1307 Medical Devices Jobs - Page 4

-Organise sales visit,bring enquiries,assist in giving demo of medical equipment to customer -Maintain relationship,support, info of doctors/hospitals -Recommend solution to client problems -Analyse competition brand -Work in team,achieve targets Required Candidate profile -Any Male with field sales experience in healthcare industry -BE/B Tech/ Diploma (Biomedical/Instrumentation/Electronics) - 1- 3 yrs exp preferably in relevant medical devices - Good technical skills

-Organise sales visit, bring in enquiries, assist in medical equipment demo -Maintain relationship, support, info of doctors/hospitals -Sell medical devices to hospitals, nursing homes -Analyse competition brand, be part of team, achieve target Required Candidate profile -Any Male with field sales experience in healthcare industry -BE/B Tech/ Diploma (Biomedical/Instrumentation/Electronics)/Science Grad. - 1- 3 yrs exp in relevant medical devices - Travelling is must Perks and benefits At par with the Best

Roles and Responsibilities Manage sales activities for Cathlab products, including stents, balloons, pacemakers, and other medical devices. Develop and maintain relationships with customers to identify their needs and provide solutions. Conduct product demonstrations and training sessions to educate customers on the features and benefits of our products. Collaborate with cross-functional teams to resolve customer issues and improve overall customer satisfaction.

As a Design & Development professional with CAD Tools knowledge, you will be responsible for conducting part feasibility studies on program parts to ensure comprehensive consideration for tool design, particularly focusing on Plastic Materials & its Properties. Your role will entail a strong working knowledge and experience in reading drawings, understanding manufacturing processes, and possessing the ability to resolve technical issues efficiently. You will be expected to address technical doubts related to software, tool design, manufacturing processes, GD&T, Drawing views, etc. Your proficiency should extend to working both independently and collaboratively within a team, demonstrating excellent communication skills throughout. Moreover, you will need to showcase your capability in developing prototypes, conducting testing to assess Mould Designs" functionality and efficiency, and selecting appropriate materials for mould construction with factors like durability, heat resistance, and cost-effectiveness in mind. It will be crucial to ensure that all mould designs adhere to quality and safety standards. Key Skills required for this role include knowledge of Medical Devices, a strong team orientation, and organizational skills. Additionally, hands-on experience with CAD Software such as Solidworks and AutoCAD will be beneficial to excel in this position.,

You are an enthusiastic and self-driven Sales Engineer needed by Cyrix Healthcare Pvt Ltd to promote and sell biomedical equipment and devices in Bengaluru. Your primary responsibilities will include achieving sales targets, nurturing client relationships, and ensuring customer satisfaction within the biomedical sector. Your key responsibilities will involve promoting and selling biomedical equipment/devices, identifying new business opportunities, generating leads through various methods such as market research and cold calling, and maintaining relationships with key stakeholders like biomedical engineers and hospital administration. Negotiating sales deals, maintaining accurate records, and staying updated on industry trends will also be crucial aspects of your role. To excel in this position, you must possess a strong knowledge of biomedical equipment/devices, demonstrate proven sales abilities in healthcare or medical devices, and exhibit excellent communication and negotiation skills. The ideal candidate should hold a qualification of BE/BTECH/Diploma in Biomedical, have 0 to 2 years of experience (freshers are also encouraged), and possess a Two Wheeler license due to the requirement of extensive travel within the assigned region. The job offers a competitive salary ranging from 25000 to 30000 p/m along with benefits such as health insurance and Provident Fund. Working hours are full-time, permanent, and in the day shift. Proficiency in English is preferred for this role. If you meet the requirements and are keen on this opportunity, please email your CV to tacyrix@gmail.com. Join us in this exciting role and make a significant impact in the biomedical industry!,

