3619 Biotechnology Jobs - Page 40

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF Funded Project in the School of Biosciences and Technology (SBST), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : Development and evaluation of Ape1 degrading peptide to sensitize genotoxic drug resistance tumor cells for apoptosis . Qualification : MSc/MTech in Biology/Biotechnology related- subjects with two years of experience. Mandatory Skills : Candidates having good knowledge in field of cancer and practical experience in animal cell culture and Western blot analysis Stipend : Rs. 37,000/- + HRA per month No. of Vacancies : 01 Posts Age Limit : 24 to 30 years Sponsoring Agency : ANRF Duration : 12 Months Principal Investigator : Dr. M. Anbalagan, Professor, School of Biosciences 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 and latest passport size photo etc. on or before ( 01/06/2025) 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.

You will be responsible for leading the scientific and technical strategy for the development of a cutting-edge biotech SaaS platform. This will involve identifying market needs in the biotech, pharma, and analytical sciences sectors, overseeing platform design, AI integration, and product development. In addition, you will be required to build strategic partnerships with academic institutions, biotech firms, and research labs, ensuring regulatory compliance and high-quality standards such as GLP, GMP, and ISO. Developing monetization models and business growth strategies will also be a key part of your role. The ideal candidate for this position will have a PhD, MSc, or MTech in Biotechnology, Bioinformatics, Life Sciences, or related fields. You should have experience in scientific R&D, biotech startups, CROs, or pharma, and exposure to SaaS, AI-driven tools, or digital solutions for biotech and life sciences. A strong network in academia, biotech, and research organizations, coupled with an interest in business strategy and scaling a tech-driven venture, will be highly beneficial. As the Chief Scientific Officer (CSO), you will play a co-founder-level role with significant ownership and strategic influence in the company. The compensation and benefits package includes competitive equity (ESOPs) or a co-founder-level stake, providing you with the opportunity to lead scientific innovation in a high-impact biotech startup. You will have the chance to build a scalable, AI-powered solution for the scientific community and shape the future of scientific research and digital transformation.,

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.),

About Us We are a deep-tech climate and biotech startup developing India’s first modular supercritical CO₂ extraction system for sustainable applications, including nutraceuticals, bioactives, and clean air solutions. We are currently building our first prototype and are looking for a hands-on engineer with expertise in pressure systems and process design to join our founding team. Role Overview As a Supercritical CO₂ Extraction Engineer, you will be responsible for designing, building, testing, and scaling our proprietary extraction system. This role requires strong mechanical and process engineering skills, along with experience or interest in high-pressure extraction systems, thermodynamics, and automation. Responsibilities Lead the design and development of supercritical CO₂ extraction hardware and components such as pressure vessels, pumps, and separators Optimize extraction parameters including pressure, temperature, and flow rates in collaboration with the R&D team Select and integrate critical components such as valves, heat exchangers, and compressors Ensure compliance with pressure vessel safety standards and develop standard operating procedures Collaborate with vendors, fabricators, and testing labs to prototype and validate designs Develop scale-up plans from laboratory systems to pilot and commercial systems Contribute to system automation and control architecture; knowledge of PLC or SCADA systems is a plus Troubleshoot technical issues during pilot runs and propose effective engineering solutions Qualifications Bachelor’s or Master’s degree in Mechanical Engineering, Chemical Engineering, or a related field Hands-on experience with pressure systems, fluid mechanics, or thermodynamics Familiarity with supercritical fluid extraction processes is a strong advantage Proficiency with CAD software (SolidWorks, AutoCAD) and simulation tools (Ansys, COMSOL) Knowledge of instrumentation, pressure testing, and material compatibility (such as SS316) Exposure to manufacturing, welding, or fabrication processes is beneficial Startup mindset: proactive, resourceful, and comfortable building from the ground up Preferred Skills Experience with CO₂ gas handling, compressors, or cryogenics Knowledge of herbal, algal, or bio-material extraction Familiarity with GMP or cleanroom protocols Passion for sustainability, biotechnology, or climate-tech innovation What We Offer Opportunity to build India’s first modular supercritical CO₂ extraction system High ownership and visibility as part of a pioneering clean-tech startup Freedom to innovate and scale your ideas Flexible work environment with a supportive team How to Apply If this opportunity excites you, you can apply directly either here on LinkedIn or by sending your CV and a short note about why you are interested in this role to hr@carbelim.io , with the subject line: Application – Supercritical CO₂ Engineer .

Job Description: Applications are invited for the post of Project Research Scientist - II (Non-Medical) for the ICMR New Extramural (First in the World Challenge) grant in the Centre for Nanobiotechnology (CNBT), at Vellore Institute of Technology (VIT). (No. EM/Dev/FIW/00252/2024 (E-Office-227016)). Title of the Project: First in the World Challenge: A Nasal Spray Formula for Pulmonary Delivery to Control Multidrug-Resistant Tuberculosis MDR-TB Qualification: The candidate must have first class in post graduate degree, including the integrated PG degrees, with three years post-qualification experience or PhD in Biotechnology experience in nanoemulsions preparation and drug delivery systems and antimicrobial studies. Stipend: Rs. 67,000 + 10% HRA (Rs. 73,700) per month, stipend will be as per Institute norms. Sponsoring Agency: ICMR, New Delhi Duration: 3 years Principal Investigator: Dr. Natarajan Chandrasekaran, Professor, Higher Academic Grade, Centre for Nanobiotechnology (CNBT), Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu Co-Principal Investigator: Dr. George Priya Doss C, Professor Grade 1, Department of Integrative Biology 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 (10/06/2025) 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.

Job Description: Applications are invited for the post of Project Research Scientist - I (Non-Medical) for the ICMR New Extramural (First in the World Challenge) grant in the Centre for Nanobiotechnology (CNBT), at Vellore Institute of Technology (VIT). (No. EM/Dev/FIW/00252/2024 (E-Office-227016)). Title of the Project: First in the World Challenge: A Nasal Spray Formula for Pulmonary Delivery to Control Multidrug-Resistant Tuberculosis MDR-TB Qualification: The candidate must have a first-class postgraduate degree, including the integrated PG degrees, relevant to nano technology, nano-delivery, biological therapeutics, pharmaceutical sciences, Biotechnology. Stipend: Rs. 56,000 + 10% HRA (Rs. 61,600) per month, stipend will be as per Institute norms. Sponsoring Agency: ICMR, New Delhi Duration: 3 years Principal Investigator: Dr. Natarajan Chandrasekaran, Professor, Higher Academic Grade, Centre for Nanobiotechnology (CNBT), Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu Co-Principal Investigator: Dr. George Priya Doss C, Professor Grade 1, Department of Integrative Biology 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 (10/06/2025) 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.

