613 Biomedical Jobs - Page 5

We are actively seeking enthusiastic and qualified Life Science graduates (B.Sc / M.Sc / B.Pharm / M.Pharm / B.Tech - Biotechnology, Microbiology, Biochemistry, etc.) for exciting opportunities in Medical Coding and Medical Billing.

ROLES & RESPONSIBILITIES To repair & maintenance of all in-house equipment. To give first hand support for the any breakdown. Keeping the records of all breakdown, servicing & AMC Maintenance of all equipment Coordinate to the company engineer for the smooth process of breakdown. Hands on training to the Doctors/Nursing staff/ operators for effective and safe use of equipment's. Handling the installation of new purchase or donated equipment. Doing the testing & commissioning of new equipment. Giving the on call support for the smooth process of users. Keep the stock for the small accessories of equipment. & maintain the records.

About ValGenesis ValGenesis is a leading digital validation platform provider for life sciences companies. ValGenesis suite of products are used by 30 of the top 50 global pharmaceutical and biotech companies to achieve digital transformation, total compliance and manufacturing excellence/intelligence across their product lifecycle. Learn more about working for ValGenesis, the de facto standard for paperless validation in Life Sciences: https://www.youtube.com/watch v=tASq7Ld0JsQ About the Role: ValGenesis is excited to invite applications for the position of Senior Validation Engineer. In this role, you will be pivotal in ensuring the compliance and quality of our innovative software solutions tailored for the life sciences sector. As a Senior Validation Engineer, you will collaborate with diverse teams to develop comprehensive validation strategies, create and execute test cases, and maintain the project quality standard. Responsibilities - Hands on work at an individual capacity leading to deliverables - Diligently work with Product, Engineering and Testing teams to gain understanding of Product functions. - Review Product Requirements including Epics, User stories, User Requirements, Software Requirements etc. - Author test cases in OQ and PQ protocols in line with the requirements and QMS guidelines - Create realistic test cases and test data based on customer usage scenarios. - Execute test cases, create defects, create deviations, and report test results. - Peer review Test cases, test data and Test designs - Work in a highly collaborative team environment, with communication across many team members. - Good understanding of the company QMS standards - Author documents in accordance with the QMS guidelines - Lead of team of people Provide ongoing guidance, allocate work, review work - Manage the Validation of a product - be responsible for the delivery quality and timelines Requirements - BE/BS degree or equivalent work experience in Computer Science, Biology, Biomedical or related field. - Must-have 5+ years of Computer System Validation and Product Software Validation testing experience in a regulated environment. - Good knowledge of Product development life cycle - Understanding of GMP, FDA and ISO regulations - Good knowledge of testing tools and Microsoft office products - Self-motivated, willing to learn new concepts, technologies, and products quickly. - Excellent interpersonal, writing and communication skills, and troubleshooting skills. - Passionate about testing, Validation, and product quality - Able to train and help colleagues with less experience; be able to lead small projects. We're on a Mission In 2005, we disrupted the life sciences industry by introducing the world's first digital validation lifecycle management system. ValGenesis VLMS revolutionized compliance-based corporate validation activities and has remained the industry standard. Today, we continue to push the boundaries of innovation - enhancing and expanding our portfolio beyond validation with an end-to-end digital transformation platform. We combine our purpose-built systems with world-class consulting services to help every facet of GxP meet evolving regulations and quality expectations. The Team You'll Join Our customers" success is our success. We keep the customer experience centered in our decisions, from product to marketing to sales to services to support. Life sciences companies exist to improve humanity's quality of life, and we honor that mission. We work together. We communicate openly, support each other without reservation, and never hesitate to wear multiple hats to get the job done. We think big. Innovation is the heart of ValGenesis. That spirit drives product development as well as personal growth. We never stop aiming upward. We're in it to win it. We're on a path to becoming the number one intelligent validation platform in the market, and we won't settle for anything less than being a market leader. How We Work Our Chennai, Hyderabad, and Bangalore offices are onsite, 5 days per week. We believe that in-person interaction and collaboration foster creativity, a sense of community, and are critical to our future success as a company.,

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Priya -9600450980 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

