1307 Medical Devices Jobs - Page 15

Analyze system requirements, user needs and system design, perform system evaluation activities (i.e. validation, verification). Transform requirements into comprehensive test protocols and automated test scripts using Python. Develop and maintain high quality non-medical device software tools in a regulated environment to support system design and system evaluation activities. Documents software development and/or test development by writing documents, reports, memos, change requests. Methods used are determined by approved procedures and standards Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving System level issues. Interact with business analysts, SMEs and QA team members Qualification & Required Skills Bachelors degree in engineering or equivalent (BE, B Tech, MCA, MSc) 8+ years of product testing experience, preferred to have experience in system testing with devices and simulators. Experience in regulated product development environment, particularly for medical devices, a plus.

Company Description: Kinexcs is an AI-driven digital health platform and wearables company with a mission to enable and empower people for mobility and a better quality of life. It is focused on reducing the burden of musculoskeletal conditions, which affects about 25% of the world's population. Their 1st product, KIMIA Recover, a continuous monitoring device for the knee joint, has obtained CE marking and HSA approval, and booked revenues from large implant companies and hospitals. It has recently won the Innomatch grant by the Temasek Foundation (one of the 6 among 256 companies across 32 countries), and is currently deployed in some of the largest public hospitals in Singapore. KIMIA Recover is a comprehensive recovery management solution providing reduction in number of hospital visits and complications. The product was also the National Winner and International Top 20 of the prestigious James Dyson Award 2020, and has gained traction with major public hospitals and orthopedic clinics. Their digital therapy platform, consisting of KIMIA Assess and KIMIA Move products, uses artificial intelligence technology for digital MSK assessment and therapy. This platform is capable of providing pre-consultation assessments and real-time exercise guidance and feedback to musculoskeletal patients, and is being adopted by some of the largest private healthcare providers in the region, along with large corporate players. Job Responsibilities: The ability to go deep on technical challenges, this role is all about understanding and building the right platform and services that power evidence driven care and richer patient experiences Lead a team through the ideation, technical development, and launch of innovative products in the domain of IoT and Medical Devices Drive product development with a team of world-class engineers and designers Attract, build, manage, and develop a talented, diverse, equitable and inclusive team of product managers and product leaders Establish shared vision across the company by building consensus on priorities leading to product execution Integrate usability studies, research and market analysis into product requirements to enhance user satisfaction Define and analyse metrics that inform the success of products Understand strategic and competitive position of the company and deliver products that are recognized best in the industry Maximize efficiency in a constantly evolving environment where the process is fluid and creative solutions are the norm Passion for working with customers to understand their scenarios and business driver Passion for working with customers to understand their scenarios and business drivers Ability to develop product plans and roadmaps, define capabilities and drive project execution Ability to build strong relationships and deliver results in cross-group projects Ability to work independently in ambiguous situations, with a strong Get it done attitude Strong problem solving and analytical skills Strong written and verbal communication skills A passion for building and supporting a diverse team that represents the diversity of our users Qualifications: MS/Bachelors degree in Computer Science or other related engineering field, or MBA. 5+ years experience in Product Management preferably in the domain of medical devices and/or IoT development. 5+ years of managing the development of robust, scalable software applications. Experience working with cross-functional teams including business, marketing, R&D, engineering, manufacturing, both internal and externally.,

Company Description Lars Medicare Pvt. Ltd. is a leading manufacturer of high-quality IV Catheters and other single-use medical devices. With CE and ISO 13485 certified production facilities, the company exports and markets products to over 70 countries. Headquartered in New Delhi, India, Lars Medicare serves world markets from branches in Dubai, UAE, and Toronto, Canada. The manufacturing facility is located in a pollution-free zone on the outskirts of New Delhi, established in 2007 as a 100% Export Oriented Unit (EOU). Role Description This is a full-time on-site role for a Domestic Sales Representative at Lars Medicare Pvt. Ltd. located in New Delhi. The Sales Representative will be responsible for day-to-day sales activities, building and maintaining relationships with domestic clients, promoting products, and achieving sales targets. Qualifications Sales, Marketing, and Customer Relationship Management skills Excellent communication and negotiation skills Ability to work independently and as part of a team Understanding of the healthcare industry and medical devices Experience in sales of medical devices is a plus Bachelor's degree in Business Administration, Sales, Marketing, or related field,