Dear Candidate , we are hiring for Biologics for the Position JR Executive . Bio burden testing of in process samples as per the specification. BET testing of water samples, in-process samples, semi-finished and finished samples as per the specification. Sterility testing of finished product. Responsible to perform the MLT testing for raw materials and water samples. Maintenance and handling of Endotoxin indicators and biological indicators. Experience on culture maintenance and VITEK2 compact system To perform the method validations for MLT, BET, Bio burden and Sterility. Injectables or biologics experience is mandatory. Male candidates are preferable. Regulatory audits exposure is mandatory. Department:- Microbiology . Exp:-2-5 Years. Des:- Jr Executive-Executive . Qua:-MSc Microbiology . NOTE : Only Male Candidates Preferable for more details please reach out Venkat -9381915043 or please share your CV to venkateswara.k@talent21.in

BI Architect About Amgen Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. About The Role Role Description: We are seeking an experienced BI Architect with expertise in Databricks, Spotfire (Tableau and Power BI secondary), AWS, and enterprise business intelligence (BI) solutions to design and implement scalable, high-performance BI architectures. This role will focus on data modeling, visualization, governance, self-service BI enablement, and cloud-based BI solutions, ensuring efficient, data-driven decision-making across the organization. The ideal candidate will have strong expertise in BI strategy, data engineering, data warehousing, semantic layer modeling, dashboarding, and performance optimization, working closely with data engineers, business stakeholders, and leadership to drive BI adoption and enterprise analytics excellence. Preferred Candidate would have extensive Spotfire experience followed by Power BI or Tableau. Roles & Responsibilities: Design and develop enterprise BI architectures and implement the architectural vision for TIBCO Spotfire at the enterprise level hosted in AWS Partner with data engineers and architects to ensure optimal data modeling, caching, and query performance in Spotfire Design scalable, secure, and high-performance Spotfire environments, including multi-node server setups and hybrid cloud integrations. Develop reusable frameworks and templates for dashboards, data models, and automation processes. Optimize BI query performance, indexing, partitioning, caching, and report rendering to enhance dashboard responsiveness and data refresh speed. Implement real-time and batch data integration strategies, ensuring smooth data flow from APIs, ERP/CRM systems (SAP, Salesforce, Dynamics 365), cloud storage, and third-party data sources into BI solutions. Establish and enforce BI governance best practices, including data cataloging, metadata management, access control, data lineage tracking, and compliance standards. Troubleshoot interactive dashboards, paginated reports, and embedded analytics solutions that deliver actionable insights. Implement DataOps and CI/CD pipelines for BI, leveraging Deployment Pipelines, Git integration, and Infrastructure as Code (IaC) to enable version control and automation. Stay up to date with emerging BI technologies, cloud analytics trends, and AI/ML-powered BI solutions to drive innovation. Collaborate with business leaders, data analysts, and engineering teams to ensure BI adoption, self-service analytics enablement, and business-aligned KPIs. Provide mentorship and training to BI developers, analysts, and business teams, fostering a data-driven culture across the enterprise. Must-Have Skills: Experience in BI architecture, data analytics, AWS, and enterprise BI solution development Strong expertise in Spotfire including information links, Spotfire Analyst, Spotfire Server, and Spotfire Web Player Hands-on experience with Databricks (Apache Spark, Delta Lake, SQL, PySpark) for data processing, transformation, and analytics. Experience in scripting and extensions Python or R Expertise in BI strategy, KPI standardization, and enterprise data modeling, including dimensional modeling, star schema, and data virtualization. Hands-on experience with cloud BI solutions and enterprise data warehouses, such as Azure Synapse, AWS Redshift, Snowflake, Google BigQuery, or SQL Server Analysis Services (SSAS). Experience with BI governance, access control, metadata management, data lineage, and regulatory compliance frameworks. Expertise in Agile BI development, Scaled Agile (SAFe), DevOps for BI, and CI/CD practices for BI deployments. Ability to collaborate with C-level executives, business units, and engineering teams to drive BI adoption and data-driven decision-making. Good-to-Have Skills: Experience with Tibco Spotfire Lead Discovery Knowledge of AI-powered BI, natural language processing (NLP) in BI, and automated machine learning (AutoML) for analytics. Experience with multi-cloud BI architectures and federated query solutions using Power BI Tableau. Understanding of GraphQL, REST APIs, and data mesh principles for enterprise data access in BI. Knowledge of AI/ML pipeline integration within enterprise data architectures. Education and Professional Certifications Bachelor’s degree with 9-13 years of experience in Computer Science, IT or related field Tibco Spotfire Certifications Power BI Certifications Tableau Certifications Soft Skills: Excellent analytical and troubleshooting skills. Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented, with a focus on achieving team goals. Ability to learn quickly, be organized and detail oriented. Strong presentation and public speaking skills. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Let’s do this. Let’s change the world. In this vital role you will be responsible for developing and leading a highly talented team that is built for delivering high-end and innovative technologies. The ideal candidate will have a consistent record of leadership in technology-driven environments using 3DEXPERIENCE Cloud platform and has a passion for fostering innovation and excellence in the biotechnology industry. Additionally, collaboration with cross-functional and global teams is required to ensure seamless integration and operational excellence. The ideal candidate will have a strong background in the end-to-end software development lifecycle and a Scaled Agile practitioner, coupled with leadership and transformation experience. This role demands the ability to drive and deliver against key organizational critical initiatives, foster a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Roles & Responsibilities: Maintain strategic relationships and strong communication with the leadership team about IS services and service roadmaps to ensure that all the customers feel informed and engaged Lead and manage large, diverse teams within a matrixed organization. Collaborate with geographically dispersed teams, including those in the US and other international locations. Foster a culture of collaboration, innovation, and continuous improvement. Develop talent, motivate the team, delegate effectively, champion diversity within the team and act as a role model of servant leadership. Responsible for managing, growing, and developing the Amgen Technology team in India, ensuring global ways of working are imbedded in the local organization Understand the decision-making process, workflows, and business and information needs of business partners and collaborators Contribute and define business outcomes + requirements, technology solutions, and services Improve activities being measured by crafting, monitoring, and optimizing relevant feedback loops through 'test & learn' activities Work with Product Owners, Service Owners and/or delivery teams to ensure that delivery matches commitments, acting as an escalation point and facilitating communication when service commitments are not met Ensure communication of key performance metrics and analysis of unmet needs Participate in collaborator and other leadership meetings, working with other parts of the organization, and functional groups to ensure successful delivery Ensure ongoing alignment with strategy, compliance, and regulatory requirements for technology investments and services Facilitate standard process sharing, ensuring ongoing alignment with the Technology & Digital strategy Provide education to new partners with regards to IT service offerings Remain accountable for ensuring overall organizational compliance to quality/compliance requirements such as GXP and Privacy Basic Qualifications: Doctorate degree / Master's degree / Bachelor's degree and 12 to 17 years of experience in Business, Engineering, IT or related field . Preferred Qualifications: Functional Skills: Must-Have Skills: Strategize, plan, and implement various phases of PLM roadmap using Dassault Systemes’ 3DEXPERIENCE platform and integrating with key enterprise platforms Strong Technical/Functional experience solutioning and supporting GMP applications across Engineering, Clinical, Commercial and Quality functions. Demonstrated hands-on experience in managing technology solutions involving one of the leading PLM solutions (Windchill, Teamcenter or 3DEXPERIENCE). Experience integrate PLM with enterprise systems such as Data Fabric, Veeva vault, SAP, MES and SCADA systems. Experience in people management and leading highly skilled matrixed teams, passion for mentorship, culture and fostering the development of talent. Must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment. Exceptional collaboration, communication and interpersonal skills to effectively manage collaborator relationships and build new partnerships. Experience in applying technology standard process methodologies: Scaled Agile (SAFe) Good-to-Have Skills: Experience in a leadership role within a pharmaceutical or technology organization Experience with configuring and customizing solutions for Requirements, CAD, Risk, EBOM, MBOM, Configuration/Variants, Recipe, MPP, Document and Change management. Experience leading data migration from various sources to 3DEXPERIENCE platforms. Experience creating solutions using Enterprise Integration Framework and usage of middleware systems such as Mulesoft, Boomi or Tibco. Extensive experience in software development lifecycle. Experience using and adoption of Scaled Agile Framework (SAFe) Strong analytic/critical-thinking and decision-making abilities. Ability to work effectively in a fast-paced, dynamic environment. Established business partnerships and IS governance practices involving senior business stakeholders Broad working knowledge of key IS domains and layers Professional Certifications: Scaled Agile Framework (SAFe) for Teams (preferred) Soft Skills: Excellent leadership and team management skills. Strong transformation and change management experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. Excellent analytical and troubleshooting skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams What You Can Expect Of Us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com

