464 Biomedical Jobs - Page 18

Purchase Review of Comparative Quotes Conducting Negotiation Meetings Co coordinating for Approval for Negotiated Work/Purchases Ensuring timely release of Purchase/Work orders Vendor Management Procurement Planning Interaction with User department Team Management Commercial tie-ups for outsourced tests Inventory Setting up of Processes Review Monitoring Stores activities to ensure the SOP is followed MIS Statutory compliance Vendor Dispute resolution Interaction with user Department Team Management Billing Planning strategizing on Pricing Approval of Discount Handling Escalations on Billing complaints Interaction with Doctors on Billing related matters Team Management Job description: Manage end to end procurement process for high end medical equipment s to and low-end equipment s Work closely with Head of Technical Operations to evaluate alternate platforms for tests to minimise cost of consumption and wastage Receive and process procurement requests from Business units i.e Hospitals, clinics, Labs, Tele Health and new projects and provide frequent updates on status of requests. Participate in procurement committee meetings and provide management with weekly reports on status of procurement requests Prepare quarterly procurement performance reports and market research reports for review by management Develop and maintain a list of approved suppliers to track quality of supplies/equipment, encourage competitive pricing and ensure timely awards and execution of contracts Develop and maintain strong professional relationships with suppliers to encourage prompt responses to requests, open dialogue and cooperation in identifying best options that add value to purchasing decisions Develop Enterprise procurement strategy for Biomedical equipment procurement and AMC/CMC contracts Liaise with suppliers to ensure adherence to contract agreements and lead corrective action plans in the instance of breach of contract Preparation and upkeep of materials database / library Evaluate product / arrange the equipment demo to users before negotiation Take on any other related duties which may be assigned

Position : Information Specialist Literature Intelligence Experience: At least 3-5 years of relevant pharma industry or research experience, working in information sciences, knowledge management or corporate library operations. Proven scientific literature searching skills with experience utilizing pharmaceutical databases and resources. Good communication and presentation skills. In addition, knowledge, and experience of working in the fields of text mining, NLP and Knowledge graphs will be preferred. Languages: Fluent spoken and written English Education: Doctor in Pharmacy or equivalent with relevant scientific background, advanced Pharmacy degree or advanced degree in Life Sciences such as Biology or Pharmacology. CTC : 11 - 14 LPA Location : Hyderabad Tenure : 6 Months Major Accountabilities Knowledge of pharmaceutical industry: effective researching of product terminology/drug nomenclature, drug class hierarchies and competitors • Product database knowledge: OVID, Embase.com, Pharmaprojects, Cortellis, Medline, Pubmed etc. • Ability to effectively construct precise drug literature search strategies • Understanding of medical terminology Proficient in alert strategy creation \• Ability to perform comprehensive review of literature and analysis of scientific and technical published literature to support health agency requests, product submissions, formulary reviews, etc. • Advanced bibliographic expertise and information management • Proficient in citation management tools, i.e. End Note • Action oriented. Ability to meet deadlines and handle multiple projects simultaneously Ability to effectively correspond written and oral, with scientific/medical associates • Ability to collaborate with global colleagues Key Performance Indicators o Timeliness project initiation, alert creation o Researching skills to develop robust search strategies. Delivery of literature intelligence solution with 100% quality and timeliness o Excellent feedback on projects from business colleagues Strong stakeholder management o Innovative mindset to drive efficiencies and develop disruptive solutions of high value. High learning agility to learn and implement the latest tools/technologies – AI, text mining, chat GPT, Knowledge graph, etc. Interested candidates share cv : busiraju.sindhu@manpower.co.in Whats App : 7013970562

Analyze and manage Healthcare data Follow international healthcare regulations Work on healthcare documentation processes with timely submission Assist in the analysis and categorization of medical data for reporting purposes

This project is based in the neonatal intensive care unit. It recruits neonates (later preterm and term) who are at risk of acute kidney injury and monitors them using a near-infrared spectroscopy device (NIRS). The machine is attached to the neonate and the readings are recorded and stored. Other demographic and clinical data variables are documented. All neonates enrolled in the study are followed up at 3, 6 and 12 months for kidney function parameters. Project Research Scientist-1 (Non Medical) Position Starting: 15th March, 2025 No. of Vacancy: one Preferred Qualifications: First class post graduate degree including integrated PG degrees Second class postgraduate degree including integrated PG degrees with PhD Basic computer operating skills Salary: 56,000 +16,800 HRA (total 72,800 pm) Language : English, Kannada, Hindi Preferable Tamil, Telugu Experience: At least 1 year experience of working in a biomedical research project Last Day for Receiving Application: 10th March, 2025 Roles and Responsibilities: To ensure all eligible neonates are included in the study To ensure complete data collection of all neonates recruited in the study. To maintain the research documents of every enrolled subject. Data entry of all the data related to the study To communicate with families during the hospital stay, and at discharge and liaise between the research team and the patient s families To communicate with families and liaise with them to ensure follow-up during the first year after discharge To support families with getting appointments for follow-up and the investigations to be done at follow-up To support timely report submission to ICMR and IEC. To maintain the documents and bills related to the expenses of the study Interested candidates may send their Resume to: The Principal Investigator ICMR NIRSneo Project