You will be working as a Senior Sales Executive in the Ultrasound Division of United Medical Solutions. Your primary responsibility will be to develop and nurture customer relationships, showcase ultrasound products, present product demos, engage in contract negotiations, and meet sales objectives within the Sangli region. To excel in this role, you should possess sales experience in the healthcare sector and have a good understanding of ultrasound equipment and medical devices. Effective communication and negotiation skills are essential, along with the ability to achieve sales targets and work within specified deadlines. Your role will also involve managing customer relationships and may require travel within the Sangli region. Ideally, you should hold a Bachelor's degree in Business, Marketing, or a related field. Experience with Customer Relationship Management (CRM) software would be beneficial for this position. If you are passionate about sales and have a keen interest in healthcare equipment, this role offers an opportunity to contribute to the growth of United Medical Solutions and deliver quality healthcare solutions to customers in Sangli.,

Greetings from Wipro!! Inviting applicant for Walk-in Drive-in Kolkata Location for Medical Device Investigator r ole Experience- 0 to 1 year Qualification- B. Pharm/ M. Pharm / Biomedical & Mechanical engineer/ BSc in Medical Imaging & Radiology Technology/master's in molecular Biology/B.SC Nursing/BDS Only the above-mentioned qualifications candidates are requested to attend the Walk in drive Current year pass out students should have original hardcopy Marksheet & Provisional Certificate Walk In Date- 12-July-25 Time to Report- 10 A.M- 1 P.M Documents to carry- Update CV & original govt. ID Card. Should mention at the top of the CV the source of information about the walk-In Walk in Address- Wipro Gate 2 - Plot no. 8&9 Block DM Sector V Salt Lake, Kolkata WB 700091- Near Salt Lake Sector V -Metro Station Candidate should have excellent Communication in English Should be ready for Fixed Night Shift Should have excellent knowledge of Medical Device

Purpose: Grow wholesales B2B business for the client in Karnataka Identify, onboard, and manage wholesale distributors and channel partners across Bengaluru/KA using product demos, trainings, and in-market activations. Meet monthly sales targets >83% Required Candidate profile The candidate must have hands-on experience in B2B Nebulizer, diapers with local market knowkedge & existing network. Build strong relationship with distributors, retailers, and hospital buyers.

Location : Surat Industry: Pharma Industry Contact:** +91 90816 99800 Biomedical Job Opening Role: Biomedical Technician / Executive Salary: 20,000 – 25,000 per month Timings: 9:00 AM – 6:00 PM Location: Pal, Surat . Required Candidate profile Medical Representative Job Opening Role: Medical Representative (MR) Salary: 20,000 – 25,000 per month Timings: 9:00 AM – 6:00 PM Location: Surat 91 90816 99800

Increase brand awareness and build a relationship with prospective and existing customers Ensure that proper advertising and marketing are done through the medical product sales Liaison with doctors, hospitals and medical staff

Requisition #: 17027 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 (ACE) team to support our customers in a new and innovative way. The landscape of customer support and learning experience is fast changing, and you will be at the forefront of this change focusing on developing and deploying solutions for our customers. The ACE team is in continuous pursuit of operating with utmost efficiency and identifies AI as one of the new paradigm shifts. In this role, you will use your engineering knowledge and the power of GenAI to streamline and accelerate AI transformation of technical support and learning and development within the ACE team. 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 impact on the success of our customers and Ansys. Key Duties and Responsibilities Apply engineering expertise and knowledge of simulation techniques to develop knowledge data related to Ansys Design Optimization and Workflow products that can be consumed by Large Language Models (LLMs). Identify gaps in existing knowledge and work with multiple subject matter experts to fill these gaps. Work with internal & external databases to develop data pipelines for developing AI models. Develop technical expertise in both Ansys Design Optimization / Workflow products and state-of-the-art GenAI technologies that are appropriate for technical support, learning and development. Follow legal and enterprise level data governance policies while handling any data. Fully document all data workflows developed towards AI powered applications and present them to the Data audit teams. Participate in other strategic team and company initiatives, as needed. Be agile and open to new responsibilities. This is a very fast paced role requiring a try often, fail fast kind of mindset. Minimum Education/Certification Requirements and Experience Bachelor s degree in Mechanical/Civil/Aerospace engineering or related field. Required minimum years of professional experience in an engineering software environment: BS+0. 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+0. Experience with Process Integration and Design Optimization platforms, and software packages like optiSLang, iSight, modeFrontier, etc. Proficiency in Python scripting and knowledge of the basics of machine learning would be a plus. Ability to work independently with minimal supervision, as well as with others in a diverse team environment. Demonstrated ability to manage multiple projects and to communicate effectively. Ability to travel domestically up to 10% of the 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.