About Amgen Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. About The Role Role Description: We are seeking a Sr Machine Learning Engineer —Amgen’s most senior individual-contributor authority on building and scaling end-to-end machine-learning and generative-AI platforms. Sitting at the intersection of engineering excellence and data-science enablement, you will design the core services, infrastructure and governance controls that allow hundreds of practitioners to prototype, deploy and monitor models—classical ML, deep learning and LLMs—securely and cost-effectively. Acting as a “player-coach,” you will establish platform strategy, define technical standards, and partner with DevOps, Security, Compliance and Product teams to deliver a frictionless, enterprise-grade AI developer experience. Roles & Responsibilities: Engineer end-to-end ML pipelines—data ingestion, feature engineering, training, hyper-parameter optimisation, evaluation, registration and automated promotion—using Kubeflow, SageMaker Pipelines, Open AI SDK or equivalent MLOps stacks. Harden research code into production-grade micro-services, packaging models in Docker/Kubernetes and exposing secure REST, gRPC or event-driven APIs for consumption by downstream applications. Build and maintain full-stack AI applications by integrating model services with lightweight UI components, workflow engines or business-logic layers so insights reach users with sub-second latency. Optimise performance and cost at scale—selecting appropriate algorithms (gradient-boosted trees, transformers, time-series models, classical statistics), applying quantisation/pruning, and tuning GPU/CPU auto-scaling policies to meet strict SLA targets. Instrument comprehensive observability—real-time metrics, distributed tracing, drift & bias detection and user-behaviour analytics—enabling rapid diagnosis and continuous improvement of live models and applications. Embed security and responsible-AI controls (data encryption, access policies, lineage tracking, explainability and bias monitoring) in partnership with Security, Privacy and Compliance teams. Contribute reusable platform components—feature stores, model registries, experiment-tracking libraries—and evangelise best practices that raise engineering velocity across squads. Perform exploratory data analysis and feature ideation on complex, high-dimensional datasets to inform algorithm selection and ensure model robustness. Partner with data scientists to prototype and benchmark new algorithms, offering guidance on scalability trade-offs and production-readiness while co-owning model-performance KPIs. Must-Have Skills: 3-5 years in AI/ML and enterprise software. Comprehensive command of machine-learning algorithms—regression, tree-based ensembles, clustering, dimensionality reduction, time-series models, deep-learning architectures (CNNs, RNNs, transformers) and modern LLM/RAG techniques—with the judgment to choose, tune and operationalise the right method for a given business problem. Proven track record selecting and integrating AI SaaS/PaaS offerings and building custom ML services at scale. Expert knowledge of GenAI tooling: vector databases, RAG pipelines, prompt-engineering DSLs and agent frameworks (e.g., LangChain, Semantic Kernel). Proficiency in Python and Java; containerisation (Docker/K8s); cloud (AWS, Azure or GCP) and modern DevOps/MLOps (GitHub Actions, Bedrock/SageMaker Pipelines). Strong business-case skills—able to model TCO vs. NPV and present trade-offs to executives. Exceptional stakeholder management; can translate complex technical concepts into concise, outcome-oriented narratives. Good-to-Have Skills: Experience in Biotechnology or pharma industry is a big plus Published thought-leadership or conference talks on enterprise GenAI adoption. Master’s degree in Computer Science and or Data Science Familiarity with Agile methodologies and Scaled Agile Framework (SAFe) for project delivery. Education and Professional Certifications Master’s degree with 6-11 + years of experience in Computer Science, IT or related field OR Bachelor’s degree with 8-13 + years of experience in Computer Science, IT or related field Certifications on GenAI/ML platforms (AWS AI, Azure AI Engineer, Google Cloud ML, etc.) are a plus. Soft Skills: Excellent analytical and troubleshooting skills. Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented, with a focus on achieving team goals. Ability to learn quickly, be organized and detail oriented. Strong presentation and public speaking skills. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