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

PCB Layout Engineer Apply Now Hyderabad, Telangana, India Job Type Full Time About the Role We are looking for experienced PCB Layout Engineer to join our team for developing a robust, scalable, and user-friendly automation system and Solutions. The ideal candidates will have hands-on experience with both PCB Design and Schematic Design and development and will be responsible for the full PCB DFM development lifecycle. Requirements Key Responsibilities: PCB Design & Layout: Develop high-quality PCB layouts from schematics using Altium Designer and other CAD tools. Prepare design files for PCB fabrication and assembly, ensuring manufacturability and adherence to design rules. Collaboration & Documentation: Work closely with the hardware engineering team to interpret schematics and design specifications. Maintain thorough documentation of design revisions and process changes. Design Verification & Optimization: Perform design reviews and implement necessary changes to meet performance and reliability requirements. Optimize board layouts for signal integrity, thermal management, and electromagnetic compatibility. Cross-functional Coordination: Collaborate with production teams to resolve any design or manufacturing issues. Coordinate with suppliers to ensure the feasibility and cost-effectiveness of PCB designs. Required Qualifications: Bachelor s degree in Electronics, Electrical Engineering, or a related field. 1-3 years of experience in PCB layout/design, preferably using Altium Designer. Strong understanding of schematic capture, component placement, routing techniques, and PCB fabrication processes. Familiarity with other CAD tools and design standards. Excellent attention to detail and problem-solving skills. Good communication skills and ability to work collaboratively in a team environment. We Offer: Competitive salary and benefits package. Opportunities for professional growth and development. A dynamic, collaborative work environment focused on innovation. Exposure to cutting-edge technologies and projects in embedded systems and IoT. How to Apply: Interested candidates are invited to submit their resume and cover letter for consideration. About the Company EURTH TECHTRONICS PVT LTD is a company that s specialized in the Manufacturing, Research and Development of innovative Consumer Electronics. Specifically, the company aims at developing and commercializing next generation Technology with various such other products in IoT, Block Chains, NFT s and Crypto spaces. Using a wide range of technologies such as electronics, embedded software, signal processing, biomedical engineering, mechanical engineering, material sciences and optics will be a day to day job. The aim of Sales and Marketing is to maintain and improve the current marketing methods in existence in the organization and to develop innovations that strengthen the organization s position in the marketplace. We currently are catering to B2B and the company envision to step in in to B2C markets. Apply Now

Role : MEP - Experience : 2years to 12years- Fit out experience Location :Hyderabad Qualification : B. E/B. Tech in Civil & Electrical/Mechanical Roles and responsibilities-MEP-INTERIOR FITOUT Review and analysis all MEP drawing materials, Schedules/programs of work, etc. Coordinating all electro-mechanical activities with the various teams on site. Review the shop drawings, construction details, product data, material samples, inspection plans, method statements, delivery schedules to confirm compliance with the requirements of the project. Reviewing submittals prior to the submission to the consultant. Ensure the civil obstruction have been cleared to the MEP contractors with MEP activities. Engage with authority at the beginning of the project to ensure that all temporary utilities (power and water) are provided on time and do the same with closing out of project to ensure the disconnection of utility services. Ensure the harmonies working relationship between the contractor and the consultants, understanding that open communication and team work are to be promoted and that an adversarial management style will be detrimental to the project. Coordinating between MEP and civil drawings at the site. Coordination and attending meeting with subcontractors, contractor & consultant, client, supplier. Materials / Work inspection to inspect with a consultant. Day to day monitoring work and planning entire work. Monitoring of work as per specification and standards. Identification of subcontractors and suppliers& collecting questions & close coordination with subcontractors. Rising IR, IIR of site MEP works for consultant approval or in case of any clarification required. Attending authority inspections as per the project schedule. Attending all testing & commissioning of MEP service Role - C & I - 2years to 12years- Fit out experience Location :Hyderabad Qualification : B. E/B. Tech in Civil-Arch Coordination with Architect and consultants for design development and site coordination . All stakeholder management and work progress monitoring onsite. Weekly and monthly meetings. with client and all stakeholders Delivering the projects as per clients agreed timelines. Quality control at all stages of the project . Checking the installations as per approved checklists. Attending the site walk for Handing over of project to the clients and rectifications of observed points. Role - EHS/Safety - 2+years Location - Hyderabad Qualification - Diploma in Industrial safety/Fire & Safety Daily EHS audit and monthly safety performance report as per company standard practices Weekly EHS walk with Project Team & EHS meeting with Project management. Preparation of minutes of meeting as per EHS guideline & QST requirements for audit Ensure site Audit report External and IMS audit with Internal audit team. Conducting daily toolbox training and various EHS training like safety induction training, Reverse training, Job specific training, BBS training, First aid training, incident accident awareness training. Conduct periodic safety inspections on all sitework locations to ensure safety procedures are in place. Preparation, implementation and submission HIRA and SOP as per the site activities. Perform and oversee the investigation of accidents, injuries, and unsafe working conditions including interfacing with workers compensation claims. Preparation, Implement and submitting of the waste management plan (solid waste, E-waste, Plastic waste, Biomedical waste, and Biodegradable waste and used oil) as per BOCW norms. Conducting emergency evacuation Mock drill and other specific mock drill (fall from height, structural collapse, scaffolding collapse, electrical shock, fire etc. ) Identify hazards and compliance with coordination of all departments. Ensure the permit system for providing access to the any work carried out from contractors or vendors. Maintaining firefighting equipment and all types of signage s in the premises Organizing and Celebrate EHS events like (National Safety Day, Fire service day/week, Road Safety Day or week and Environmental day. )