We’re Hiring at Siemens Healthineers! Join us in shaping the future of healthcare with integrity, precision, and purpose. We are looking for Area Sales Professional to join our team in Hyderabad. About the Role Siemens Healthineers India is looking for Area Sales Professional for the Point of Care (PoC) portfolio of its Diagnostics business. Role & Responsibilities Plans sales volumes and potentials of all customers in the assigned region. Provides information via CRM for forecasts and planning. Analyzes the specific market conditions and builds a sound market related network of stakeholders. Spots opportunities for Point of Care products. Prepares customer contact, builds and maintains a customer focused network. Prepares / coordinates and negotiates proposals in cooperation with proposal mgmt. / other involved professionals and management. Coordinates the realization of assignments, may coordinate and contribute to set up respective product developments and Key Projects. Completes sales and revenue related key reporting. Contributes to the development of After-Market business in the region. Point of contact to customers in commercial matters and influences collaboration within the organization to secure customer support. To work in coordination with channel partners and support them in closing the deals. To align for product demonstration and arrange for requisite approvals. Responsible for maintaining the market share in the respective geographies. Ensuring that the receivables from sales operations are collected within time. Experience & Educations Bachelor's Degree or higher in Engineering (Preferred), Bachelor of Science / Biomedical or related field with 5-7 years of experience in Point of care Diagnostics/ Lab Diagnostics/medical devices. Key Skills & Tools Strong understanding of healthcare product lines, POC Diagnostics and technology. Expert in customer exposure & account management best practices. Demonstrate ability to work independently & within a team. Ability to handle Dealer Distributor network. Good Territory knowledge -Andhra Pradesh & Telangana

Applications are invited for the post of one Junior Research Fellow (JRF) for the Anusandhan National Research Foundation (ANRF) -Prime Minister Early Career Research Grant Scheme project in the Centre for Biomaterials, Cellular and Molecular Theranostics (CBCMT), at Vellore Institute of Technology (VIT), Title of the Project : Unveiling and Reprogramming the Cellular Package Mechanism of Tumor Extracellular Vesicles to Combat Cancer Metastasis. File : (ANRF/ECRG/2024/006012/LS). Qualification : M.Sc., /M. Tech., (Biomedical Science, Biotechnology, Biochemistry and Nanotechnology) with a minimum of 55% marks. Preference will be given for students with NET and/or GATE qualifications. Desirable (if any) : Candidates with research experience in cell culture, molecular biology and nanomedicine Stipend : For NET/GATE Qu For NET/GATE Qualified candidates: Rs. 37,000/- + 10% HRA per month for the first two years and Rs. 42,000/- + 10% HRA per month for the third year. For other Candidates: Institutional norms will be applicable. Sponsoring Agency : Anusandhan National Research Foundation (ANRF) -Prime Minister Early Career Research Grant Scheme, Government of India No. of Positions : 1 Duration : 3 Years Principal Investigator Dr. Arunkumar Pitchaimani, Ph.D., Assistant Professor & Ramalingaswami Fellow, Centre for Biomaterials, Cellular and MolecularTheranostics (CBCMT), Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu, India. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo, etc. on or before (04/07/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date, which will be intimated by email. The selected candidate will be expected to join at the earliest.

Applications are invited for the post of Junior Research Fellow (JRF) for the ANRF (SERB), Govt. of India, Funded Project in School of Biosciences and Technology, VIT, Vellore. Title of the Project : Phosphorylation dependent regulation of Arginine and Glutamine rich protein-1 (ARGLU1) by P21 activated kinase-1 (PAK1) - a regulatable molecular switch with therapeutic potential in breast cancer File : CRG/2022/000911 Qualification : M.Sc in Biochemistry/Genetics/ Molecular Biology Desirable (if any) : Prior experience in Animal Studies & Cell line analysis and training in abroad university Stipend : 31,000 Sponsoring Agency : ANRF (SERB), Govt. of India No. of Positions : 1 Duration : 3 Years Principal Investigator Dr. Ganesh Venkatraman Professor, Department of Biomedical Sciences School of Bio Sciences and Technology (SBST) VIT, Vellore 632 014, Tamil Nadu. . on or before (25/06/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date, which will be intimated by email. The selected candidate will be expected to join at the earliest.