As a Design Quality Engineer at our company, your primary responsibility will be to develop, establish, and maintain quality engineering methodologies, systems, and practices that align with BSC, customer, and regulatory requirements. You will serve as a Quality representative to enhance awareness, visibility, and communication on quality initiatives, supporting departmental, functional, site, divisional, and corporate quality goals and priorities. Your role will involve providing focused quality engineering support within new product development, operational, or system/services support. In this position, you will collaborate with sustaining project teams and engage in design quality engineering throughout the entire product cycle. Your duties will include ensuring the creation and proper execution of Project/Sustaining Quality Deliverables, such as Project Design & Development Plan, Risk Management Plan, Hazard Analysis, Use and Design FMEA, Field Assessment Plan, and Software Validation Plan. Additionally, you will work on product Design History File (DHF), design input, design output, product risk management, usability, verification, and validation efforts for commercial products. Furthermore, you will be responsible for managing electronic document control and version control on all project-related documents, ensuring adherence to quality systems and design assurance Standard Operating Procedures (SOPs), and providing quality and regulatory compliance guidance to product development or design change project teams. You will lead the implementation of assurances, process controls, and Corrective and Preventive Action (CAPA) systems to meet or exceed internal and external requirements. As an effective communicator and team member, you will support quality disciplines, decisions, and practices while applying sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues. Your role will also involve assisting in the development and execution of streamlined business systems to effectively identify and address quality issues. In all your actions, you will demonstrate a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures. As a Design Quality Engineer, you will be expected to have expanded conceptual and technical knowledge in the Medical Device Design Quality domain, broaden your capabilities in applying concepts in your job function, demonstrate working knowledge of business and industry practices, and company processes to accomplish your work. You will be accountable for your contributions and meeting objectives, with no supervisory responsibility. Your role will involve planning and organizing non-routine tasks with approval, initiating or maintaining work schedule and priorities, organizing project assignments, and maintaining project schedules. You will use judgment to solve problems in straightforward situations, working under general direction from more senior-level roles or managers. Your interactions and communications will primarily involve explaining factual information of limited complexity to others in straightforward situations and organizing, presenting, and explaining data/information to internal audiences.,

Join our team at Medekom Ventures Pvt. Ltd. and embark on a journey at the forefront of Medical Device Innovation! As a Service Engineer for Medical Devices, you will play a crucial role in the installation, commissioning, maintenance, and servicing of High-end Medical Equipment. This position requires extensive travel and is based in Hyderabad. To be successful in this role, you should have 2-5 years of experience and hold a BE/B-Tech degree in Biomedical, Mechanical, or Electronics. Alternatively, a Diploma Holder with significant experience in the field of medical devices may also be considered. Key qualifications for this position include customer handling experience, customer orientation, the ability to work under pressure, and adept problem-solving skills. A strong sense of teamwork is essential, and knowledge of computer software/hardware installation will be advantageous. If you are looking to make a meaningful impact in the field of Medical Device Innovation and possess the necessary qualifications and experience, we invite you to join our dynamic team at Medekom Ventures Pvt. Ltd. Visit our website at https://www.medekom.com for more information.,

At Infosys, we pioneered and perfected the global delivery model, introducing to our customers the ability to move technology work to different locations where talent is readily available, and quality is both impeccable and cost competitive. Over the years we have applied this model to a full range of services - both technical and business. Our IT services such as application integration, testing, maintenance and infrastructure management ensure your operations are fully optimized. Our business process outsourcing and management services, such as customer service delivery, human resource outsourcing and procurement handling, drive down process costs while greatly enhancing their efficiencies. Most importantly, as part of our strategic sourcing approach, these services free up resources that can then be deployed to drive transformation and innovation initiatives Location for this position is Pune, Maharashtra , IN. Must work from office Experience required: 4-8 years of relevant experience. Responsibilities: Automate end-to-end test cases for connected systems using Selenium-Python . Prepare and execute system integration testing scenarios. Conduct peer reviews of test objectives, scenarios, and automated scripts. Strong understanding of object-oriented programming (OOP) concepts. Prepare requirement traceability matrices. Test web-based applications across different devices and browsers. Experienced in Web and Mobile Applications Automation testing Design, write, and execute automated test scripts. Identify, document, and track bugs and issues. Collaborate with cross-functional teams to ensure high-quality software delivery. Continuously improve test automation processes and frameworks. Preferred: BE/BTECH in Computer Science or related field (or equivalent experience). 3+ Years strong Selenium with python experience 2 years of Python programing experience Mobile App automation testing using APPIUM (nice to have) Knowledge of continuous integration/continuous deployment (CI/CD) pipelines. Familiarity with Agile development methodologies. Proven track record in automation testing and quality assurance. Excellent problem-solving skills and attention to detail. Strong communication and teamwork abilities. Experience in the Medical Device industry or IOT is preferred.