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

Novartis Biomedical Research is seeking an experienced and highly motivated data and MLOps scientist/engineer/wizard to help us push the frontiers of data science and machine learning for Life Sciences and drug discovery. Within the Research Informatics division on Biomedical Research, you will take on a hands-on data scientist role at the intersection of science, R&D and real-world impact. You will be a part of a truly unique organization with an inter-disciplinary team made up of accomplished scientists who are at the forefront of AI/ML in drug discovery. You will have the opportunity to shape the next wave of drug discovery, combining insights from a wealth of data modalities including various omics datasets (genomics, transcriptomics, proteomics), spatial omics technologies, compound structures, protein sequences and structures, compound activity, protein structures, measurements from cellular experiments and safety studies, histopathology, clinical imaging, and clinical readouts. This is a senior individual contributor role and will require demonstrated and current hands-on experience in Python, R, cli/shell scripting, diverse ML workflows, who can perform under minimum supervision in a highly collaborative environment. Job Description Key Responsibilities: Collaborate closely with data scientists and subject-matter experts to fulfill data and computational needs. Validate and ensure the accuracy and quality of data by cleaning, shaping, and sometimes analyzing, normalizing, and conforming it to existing models and vocabularies. Identify and rectify data inconsistencies and irregularities. Design data models and prepare data artifacts to effectively meet business needs. Promote culture of transparency and communication regarding data modifications, lineage, and definitions to all stakeholders Essential Requirements : Python and/or R, and any other scripting language. Experience with HPC, cloud (AWS) workflows, setup and deployments. Experience deploying ML models along with resolving package dependencies) from github, huggingface, etc., successfully. Experience with DevOps, MLOps Demonstrable data management expertise in relational, document, column and graph datastores. Experience building ETL processes in high-performance environments like Databricks, AWS, Snowflake. Experience with python ML frameworks: Pytorch, tensorflow is a plus. Experience with several bioinformatics tools for sequence matching, alignment, clustering is a plus. data imputation and visualisation methods. Strong background in extracting relevant data from diverse sources (excel sheets, powerpoint, csv, database queries, etc.) with varying formats and potentially missing or mislabeled information. Experience and familiarity with various data types, including images, tabular, unstructured, and text. Experience working with other subject matter experts to actively solicit information needed to harmonise datasets into machine learnable form. Experience in document mining and processing diverse data sources. Experience working with several large public scientific (preferably biology-related) data sources is a plus. Experience with validating the data accuracy and quality of data by cleaning, shaping, analyzing, normalizing, and conforming it to existing models and vocabularies. Strong interest in the latest relevant literature and application of ML and data science to the biological sciences, is a plus. Understanding and working vocabulary about common machine-learning concepts (training sets vs. test sets, over/under fitting, bias, annotations, feature extraction, RAG, LLMs, classifiers, and so on) Excellent English-language oral and written communication skills. Proactive communication habits: asking questions and seeking clarifications when necessary. Desirable Requirements: BS in Computer Science, Informatics or similar, or equivalent practical experience. Fluency in English You ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https: / / www.novartis.com / careers / benefits-rewards Skills Desired Algorithms, Computer Programming, Computer Science, Computer Vision, Data Science, People Management, R&D (Research And Development), Solution Design, Waterfall Model

