team,achieve results Required Candidate profile -Any Male with field sales experience in healthcare industry -BE/B Tech/Bsc/BPharm/Dip-Engg - 1- 4 yrs experience - Good communication,presentation & negotiation skill -Age under 35 -2 wheeler must Perks and benefits Other benefits and Incentves

You will be responsible for sales lead generation to closing the deal by meeting Ophthalmic Surgeons / Eye Hospitals for our entire range of Ophthalmic Equipments.

Siemens Healthineers has openings for full time Data scientist to support development of AI-based applications for products in Healthcare. The candidate would be working on one of the AI applications within the AI-Rad Companion suite of clinical AI applications. The role of the data scientist is to be a bridge between the research teams developing Medical Imaging related AI algorithms, the engineering teams productizing it, the Regulatory team filing for country regulatory clearances and the clinical customers. Clear understanding of the fundamentals of medical imaging, radiology in particular is essential to perform the role. Understanding of the regulatory clearances and it s needs for supporting evidence for AI algorithms is necessary as the person facilitates these inputs working closely with the research team and regulatory teams. High level Understanding of the AI and it s applications in clinical context is essential to bring the information related to performance and reliability metrics. Work closely with the clinical evaluation report writers to provide insights into the AI application. The applicant will join our innovation group in solving exciting and challenging research problems with real-world medical applications that require Data science. Our group develops medical image, text analytics and AI applications supporting clinicians and other medical professionals. We are well recognized for delivering cutting-edge intelligent solutions. Responsibilities: Contribute the development of Artificial Intelligence solutions for medical imaging Support the product development and deployment of research prototypes Support Scientific evaluation, setup and manage algorithm validation pipeline Education: Recently acquired Masters or PhD in Computer Science, Electrical Engineering, Optimization, Mathematics or Statistics. Experience: 4+ Years of experience Skills/Competency: Strong programming ability in both scripting and object-oriented programming languages is required (C/C++, C#, python, R) Working knowledge of deep learning frameworks and libraries like pytorch, caffe, tensor flow and high-level APIs like Keras is preferable but not required Prior exposure to machine learning and related fields is preferable but not required Motivated, self-driven and with a strong ability to learn independently Exhibits strong problem-solving skills Self-directed and actively takes initiative Familiar with DICOM & Medical Raw image formats and its applications Familiar with Data science tools Strong knowledge of regulatory needs related to medical devices, AI products in healthcare

Minimum 01 Year Experience in Accounts Salary : 18k to 20k Functional Area : Accounts Industry: Medical Devices/ Equipment Employment Type : Permanent Job, Full Time Job Location : WZ-1, Phool Bagh, Rampura, Near Ashok Park Main Metro Station, Delhi 110035. Education: Minimum Graduate. Tally working is mandatory. Job Description: Bank Reconciliation Day to Day Accounting Inter Accounts Reconciliation Preparation of Profit & Loss Accounts & Balance Sheet, TDS, Income Tax Desired Candidate Profile: Candidate should have sound knowledge of Tally and Accounting. Computer Skills on Excel and Word is mandatory Candidate should able to make draft of emails and email communication. Candidate s communication skills should be good. Company Profile: One of the leading manufacturers and suppliers of Orthopedic Implants and instruments, founded in 1987 and has a manufacturing unit at Rai Industrial Area, District Sonipat, Haryana, and Corporate Office in Phool Bagh, Rampura, New Delhi Near Ashok Park Main Metro Station. Note: Kindly mail your resume at hr@siora.net. Our HR team will call you for the interview if your resume is selected.

Education: Diploma in Mechanical Key skills: Mechanical Diploma with Excel Knowledge mandatory. Desired Candidate Profile: The candidate should have a minimum of 03 years experience in Production Planning Control with Computer Skill Excel. Skilled to read Engineering Drawings Skilled in operating Measurement Instruments like Vernier Caliper, Micrometer, Profile Projector, use different types go and no-go gauges. Knowledge of Computer Applications like Word and Excel.