Job Description Position: Medical Coder -Work from Home Ct: HR Kamatchi - 8925264660 Job Description:Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books. Requirement: knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills No of vacancy: 500 Eligibility: Nursing GNM/DGNM Life science graduates Pharmacy Physician assistant Bio medical Engineers Bio chemistry Bio technology Bio informatics Micro biology Zoology and Advanced zoology Biology Botany Plant biotechnology Genetics Food and Nutrition Paramedical Physiotherapy M.Sc. Clinical Nutrition M.Sc. Human Genetics M.Sc. Medical Laboratory Technology M.Sc. Medical Sociology M.Sc. Epidemiology M.Sc. Molecular Virology M.Sc. Biostatistics M.Sc. Blood Banking Technology M.Sc. Rgnerative Medicine M.Optom. M.Sc. Genetic Counseling M.Sc. Radiolog & Imaging Technology M.Sc. Medical Biochemistry M.Sc, Medical Microbiology M.Sc. Clinical Care Technology M.Sc. Clinical Care Technology M.Sc. Medical Physics B.Sc. - Accident & Emergency Care Technology B.Sc. - Audiology & speech Language Pathology B.Sc. - Cardiac Technology B.Sc. - Cardio Pulmonary Perfusion Care Technology B.Sc. - Critical Care Technology B.Sc. - Dialysis Technology B.Sc. - Neuro Electrophysiology B.Sc. - M.L.T. B.Sc. - Medical Sociology B.Sc. - Nuclear Medicine Technology B.Sc. - Operation Theatre & Anaesthesia Technology Bachelor of Science in Optometry B.Sc. - Physician Assistant B.Sc. - Radiology Imaging Technology B.Sc. - Radiotherapy Technology B.Sc. - Medical Record Science B.Sc. - Respiratory Therapy B.Sc. - Fitness and Lifestyle Modifications Accident & Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre & Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology & Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Salary 15K to 17K (fresher) To 50K (experienced) Pm (Incentives && Benefits as per Corporate Standards) 4K fixed hike after six months Other Benefit: 1. Pick Up & Drop Facility 2. Food Facility 3. Day Shift 4. Weekend Off Reach us : HR Kamatchi 8925264660 Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Jobs for Passed outs Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital Perks and Benefits Incentives & Benefits as per Corporate Standards

ct Us: HR Shanmuga Priya 8072891550 This Role is Open to Fresh Graduates with Excellent English Communication Skills. you should have At Least a Diploma/degree in Any Field DESCRIPTION Medical Coding is the Fastest-growing Profession in the Healthcare Industry Today. It is a Niche Specialization and the Demand for Trained and Certified Medical Coders is Increasing Exponentially and Bound to Increase in Upcoming Years, Especially in India. you Pay Strong Attention to Details and are Capable of Delivering Top-quality Work you are Goal-oriented and Thrive in Fast-paced Environments maintains a Working Knowledge of Cpt-4, Icd-10-cm, and Icd-10-pcs Coding Principles, Governmental Regulations, Uhdds (uniform Hospital Discharge Data Set) Guidelines, Aha Coding Clinic Updates, and Third-party Requirements Regarding Coding and Documentation Guidelines Methodology Identify cases eligible for medical reviews and assign these to appropriate reviewers. Reach out to the client for any problems identified in the cases for review. Adhere to Utilization Review Accreditation Commission (URAC), jurisdictional, and/or established MediCall best practice UM time frames, as appropriate. Adhere to federal, state, URAC, client, and established MediCall best practice WCUM time frames, as appropriate. Develop a complete understanding of the Medical management Procedures. Perform medical review assessment (MRA) on utilization of health services (eg healthcare plans, workers compensation products etc) in an accurate, efficient and timely manner while ensuring compliance with utilization management regulations and adherence to state and federal mandates. Provide succinct negotiable points based on the submitted medical records that identify necessary medical treatment, casually related care, response or lack of response to treatment, etc. Identify missing records and information that are necessary in the completion of the medical review assessment. Adhere to Department of Labor, state and company timeframe requirements. Coordinates physician reviewer referral as needed and follows up timely to obtain and deliver those results. Track status of all utilization management reviews in progress and follow up on all pending cases. Work closely with management team in the ongoing development and implementation of utilization management programs. Respond to inbound telephone calls pertaining to medical reviews in a timely manner, following client a established protocols. Process customer calls consistent with program specified strategies and customer satisfaction measurements to include but not limited to proper answering procedure, eg opening and closing remarks. Learn new methods and services as the job requires. Required Skills Medical Coding Freshers Medical Coder Pharmacy Physiotherapy, BPT, MPT Staff Nurse Biotechnology, Biomedical Engineer, Biochemistry Microbiologist, Biology HR Shanmuga Priya 8072891550