Perform engineering tasks including medical design, research, and prototyping. Create CAD models/drawings, design solutions to meet client goals, and produce detailed documentation and realistic renderings using Solid Edge, SolidWorks, and AutoCAD. Required Candidate profile -Team work in finalizing parts & components -Design of 2D, 3D plastic and metal components -Coordinating to finalizing with supplier & vendors for quality -Assisting while testing and improvising

A Day in the Life Careers that Change Lives Be a part of the Medtronic Engineering and Innovation Center (MEIC) in Hyderabad by applying your skills to the growth, development, and sustaining efforts of Medical Devices products within the center. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations A Day in the Life As an R&D Engineer II of the MEIC, you will collaborate with the sustenance and engineering teams globally. You will enable Product Development, Medical Devices Design Controls, and Medical Device Regulation activities in close conjunction with the global teams. Medtronic is a world leader in providing health care products that benefit individuals well-being. Our organization contributes directly to this mission. Our business is growing significantly as the market demands reliable medical devices which look and feel more like consumer devices. As a result, we need an Engineer II who will ensure we deliver the best on-time with high quality for our products. Key Requirements: Should have good knowledge on Medical Device Regulations and experience in Gap Assessment and Remediation activities Must be able to communicate well with cross-functional team members, and be able to efficiently collaborate with team members to achieve project goals, and contribute positively to the engineering community. Should be able to implement new standards across all product families. Engineer II is expected to have the appropriate knowledge on product development and cross-functional aspects. Responsible for supporting the Product Development Team with application Medical devise standards/regulations to new products under development. Should have basic knowledge of project management and be able to plan and schedule project activities. Works independently with general supervision on larger, moderately complex projects / assignments. Must-Have : Bachelor s degree in Mechanical / Production / Bio Medical Engineering with 3 to 6 years of relavent experience. Good knowledge on medical device regulations like IEC-60086, ISO-22442, FDA Guidance etc. Very good verbal communications to interact with global partners. Basic knowledge in Concept & Product Development. Nice to Have : Medical Device Experience Master Degree GD&T Knowledge CAD (CREO) application experience 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

Summary -Monitors and audits the company s drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against product labeling. Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide trending and safety signal detection and assessment. Supports all clinical trial activity and post marketing. About the Role Major accountabilities: Global and /or regional, cross-functional leadership of assigned pharmacovigilance processes across Novartis

Innovation starts from the heart. Heart valve disease impact millions of lives, spanning all ages and geographies. As communities globally address the opportunities and challenges of cardiovascular care, telling a compelling and authentic story is more crucial than ever. Beyond raising awareness, our Marketing teams build lasting, trusted relationships with medical professionals and industry stakeholders to ensure patients can receive the treatments they need. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. How you will make an impact: Lead the execution of country marketing plan to achieve local business goals Drive the implementation of new product and indication launches and ensure strong launch execution Evaluate local needs of the commercial and clinical teams in alignment with the marketing plan, including delivering field training and clinical marketing activities Maintain contact with local KOLs and develop high quality relations with other health care professionals, develop event strategy, aligned with local dynamics/needs and EU event strategy Lead the implementation of assigned Therapy Development initiatives and Economic Value campaigns Lead the creation of localized marketing materials Assess market dynamics and analytics (e.g, market size and trends, competitive situation, reimbursement) in close collaboration with Business Analyst in the country What you will need (Required): Bachelors Degree in marketing, economics, biomedical engineering or relevant fields with minimum 8 years of related marketing experience in Medical Devices is required Masters Degree or equivalent in additional Healthcare related (scientific or engineering) post-graduate degree a plus, with minimum 6 years of related marketing experience in Medical Devices is required Medical devices experience in Cardiovascular/Cardiology is an added advantage What else we look for (Preferred): Proven successful project management skills Proven expertise in Microsoft Office Suite Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives Extensive knowledge of own area within the organization while contributing to the development of new concepts, techniques, and standards Extensive understanding of related aspects of marketing concepts and principles Extensive understanding of broad market research designs, develops market research programs coordinating with the global VOC manager and demonstrates an in-depth understanding of commercial goals behind research Ability to forecast product lines for short-term and long-term accuracy based on market development, sales trends, competition and changing market dynamics. Ability to assess and understand market share, pricing, ASPs, competitive dynamics Possess strong clinical knowledge, experience and knowledge of the clinical areas where Edwards products are used or intended to be used, understand the purchasing process and challenges for product adoption in complex healthcare networks Strict attention to detail Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization Ability to manage competing priorities in a fast paced environment Ability to represent leadership on sections of projects within a specific area working closely with cross-functional team, marketing peers and leaders and managing needs and messaging to upper management Ability to maintain a strong relationship with the regional sales team, clinical specialists, governmental affairs, clinical economics and training to ensure effective and optimal integration of efforts Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