As the Sales Head for Medical Devices & Diagnostic Equipment, you will be responsible for leading the sales and business development efforts in Telangana and AP. Your primary focus will be on establishing a network of institutional customers, clinics, and medical device outlets/pharmacies, as well as engaging with doctors in the region. You should bring a strong background in the medical devices business to effectively drive revenue, implement sales strategies, manage teams, foster customer relationships, and oversee credit management. With 6-7 years of relevant experience, you will play a key role in expanding our presence in the Medical Devices | Diagnostics industry. Your key responsibilities will include strategizing and executing sales plans, identifying new business opportunities, and ensuring the overall growth of the sales department. Your leadership will be instrumental in achieving targets and establishing a strong foothold in the market. If you are a dynamic and results-driven individual with a passion for the healthcare industry, this opportunity offers you a platform to make a significant impact and drive the success of our sales and business development initiatives in the medical devices sector.,

India's Hiring for Big Healthcare Enterprise KTPL Technologies Private Limited. Position Hiring: Biomedical Service Engineer No. of Vacancies: 20 Company Profile: About KTPL Technologies Pvt. Ltd.: Founded in 1993 by the late Mr. Vikram Kirloskar with the name of Kirloskar Theratronics Pvt. Ltd. and further changed to KTPL Technologies (formerly Kirloskar Technologies Pvt. Ltd.) w.e.f . began its journey with a vision to transform Indias healthcare landscape through advanced medical technologies and solutions. What started as a modest venture with a team of 15 employees across three locations has evolved into a robust organization of 650+ professionals, delivering excellence across India and globally. Over the past 30 years, KTPL has built a reputation for reliability, customer focus, and pioneering spirit. The company has served more than 75,000 customers , spanning leading public and private healthcare institutions, and has successfully executed international healthcare technology projects. In 2024, KTPL entered an exciting new phase under the leadership of renowned businessman Mr. Kamal Gupta , who took over the company with a vision to scale new heights, strengthen the foundation, and accelerate KTPL's journey toward global excellence. Job Responsibilities: Service Support: Responsible for providing periodic maintenance services, timely resolution for equipment malfunctions, troubleshooting, and repair of electronic and electromechanical equipment onsite service. Preventive and Corrective maintenance of Biomedical Equipment. Coordinate with service contractors for maintenance, calibration, and collection of service documents. Training customers on equipment operation, maintenance procedures and process related to the upkeep of equipment. Key Account/Customer Relationship Management: Responsible for building and managing key customers as well as building and strengthening customer relations by timely follow-up and support to the customers. Responsible for the closure of all assigned calls. Timely submission of documents (service reports, PM reports, etc.) to the branch office. Responsible for the daily scheduling of engineers and providing daily updates to BSM. Follow up with the service coordinator for spares required to rectify the equipment. Responsible for grooming of Engineers technicians reporting to him. Education and Experience Requirements: B.E/B.Tech in Biomedical Engineering/ Medical Electronics/ Electronics & Electrical / Electronics & Telecommunication, and Instrumentation. Diploma in Electronics Engineering, Electronics & Telecommunications, or Electrical Engineering. Experience: 3 Years+ Expertise in the repair, calibration, and maintenance of medical equipment. High level of customer focus and good communication skills with a pleasing personality. Self-motivated and self-directed with the ability to create and manage their own schedule. WE REQUIRE AMBITIOUS PEOPLE WITH PROFESSIONAL IMAGE, GOOD ATTITUDE, AND MENTALITY TO GROW WITH THE COMPANY. Salary Range: Salary will not be a constraint for the right candidate, and it may vary based on experience and skill set.

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

Role Overview: We are seeking a dynamic and visionary CEO to lead our growth in the medical devices sector focused on IVF and Urology. The ideal candidate will bring a rare blend of strategic acumen, operational expertise, and a deep understanding of the healthcare ecosystem. Key Responsibilities: Lead the companys strategic direction and overall operations with full P&L responsibility. Drive national and international marketing initiatives for global brand positioning and market penetration. Oversee regulatory compliance across domestic and international markets. Ensure operational excellence across supply chain, logistics, purchase, and manufacturing. Build and lead high-performing cross-functional teams across departments. Identify and unlock new business opportunities and partnerships. Manage investor relations and provide timely business performance insights. Foster a culture of innovation, integrity, and ownership. Ensure customer-centric product development and service delivery. Lead expansion plans in India and key global markets. Guide the company through complex challenges with a solution-oriented approach. Monitor industry trends and emerging technologies in IVF & Urology. Maintain strict adherence to quality assurance and production protocols. Create a high-impact corporate culture focused on accountability and excellence. Represent the company at key forums, industry events, and conferences. Collaborate closely with R&D, sales, and clinical teams for holistic product success. Develop and manage scalable business processes and reporting systems. Act as the face of the organization for strategic collaborations and alliances. Demonstrate strong ownership mindsettreat the business as your own. Be a go-getter and growth catalyst, committed to the companys long-term vision.