About Amgen Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. About The Role The MAC Reference Librarian will be responsible for managing the digital Reference Library and Match Text Library within the Veeva Global PromoMats system, while adhering to internal guidelines, SOPs (Standard Operating Procedures), policies and industry regulations. Roles & Responsibilities: Manage Reference and Match Text Libraries for multiple US MAC Teams Adding new Match Text records and adjusting existing records. Manage Amgen Label Reference documents in Veeva Organize annual reviews Supports Global Initiative/Other MAC related projects. Expert in MAC Reference Requirements and Veeva Reference & Annotation (R&A) technology. Performs Quality Check on all References uploaded into the Reference Library to ensure aligned to R&A requirements Builds & maintains strong relationships with project Sponsors (owners), Reviewers, agencies, and other MAC Cross functional partners while also providing training on Reference Library and Linking requirements & identify Reference QC issues Collaborates with Material Compliance Managers (MCM) to understand BU/Product business priorities and elevate process issues that arise Collaborates with MCA to identify and correct Reference QC issues Partners with SciComm to update Links to Reference Anchors in MAC materials Manage the MAC Reference Library email Inbox. Create and manage associated work instructions. Facilitate weekly Reference Library Office Hours Reports to the Director of Material Compliance in Regulatory Affairs Required Knowledge and Skills: Ability to foster collaboration, work effectively on cross-functional teams, and consistently deliver on-time. Strong oral and written communication skills; strong interpersonal skills; demonstrated time management and decision-making skills. Critical thinking and problem-solving skills Quick learner, proactive, takes initiative. Distinguishes proper balance between strategic and tactical thinking. Strong experience with Project Management tools, methodologies, and practices Proven ability to manage in a highly fluid, interactive, matrix environment. Authoritative command of complexity and ambiguity, ability to see the big picture, ability to collect, digest and assemble information to enable relevant business analysis and influence decision-making. Identify continuous process and system improvements to save time and cost to Amgen. Preferred Knowledge and Skills: An understanding of the pharmaceutical commercialization process and knowledge of the legal and regulatory guidelines affecting promotion of prescription products Project management experience in the Pharmaceutical, Biotechnology or other Healthcare-related field, or other regulated industries Experience with Microsoft Office 365 (e.g. Word, Excel, Outlook, and PowerPoint), Adobe products (e.g. Adobe Photoshop, Illustrator, and Acrobat Pro), and Veeva PromoMats Experience managing medical reference support for marketing materials that are produced at high volumes. Experience managing digital library and medical references. Basic Education and Experience: Bachelor’s degree and 6 years of related experience OR Associate’s degree and 10 years of related experience Preferred Education and Experience: Bachelor’s degree and 6 years of related experience Experience working in a Global Regulatory Affairs organization AIN working hours for this position: This position supports the Regulatory Promotion and Material Compliance activities serving Amgen’s US Business Operations and thus the AIN working hours will need to be flexible with occasional overnight work time when needed to support product launches and new indications. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

About Amgen Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. About The Role The Digital Governance team supports the Global Regulatory Affairs and Strategy organization in the constant pursuit of Execution Excellence. They do this by managing the tracking and documentation of Amgen’s global digital sites and projects for compliance purposes. The Sr. Associate – Digital Governance will support the Digital Governance Business Process Owner (DSR BPO) in maintaining the accuracy of Amgen’s global digital site database. They are responsible for ensuring database records are kept up to date, responding to inquiries for database reports, following up on pending actions, and assisting users with process-related questions. This role will be on a flex shift to allow for live training and collaboration. Roles & Responsibilities: Support tracking and documentation of Amgen’s global digital sites and projects for compliance purposes Promote compliance for Amgen’s digital and social media asset inventory Provide guidance to inquiries regarding Amgen’s global digital database Assign training as needed to Amgen employees who manage or support digital assets Update formal process documents (SOPs, guidance/training documents) as needed Quality check digital assets against database information to ensure accuracy Follow up on overdue database task assignments Work with Domain Law to register Amgen URLs Support Digital Governance management in identifying areas of risk and concern Execute and document effectiveness checks Support corrective actions and regulatory inspections Maintain weekly and quarterly database reports Test digital site contact information to ensure compliance Provide Project Management support to key initiatives Maintain project management standards and methodology Provide change management support to key initiatives Required Knowledge and Skills: Deep knowledge of Veeva PromoMats database management processes Excellent written/oral communication skills and attention to detail Strong problem-solving skills and the ability to navigate complex situations Adaptability to assist in meeting urgent goals in a complex environment Familiarity with pharmaceutical regulatory compliance requirements (US and global) Experience with social media and website management Knowledge of Excel Ability to work collaboratively in a team environment Project Management Change Management Preferred Knowledge and Skills: Understanding of pharmaceutical regulatory compliance requirements in a global database environment Awareness of social media requirements and processes Basic Education and Experience: Master’s degree OR Bachelor’s degree and 3 years of related experience OR Associate’s degree and 5 years of related experience Preferred Education and Experience: Master’s or bachelor’s degree Experience working in a Global Regulatory Affairs or Pharmacovigilance organization AIN working hours for this position: This position supports the Regulatory Promotion and Material Compliance activities serving Amgen’s US Business Operations and thus the AIN working hours will need to be flexible with occasional overnight work time when needed to support product launches and new indications. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Job description Greetings from Indira IVF!!! Position- Lab Asst - Andrology Qualification- B.Sc. - Biotechnology/ Microbiology Experience- 1 to 4 Years Job Timing - 9 am to 6 pm Salary- Best in the industry

Position: Business Development Specialist Location: Bangalore Employment Type: Full-Time, Work from Office Qualification: Bachelor's, Master's degree in Biotechnology, Life Sciences, or related field ( MSc, BTech, MTech) Experience: 0-1 Year Immediate Joiners will be given preference Job Responsibilities  Identify new sales opportunities through inbound and outbound calls.  Reach out via cold calls and emails to explore potential sales avenues.  Meet and exceed quarterly milestones while successfully closing sales.  Study accounts regularly, identifying key players in the biotech and life science sector.  Collaborate with team members to work towards closing deals.  Maintain a detailed prospect database.  Conduct offline demonstrations to showcase our offerings and secure deals. As an Inside Sales Specialist at Biotecnika, you will play a crucial role in driving sales for our innovative products and services. Your responsibilities will include:  Customer Engagement: Interact with potential customers, understand their needs, and effectively communicate the value of Biotecnika's offerings.  Sales Generation: Proactively identify and pursue new business opportunities to meet and exceed sales targets.  Product Knowledge: Stay updated on Biotecnika's products and services to provide accurate information to customers and address their queries.  Relationship Building: Cultivate and maintain strong relationships with clients to ensure satisfaction and foster long-term partnerships.  Market Analysis: Keep abreast of industry trends, competitor activities, and market demands to identify new opportunities. Educational Requirements  Bachelor's, Master's degree in Biotechnology, Life Sciences, or related field (BSc, MSc, BTech, MTech).  Previous experience as an Inside Sales Specialist is advantageous.  Demonstrated success in meeting and exceeding sales quotas.  Strong communication and phone skills.  Familiarity with web presentation tools and Customer Relationship Management (CRM) systems. Skills  Excellent interpersonal and communication skills.  Proven ability to work in a goal-oriented, fast-paced environment.  Proficiency in using web presentation tools.  Strong analytical skills to identify key players in the industry.  Prior experience with Customer Relationship Management (CRM) systems.  Self-motivated and results-driven. Join Biotecnika and be a part of a vibrant team that is at the forefront of innovation in the biotech industry. Your passion for sales and commitment to excellence will be rewarded in an environment encouraging professional growth and development.  Venue: Biotecnika Info Labs Pvt Ltd, 1218, 11th A Cross Rd, Vanganahalli, 1st Sector, HSR Layout, Bengaluru, Karnataka 560102 Biotecnika is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