About Vantive Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don t settle for the mediocre. Each of us is driven to help improve patients lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Job Summary Job Title - Senior Engineer, Acute Disposables Location - Whitefield, Bangalore Shift - General Job Description You will be responsible for developing solutions to challenging issues associated with the design, development, and sustenance engineering for our new and existing Disposables for the Acute Therapies product portfolio. The successful candidate will possess solid hands-on technical abilities, an excitement and energy for product development, and a passion for their work and the impact it has on meeting the needs of patients. Project tasks involve development and maintenance of risk management files. Active support in Engineering change management with focus on risk, root cause analysis, solutions for CAPAs, NCRs, design implementation, verification & validation, standards compliance activities to ensure maintenance of state of the Art also from risk management perspective. Projects also include the development of new functions and features to be integrated into the existing products/new products. Essential Duties and Responsibilities: Leads the evaluation and development of Disposables on assigned projects with focus on risk management. Owns and maintains the risk management files for the assigned product families. Manages all technical complexities of the work, and effectively communicates with all project team members and stakeholders. This includes reporting pertinent information at key milestones. Collaborates with cross functional team (e.g., Quality, regulatory, clinical) to ensure the proper deployment of risk management activities. Manages and prioritizes multiple projects and tasks. Develops solutions and approaches to complex problems through application and adaptation of state-of-the-art techniques. Able to clearly present moderately complex concepts and tailor communication to audiences, including senior management. Organizes and presents solutions from risk management perspective without assistance. Oral and written communication is well planned, organized and has a clear logical flow. Ensures successful integration of disposables design elements from risk management perspective into the overall system. Resolves competing constraints between interrelated functions (R&D, purchasing, manufacturing, regulatory, marketing, etc.) required to complete the risk management tasks. Creates and maintains design documentation that includes requirements, specifications, verification reports, Bill of Materials, detailed engineering drawings, study reports and all documents that contribute to DHF of the product family. Leads troubleshooting and problem-solving efforts of the products associated with field performance and manufacturing ensuring acceptable risk profile of the device is maintained throughout the entire product lifecycle. Support, from risk management perspective, the necessary testing required to validate the safety and effectiveness of the design(s). Education & Experience Graduate or Postgraduate in Mechanical Engineering/ Polymer Technology/Plastic Technology/Bio Medical engineering or Equivalent Minimum of 6 years of relevant experience, Prior experience of technical leadership in Sustenance/New product development in Critical care Medical device domain is a plus. Experience in a regulated industry preferably medical devices and familiarity with ISO 13485, and ISO 14971 Qualifications Proficiency with MS Office and other office productivity tools. Self-directed, resourceful, and able to work on multiple projects and priorities. Strong organization, attention to detail, and documentation skills. Strong hands-on lab skills, and prototype fabrication skills. Very adept at grasping and solving complex problems using root-cause analysis techniques. Previous experience on product risk management is a plus. Ability to objectively identify technical solutions, and make sound engineering decisions. Clear and effective communication (written and oral) and presentation skills. A proven track record of effectiveness in a fast-paced environment. Proven ability to create results within budget, timeline, and product/project deliverables. Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Job Summary Job Title -Research Associate III Location - Whitefield, Bangalore Shift - General Job Responsibilities: Act as Product Design Owner (PDO) within its product family and technical expert for projects in development and lifecycle management activities within R&D Kidney Care Solutions Development Organize, plan and execute sustaining activities in compliance with current QA/ environmental/ regulations and standards Provide technical leadership, mentor and guide the change owners and Project Leads within its product family in order to get tasks accomplished according to plans, milestones and business needs Responsible for development and delivery of plastic materials and mechanical testing, writing of verification test protocols, test cases and reports Troubleshooting, root-cause-analysis and problem-solving related to material aspects of the products associated with field performance and manufacturing Review and approve Design Control documentation for projects in development and sustaining activities. Responsible and accountable for the design history files of a given product family Establish, maintain and update technical specification describing product appearance, characteristics and functions, and associated verification and validation documents Organize, plan and follow the execution of product changes, supplier changes and labelling tasks related to life cycle management projects Support Product Risk Owners with the Design related information and associated failure modes and risks arising from any of the design changes for a given product family Support worldwide product registration and launch following international/regional/national regulations; provide technical support to authorities questions Provide technical leadership for products/process/cost improvements related to life cycle management projects Provide resource estimation and forecast Ensure good internal and cross-functional communication at a global front and regular status update of projects Qualifications and Skills Masters in chemistry or Polymer science with at least 10 years of relevant experience or Ph.D. in relevant sciences discipline with at least 7 years of relevant experience. Excellent English verbal and written communication skills Exposure to medical devices and drug products Proficient with polymeric materials testing methodologies, such as, FTIR, GC-MS, HPLC, tensile testing etc Good knowledge of product development stages and life cycle management: development, stability, clinical, registration, process transfer, production, suppliers, customer service Good knowledge of Design Control documentation and process Prior experience of product design owner (PDO) / Material SME role for pharmaceutical products and medical devices Demonstrated project/program leadership in medical device / drug industry Exposure to Product Risk Management for medical devices and drug products Working knowledge of international/regional/national regulations and standards Experience in project management and stakeholder management at a global front Must be able to able to carry out strategy and vision set by upper management and be able to communicate the vision to more junior associates. Ability to work independently. Equal Employment Opportunity Vantive is an equal opportunity employer. Vantive evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.