Welcome to the era of Velsera! Seven Bridges, Pierian UgenTec have combined to become Velsera. Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision RD, expand access to, and more effectively leverage analytics at the point of care. We unify technology-enabled solutions and scientific expertise to enable a continuous flow of knowledge across the global healthcare ecosystem. This interweaves diverse biomedical communities, allowing them to build upon each other s success and accelerate medical breakthroughs that positively impact human health. With our headquarters in Boston, MA, we are growing and expanding our team which located in 14 different countries! What will you do Train, fine-tune, and deploy Large Language Models (LLMs) to solve real-world problems effectively. Design, implement, and optimize AI/ML pipelines to support model development, evaluation, and deployment. Collaborate with Architect, software engineers, and product teams to integrate AI solutions into applications. Ensure model performance, scalability, and efficiency through continuous experimentation and improvements. Work on LLM optimization techniques, including Retrieval-Augmented Generation (RAG), prompt tuning, etc. Manage and automate the infrastructure necessary for AI/ML workloads while keeping the focus on model development. Work with DevOps teams to ensure smooth deployment and monitoring of AI models in production. Stay updated on the latest advancements in AI, LLMs, and deep learning to drive innovation. What do you bring to the table Strong experience in training, fine-tuning, and deploying LLMs using frameworks like PyTorch, TensorFlow, or Hugging Face Transformers. Hands-on experience in developing and optimizing AI/ML pipelines, from data preprocessing to model inference. Solid programming skills in Python and familiarity with libraries like NumPy, Pandas, and Scikit-learn. Strong understanding of tokenization, embeddings, and prompt engineering for LLM-based applications. Hands-on experience in building and optimizing RAG pipelines using vector databases (FAISS, Pinecone, Weaviate, or ChromaDB). Experience with cloud-based AI infrastructure (AWS, GCP, or Azure) and containerization technologies (Docker, Kubernetes). Experience in model monitoring, A/B testing, and performance optimization in a production environment. Familiarity with MLOps best practices and tools (Kubeflow, MLflow, or similar). Ability to balance hands-on AI development with necessary infrastructure management. Strong problem-solving skills, teamwork, and a passion for building AI-driven solutions. Our Core Values People first. We create collaborative and supportive environments by operating with respect and flexibility to promote mental, emotional and physical health. We practice empathy by treating others the way they want to be treated and assuming positive intent. We are proud of our inclusive diverse team and humble ourselves to learn about and build our connection with each other. Patient focused. We act with swift determination without sacrificing our expectations of quality . We are driven by providing exceptional solutions for our customers to positively impact patient lives. Considering what is at stake, we challenge ourselves to develop the best solution, not just the easy one. Integrity. We hold ourselves accountable and strive for transparent communication to build trust amongst ourselves and our customers. We take ownership of our results as we know what we do matters and collectively we will change the healthcare industry. We are thoughtful and intentional with every customer interaction understanding the overall impact on human health. Curious. We ask questions and actively listen in order to learn and continuously improve . We embrace change and the opportunities it presents to make each other better. We strive to be on the cutting edge of science and technology innovation by encouraging creativity. Impactful. We take our social responsibility with the seriousness it deserves and hold ourselves to a high standard. We improve our sustainability by encouraging discussion and taking action as it relates to our natural, social and economic resource footprint. We are devoted to our humanitarian mission and look for new ways to make the world a better place. Velsera is an Equal Opportunity Employer: Velsera is proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, colour, gender, religion, marital status, domestic partner status, age, national origin or ancestry.

Welcome to the era of Velsera! Seven Bridges, Pierian UgenTec have combined to become Velsera. Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision RD, expand access to, and more effectively leverage analytics at the point of care. We unify technology-enabled solutions and scientific expertise to enable a continuous flow of knowledge across the global healthcare ecosystem. This interweaves diverse biomedical communities, allowing them to build upon each other s success and accelerate medical breakthroughs that positively impact human health. With our headquarters in Boston, MA, we are growing and expanding our team which located in 14 different countries! What will you do 1. AI Model and Pipeline Validation Design and implement test plans and test cases for AI frameworks to ensure comprehensive validation of functionality, accuracy, and performance. Validate AI model outputs, identify discrepancies, and report bias in results. Ensure end-to-end validation of data pipelines, including data ingestion, preprocessing, transformation, and model deployment. Identify and resolve functional and non-functional issues in AI models and data workflows. 2. Test Automation Scripting Develop and execute automated test scripts using Python. Utilize test automation tools like Selenium, PyTest, or similar frameworks to enhance testing efficiency. Implement CI/CD testing frameworks for AI/ML pipelines. 3. Cloud-Based AI Testing Conduct AI application testing on cloud platforms such as AWS, Azure, and Google Cloud. Ensure AI model performance remains optimal across different environments and scenarios. Validate large datasets, ensuring data preprocessing, augmentation, and quality assurance. 4. AI/ML Model Performance Testing Identify and report bottlenecks in AI models. Conduct stress testing for AI models in real-world use cases. 5. Collaboration Quality Assurance Work closely with AI/ML engineers, data scientists, and software engineers to define quality standards. Contribute to compliance with AI-related regulatory and industry best practices. Document and maintain test cases, defect reports, and validation procedures for AI systems. What do you bring to the table Strong experience in designing and implementing test cases for AI frameworks. Experience in validating AI model outputs and identifying discrepancies or biases. Attention to detail in identifying functional and non-functional issues in AI models. Proficiency in scripting and developing automated test scripts using Python Hands-on experience with test automation tools (Selenium, PyTest, etc.). Experience with cloud-based testing platforms (AWS, Azure, Google Cloud). Preferred Skills: Familiarity with validating large datasets and ensuring data quality. Knowledge of AI/ML model evaluation tools like TensorFlow, Keras, PyTorch. Experience in performance testing of AI models in diverse environments. Our Core Values People first. We create collaborative and supportive environments by operating with respect and flexibility to promote mental, emotional and physical health. We practice empathy by treating others the way they want to be treated and assuming positive intent. We are proud of our inclusive diverse team and humble ourselves to learn about and build our connection with each other. Patient focused. We act with swift determination without sacrificing our expectations of quality . We are driven by providing exceptional solutions for our customers to positively impact patient lives. Considering what is at stake, we challenge ourselves to develop the best solution, not just the easy one. Integrity. We hold ourselves accountable and strive for transparent communication to build trust amongst ourselves and our customers. We take ownership of our results as we know what we do matters and collectively we will change the healthcare industry. We are thoughtful and intentional with every customer interaction understanding the overall impact on human health. Curious. We ask questions and actively listen in order to learn and continuously improve . We embrace change and the opportunities it presents to make each other better. We strive to be on the cutting edge of science and technology innovation by encouraging creativity. Impactful. We take our social responsibility with the seriousness it deserves and hold ourselves to a high standard. We improve our sustainability by encouraging discussion and taking action as it relates to our natural, social and economic resource footprint. We are devoted to our humanitarian mission and look for new ways to make the world a better place. Velsera is an Equal Opportunity Employer: Velsera is proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, colour, gender, religion, marital status, domestic partner status, age, national origin or ancestry.