India - Hyderabad JOB ID: R-218572 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jul. 11, 2025 CATEGORY: Information Systems Let’s do this. Let’s change the world. In this vital role you will be responsible for developing and leading a highly talented team that is built for delivering high-end and innovative technologies. The ideal candidate will have a consistent record of leadership in technology-driven environments using 3DEXPERIENCE Cloud platform and has a passion for fostering innovation and excellence in the biotechnology industry. Additionally, collaboration with cross-functional and global teams is required to ensure seamless integration and operational excellence. The ideal candidate will have a strong background in the end-to-end software development lifecycle and a Scaled Agile practitioner, coupled with leadership and transformation experience. This role demands the ability to drive and deliver against key organizational critical initiatives, foster a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Roles & Responsibilities: Maintain strategic relationships and strong communication with the leadership team about IS services and service roadmaps to ensure that all the customers feel informed and engaged Lead and manage large, diverse teams within a matrixed organization. Collaborate with geographically dispersed teams, including those in the US and other international locations. Foster a culture of collaboration, innovation, and continuous improvement. Develop talent, motivate the team, delegate effectively, champion diversity within the team and act as a role model of servant leadership. Responsible for managing, growing, and developing the Amgen Technology team in India, ensuring global ways of working are imbedded in the local organization Understand the decision-making process, workflows, and business and information needs of business partners and collaborators Contribute and define business outcomes + requirements, technology solutions, and services Improve activities being measured by crafting, monitoring, and optimizing relevant feedback loops through 'test & learn' activities Work with Product Owners, Service Owners and/or delivery teams to ensure that delivery matches commitments, acting as an escalation point and facilitating communication when service commitments are not met Ensure communication of key performance metrics and analysis of unmet needs Participate in collaborator and other leadership meetings, working with other parts of the organization, and functional groups to ensure successful delivery Ensure ongoing alignment with strategy, compliance, and regulatory requirements for technology investments and services Facilitate standard process sharing, ensuring ongoing alignment with the Technology & Digital strategy Provide education to new partners with regards to IT service offerings Remain accountable for ensuring overall organizational compliance to quality/compliance requirements such as GXP and Privacy Basic Qualifications: Doctorate degree / Master's degree / Bachelor's degree and 12 to 17 years of experience in Business, Engineering, IT or related field . Preferred Qualifications: Functional Skills: Must-Have Skills: Strategize, plan, and implement various phases of PLM roadmap using Dassault Systemes’ 3DEXPERIENCE platform and integrating with key enterprise platforms Strong Technical/Functional experience solutioning and supporting GMP applications across Engineering, Clinical, Commercial and Quality functions. Demonstrated hands-on experience in managing technology solutions involving one of the leading PLM solutions (Windchill, Teamcenter or 3DEXPERIENCE). Experience integrate PLM with enterprise systems such as Data Fabric, Veeva vault, SAP, MES and SCADA systems. Experience in people management and leading highly skilled matrixed teams, passion for mentorship, culture and fostering the development of talent. Must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment. Exceptional collaboration, communication and interpersonal skills to effectively manage collaborator relationships and build new partnerships. Experience in applying technology standard process methodologies: Scaled Agile (SAFe) Good-to-Have Skills: Experience in a leadership role within a pharmaceutical or technology organization Experience with configuring and customizing solutions for Requirements, CAD, Risk, EBOM, MBOM, Configuration/Variants, Recipe, MPP, Document and Change management. Experience leading data migration from various sources to 3DEXPERIENCE platforms. Experience creating solutions using Enterprise Integration Framework and usage of middleware systems such as Mulesoft, Boomi or Tibco. Extensive experience in software development lifecycle. Experience using and adoption of Scaled Agile Framework (SAFe) Strong analytic/critical-thinking and decision-making abilities. Ability to work effectively in a fast-paced, dynamic environment. Established business partnerships and IS governance practices involving senior business stakeholders Broad working knowledge of key IS domains and layers Professional Certifications: Scaled Agile Framework (SAFe) for Teams (preferred) Soft Skills: Excellent leadership and team management skills. Strong transformation and change management experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. Excellent analytical and troubleshooting skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. and make a lasting impact with the Amgen team. careers.amgen.com

Job Description Job Summary: The Quality Assurance Associate Director will support a technical team interfacing between our Company and External Partners in the Biologics Drug Substance and Drug product manufacturing area. This individual will be responsible for ensuring that all quality assurance processes, and compliance requirements are met during technical transfers to and from External Partners and throughout the continuous commercial manufacturing process at External Partner sites. Key Responsibilities: Quality Oversight: Report to the Quality lead (or delegate) and provide general direction on quality goals and objectives, functioning independently to ensure oversight of all quality-related issues at External Partner site. Regulatory Compliance: Ensure that all quality assurance activities comply with regulatory requirements (FDA, EMA, etc.) and internal quality standards throughout the product lifecycle, including during facility start-up and technical transfers. Manufacturing Support: Provide ongoing quality support to External Partners by resolving quality issues, performing proactive analysis of process performance, and developing plans to ensure compliance and quality meet capacity needs. Collaboration: Work collaboratively with Biologics Quality Operations and other relevant teams within the Focused Factory to support the product lifecycle and address quality-related matters. Validation Strategies: Support and oversee validation strategies for new and existing products, ensuring compliance with best practices in quality assurance. Technical Review: Conduct a calibrated technical review of External Partners’ process change requests, deviations, protocols, and Master Batch Record changes to ensure compliance with quality standards. Issue Resolution: Troubleshoot quality-related manufacturing issues and support investigations using scientific problem-solving methodologies. Efficiency Improvement: Work with Operations, Quality, and External Partners to develop more efficient methods to meet regulatory requirements while ensuring quality standards are upheld. Quality Management System: Ensure adherence to the highest quality, compliance, and safety standards by participating in and complying with our Manufacturing Division Quality Management System requirements. Partner Engagement: Collaborate with External Partners to achieve business goals while fostering a common culture that prioritizes quality and compliance for both organizations. Education Minimum Requirement: Bachelor’s or master’s degree (or equivalent) in Chemical/Biochemical Engineering, Biotechnology, Microbiology, Pharmaceutical Science, Life Sciences, or a related field. Required Experience and Skills: Proven experience in highly regulated manufacturing environments with a minimum of 15 years of experience in quality assurance within biopharmaceutical operations, particularly related to Drug substance and drug product manufacturing and validations. Strong knowledge of quality systems, regulatory compliance, and quality assurance practices in the biopharmaceutical industry. Familiarity with change management processes and regulatory support planning. Experience in process validations, cleaning validations, and the associated quality documentation requirements. Proficiency in large molecule manufacturing, in process controls, analytical testing, validations, batch records review and release. Ability to perform risk assessments and develop strategies for continuous improvement initiatives. Proficient in computer system validations, equipment validations, area qualification, Audits, batch release procedures. Effective communication skills for managing partnerships and addressing quality concerns. Preferred Experience and Skills: Familiarity with high-performance organizational tools and a strong understanding of digital manufacturing processes, computer system validation requirements, and quality management within biologics production and quality. Experience with quality management software and metrics analysis to drive performance improvements. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Biotechnology, Change Management, Cross-Cultural Awareness, Cross-Functional Teamwork, Digital Manufacturing, GMP Training, Good Distribution Practice (GDP), Immunochemistry, Inspection Readiness, IS Audit, Management Process, Manufacturing Compliance, Manufacturing Environments, Manufacturing Quality Control, Microbiology, Product Lifecycle, Quality Assurance (QA), Quality Auditing, Quality Management, Quality Management Standards, Quality Metrics, Quality Standards, Quality Systems Compliance {+ 2 more} Preferred Skills: Job Posting End Date: 08/11/2025 A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R357786