Job Description Summary Responsible for developing, implementing, and leading the supplier strategy for products within the Molecular Imaging and Computed Tomography (MICT) business unit. This role involves driving and cultivating strategic relationships through strong technical and market expertise. Key responsibilities include setting, refining, and executing the long-term sourcing strategy and operating plan throughout the product life cycle. Manages a team of sourcing professionals. This position collaborates closely with Commodity Sourcing, Supplier Quality, Finance, Manufacturing Operations, and Engineering to deliver products to our customers with a focus on total cost mindset. Additionally, this role ensures that we maximize the value derived from our supplier partnerships. . Job Description Essential Responsibilities Driving the sourcing strategy to deliver a competitive advantage, including the implementation of strategic supplier initiatives. This encompasses supplier selection, development, and consolidation to ensure sourcing optimization and overall supplier performance. Leading specific sourcing activities with full accountability for procurement and achieving material deflation targets by setting strategic direction and execution for program and commodity sourcing professionals. Serving as the key point for all supply chain issues, including the management of New Program Introduction (NPI) deliverables necessary to establish an optimal supply chain focused on strategic suppliers, with the objective of achieving robust NPIs. Responsible for risk management within the supplier base, ensuring compliance with all quality standards. Developing strategies and driving negotiations to meet the businesss quality, fulfillment, and productivity requirements. Leading a team of sourcing professionals to meet the business units sourcing deliverables. Contributing to the improvement of procedures, methodologies, and tools already in place within the department. Advocating for LEAN principles and practices, including Problem Solving Reports (PSR). Required Qualifications Master s degree in supply chain, engineering or business administration with proven experience in commercial (sourcing, sales), supply chain. Over 10 years of extensive experience in Sourcing and Procurement within the medical devices industry or a closely related sector. Desired Characteristics Strong oral and written communication skills Strong negotiation skills. Ability to energize, develop and build rapport at all levels within an organization. Strong interpersonal and leadership skills. Demonstrated ability to analyze and resolve problems. Demonstrated ability to lead programs / projects. Strong business acumen and capacity to understand complex market dynamics (supplier/partner/customer relationships). Ability to document, plan, market, and execute programs. Established project management skills. Inclusion and Diversity We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you d expect from an organization with global strength and scale, and you ll be surrounded by career opportunities in a culture that fosters care, collaboration and support. Disclaimer: GE HealthCare will never ask for payment to process documents, refer you to a third party to process applications or visas, or ask you to pay costs. Never send money to anyone suggesting they can provide employment with GE HealthCare. If you suspect you have received a fraudulent call , please fill out the form below: https: / / www.ge.com / careers / fraud #LI-SB1 #LI-Onsite Relocation Assistance Provided: Yes