Welcome to the era of Velsera! Seven Bridges, Pierian UgenTec have combined to become Velsera. Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision RD, expand access to, and more effectively leverage analytics at the point of care. We unify technology-enabled solutions and scientific expertise to enable a continuous flow of knowledge across the global healthcare ecosystem. This interweaves diverse biomedical communities, allowing them to build upon each other s success and accelerate medical breakthroughs that positively impact human health. With our headquarters in Boston, MA, we are growing and expanding our team which located in 14 different countries! What will you do Lead and participate in collaborative solutioning sessions with business stakeholders, translating business requirements and challenges into well-defined machine learning/data science use cases and comprehensive AI solution specifications. Architect robust and scalable AI solutions that enable data-driven decision-making, leveraging a deep understanding of statistical modeling, machine learning, and deep learning techniques to forecast business outcomes and optimize performance. Design and implement data integration strategies to unify and streamline diverse data sources, creating a consistent and cohesive data landscape for AI model development. Develop efficient and programmatic methods for synthesizing large volumes of data, extracting relevant features, and preparing data for AI model training and validation. Leverage advanced feature engineering techniques and quantitative methods, including statistical modeling, machine learning, deep learning, and generative AI, to implement, validate , and optimize AI models for accuracy, reliability, and performance. Simplify data presentation to help stakeholders easily grasp insights and make informed decisions. Maintain a deep understanding of the latest advancements in AI and generative AI, including various model architectures, training methodologies, and evaluation metrics . Identify opportunities to leverage generative AI to securely and ethically address business needs, optimize existing processes, and drive innovation . Contribute to project management processes, providing regular status updates, and ensuring the t imely delivery of high-quality AI solutions. Primarily responsible for contributing to project delivery and maximizing business impact through effective AI solution architecture and implementation . Occasionally contribute technical expertis e during pre-sales engagements and support internal operational improvements as needed. What do you bring to the table A bachelors or masters degree in a quantitative field (e.g., Computer Science, Statistics, Mathematics, Engineering) is required . The ideal candidate will have a strong background in designing and implementing end-to-end AI/ML pipelines, including feature engineering, model training, and inference. Experience with Generative AI pipelines is needed . 8+ years of experience in AI/ML development, with at least 3+ years in an AI architecture role. Fluency in Python and SQL and noSQL is essential. Experience with common data science libraries such as pandas and Scikit-learn, as well as deep learning frameworks like PyTorch and TensorFlow, is required. Hands-on experience with cloud-based AI/ML platforms and tools, such as AWS (SageMaker, Bedrock), GCP (Vertex AI, Gemini), Azure AI Studio, or OpenAI, is a must . This includes experience with deploying and managing models in the cloud. Our Core Values People first. We create collaborative and supportive environments by operating with respect and flexibility to promote mental, emotional and physical health. We practice empathy by treating others the way they want to be treated and assuming positive intent. We are proud of our inclusive diverse team and humble ourselves to learn about and build our connection with each other. Patient focused. We act with swift determination without sacrificing our expectations of quality . We are driven by providing exceptional solutions for our customers to positively impact patient lives. Considering what is at stake, we challenge ourselves to develop the best solution, not just the easy one. Integrity. We hold ourselves accountable and strive for transparent communication to build trust amongst ourselves and our customers. We take ownership of our results as we know what we do matters and collectively we will change the healthcare industry. We are thoughtful and intentional with every customer interaction understanding the overall impact on human health. Curious. We ask questions and actively listen in order to learn and continuously improve . We embrace change and the opportunities it presents to make each other better. We strive to be on the cutting edge of science and technology innovation by encouraging creativity. Impactful. We take our social responsibility with the seriousness it deserves and hold ourselves to a high standard. We improve our sustainability by encouraging discussion and taking action as it relates to our natural, social and economic resource footprint. We are devoted to our humanitarian mission and look for new ways to make the world a better place. Velsera is an Equal Opportunity Employer: Velsera is proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, colour, gender, religion, marital status, domestic partner status, age, national origin or ancestry.