COMPANY BACKGROUND Akero Therapeutics is a clinical stage biopharmaceutical company focused on discovering and developing transformational treatments for patients with serious metabolic diseases marked by high unmet need. Our current focus is on advancing our lead program efruxifermin (EFX) to provide a powerful new treatment for patients with MASH(metabolic dysfunction-associated steatohepatitis). We are a team of problem solvers dedicated to pursuing bold scientific approaches to build a brighter future for patients. Our diverse skill sets and backgrounds, desire to learn from each other and collaborative spirit breed a culture where everyone feels inspired to bring their best thinking to work, and to bring out the best in others. Job Summary The Associate Director of Statistical Programming will be a key member of the clinical development team responsible for ensuring the accuracy and timeliness of programming deliverables for clinical studies. The incumbent will lead and manage statistical programming activities for clinical trial reporting, integrated safety/efficacy analysis, and global regulatory submissions. In addition, the incumbent will possess strong technical understanding of programming principles, documentation, SDTM/ADaM structure, and ICH GCP requirements. The main responsibilities of this position include development of analysis and dataset specifications, vendor management, and QC of key deliverables provided by CRO vendors while adhering to planned project timelines. As a key member of the clinical development and cross-functional teams, this position demands strong collaborative and communication skills, including the ability to engage with a diverse range of internal and external stakeholders. Job Responsibilities Review and lead quality control (QC) of SAS programming deliverables and vendor management of CROs Development and manage timelines for statistical programming deliverables and associated documentation. Perform ad hoc analyses as requested. Represent statistical programming function at internal and external meetings Develop overall strategy regarding preparation and standardization of data packages for BLA submission(s) Qualifications Master’s degree or PhD in Statistics, Biostatistics, Mathematics, or other field with significant quantitative and scientific component. Exceptional BS-level candidates with commensurate industry experience may be considered. 8 years or more direct biotechnology or pharmaceutical industry experience in statistical programming, including vendor management experience (e.g. CROs) Expertise in CDISC (SDTM/ADaM) standards and implementation, regulatory requirements, and ICH GCP. Recent experience with BLA/NDA/MAA submission, as well as ISS/ISE development experience, is highly desirable Familiarity with hepatology, gastroenterology, or cardiometabolic therapeutic area is desirable Technical Requirements and Skills Proficient in MS Office Suite (Word, Excel and Power Point) Expertise in SAS programming (SAS base, macro, etc.), SDTM/ADaM data standards and documentation, and quality control. Fluency in at least one other statistical programming language such as R or Python, is a plus. Strong interpersonal and communication skills; proactive approach. Demonstrated problem solving skills (including taking ownership to ensure timely resolution with vendors), a strong sense of urgency, keen attention to detail, and the ability to successfully execute in an environment under time and resource pressures. Able to work both independently and in a team environment. Ability to work collaboratively with CROs and lead oversight of outsourced programming activities. Familiarity with modern ML/AI methodology (e.g. deep learning) and applications is a plus Detail-oriented, with good organizational, prioritization, and time management proficiencies, and able to work on multiple projects simultaneously. Ability to travel if needed (<20%) Compensation Below is the pay range for this position that we reasonably expect to pay. Individual compensation is based on a number of factors including, experience, education and skill set, and geographic location. This range is for the San Francisco Bay Area, California location and may be adjusted to the labor market in other geographic areas. Pay range: $200,000 - $209,000 per annum Special Advisory The FTC has an advisory out on the domain @akerotxhr.com and the email address akerotx@consultant.com. If you are contacted by any individual or group using email addresses or other contact information that incorporate “akerotx” but do not use our exact domain, akerotx.com, please submit a report to the FTC.