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. The mission of our Sustaining R&D team is to protect Endoscopy revenue through our guiding principles of quality, compliance, business continuity and cost reduction. As a member of our team, the R&D Manager II will manage a team of engineers primarily supporting the Endoscopy products made at Boston Scientific s Coyol plant in Costa Rica. He/she will build and lead a high-performing team of engineers located in Coyol, Costa Rica, and execute sustaining projects with cross-functional team members located in Coyol and Marlborough. Your task will be to guide these R&D engineers through continued growth of our product and projects portfolio, in day-to-day technical and business-level decision making, and in hiring and developing top talent. The ideal candidate is expected to have proven the ability to lead and build trust with direct reports, peers and business stakeholders. The candidate demonstrates strong leadership and decision-making skills within a cross-functional core team. Your responsibilities include: Assists in functional deliverables as needed and ensures technical excellence for Sustaining R&D. Provides guidance and approval regarding technical strategies and approaches. Assists in identifying new opportunities to drive Value Improvement Projects and Complaint Reduction efforts. Provides guidance and training to staff, assists subordinates in attaining career goals, motivates individuals to achieve results, and recruits and maintains a high-quality staff. Assists in and/or completes the development of budgets and monitors spending for the Sustaining efforts in Coyol. Assists in identifying and developing department tools and systems. Assists in and/or determines appropriate staff levels, schedules and resources. Works with project managers to understand priorities and plans resource and time allocation accordingly. Collaboratively determines project staff assignments and schedules work to meet completion dates and R&D deliverables. Maintains and enhances cross-functional team relationships. Works cross-functionally in identifying and resolving technical issues. Monitors and evaluates project and department progress and results. Leads and mentors a group or team of employees in the achievement of organizational goals. Guides, coaches, and develops direct reports, and drives best practices throughout the organization. Fosters a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives. May direct and control the activities and budget of one or more functional areas, divisions, product groups, projects/programs and/or operations. What we re looking for in you: 5+ years technical leadership roles, preferably in medical device industry 3-5 years experience in direct people leadership Bachelors required. Preferably in Mechanical Engineering or Biomedical Engineering degree A positive attitude, innovative and creative thinker. Ability to transparently and concisely communicate technical issues and risks across all levels of the organization Experience developing a company culture of knowledge driven product development & engineering excellence Working knowledge of complex mechanical design principles and FDA/BSI regulated medical device design controls Familiarity with statistical analysis and data driven decision making. Understanding of IEC60601 requirements/constraints for mechanical system design is preferred Track record of strong cross-functional collaboration, influence, and project management enabling highly effective project teams Practiced problem solver, proficient in problem solving methodologies (i.e. Six Sigma, DOE, etc.) Passion to learn new technologies and find new solutions Passion for understanding and solving problems for end users and for team member subordinate Takes initiative and acts quickly to drive solutions Solid English/Spanish skills Travel - 15% Requisition ID: 606852 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!

Audit Score Overall summary of the audit score, should meet the targeted values (Monthly) Documentation Consent for all including Data privacy, dialysis prescription, medication prescription, handbooks (100% Compliance) Infection control (90% Compliance) Reprocessing, BMWS, Machine maintenance, Medication Management, Complication Management & Concentrates Preparation Action and closure on NC s (With in DRR, Consumption report. Efficiency (Support to Sr Tech/Clinic In charge to achieve minimum 80%) Cost optimization: Proper utilization of Consumable per treatment, Electricity, water, proper Management of patient and staff roster, repair & maintenance cost by proper handling of machines/equipment s (Support to Sr Tech/Clinic In charge/Admin Executive to achieve the organization Goal) 100% adherence to Lab entries, treatment completeness and patient admission etc in EuCliD Patient Care Management Patient Satisfaction survey score - Quarterly (Satisfaction rating minimum 4.5 out of 5) Patient Dropout and Patient Transfer (Should not be more than 3%) RQMT reporting (100% incidents as per policy need to be report to Sr Tec/Operations) LAB compliance (Serology should be done once in 3 months and Monthly LAB s as per Nephrologist written prescription) Vaccination of patients (As per FMC policy) Support in Implementing and Achieving clinical KPI targets with collaboration with Nephrologist. Patient routine assessment Infection Control Reprocessing Bio Medical waste Machine Disinfection and Maintenance Risk Management Crash cart maintenance Emergency Equipment maintenance Adherence - Company Policies Ensure adherence to company s time & attendance policy Ensure adherence to company s code of conduct & Compliance Maintain the team camaraderie Drive effectively the positive environment for Unit Training: 90% to attendance in training Work Instruction- Compliance to be 100% Attend all hands-on skills Pre-& Post assessment to score above 80% Participate in mock drills in hospitals (90% attendance)

Manager Health Academics | SVYM (Swami Vivekananda Youth Movement) Manager Health Academics Position Summary: Undertake health related academic courses, skilling and training programs Looking for Manager Health Academics Position Summary: Operationalize and manage Health-related academic courses, skilling and training programs, organise continuing medical education and other health-related professional development programs undertaken by SVYM s Vivekananda Memorial Hospital in Saragur Qualification & Experience: Master s Degree Holder in Health Sciences (MPH/MSW or any other postgraduate in Biomedical Sciences) and at least 2 years work experience in the medical/paramedical higher education institutions/ecosystem or in development sector Key Skills: Program Management and Administrative Skills Effective communication (Kannada & English) and stakeholder management skills Organisational and people management skills Outcome and Service Orientation Knowledge of MS Office and basic computer skills Working knowledge of Financial management Ability to write project proposals & report Technical understanding of health-related higher education ecosystem Willing to travel whenever necessary Work Location: Vivekananda Memorial Hospital (VMH), Hanchipura road, Saragur town & taluk Mysuru district Apply for this Job: Upload Your Resume (File types: PDF, Doc, Docx. 5mb Filesize limit)