US (FDA) Regulatory Support: Prepare and submit: 510(k) premarket notifications,PMA,supplements or De Novo requests (if applicable),Support establishment registration Medical device listing, Ensure compliance with 21 CFR Part 820 (QSR) and UDI Office cab/shuttle Annual bonus Health insurance Provident fund

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries CORE JOB RESPONSIBILITIES Business generation & development: Achieve monthly, quarterly, half yearly and yearly sales target by promoting companys products ethically to customers as per the business plan, also ensure Doctor / Customer Call average as per the customer management plan of the division Organizing Camps (CME) as per the division strategy and customer needs Facilitate the process of successful new product launch. To create and update customer list as per the therapy and product of the division. Ensure Ipad adoption (if applicable) as per division norms and adherence to CLM calls Brand Management: Prescription audit for Abbott brands and other competitors brands Generate POBs for Abbott brands as per the business plan REQUIRED EXPERIENCE BSc/ B. Pharm or Any Graduate with minimum 2 years of prior experience as a Medical Representative PREFERRED EXPERIENCE Candidate with prior/current experience in the same therapy. Candidates from MNC and top Indian Pharma companies will have added advantages. Fluent and confident in communication LOCATION: India > Guwahati : Pushpanjali Arcade, Near ABC Bus Stop t

Job Description Job Summary Job Title Research Scientist - I Location Whitefield, Bangalore Shift General Your Role at Vantive: The successful candidate for this role will be part of the Analytical Chemistry and Stability (ACS) team and will bring hands-on and technical leadership experience in Elemental analysis for medical devices and drug products. This Research Scientist role will entail utilization of expertise in analytical chemistry, Atomic Absorption (AA), Inductive Coupled Plasma techniques (ICP-OES, ICP-MS) and other appropriate techniques to perform gap assessments for medical device and drugs requirements and support change control activities across the Renal and Acute Care businesses within Vantive. The successful candidate is expected to also have a strategic mindset and will work closely with regulatory, quality, preclinical and product design owning leaders to enable investigations of trace level Elemental Analysis in drugs & devices to support on-market or new product programs. This role will also include planning and performing laboratory work in AA, ICP-MS and ICP-OES, including independent execution of laboratory studies at in-house or external labs for Method Development and Validations. The candidate will likely act as study director for multiple studies at any given time and is expected to be able to do wet chemistry, AA, ICP-MS and ICP-OES hands-on as required from time to time for efficient and effective execution of the program. The individual will author required reports (internal documentation and regulatory submissions) following pertinent internal and external guidelines that ensures safety and compliance of drugs or devices that Vantive makes. The candidate is expected to stay abreast of emerging sciences and technologies that influence chemical characterization for medical devices and drugs through active participation in relevant external forums / societies. Essential Duties and Responsibilities. Develop strategies to effectively apply a risk-based scientific approach within a regulatory framework to support trace level Elemental analysis projects and change control activities. Develop and Validate Methods for Elements and Elemental Impurities using the ICP-OES, ICP-MS and other relevant techniques. Define strategy for conversion of legacy AA methods to ICP and prove the equivalency between two techniques by following appropriate statistical methodologies. Collaborate with a multidisciplinary team of subject matter experts (e.g. ACS, E&L, Materials, Biocompatibility, and Toxicology) to develop trace level Elemental analysis strategies that align to regulatory requirements for medical devices and drug products. Participate in ACS change control impact assessments when applicable to trace Elemental impurities analysis and work with cross functional team members (design owners, E&L SMEs, materials, preclinical, etc.) to determine a comprehensive testing strategy through writing impact assessments, gap assessments, technical rationales and documents related to such change controls. Maintain and apply current knowledge of relevant Quality System Regulations and other regulatory requirements related to chemical characterization of product development, design and safety. Interact across functions (Design Owning Organization, Project Management Organization, Regulatory Affairs, Preclinical, etc.) to understand products and therapies, as well as business, technical, and regulatory requirements to meet project needs. Should have knowledge, experience, and responsibilities on the matter that are essential for ensuring Manufacturing Plants can escalate and share any concerns regarding compliance to quality system for Management and Control of Elemental Impurities and Elemental Impurity Risk Assessments . Qualifications. -Demonstrated experience in applying Elemental Impurity analysis methods and tools as part of R&D -Knowledge of regulatory expectations related to Elemental analysis for drugs and devices. -Performing change control in a GMP environment. -Experience in working in global cross-functional teams for trace Elemental Impurities analysis projects - independent problem solver who can use a methodical approach to develop solutions and make recommendations. Education and/or Experience. Bachelor s degree in scientific discipline (Analytical or Organic chemistry preferred) with a minimum 14 years of experience, or MS with a minimum 7 years of experience or PhD with a minimum 3 years of relevant experience.