Overview: Dozee Health AI is a pioneer in Contactless Remote Patient Monitoring (RPM), proven to drive transformation at scale. Headquartered in Bengaluru, India, Dozee has emerged as India’s no. 1 RPM Company. We are seeking visionary individuals to help us in this very exciting journey. As a part of our dynamic team, you’ll have the opportunity to collaborate with top healthcare providers in the country, applying AI-powered RPM solutions to tackle some of the most pressing challenges in healthcare - enhancing staff efficiency, improving patient outcomes, and pioneering the next generation of care models. Responsibilities Plan, establish and maintain a Quality Management System in accordance with EN ISO 13485 Implement regulatory strategies for maintaining compliance with established standards like IEC 60601, IEC 62304, US FDA and CE Marking, etc Prepares dossiers and device master files for regulatory submissions Follow the Medical Device Act by CDSCO and other relevant regulations related to products developed and provide directions for compliance to the organization. Work with different teams to setup Quality policies and standards Ensuring all established quality and delivery commitments are met such as working within FDA regulations, Design Control and ISO Standards. Training and ensuring all assigned employees are aware of and comply with company policies, government procedures, and regulations. Working closely with product development and product transfer teams Supplier Audit and Qualification. Assist with Management Review meetings including generation of quality metrics and coordinating the review. Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal procedures to assure compliance for QMS. Lead audit and inspection preparation, resolution of audit and inspection findings with relevant stakeholders through all stages of the audits. Coordinate CAPA's meetings and provide assistance to the corrective action owners to ensure effectiveness. Ensure employee training compliance to Corporate and site-level QMS. May be responsible for preparing and facilitating quality related training programs for employees. Requirements Educational Qualification- B.Tech Minimum 3-5 years of experience in Medical Device Regulation. Experience with international medical device regulatory approvals and submissions Experience supporting regulatory agency inspections and Notified Body Audits in an SME role Demonstrated knowledge of US FDA, EU MDR, ISO 13485 Quality Management System and ISO 14971 Risk Management for Medical Devices as well as IEC 62304 Ability to analyze and interpret standards, technical procedures, professional journals and governmental guidance and regulation documents Proven experience in new medical device registrations and filings Working experience with CDSCO, Notified body and other associations for medical device regulation Able to constructively collaborate with cross-functional teams Working knowledge of quality assurance methodologies Knowledge of commonly-used concepts, practices, and procedures for a full product development life-cycle and Medical Device Quality Management System. Support compliance assessments to ensure quality and regulatory requirements are successfully implemented and maintained. Providing guidance to the team to interpret regulatory requirements for various life-cycle stages of the project Drive Good Documentation practices Ability to follow instructions, work independently, or function in a team as needed Highly organized, process orientated and adherence to standard process. Exhibit good leadership across departments and teams. Good time management and project management. Collaborative and a team player Good interpersonal, listening and communication skill Vision & Mission Save Million lives with Health AI Dozee is India’s leading AI-Powered contactless Remote Patient Monitoring (RPM) and Early Warning System (EWS). A solution that continuously monitors patients and provides early warnings of clinical deterioration, enabling timely interventions and enhancing patient safety in hospitals, nursing facilities and patient homes. A "Made in India for the World" solution, Dozee has pioneered the world’s first non-contact blood pressure monitoring system. Trusted by leading healthcare providers in India, the USA, and Africa, Dozee is transforming patient safety and care by enhancing outcomes and reducing costs. Dozee is adopted by 300+ hospitals and monitors 16000+ beds across 4 countries . Dozee has monitored over 1 Mn Patients, Delivered 35000+ Life Saving Alerts and Saved 10 Mn+ Nursing Hours. Videos Science Behind Dozee : Ballistocardiography & Artificial Intelligence - 100 Dozee deliver 144 life saving alerts and INR 2.7 Cr of saving - Sattva Study Dozee saves life of a mother at home Leading Healthcare Game changers work with DozeeI Introducing Dozee VS - Dozee Shravan - A clinical grade RPM service Dozee in News: Bloomberg - Oct 21, 2024 From AI Beds to Remote ICUs, Startups are plugging India's health Gaps News18Oct 26, 2024 Now, You Can Remotely Monitor Your Loved Ones in Hospital With Bengaluru Start-Up's 'Shravan' Analytics India MagazineOct 29, 2024 Dozee Harness AI for Personalised Patient Care ET HealthWorldSep 16, 2024 We trust AI everyday - From Google Maps to Smartphones, So why not use it to enhance patient safety in healthcare? BW healthcareworldOct 29, 2024 Dozee's AI-Powered System Predicts Patient Deterioration 16 Hours in Advance A tertiary care hospital study published in JMIR , validated Dozee’s Early Warning System (EWS), showing it identified 97% of deteriorating patients, provided alerts ~19 hours in advance , and generated 5x fewer alerts, reducing alarm fatigue and improving patient outcomes. A study at King George Medical University, Lucknow, and published in Frontiers in Medical Technology demonstrated that Dozee’s automation can potentially save 2.5 hours of nursing time per shift , improving workflow efficiency and allowing more focus on patient care. A study on remote patient monitoring in general wards published in Cureus found that 90%+ of healthcare providers reported improved care and patient safety, 74% of patients felt safer , and there was a 43% increase in time for direct patient care. Research by Sattva , an independent consulting firm, demonstrates Dozee's substantial impact: for every 100 Dozee-connected beds, it can save approximately 144 lives , reduce nurses’ time for vital checks by 80% , and decrease ICU average length of stay by 1.3 days. Key Highlights Founded : October, 2015 Founders : Mudit Dandwate, Gaurav Parchani Headquarters : Bangalore, India \u007C Houston, USA \u007C Dubai, UAE Key Investors & Backers : Prime Ventures, 3one4 Capital, YourNest Capital, Gokul Rajaram, BIRAC (Department of Biotechnology, State Bank of India, and Dinesh Mody Ventures, Temasek Foundation, Horizons Ventures Stage : Series A+ Team Strength : 280+ Business : Providing Continuum of care with AI-powered contactless Remote Patient Monitoring (RPM) and Early Warning System (EWS) for Hospitals and Home. Certifications & Accreditations : ISO13485:2016 Certified, ISO27001:2022 Certified, CDSCO Registered, FDA510K Cleared for the flagship product Dozee Vitals Signs (VS) measurement system and SOC2 Type II Certified Achievements: Forbes India 30 under 30 Forbes Asia 100 to Watch - Times Network - India Health Awards 2024 for AI innovation in Bharat Healthcare tech BML Munjal Award for Business Excellence using Learning and Development FICCI Digital Innovation in Healthcare Award Anjani Mashelkar Inclusive Innovation Award Marico Innovation For India Award. To know more about life@dozee, click here . Disclaimer: Dozee is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.” Dozee does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. Dozee will not tolerate discrimination or harassment based on any of these characteristics