Job_Description":" Location: Salem (Onsite) Department: Engineering Reports To: Director of AI / Chief Technology Officer Type: Full-time About the Role We are seeking a highly skilled Senior AI/ML Developer to lead the development of advanced machine learning solutions focused on medical data summarization. You will build systems that convert complex, unstructured healthcare datasuch as electronic health records (EHRs), clinical notes, and imaging reportsinto accurate, structured summaries that improve decision-making and streamline patient care. Key Responsibilities - Design, train, and deploy NLP and ML models for summarizing medical records, physician notes, lab data, and radiology reports. - Develop end-to-end ML pipelines for medical data ingestion, preprocessing, information extraction, and summarization. - Fine-tune transformer-based models (e.g., BERT, BioBERT, ClinicalBERT, GPT, LLaMA) for domain-specific NLP tasks. - Apply techniques such as named entity recognition (NER), relation extraction, summarization, and prompt engineering. - Collaborate with clinical informatics experts, data engineers, and product managers to ensure models are clinically relevant and accurate. - Evaluate model performance with healthcare-specific metrics (e.g., ROUGE, BLEU, clinical accuracy). - Ensure solutions meet HIPAA and other healthcare data privacy and security standards. - Mentor junior team members and review code and ML solutions for performance and compliance. Requirements Minimum Qualifications - Bachelors or Masterin Computer Science, Data Science, Biomedical Engineering, or a related field. - 3+ years of experience in machine learning, with a focus on NLP or medical AI. - Proficiency in Python and ML libraries such as PyTorch, TensorFlow, Scikit-learn, Hugging Face Transformers. - Experience with healthcare data formats and standards (e.g., HL7, FHIR, ICD-10, SNOMED CT). - Strong foundation in deep learning, transformers, and sequence models. - Experience deploying models to production environments (cloud, containers, APIs). - Familiarity with privacy and compliance frameworks (HIPAA, GDPR in medical contexts). Preferred Qualifications - Bachelors/Masters Degree or equivalent research/industry experience. - Experience with clinical NLP tools (e.g., cTAKES, MedSpaCy, MetaMap). - Familiarity with MLOps tools and workflows (MLflow, DVC, Airflow). - Publications or contributions to open-source projects in medical AI. - Prior work on medical summarization, LLM fine-tuning, or clinical decision support systems. Tools & Technologies You May Use Languages/Libraries: Python, PyTorch, TensorFlow, Scikit-learn, Hugging Face, Spacy Cloud & MLOps: AWS/GCP, Docker, Kubernetes, MLflow Healthcare-Specific: FHIR, HL7, DICOM, BioBERT, ClinicalBERT Data Handling: Pandas, SQL, Spark, DVC, Airflow Benefits Benefits - Competitive salary with performance-based bonuses - Health insurance - Annual learning & development budget - Opportunities to work on real-world healthcare problems that impact live ","

Applications are invited for the Post of Junior Research Fellowship (JRF) for the DST_SERB Funded Project in the School of Electronics Engineering (SENSE), FILENO. CRG/2023/005678, Vellore Institute of Technology (VIT). Title of the Project : EEG-based investigation of the fundamental frequency coding for source segregation in elderly normal-hearing adults. Qualification : First division Masters Degree in Electronics and Communication Engineering or equivalent with specialization in Signal Processing or B.Tech. in ECE/EIE/EEE/ETC from a recognized University or equivalent. Desirable: GATE/NET qualified; however, non-GATE/NET candidates are also encouraged to apply. Describe if any Candidates must have strong knowledge of Signal Processing and MATLAB software. Additionally, knowledge of Deep Neural Networks will be given more preference. The candidate will acquire the neural representations of speech signals using the EEG device from human subjects (younger and older subjects), apply signal processing techniques to these neural representations to test the hypotheses, and will be responsible for writing project reports, papers, and coordinating project activities. Stipend : 31,000/- (for starting 6 months) and 35,000 (last year) per month for GATE/NET-qualified candidates . Sponsoring Agency : DST-SERB, Government of India. Duration : 1.5 years Principal Investigator : Dr. Anantha Krishna Chintanpalli , Professor in Communication Engineering, School of Electronics Engineering, Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu. Co-Principal Investigator : Dr. R. Sivakumar Professor in Sensor and Biomedical Technology School of Electronics Engineering Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Send your CV along with relevant documents about the details of qualifications, scientific accomplishments, experience (if any), and the latest passport-size photo on or before 27/06/2025. Apply online http://careers.vit.ac.in. No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date, which will be intimated by email. Candidates will be shortlisted based on their merit and as per the requirements of the project. The selected candidate will be expected to join on or before 1 st August 2025. The selected candidate may be permitted to register for the PhD program of VIT Vellore subject to fulfilling the requirements of the PhD qualification process as per the institute norms.