Job Responsibilities: Act as Solution Lead and Technical expert for new product development projects and lifecycle management activities within R&D Kidney Care Drug Products Organization. Organize, plan and execute product development or sustaining activities in compliance with current QA/ environmental/ regulations and standards. Provide technical leadership, mentor and guide the execution scientists in order to get tasks accomplished according to plans, milestones and business needs. Review and approve Design Control documentation as per the quality procedures and industry standards. 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 product development or 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 resource estimation and forecast to the project managers or project leaders. Ensure good internal and cross-functional communication at a global front and regular status update of projects Qualifications and Skills Master s in chemistry or M. Pharm. with at least 10-12 years of relevant experience or Ph.D. in pharmaceutical or relevant sciences discipline with at least 7-10 experience in solution development of parenteral formulations. Excellent English verbal and written communication skills Exposure to medical devices and drug products 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 Demonstrated project/program leadership in drug/pharmaceutical products 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.

We're hiring Territory/Area Sales Managers for Medical devices or Medical Equipment company for Multiple Locations: Delhi (M/F), Chandigarh/Ludhiana(M), Jaipur(M), Lucknow(M), Mumbai(M/F), Pune(M), Bangalore(M), Chennai(M)

HCLTech WalkInDrive In Chennai for Mechanical Engineers on 26th July Saturday. CONSIDER THIS AS CALLLETTER Medical Mechanical DHF/ windchillPLM/Design Verification/Control Engineer- WalkIN on 26th July in Chennai Shollinganallur Join a team that values innovation, growth, and impactful work. Dont miss the chance to work with cutting-edge Project in SME and be a part of something transformative! Drive Date:26th July Saturday (9AM-2PM) Skill1: #DHF #remediation #DHFremediation Skill2: #Designcontrol #designverfication #designvalidation Skill3: #WindchillPLM in medical domain Contact Person: Katherine Sylvia Venue Location: #HCLTech Elcot Sez, 602/3, 138, Medavakkam High Road, Sholinganallur, #Chennai -600119 Position:Mechanicaldesign (Lead, Technical Lead) Experience: 2.5-9 years Job Location:Chennai Skill : Medical device, Design control, Design Verification, DHF, MDR, ISO13485, Risk management, DHF Remediation, WindchillPLM #changeorder #Designhistoryfiles #JD : B.E / B.Tech or higher education in Mechanical Engineering #EXPERIENCE : Sustaining Engineers should have Medical Device #DesignControls , #Design verification & Validation experience of 3 to 7 years. Adept with #DesignControlprocess for #MedicalDevices . Led Change Qualification projects for medical devices, working with multi-cultured CFT. Experience developing test protocols and test plans Ensures quality of deliverables, including design, data summary and interpretation and report generation. Expertise in #MechanicalEngineering basics. #RiskManagement (Proactive risk identification and mitigation planning) Self-motivated and capable of working independently & Strong project management skills. Knowledge on #ISO13485 would be an added advantage. Excellent Oral and written Communication (MUST prove Technical writing skills with samples and/or assessment during the interview) & Interpersonal skills #SOFTWARETOOLS : #Mechanical #SolidWorks , #2D #ToleranceStackup , MS Word/ Excel/ Power point, #Skill2#JD : #DHFRemediation Experience in gap assessment process such as Testing gap assessment, Standards gap assessment, Requirements gap assessment Knowledge in Design History File remediation #Skill3#JD : #windchillPLM #medicaldomain #BOMstructure #Changeorder Create, Revise, Release parts (ZFIN, ZRAW, ZSMI, ZMOD, ZNVL) in Wind-chill according to the requirements defined in WI Create, Revise, Release Documents (Protocols, Reports, FAB, TRAV, PFMEA, IFU, Drawing Specification, Device tracking kit etc) in Wind-chill according to the requirements defined in WI Update Document and Part structure Create, Update BOM structure Create Change order with change description and justification for change. Assign Change Activity Assignee and Peer Reviewer. Assign approvers to the Change Implementation Board for change orders per the approval requirements. Create manual Pre- and Post-Release Adhoc Tasks Follow up with approvers to get the COs reviewed and approved Release of the Change Orders in Wind chill #Contact Person: #KatherineSylvia Interested candidates can share their CV on below mail id Katherinesylvia.k@hcltech.com with Below details Current Company, Current CTC, Expected CTC, Notice Period, Location . CONSIDER THIS AS CALLLETTER