Position Title: Sales Executive- Holmium Laser Branch Locations: Ranchi, Patna and Delhi Vacancies: 3 Roles & Requirement 1-6 years Experience in sales Segment: Urology Products: Holmium Laser, Thulium Fiber Laser, Morcellator, Laparoscopy, Endoscopy, Urology Scopes etc. Diploma/Degree in Biomedical or Electronics Good Experience in medical devices/equipment's sales Application Process: Interested candidates should submit their resume to recruitment@allengersglobal.com or WhatsApp : 8288806351 Only shortlisted candidates will be contacted for further consideration.

Position Title: Sales Executive Branch Locations: Ranchi, Guwahati and Dehradun Vacancies: 3 Roles & Requirement 1-6 years Experience in Sales Segment: Cardiology and Neurology Products: TMT, MPM, ECG, Holter, EEG, EMG and PSG Diploma/Degree in Biomedical or Electronics Good Experience in medical devices/equipment's sales Application Process: Interested candidates should submit their resume to recruitment@allengersglobal.com or WhatsApp : 8288806351 Only shortlisted candidates will be contacted for further consideration.

About the Role: We are hiring a Product and Sales Specialist for one of the DSS Group companies - NeoDx Biotech Labs, a prominent manufacturer of molecular diagnostics kits . This role is crucial for supporting healthcare professionals in accurate disease detection and management. The ideal candidate will have strong technical knowledge in molecular diagnostics, especially RT-PCR, and experience in key account management, distributor/channel partner development, and revenue generation within the healthcare or diagnostics industry. The position involves driving market penetration, providing application support, and ensuring customer satisfaction. A techno-commercial approach, combining business development with technical expertise, is essential for success in this role. https://www.linkedin.com/company/neodx/ Locations: Delhi, Jaipur, Bhopal, Kolkata, Visakhapatanam/Hyderabad Positions open: 05 Key Responsibilities: Identify and onboard key accounts for RT-PCR diagnostic kits. Develop and execute strategies to achieve revenue targets and business growth, account creation by product management and technical support. Work closely with hospitals, diagnostic labs, oncologists, microbiologists, and research institutions to drive product adoption. Conduct competitor analysis and market intelligence to position NeoDx products effectively. Build and nurture relationships with KOLs (Key Opinion Leaders) to enhance brand credibility and market influence. Demonstrate a strong technical understanding of Real-Time PCR technology, including assay principles, troubleshooting, and workflow optimization. Conduct product demonstrations, technical presentations, and training sessions for customers and channel partners. Support customers with troubleshooting, workflow optimization, and assay validation in clinical and research settings. Collaborate with R&D, Quality, & Regulatory teams to provide field insights for product improvements. Job Specification: Strong understanding of RT-PCR principles, applications, troubleshooting, and assay optimization. Excellent presentation, negotiation, and relationship management skills. Frequent travel to engage with customers and partners. Educational Qualification: Masters Degree / Engineering / Ph.D. in Biotechnology, Molecular Biology, Life Sciences, or a related field.

About the Role We are looking for a dynamic Senior Service Engineer/Area Service Manager to join our team and drive excellence in post-sales service, customer support, and technical operations. This role is crucial in maintaining customer satisfaction and ensuring optimal performance of our equipment and solutions. You will be the go-to expert for installations, troubleshooting, and maintenance activitiesensuring uptime, efficiency, and service quality. As a key player in our technical support team, you'll work closely with sales, product, and engineering teams to uphold our service standards and brand reputation. Location:Mumbai Key Responsibilities Independently manage installation, calibration, maintenance, and repair of assigned equipment/systems at customer sites across West India region. Provide on-site and remote technical support to customers, ensuring high uptime and operational efficiency. Analyze service issues, identify root causes, and implement effective solutions. Maintain detailed service logs, reports, and documentation in compliance with company policies. Train end-users on operation and basic maintenance. Collaborate with cross-functional teams to improve service strategies and escalate critical issues. Participate in Foreign & Domestic service training programs to keep up with new technologies and product updates. Qualifications & Skills Degree/Diploma in Engineering (Electronics / Instrumentation preferred) Minimum 5+ years of hands-on field service experience , preferably in diagnostics, medical devices, or automation systems Strong problem-solving skills and ability to work independently Excellent verbal and written communication skills Ability to manage priorities and deliver under pressure Willingness to travel extensively (regional/national, as needed) Familiarity with CRM tools and service documentation processes Why Join Us? Opportunity to work with cutting-edge technologies and leading global brands Be part of a high-performance service team focused on customer satisfaction Regular training and growth opportunities

