2347 Life Sciences Jobs - Page 19

As the Engineering Manager, you will lead a talented, cross-functional team of engineers and data scientists to design and develop transformative solutions for our Personalization Science products. Your role will focus on the application of advanced AI technologies, specifically LLMs and NLP, to enhance existing product capabilities and develop new capabilities for our clients. You will be instrumental in setting technical direction, fostering team collaboration, and ensuring project alignment with strategic business goals. Responsibilities: - Team Leadership: Recruit, mentor, and manage a team of software engineers and data scientists, fostering a collaborative and high-performance culture. - Technical Guidance: Provide expertise in LLMs, NLP, and machine learning (ML) technologies to guide the team in developing and implementing innovative solutions. - Project Management: Oversee the end-to-end delivery of product features, from ideation and prototyping through development, deployment, and optimization. - Collaboration: Work closely with Product, and other cross-functional teams to align technical initiatives with business objectives and ensure seamless integration with our other solutions. - Strategy Development: Define and implement technical strategies for NLP and LLM applications, staying abreast of industry advancements and evolving best practices. - Quality Assurance: Ensure high standards for code quality, testing, and reliability, balancing innovation with the need for robust, scalable production systems. - Continuous Improvement: Drive an agile development process with continuous improvement, focusing on both individual and team development, system refinements, and process optimization. Qualifications: - Education: Bachelor s degree in computer science, engineering, or equivalent work experience - Experience: 8+ years in software engineering or data science, with 3+ years in a leadership or management role - Technical Expertise: Strong background in LLMs, NLP, and machine learning frameworks (e.g., TensorFlow, PyTorch, Hugging Face), with experience in deploying production-level solutions. - Project Management Skills: Proven experience managing cross-functional teams with agile methodologies (i.e. SCRUM) - Communication Skills: Excellent interpersonal and communication skills with a track record of working effectively across functions. - Problem-Solving Skills: Analytical mindset with a strong ability to tackle complex, abstract problems and drive impactful solutions. - Preferred Skills: Familiarity with cloud platforms (e.g., AWS, GCP), MLOps best practices, and deployment of scalable AI models in production environments.

Conduct research to define targeted customer segments and determine the key values that drive buying behavior for each segment.To plan and develop marketing strategies for target customer segment.Team working spirit and abilit Required Candidate profile Proven work experience in sales and developing customer relationships. Experience in sales (preferably lab instruments Willingness to travel (above 80%)

Knowledge Park Pvt Ltd is looking for Assistant Teacher- Computer Science to join our dynamic team and embark on a rewarding career journeySupport classroom management: Assistant teachers assist in maintaining discipline and order within the classroom. They help enforce rules and routines, manage student behavior, and address any disruptions or conflicts that arise.Assist in lesson preparation: Assistant teachers collaborate with the lead teacher to develop and prepare instructional materials, lesson plans, and activities. They may also help set up and organize classroom resources, such as books, visual aids, and technology.Provide individualized attention: Assistant teachers work closely with students to provide one-on-one or small group support. They may assist students with assignments, reinforce concepts taught by the lead teacher, and provide additional guidance or clarification when needed.Support student assessments: Assistant teachers may assist in assessing student progress and performance. They may help administer tests or quizzes, grade assignments, record student data, and provide feedback to the lead teacher regarding student strengths and areas for improvement.Foster a positive learning environment: Assistant teachers contribute to creating a welcoming and inclusive classroom environment. They support student engagement and participation, encourage positive social interactions, and promote a sense of respect and cooperation among students.Assist with classroom logistics: Assistant teachers may help with practical tasks, such as taking attendance, organizing student records, managing classroom resources, and maintaining a tidy and organized learning space.