You are an experienced Medical AI Analyst with 2-6 years of experience, adept at working with CT scans on AI platforms. Your role involves data labeling, meticulous observation, and attention to detail when utilizing AI tools for tasks, especially focusing on biomarkers. Analyzing radiology images, tracing, tracking, and marking essential scan details are crucial aspects of your responsibilities. You are responsible for delivering accurate outputs to clients, demonstrating proficiency in presenting CT scans of patients with asthma and lung cancer, and providing biomarker solutions. Your expertise includes precise data collection through navigation and tracking processes using AI-powered software, ensuring quality and efficiency. Coding reports in electronic data forms within Salesforce is within your skill set. Understanding medical images and datasets while aligning with project guidelines is vital for successful project completion. You will be working at iMerit, a leading global provider of data services for Artificial Intelligence in Healthcare. The company's Medical Division collaborates with prominent pharmaceutical companies, medical device manufacturers, and hospital networks to facilitate advancements in Machine Learning. iMerit has a proven track record of supporting cutting-edge technologies like digital radiology, digital pathology, clinical decision support, and autonomous robotic surgery. Recognized as a Great Place to Work for three consecutive years, iMerit fosters an inclusive work culture that promotes professional growth and goal achievement. Emphasizing gender equality, over 50% of the company comprises Women in Tech who actively contribute to innovative AI technologies across various industries. Joining iMerit means becoming part of a dynamic team in a fast-growing technology company, driving advancements in data enrichment, annotation, and labeling for AI and Machine Learning. As a full-time employee, you can benefit from health insurance, leave encashment, paid sick time, Provident Fund, and work-from-home opportunities. Operating on a fixed shift schedule, you will thrive in a collaborative environment focused on technological innovation and career development. For further details and to explore career opportunities, please visit www.imerit.net. (Note: The job type is Full-time, and the application question pertains to the applicant's Highest Qualification. The work location is in person.),

Provides advanced technical support, including comprehensive troubleshooting and escalation support, ensuring accurate diagnostics and resolutions while strictly adhering to regulatory guidelines and safety protocols. Conducts in-depth diagnostics and repairs on complex medical devices, ensuring minimal downtime and optimal performance to meet the critical needs of healthcare providers and patients. Understands implications of work, makes recommendations for solutions, and utilizes experience and in-depth knowledge to complete a wide range of tasks in resourceful and effective ways. Exercises within established procedures, utilizes specialized skills to perform in-depth analysis of assigned tasks, identifying key issues and patterns and resolves moderately complex problems to drive results. Executes thorough pre-visit preparation, ensuring that all necessary parts, tools, and diagnostic information are available to achieve resolution in first visit and enhance customer satisfaction. Handles customer escalations and complaints by following established processes, ensuring accurate information capture, timely resolution, and maintaining high levels of customer service. Takes initiative with medium to high technical complexity support tasks, making informed decisions within defined frameworks to deliver effective solutions and improve device functionality. Engages actively in continuous improvement initiatives, sharing complex solutions and technical knowledge to enhance service quality, efficiency, and team performance. Provides technical mentorship and guidance to junior technicians, sharing expertise, best practices, and technical procedures to improve overall team capabilities and service outcomes. Collaborates with cross-functional teams and the wider organization to identify opportunities for sales or value-added services, supporting business goals and enhancing customer relationships. Minimum required Education: B.E. or B.Tech Minimum required Experience: Minimum 4 years of experience in IT, Network Diagnosis, System Connectivity, Remote Service within Engineering, Medical, Diagnostic Imaging service environment or Electromechanical Industries or Science related environment or equivalent. Preferred Education: Associate Degree in Biomedical/Electronics or related field or equivalent combination of education and experience; Preferred Experience: Minimum 4 years of experience in IGT/MRI/CT (Diagnostic Imaging) service environment or minimum 4 years of experience in Electromechanical industries. with OEM experience preferred, Preferred Skills: Troubleshooting Documentation & Reporting Continuous Improvement Product Installation Product Repair & Maintenance IT Networking Regulatory Requirements Engineering Fundamentals Remote Support Tools & Techniques