Embedded Software Team Lead / Manager Apply Now Hyderabad, Telangana, India Job Type Full Time About the Role We are looking for experienced Embedded Software Manager to join our team for developing a robust, scalable, and user-friendly automation system. The ideal candidates will have hands-on experience with both Hardware and IoT development and will be responsible for the full Product development lifecycle Requirements Job Summary: Eurth Tech is seeking an experienced and dynamic leader to drive our Embedded Software Development Team. The successful candidate will be responsible for managing the team, overseeing the development of embedded systems and IoT solutions, and ensuring high quality and timely delivery of projects. This role combines technical expertise with strong leadership and project management skills. Key Responsibilities: Team Leadership Mentoring: Lead, mentor, and manage a team of embedded engineers. Facilitate professional growth and provide technical guidance. Project Management: Oversee project planning, timelines, and resource allocation. Ensure projects are delivered on time and meet quality standards. Technical Oversight: Drive the design, development, and maintenance of embedded systems and software. Ensure adherence to best practices through rigorous code reviews and testing. Collaboration: Coordinate with cross-functional teams including hardware, product management, and quality assurance. Communicate project progress, challenges, and milestones to senior management. Process Improvement Innovation: Develop and implement process improvements to boost efficiency and quality. Stay updated with industry trends to drive innovation and enhance our technical strategy. Documentation Compliance: Oversee the creation and maintenance of technical documentation and ensure compliance with industry standards. Required Qualifications: Bachelor s or Master s degree in Electrical Engineering, Computer Engineering, or a related field. Minimum of 5 years of experience in embedded software development. Proven experience in a leadership or team management role. Strong programming skills in C/C++ and familiarity with Python. Expertise in microcontroller programming, peripheral interfaces, and wireless communication protocols (Bluetooth, Wi-Fi). Working knowledge of real-time operating systems and Linux-based systems. Experience with agile methodologies and version control systems (e.g., Git). Excellent communication, analytical, and problem-solving skills. We Offer: Competitive salary and benefits package. Opportunities for career advancement and professional development. A dynamic, fast-paced, and collaborative work environment. The chance to work on cutting-edge technology and contribute to impactful projects. How to Apply: Interested candidates are invited to submit their resume and cover letter for consideration. About the Company EURTH TECHTRONICS PVT LTD is a company that s specialized in the Manufacturing, Research and Development of innovative Consumer Electronics. Specifically, the company aims at developing and commercializing next generation Technology with various such other products in IoT, Block Chains, NFT s and Crypto spaces. Using a wide range of technologies such as electronics, embedded software, signal processing, biomedical engineering, mechanical engineering, material sciences and optics will be a day to day job. EURTH TECHTRONICS PVT LTD is a company that s specialized in the Manufacturing, Research and Development of innovative Consumer Electronics. Specifically, the company aims at developing and commercializing next generation Technology with various such other products in IoT, Block Chains, NFT s and Crypto spaces. Using a wide range of technologies such as electronics, embedded software, signal processing, biomedical engineering, mechanical engineering, material sciences and optics will be a day to day job. Apply Now

Job Location: Kolkata Job Type: Full Time Qualification: Any Graduate/B.Sc (Chemistry)/ B.Sc (Biotechnology) Bachelors degree in Chemistry/Bio Chemistry/Bio Tech Experience: 5 - 10 Years Job Overview Accurex Biomedical is seeking an experienced and driven Regional Sales Manager (RSM) to lead and expand our sales operations in the Eastern India region. The RSM will be responsible for developing sales strategies, managing distributor networks, and driving revenue growth while maintaining strong customer relationships. Key Responsibilities Industry Experience: 5+ years in IVD, Diagnostics, or Medical Devices Sales. Strategic sales plans to achieve revenue and market share targets. Prior experience managing teams and handling distributor networks. Strong ability to communicate negotiates, and close deals effectively. Familiarity with the Eastern India market, customer base, and sales channels. Should be open to frequent travel across the assigned region. Understanding of diagnostic instruments, reagents, and laboratory workflows What We Offer Opportunity for growth and development Dynamic and collaborative work environment Salary Competitive salary package: Up to 8 LPA (Based on experience qualifications). Apply Here