Project Staff Walk-in-Interview (Advt. No.: MMP025302/WP02/DRC/2025/01) Total Number of Posts: 02 Interview Date: 24th July 2025; Thursday at 10.00 AM Post code: PAT-I Post Name: Project Associate I (PAT-I) Number of posts: 02 Essential Qualification: Master's degree (M.Sc.) in Microbiology/Biotechnology / Biochemistry Preferred experience: Basic knowledge of PGPRs, microbial community-NGS, metabolite profiling skills/ethics to execute/deal with the experimentations Emoluments: (a) ₹. 31,000/- + HRA for those candidates who have qualified CSIR-UGC / ICAR / ICMR NET including lectureship/assistant professorship or GATE or those who have qualified National level examinations conducted by Central Government Department like DBT/DST or equivalent and/or their Agencies/Institutions (b) ₹ 25,000/- + HRA for others who do not fall under (a) above Job description: Selected candidate will work in the CSIR-sponsored project entitled “ Bioresource Conservation and Prospection (MMP025302) ” in WP-02 “ Bio-prospection of Mangroves”. The candidates are expected to design/ execute the experiments as well as visit the mangrove growing sites to fulfill the project objectives. Age limit: 35 years as on the date of interview (age relaxation as per CSIR rule). Other details: Duration: This position is purely temporary, initially for one year and subsequently extendable based on work performance up to project duration, whichever is earlier. It does not confer any right or claim for absorption in CSIR-CSMCRI. This post is purely temporary and co-terminus with the project. The engagement of a project staff in different projects either in the CSIR - Central Salt & Marine Chemicals Research Institute, Bhavnagar or different Laboratories/Institutes of CSIR taken together shall not exceed 06 years in any case. It would, therefore, not confer any right/claim implicit or explicit for any candidate for claiming extension or absorption in CSIR-CSMCRI, Bhavnagar. Interview Details: Interested candidates should appear before the Selection Committee for an interview/written test at CSIR-Central Salt and Marine Chemicals Research Institute, G. B. Marg, Bhavnagar-364002 (Gujarat) on 24 th July 2025, Thursday at 10.00 AM in the institute. Required Documents: Please bring an application with full particulars, including: Full name and postal address with email and phone number (application form attached), Date of birth and recent photograph. Educational qualifications and experience (if any) with photocopies of certificates/testimonials. Also, bring the following original documents (compulsory): Certificates and mark sheets (Degree/Diploma, etc.) of educational qualifications and proof of date of birth mentioned in the application (degree certificate is compulsory). GATE/NET Score Card, validity of the score, and details of seminars/projects done in the Master’s course. Experience certificates and testimonials. "No Objection Certificate" from the present employer if employed in a Government/Semi-Government or Autonomous Organization. For queries, please email drchaudhary@csmcri.res.in. No TA/DA will be provided for attending the interview.

Title: Senior Manger - API Supply chain team Date: Jul 11, 2025 Location: Dewas API - Supplychain Company: Sun Pharmaceutical Industries Ltd Role: Senior Manger – API Supply chain team Qualification: B.E. (Chemical) – preferred OR M. Sc (Chemistry) / Biotechnology / Microbiology OR B.Sc.+ MBA (Operations) Experience: Chemical Engineer with 3-4 years of experience OR candidate from other educational background with 6-9 years of experience Department: API Supply chain team Industry Preference: Pharma, Chemical, Paint, Agro, Speciality Chemicals Job Location: Andheri, Mumbai Areas of responsibilities: Capacity Planning & Capacity Effective Utilization Campaign Planning Business Continuity – De risking Plan (OS to IH, IH to OS), AVD Plan Implementation Site Transfer- API & Intermediate Cost Reduction Batches – MRP -à Commercial Supply NPL, Filling & Query Batches Supply management SCM Process maturity - Norms Setting, Cost to Serve, Planning Master Data Controller Chronic Supply Issues Resolution Responsible for Team Development & people Management - Training/ capability development of team Internal Interactions (within the organization) - Plants, RA, Procurement, R&D , Quality, LCM

We are seeking dynamic and motivated fresher to join our Field Sales team as Sales Specialists . This role offers an exciting opportunity to kickstart a career in scientific sales while actively contributing to the growth of cutting-edge biotech and life sciences solutions. Bachelor’s or Master’s degree in Biotechnology, Biomedical Engineering, Life Sciences, or a related field. Experience - 0 to 3 Years Strong interest in sales and client-facing roles within the scientific domain. Excellent communication, interpersonal, and presentation skills. Willingness to travel extensively within Andhra Pradesh. Must be self-driven, organized, and eager to learn. Two-wheeler with a valid driving license is preferred. Send your resume to Sales@nexgentechnologies.co.in Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹25,000.00 per month Work Location: In person Expected Start Date: 01/08/2025

Ct: HR SRIMATHI:7358425167 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM and CPT code Eligibility:Any lifescience,paramedical & medical UG/PG

Company Description At Proton Health, we are dedicated to revolutionizing preventive health by providing cutting-edge genetic testing kits. As the exclusive marketing partner for MyDNA by Lords Mark Microbiotech, we offer personalized insights into health and well-being. Our mission is to make genetic testing and gut microbiome testing accessible and actionable, empowering individuals to take control of their health through understanding their genetic and gut makeup. We leverage the latest advancements in genomics to inform better healthcare decisions and achieve superior outcomes. While we focus on these testing solutions, we are committed to expanding our healthtech product portfolio, continuously promoting innovative solutions. Role Description This is a full-time hybrid role for the Head of Sales and Business Development located in the Mumbai Metropolitan Region, with some work-from-home flexibility. The Head of Sales and Business Development will oversee sales strategies, manage key accounts, and drive business growth. Responsibilities include developing and executing sales plans, identifying and pursuing new business opportunities, and analyzing market trends to inform strategic decisions. Qualifications Sales and Sales Management skills Account Management and Team Management experience Strong Analytical Skills Excellent communication and interpersonal skills Proven track record in achieving sales targets Ability to work independently and in a team environment Experience in the healthtech or biotechnology industry is a plus Bachelor's degree in Business, Marketing, or a related field

Company Description AAKAR Scientific Pvt. Ltd. is an ISO 9001:2015 certified company specializing in laboratory furniture manufacturing and supply in India. With a focus on Pharma, Healthcare, Biotechnology, and other sectors, AAKAR Scientific provides turnkey lab solutions and a wide range of lab furniture and equipment. The company's dedication to technological innovation has earned the trust of over 10,000 users. Role Description This is a full-time on-site Sales Manager role located in Gujarat, India at AAKAR Scientific. The Sales Manager will be responsible for driving sales of laboratory furniture and Fume Hood to clients in various sectors. Daily tasks include prospecting, client meetings, preparing proposals, and closing deals to meet sales targets. Qualifications · Sales and Business Development skills · Client Relationship Management skills ( communication with internal and external customers) · Experience in selling lab furnishing projects · Excellent communication and negotiation skills · Bachelor's degree in Business Administration, Sales, or related field · Knowledge of laboratory furniture · Fulfilling the Targets · Preparation of drawing and quotation · Order negotiation · follow up the quotations · Interacting with customers · preparing BOQ, · payment collections 📩 Apply now at ssbu@aakarscientific.com 📞 Contact: +91 99099 23484

We are seeking dynamic and motivated fresher to join our Field Sales team as Sales Specialists . This role offers an exciting opportunity to kickstart a career in scientific sales while actively contributing to the growth of cutting-edge biotech and life sciences solutions. Bachelor’s or Master’s degree in Biotechnology, Biomedical Engineering, Life Sciences, or a related field. Experience - 0 to 3 Years Strong interest in sales and client-facing roles within the scientific domain. Excellent communication, interpersonal, and presentation skills. Willingness to travel extensively within Andhra Pradesh. Must be self-driven, organized, and eager to learn. Two-wheeler with a valid driving license is preferred. Send your resume to Sales@nexgentechnologies.co.in Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹25,000.00 per month Work Location: In person Expected Start Date: 01/08/2025