Post : Biomedical Engineer Qualification : D iploma in Biomedical Experience: Experienced Location: PARIALA Remuneration : Best in hospital industry Job Responsibilities: Provides technical support Responds to user inquiries Maintains biomedical machine and equipment Generates reports on machine performance Trains machine operators on proper usage of equipment liaising with medical and scientific staff and patients to understand their needs designing, developing and testing products, equipment and devices that will address medical problems cost efficiently designing, testing and implementing new medical procedures, such as computer-aided surgery and tissue engineering managing clinical trials of new devices and equipment working with manufacturers of devices and their marketing teams investigating ways to market new products maintaining equipment and training staff to use it safely responding to queries and resolving problems with devices writing reports and documentation Installing and modifying medical equipment and instruments within hospitals, health centres, and extended care facilities Ensuring the safety of medical equipment used for diagnosis, treatment, and monitoring of patients Design and develop devices to assist with a physical disability, such as prostheses Design and evaluate the efficacy of medical devices, such as pacemakers, dialysis machines, and patient monitors Study medical systems and products to prepare and present reports to research groups, hospital boards, or professional associations Develop and improve medical technology, such as surgical lasers and artificial hips and knees Supervision of biomedical technicians and technologists Interested candidate can attend walking interview at 11:00am or send their resume at gurgaon@parkhospital.in Regards HR Team

Key responsibilities include generating new business opportunities to meet assigned targets, managing collections and accounts receivables, and ensuring effective handling of the company’s product portfolio. Looking for Dental domain. Required Candidate profile Any Graduate Should have min 3 Years of experience in sales in Dental Industry (Dental Implant / Dental Material / Dental Pharma)

As a member of our team, you will be responsible for designing, developing, and maintaining medical devices and systems. Your primary focus will be collaborating with medical professionals to guarantee the safety and effectiveness of the products you work on. To qualify for this role, you must have completed your 10+2 education with a Science background. Additionally, you are required to possess a bachelor's degree in fields such as B. Tech Biomedical Engineering, B.Sc Biomedical Engineering, or other related courses. This educational background will provide you with the necessary knowledge and skills to excel in this position.,

The position of Medical Device Sales Representative at Seawolf Technologies in Mumbai is a full-time hybrid role, offering the flexibility of remote work. As a Sales Representative, you will be tasked with the promotion and sales of medical devices within the orthopedics field, primarily focusing on operating rooms and medical professionals. Your responsibilities will include cultivating relationships, showcasing product features, and meeting sales objectives. To excel in this role, you should possess a background in Medical Sales and demonstrate strong Sales skills. Experience in Orthopedics and Operating Room environments is crucial, along with a solid understanding of Medicine and medical devices. Effective communication and interpersonal abilities are essential for engaging with clients, while your capacity to work both independently and collaboratively will be advantageous. Proficiency in negotiation and closing sales is key to succeeding in this position. A Bachelor's degree in a related field is required for this role, and prior experience in medical device sales would be considered a valuable asset. If you are a dynamic professional seeking a challenging opportunity in the sales of medical devices, this role at Seawolf Technologies could be the ideal fit for you.,

As a Content Writer with 2-5 years of experience in the Healthcare, Pharma, or Medical background, you will be responsible for creating engaging and informative content related to medical devices, with a particular focus on ECG and other smart devices. Your role will involve ensuring that the content is accurate, well-researched, and tailored to the target audience. You should have a deep understanding of medical terminology and concepts, along with the ability to communicate complex information in a clear and concise manner. Additionally, you should be detail-oriented, creative, and able to work effectively both independently and as part of a team. Candidates with no employment gaps and based in Mumbai will be preferred for this permanent position. The ideal candidate will have a total of 5 years of work experience, with at least 3 years dedicated to content writing specifically. The work location for this role is in person, with both fixed and rotational shifts available. If you meet the criteria and are passionate about creating content that educates and inspires in the healthcare industry, we encourage you to apply for this exciting opportunity.,