Job Description – 1.Electronics Component Fault Finding, Installations & Servicing 2.Understand Software and Drivers Required for Electronic System. 3.Capable of applying knowledge to troubleshoot and propose solutions for electronics- related issues

Refer Medical Records and assign ICD-10-CM, CPT, HCPCS Codes Clinical Documentation Review Medical Coding and Medical Billing

We are Hiring Medical Sales Representative for the for renowned Italian MNC Vacant Head Quarters: BHOPAL, CUTTACK, THALESSERY Qualification : Any Graduate JOB DESCRIPTION 1. Meeting doctors, Retailers & wholesalers, promotion and demand generation for the requisite product portfolio. 2. To implement the sales strategies in the respective territory of the Company. 3. To collect the various relevant market information & submit it to the ABM. 4. To respect and work within the systems and the values of the company. Thanks & regards HR APLE PHARMA Aastha Mishra / Arpita 8950013071, 9051370786 Share your CV at resume@aplepharma.com Required Candidate profile Should be confident, good in communication skills, Note: You can also share references of Medical representatives working in Pharma & interested for Medical Device segment.

Aster Medcity is looking for Assistant Manager - Biomedical to join our dynamic team and embark on a rewarding career journey. Ensuring company policies are followed. Optimizing profits by controlling costs. Hiring, training and developing new employees. Resolving customer issues to their overall satisfaction. Maintaining an overall management style that follows company best practices. Providing leadership and direction to all employees. Ensuring product quality and availability. Preparing and presenting employee reviews. Working closely with the store manager to lead staff. Overseeing retail inventory. Assisting customers whenever necessary. Organizing employee schedule. Ensuring that health, safety, and security rules are followed. Ensuring a consistent standard of customer service. Motivating employees and ensuring a focus on the mission. Maintaining merchandise and a visual plan. Maintaining stores to standards, including stocking and cleaning. Completing tasks assigned by the general manager accurately and efficiently. Supporting store manager as needed.

Park Group is looking for Bio Medical -Technician to join our dynamic team and embark on a rewarding career journey Conduct routine inspections and troubleshooting of hospital equipment Ensure compliance with healthcare safety regulations Collaborate with healthcare professionals for equipment optimization

Park Group is looking for Bio Medical - Engineer to join our dynamic team and embark on a rewarding career journey Ensure compliance with healthcare and safety regulations Conduct research to improve medical technologies Support hospitals with technical expertise for medical systems

Park Group is looking for Bio Medical -Incharge to join our dynamic team and embark on a rewarding career journey Ensure compliance with healthcare industry standards Manage a team of technicians for efficient service Coordinate with medical teams for equipment needs

Maintain all statutory & operational records. Testing of all machineries by chattered engineer as per factory act. Prepare yearly budget Responsible for handling Bio-medical waste from receiving till treatment.

Title of the Project : Development and Evaluation of Intelligent Robot-Assisted Upper Limb Therapy System Qualification : Bachelor s/ Master s/ PhD degree in Computer Science, Biomedical Engineering, or related fields, or significant practical experience in Robotics, Explainable AI, and Rehabilitation. Relevant skills in either one is also considered. Describe if any In-depth knowledge about robotics, forward and inverse kinematics, and control systems Hands-on experience with designing and implementing Explainable AI-ML models Programming skills in python, MATLAB, and C#