Applications are invited for the Post of Project Technical Support-III for the ICMR Funded Project in the School of Bio Sciences and Technology (SBST), at Vellore Institute of Technology (VIT), ( IIRP-2023-3019 dated 04-04-2025) Title of the Project : Preparation and Evaluation of Wound Dressing Material and Topical Ointment Using Magnetosome Conjugated Lemon Grass Extract (MLGE) Qualification : First Class Post-Graduate (PG) Degrees (M.Tech., M.Sc.,) degrees in Biotechnology /Botany /Microbiology or equivalent Describe if any Candidates having knowledge and hands-on experience in the area of animal work/herbal formulations / nanoformualtions / cell culture work will be preferred. Publication records relevant to the field. Fluent in English, both written and spoken. Stipend : Rs. 28,000/- + 10% HRA of Rs. 2800/- Total Rs. 30,800/- per month Sponsoring Agency : ICMR Duration : 11 Months or till the completion of project Principal Investigator : Dr. K. Suthindhiran , Professor, Department of Biomedical Sciences, School of Bio Sciences and Technology Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu. Co-Principal Investigator : Dr. M. A. Jayasri, Associate Professor, Department of Biomedical Sciences, School of Bio Sciences and Technology Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc on or before ( 16/04/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Knowledgeable, developing intermediate level technician performing normal functions under general supervision. Performs scheduled and unscheduled semi-routine repair, maintenance activities and operational condition of all medical equipment, water systems and the physical plant in assigned facilities that ensure patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer s documentation, industry standards and local, state and federal regulatory requirements. Performs cost containment activities related to repair and maintenance and monthly Technical CQI/QAI duties. Functions as an equipment trouble-shooter to identify and ensure resolution to problems. PRINCIPAL DUTIES AND RESPONSIBILITIES: Under general supervision, performs moderate scope semi-routine tasks in nature requiring full knowledge of general aspects of the job, including but not limited to the following: Repair and Maintenance: Performs and/or oversees timely maintenance, troubleshooting, and repair activities to water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as required and recommended by the manufacturer and established company policy and procedures, including maintaining aesthetics of the equipment and water room. Coordinates and completes scheduled and unscheduled repair and maintenance of physical plant by company approved vendors. Oversees maintenance of all ancillary devices assuring it follows manufacturer s recommendations and in compliance with company policies and procedures, industry standards and local, state and federal regulatory requirements. Acts as equipment trouble-shooter , identifying where problems exist and recommending resolution as needed utilizing acquired knowledge of company machinery, equipment, and systems. Purchases and maintains an inventory of service parts using approved sources and ensures RGA and warranty parts are returned in a timely manner. Performs water/dialysate sample collection and processing, and reviews, evaluates, and reports quality results per applicable policies and procedures. Documents all daily, weekly, monthly repair and maintenance activity/repairs per applicable policies and/or procedures. Oversees and updates project tracking or other company tracking/documentation systems as assigned. Regulatory Compliance: Performs monthly Technical CQI/QAI duties. Analyzes, assembles, and assimilates information and data for the CQI/QAI process and leads technical discussion, including reporting outcomes and creating and implementing improvement plans. Collaborates with facility staff to ensure all regulatory and OSHA requirements are met. Reviews water system documentation to verify compliance (i.e. readings are within parameters). Performs daily, weekly, and monthly trend analysis on the water system, anticipating appropriate action to assure system functions as designed. Identifies instances where company policy and procedures are not being met including escalation of issues to next level management. Medical Supply Inventory: Manages Program s Medical Supply Inventory by managing par values, making sure program has the correct inventory to support the patient treatments, performing physical inventory counts and generating a physical inventory report. Miscellaneous, Operational and Educational: Must maintain water treatment equipment qualification by completing Annual Water Training. Supports clinical education by administering return demonstrations during Annual Water Training. Must maintain current required certifications. Monitors and reviews patient care staff s technique for testing water system, assuring tests and documentation meet policy and comply with manufacturer s specifications for the devices and test equipment used. Attends and successfully completes all technical training programs required by state/federal regulations and company policy. Refer to Biomedical Technician Career Pathway Department Operating Guideline for full list of training requirements. Transports equipment as needed. Escalates issues to supervisor for resolution, as deemed necessary. Acts as a mentor, role model and resource for technical staff by setting an example of appropriate behavior, work habits and attitudes towards patients, coworkers, and management. At supervisor s discretion, assists technical staff with general tasks that require a better understanding of functions and provides mentorship and training to new technical staff. Works toward becoming subject matter expert in one or more areas through continued learning in professional subjects. Other related duties as assigned. PHYSICAL DEMANDS AND WORKING CONDITIONS: The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Employees are required to take the Ishiharas Color Blindness test as a condition of employment. Note that, failing the Ishihara Test for Color Blindness does not preclude employment. The Company will consider whether reasonable accommodations can be made. Position involves active work including lifting, bending, walking and standing for considerable lengths of time. The use of dollies or other equipment is mandatory when moving heavy weight items. May be required to frequently lift items weighing up to 50 lbs. as high as 5 feet. There is potential exposure to chemicals and infectious materials. Scope of work includes high voltage equipment. Personal Protective Equipment (PPE) is provided by the company. Work environment is typically air temperature controlled with moderate noise levels. May be required to work in various outdoor elements. Evening and weekend availability, as well as ability to take on-calls are required. Overnight travel may be required. SUPERVISION: None EDUCATION AND REQUIRED CREDENTIALS: High school diploma or G.E.D. required. Successful completion of the Biomedical Technician Education Curriculum and Practicum. Associate or Bachelor Degree in electronics / biomedical technology, or equivalent a plus. Nephrology/Biomedical Industry Technical Certifications preferred - Board of Nephrology Examiners Nursing and Technology (BONENT), Certified Hemodialysis Technician (CHT), National Nephrology Certification Organization (NNCO), Certified Biomedical Nephrology Technician (CBNT), Water Quality Association (WQA) Water Treatment Specialist (WTS), Association for the Advancement of Medical Instrumentation (AAMI), Certified Biomedical Equipment Technician (CBET) Valid Drivers License issued in the employee s state of residence required. EXPERIENCE AND REQUIRED SKILLS: 1 - 2 years as a Biomedical Technician level I with successful completion of all required training, education curriculum and practicum and meet all other promotion requirements as outlined in the Biomedical Technician Career Pathway Department Operating Guideline. Or 2+ years directly related experience working in an industrial/medical technical setting, 1+ years directly related experience with an Associate Degree in electronics/biomedical technology, or Bachelor Degree in electronics/biomedical technology with no experience - Must successfully complete all required training, education curriculum and practicum within the first 24 months from date of hire / job entry date. Manual dexterity required - ability to use common hand tools and small power equipment. Strong verbal and written communication skills with the ability to comprehend and communicate in the English language. Proficient computer skills with the ability to navigate through common operating systems, such as Microsoft Office, SAP and TMS products. Ability to work a flexible schedule including nights, weekends and holidays.