Surgical Sales Specialist We're seeking a Surgical Sales Specialist to educate customers on our products, build strong relationships, and drive sales in a fast-paced healthcare environment. You'll manage distribution, gather market data, and help expand our reach. Qualifications: Bachelor's degree (preferred: B.Tech/B.E., B.Sc., B.Pharma) with 2-3 years of post-grad sales/marketing experience, ideally in healthcare/surgical. Skills: Self-motivated, excellent communicator, strong selling and customer relationship skills. Bonus if you're comfortable in an Operating Theatre and keen to learn clinical details.

Internship Alert! Join our Biomedical Engineering Dept. for hands-on training in hospital equipment maintenance. Final-year students/freshers can apply. Send CV to bme@nshhospital.com Duration: 36 months | Certificate provided

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing whatever your ambitions. Location: Chennai, India Responsibilities: Candidate with technical and selling skills in medical devices is preferred. Able to exhibit technical knowledge and business knowledge of the medical device industry (BSC and competitors). Visit external and internal customers of Boston Scientific on a regular and planned basis to promote products and services to achieve monthly, quarterly and yearly sales targets, as agreed with the Manager. Manage existing customer base and acquire new customers in the assigned territory without appreciable direction. Independently plan and develop the market for existing and new products according with divisional goals and objectives, through execution, while optimizing available tools. Support the PI lines of business and help organization achieve the desired sales objectives Establish and maintain positive and cooperative working relationships with customers, conducting his or herself in a professional and responsible manner at all times. Conduct customer CMEs, product demonstrations and in-service programs to ensure customer satisfaction. Execute the required job on timely basis such as SFDC. To assist the physicians for cath lab procedures relevant to PI wherever required/requested in the entire territory Involve in clinical discussion with the respective Physicians like Interventional Radiology, Vascular Surgeons, Interventional Cardiologist, Interventional Neurologist and Interventional Nephrologist regarding the technical specifications Establish relationships with KOLs in the territory and execute engagement plans in line with marketing. Work closely with the tender management team to ensure that we can timely lock in tenders with our specifications and win. Help BSC to execute the operations in case of direct supplies and ensure smooth supplies/transactions. Work closely with dealer and their team to ensure smoother operations and train dealer person on BSC PI Portfolio. Candidate will manage the territory with integrity and in accordance with our Code of Conduct Requirements: Bachelor s degree in business or sciences and minimum 5 years of experience in medical devices consumables or super specialty products ( dealing in IR or Vascular surgery only) experience. Candidate will be based at Chennai City only. Candidate should have working experience in Chennai, Vellore and Pondicherry. Track record of achieving annual sales numbers. Existing relationships within the industry specialty/ KOLs will be preferred. Basic understanding of hospital purchase procedures and Govt. tenders of Tamil Nadu state. Ability to proactively manage the business and able to quickly understand new tasks for execution. Ability to build positive working relationships, both internally and externally. Able to assist the patient procedures in cath lab / OT setting. Able to travel continuously in the territory, Travel experience within Tamil Nadu state geography is preferred Requisition ID: 608753 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