Summary We are seeking a highly skilled AI Architect to design and implement cutting-edge Generative AI (GenAI) solutions tailored for the pharmaceutical and life sciences industry. This role will be responsible for defining AI strategies, selecting and fine-tuning generative AI models, and ensuring seamless integration with enterprise systems to enhance drug discovery, clinical trials, regulatory compliance, and patient-centric solutions. The AI/GenAI Architect will collaborate closely with data scientists, engineers, and business stakeholders to develop scalable, compliant, and high-performance AI applications that leverage large language models (LLMs), multimodal AI, and AI-driven automation. About the Role Key Responsibilities GenAI Strategy & Roadmap: Define and implement a generative AI architecture and roadmap aligned with business goals in pharma and life sciences. Solution Design: Architect scalable GenAI solutions for drug discovery, medical writing automation, clinical trials, regulatory submissions, and real-world evidence generation. LLM Development & Optimization: Work with data scientists and ML engineers to develop, fine-tune, and optimize large language models (LLMs) for life sciences applications, such as scientific literature analysis, regulatory intelligence, and patient engagement. Cloud & On-Prem AI Infrastructure: Design GenAI solutions leveraging cloud platforms (AWS, Azure, GCP) or on-premise infrastructure while ensuring data security and regulatory compliance. MLOps & Deployment: Implement best practices for GenAI model deployment, monitoring, and lifecycle management within GxP-compliant environments. Compliance & Governance: Ensure GenAI solutions comply with regulatory standards (FDA, EMA, GDPR, HIPAA, GxP, 21 CFR Part 11) and adhere to responsible AI principles, including bias mitigation and explainability. Performance Optimization: Drive efficiency in generative AI models, ensuring cost optimization and scalability while maintaining data integrity and compliance. Stakeholder Collaboration: Work with cross-functional teams, including platform teams, and Drug Development teams, to align GenAI initiatives with enterprise and industry-specific requirements. Research & Innovation: Stay updated with the latest advancements in GenAI, multimodal AI, AI agents, and synthetic data generation to incorporate emerging technologies into the company s AI strategy. Required Qualifications Bachelors or Masters degree in Computer Science, AI, Data Science, Bioinformatics, or a related field. Experience: 8+ years in AI/ML development with at least 2 years in an AI Architect or GenAI Architect role in pharma, biotech, or life sciences. Technical Expertise: Strong proficiency in Generative AI, large language models (LLMs), multimodal AI, and deep learning for pharma applications. Hands-on experience with AI/ML frameworks (TensorFlow, PyTorch, Hugging Face, LangChain, Scikit-learn, etc.). Experience with data engineering, ETL pipelines, and big data technologies (Spark, Kafka, Databricks, etc.). Proficiency in programming languages such as Python, R, or Java. Knowledge of cloud AI services (AWS Bedrock, Azure OpenAI, Google Vertex AI). Deploy a Lightweight LLM in a Pharma SaaS Platform MLOps & DevOps: Familiarity with CI/CD, containerization (Docker, Kubernetes), vector databases, and real-time model monitoring. Regulatory & Ethical AI: Understanding of AI governance, responsible AI principles, and compliance requirements for GenAI in pharma. Problem-Solving: Strong analytical and problem-solving skills with the ability to design innovative GenAI solutions for life sciences use cases. Communication & Leadership: Excellent communication skills to articulate GenAI strategies and solutions to technical and non-technical stakeholders. Preferred Qualifications Experience in GenAI applications for medical writing, automated clinical trial protocols, drug discovery, and regulatory intelligence . Knowledge of AI explainability, retrieval-augmented generation (RAG), knowledge graphs, and synthetic data generation in life sciences. AI/ML certifications from AWS, Google, or Microsoft. Understanding of biomedical ontologies, semantic AI models, and federated learning . Exposure to fine-tuning the LLM models will be a big plus Exposure to SLM or domain LLM model will be a big plus BioGPT & PubMedBERT: NLP for biomedical literature and clinical trial analysis Custom SLMs: Fine-tune Mistral 7B, Phi-2, or Gemma on pharma datasets

Title: PV Scientist - Senior ExpertLocation: Bangalore Purpose of the Role: We are seeking a highly motivated and skilled Pharmacovigilance Scientist to collaborate with global safety leads and program safety leads This role is essential for providing integrated medical safety strategies for assigned investigational and core (high-risk) marketed products, including input into safety aspects of clinical development, risk management, and benefit-risk management Your roleSignal Detection and Management:Perform safety monitoring using dedicated tools (eg, Spotfire, EVDAS, Empirica Signals) for signal detection Review and analyze clinical and safety database outputs; interpret aggregate safety data from clinical trials and post-marketing sources Review scientific literature for safety surveillance and signal detection Support the analyses of safety signals, contribute to authoring signal evaluation reports, and participate in relevant safety governance meetings Support communication of findings from Emerging Safety Issue Reports to external stakeholders RMP Updates and Periodic Safety Reports:Retrieve/summarize data from various sources in support of authoring and providing content for Risk Management Plans (RMPs) and periodic safety reports Support local adaptation of RMPs and respond to health authority questions Submissions and Safety Variations:Contribute to delivery of safety relevant documents of the Common Technical Document (CTD) Contribute to ISS/SCS IAP, health authority briefing documents, and product information and clinical overview addendum Clinical Trial Activities: Provide input into safety sections of the Investigational Medicinal Product Dossier (IMPD), Investigators Brochure (IB), and Informed Consent Form (ICF) Support delivery of safety-related input for clinical trial documents, including protocols and reports Provide safety related input for data monitoring committees with safety-related documentation Other Activities:Respond to queries from auditors/inspectors and participate in interviews Contribute to the design and implementation of post-authorization safety studies Develop and maintain MedDRA CMQs for signal analysis and aggregate safety data Create product-specific training for internal and external stakeholders Provide expert input into process standardization and improvement within GPS and GD Who you are: Experience Required:MD, or PhD/advanced science degree or tertiary level qualifications in a biomedical/health related field Fluent in written and spoken English Qualification:Over 4 years of Pharmaceutical industry experience or similar (egHealth Authority) Experience in Pharmacovigilance risk management in both clinical development and post-marketing areas, including submission experience Ability to work collaboratively in a global team environmentTech savy with strong analytical and communication skills