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

Detailed job description - Skill Set: Technically strong hands-on Self-driven Good client communication skills Able to work independently and good team player Flexible to work in PST hour(overlap for some hours) Past development experience for Cisco client is preferred.

Job Summary In this role, you will be responsible for supporting new product development and technology initiatives in the Advanced Technology and Design Engineering Team. This role will provide Mechanical Engineering support to a multidisciplinary team of Mechanical, Biomedical, and System Engineers in collaboration with Hardware, Firmware, and Industrial Engineers. The team conducts research and support s visualization of new and innovative conceptual products by modeling, designing, specifying, and integrating electrical/mechanical components into system-level designs. This level role provides the opportunity for exposure to fundamental mechanical engineering principles and concepts. Essential Duties and Responsibilities With guidance, support and supervision from Leads and Sr. Engineers, Provides mechanical engineering support to a global team of multidisciplinary engineers to develop multiple new product concepts with committed timelines and project goals per established governance policies, best practice, and guidelines. Functions as a Mechanical Engineering resource to the Project Team. Supports projects as assigned by the Engineering Manager. Generates 3D CAD models and 2D drawings of product concepts. Prepares and presents detailed technical presentations, reports and design documentation as required. Generate intellectual property referenced to the mechanical design. Generates reports to document test findings, learnings, and research efforts. Estimates technical requirements and breaks down work to user stories and tasks. Plans, develops, tests, deploys different solutions in a DevOps environment. Work on various prototypes, or proof of concept, to test solution. Solve routine and standard problems. Other relevant duties as assigned. Additional Responsibilities Must be able to interpret data, reading or writing, public speaking express or exchange ideas with employees, understand direction and adhere to established procedures Must be able to own and be held responsible for assigned activities while contributing to a team and collaborating with others across multiple business functions This position requires a highly organized person who is articulate and personable, is technically sound, acts as a resource for other team members, is willing to grow in an agile environment, and demonstrates initiative and commitment to quality in all tasks. Education Bachelor s degree with emphasis in Mechanical Engineering or equivalent experience. Work Experience No min required required Preferred Knowledge, Skills and Abilities Basic understanding of Engineering principles. Mechanical Engineering & Design Skills Early Concept Development and Prototyping Proficient with Solid works, FEA Software, Microsoft Office suite software Knowledge of Six Sigma DFSS Techniques Knowledge of Mathcad, LabView, or other Modeling Tools and experience Exposure to DFMEA, PFMEA and other Risk Management Tools Exposure to DOE, Statistical Analysis, Minitab experience preferred. Demonstrated ability to work with team members across functional groups. Strong multi-tasking skills and ability to juggle/prioritize multiple programs. License and Certifications Travel Requirements None: No travel required 10%: Up to 26 business days per year Physical Requirements Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects. Additional Requirements

About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About the role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturers quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* About you Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology In addition to a relevant educational degree, candidates must have a minimum 4 years work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.