A Day in the Life Collaborating with cross-functional teams to develop comprehensive product risk management files, including the risk management plan, Hazard Analysis, DFMEA, and risk management report, adhering to ISO 14971 standards. Responsible for maintaining highest standards of product reliability and patient well-being through gather and analyze data, write reports, and communicate with regulatory agencies on ensuring product safety. Responsibilities may include the following and other duties may be assigned: Capability to conduct thorough reviews of new and modified product design documentation, assessing quality characteristics such as manufacturability, serviceability, testability, reliability, and compliance with product requirements. Subject matter expert in risk management for designated medical device products or platforms. Ensuring compliance with FDA Quality System Regulations, EU MDR, ISO 13485, ISO 14971, IEC 60601, and other relevant industry standards during product development and changes. Reviewing Design History Files and Technical Files to ensure alignment with applicable requirements. Collaborate with cross-functional teams to gather and analyze data related to the performance and safety of medical devices and independently develop Periodic safety update plan and reports. Partner with regulatory affairs and medical experts to ensure accurate and timely submission of PSURs to regulatory authorities. Continuously monitor and stay updated with evolving safety regulations and guidelines to ensure PSUR compliance. Familiar with Literature review, PMCF, IMDRF coding, CAPA and NCMR. Hands on experience in signal evaluation trending and reports, preliminary code reviews for the product complaints on periodic basis. Delivering presentations on project status and issues to the QA organization and providing training to other departments on relevant procedures and policies. Participating in audits and demonstrating the ability to effectively contribute as a team player in various roles, including contributor, subject matter expert, leader, and facilitator. Provide Quality support to facilitate resolution of product complaints and/or safety issues Previous experience working in a cross-functional team environment. Familiar with statistical software tools (Minitab) Develop templates and trainings based on the quality system regulations, applicable standards and guidance. Independently review all deliverables to ensure compliance with development process and the standard. Demonstrates ability to effectively play multiple roles on a cross-functional team including contributor, subject matter expert, leader, facilitator. Hands-on experience on complaints analyis, Post market surveillance, Design Controls for Medical Devices. Required Knowledge and Experience B E or B. Tech in Mechanical/Biomedical Engineering Minimum 4-6 years of quality engineering experience or equivalence and overall 6-8 years of experience. Familiar with ISO 9001, ISO 13485, ISO 14971, IEC 60601, 21 CFR part 820, 21 CFR part 11, EUMDR and product specific industry standards. Working knowledge of and auditing experience to the FDA Quality System Regulation, ISO 13485, and the Medical Device Directive. Good verbal and written communication skills Understanding of post-market surveillance processes and adverse event reporting. Knowledge of risk management principles and hazard analysis in the context of medical devices. 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

Designation - ESI Executive Scientific Information Eligibility Criteria - Any Graduate with minimum 2 to 3 years experience in sales of Medical devices / OTC products in the same area. Should have good communication skills. Stability should be there. Will be responsible for meeting with Retailers, Distributors, whole sellers, Doctors. So should have experience in same. Salary - 3.30 LPA (Non Metro cities) + Good Allowances + Good Incentives 3.75 LPA (Metro cities Bangalore, Hyderabad, Chennai) + 60,000 Rs Metro Bonus + Good Allowances + Quaterly Incentives Locations - ESI North Hyderabad, South Hyderabad, Hyderabad West, Chennai West, Chennai South, Chennai Central, Mangalore, Calicut North, Calicut North

What We Want You To Do Approve new equipment through testing, ensuring standards and compliance Install new equipment by setting, adjusting, calibrating, and testing functionality Maintain equipment by following preventive maintenance schedules, performing tests, troubleshooting, and resolving malfunctions Calls for special equipment service, evaluates service contracts and maintains equipment inventories. Directs biomedical equipment operation by providing equipment operation demonstrations, instructing other staff in use and care of equipment and answering questions. Evaluates proposed equipment by conducting tests and evaluations. Maintains supplies inventory by checking stock, anticipating needs, placing and expediting orders, and verifying receipt. Compile, analyze, and summarize data to prepare biomedical reports, highlighting information and trends Write reports and documents describing protocols, policies, maintenance, standards for use and repair of biomedical tools, machinery, and software Requirements Proven work experience in biomedical equipment quality control and quality assurance. Have an understanding of quality control, quality assurance and quality checks. Awareness of ISO 15189 and ISO 13485 & other regulatory requirements. Skills Keen attention to details. Ability to critically evaluate the requirements of the relevant ISO standards.. Ability to work independently with minimal supervision as well as collaboratively in a team environment. Strong analytical and problem-solving abilities. Ability to execute tasks and document information independently. Excellent organizational and time management skills with the ability to prioritize tasks effectively Strong interpersonal and communication skills with the ability to interact professionally with diverse stakeholders Skills : problem-solving abilities , genomics , organizational skills,quality control,iso 13485,analytical skills,communication skills,time management,iso,iso 15189,keen attention to details,interpersonal skills,quality assurance

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)