Job Overview Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager. Essential Functions Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that dont require extensive programming expertise) with guidance. May serve in the role of back-up to a DOC or DTL. May conduct data review. May write and resolve data clarifications. May lead database audit team. May develop and test databases and edit specifications. May perform testing of programming. May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team." Qualifications Bachelors Degree Clinical, biological or mathematical sciences, or related field Req Equivalent combination of education, training and experience in lieu of degree. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Pall Corporation, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation. Learn about the Danaher Business System which makes everything possible. The Engineer, Cloud Hosting is part of IT Infrastructure team and will be located in Pune, India. In this role, you will have the opportunity to: Install, upgrade, and maintain SQL Server databases; track and apply patches and CUs with minimal impact. Monitor performance using SSMS, Profiler, and AWS Compute Optimizer; configure alerts and resolve issues. Implement and document disaster recovery strategies; ensure regular testing and compliance. Ensure security compliance, support audits, and respond to SQL-related support tickets per SLA. Automate routine tasks and develop a strategic roadmap for SQL infrastructure improvements. The essential requirements of the job include: 5+ years of experience administering large number of Microsoft SQL Servers in enterprise environments. Proficiency with centralized management tools like SQL Server Management Studio, SQL Profiler, and monitoring tools (e.g., AWS Compute Optimizer) Experience with backup/recovery strategies, patch management, and performance tuning Strong understanding of database security, compliance, and audit readiness AWS certification or demonstrated knowledge of AWS services relevant to SQL Server hosting and monitoring Join our winning team today. Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Summary: We are looking for a highly motivated Compliance Software Implementation Specialist with experience in healthcare regulatory standards to lead the implementation of compliance platforms at Ambulatory Surgery Centers (ASCs) . The ideal candidate will be responsible for requirement gathering, software configuration, end-user training, and ongoing system support. This role requires strong coordination between clinical, IT, and administrative teams. Key Responsibilities: Lead and manage the implementation of compliance software at ambulatory surgery centers (ASCs). Gather requirements and configure the software to meet regulatory, accreditation, and facility-specific needs. Train ASC staff on system use, workflows, and compliance documentation. Ensure adherence to regulatory standards (e.g., CMS, AAAHC, Joint Commission). Provide ongoing support, troubleshooting, and optimization of the platform. Coordinate with internal IT teams, ASC administrators and super users. Document workflows, changes, and implementation outcomes. Required Skills & Qualifications: Experience with healthcare or compliance software (e.g., incident reporting, infection control, credentialing) Familiarity with ASC regulations: CMS, AAAHC, Joint Commission Strong project management and stakeholder communication skills Ability to train clinical and non-technical staff Basic technical aptitude in software configuration and system integration Excellent verbal and written communication skills Strong attention to detail in regulatory and documentation practices Educational Qualification Bachelor s degree in Nursing, Life Sciences, Healthcare Administration, Engineering, or a related field Additional certifications in healthcare compliance or project management are a plus

When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services. Job Title Director - Data Analytics Location(s) Mumbai Preferred Characteristics Experience within Life Sciences, Diagnostics, Healthcare, or related scientific industries. Direct experience in designing and implementing solutions specifically for data platform modernization. Experience managing globally distributed teams. Experience implementing DataOps and CI/CD practices within a data engineering context. Ability to balance operational excellence with innovation, driving both cost efficiency and business value creation. Ability to drive outcomes in a highly complex matrix environment which is often amorphous. Lead and develop a high-performing global team of functional experts, technical leads, and application managers. Foster a culture of accountability, collaboration, innovation, and customer focus. Continuously upskill the team to stay aligned with evolving technology trends and business needs. Key Responsibilities: Platform Stabilization & Operational Excellence: Accountable for stable, reliable, and secure operations across all Datawarehouse applications, ensuring adherence to defined SLAs and KPIs. Assess the current data platform architecture, identify bottlenecks, and implement solutions to ensure high availability, reliability, performance, and scalability. Establish robust monitoring, alerting, and incident management processes for all data pipelines and infrastructure. Drive initiatives to improve data quality, consistency, and trustworthiness across the platform. Oversee the operational health and day-to-day management of existing data systems during the transition period. Manage relationships with strategic vendors across the enterprise applications landscape, ensuring strong performance, innovation contributions, and commercial value. Platform Modernization & Architecture: Define and execute a strategic roadmap for modernizing PerkinElmers data platform, leveraging cloud-native technologies (AWS, Azure, or GCP) and modern data stack components (e.g., data lakes/lakehouses, Data Fabric/Mesh architectures, streaming platforms like Kafka/Kinesis, orchestration tools like Airflow, ELT/ETL tools, containerization). Lead the design and implementation of a scalable, resilient, and cost-effective data architecture that meets current and future business needs. (DaaS) Champion and implement DataOps principles, including CI/CD, automated testing, and infrastructure-as-code, to improve development velocity and reliability. Stay abreast of emerging technologies and industry trends, evaluating and recommending new tools and techniques to enhance the platform. Leadership & Strategy: Build, mentor, and lead a world-class data engineering team, fostering a culture of innovation, collaboration, and continuous improvement. Develop and manage the data engineering budget, resources, and vendor relationships. Define the overall data engineering vision, strategy, and multi-year roadmap in alignment with PerkinElmers business objectives. Effectively communicate strategy, progress, and challenges to executive leadership and key stakeholders across the organization. Drive cross-functional collaboration with IT, Security, Enterprise Apps, R&D, and Business Units. Data Monetization Enablement: Partner closely with business leaders, enterprise app teams, and other business teams to understand data needs and identify opportunities for data monetization. Architect data solutions, APIs, and data products that enable the creation of new revenue streams or significant internal efficiencies derived from data assets. Ensure robust data governance, security, and privacy controls are embedded within the platform design and data products, adhering to relevant regulations (e.g., GDPR, HIPAA where applicable). Build the foundational data infrastructure required to support advanced analytics, machine learning, and AI initiatives. Basic Qualifications Required Qualifications & Experience Bachelors or Masters degree in Computer Science, Engineering, Information Technology, or a related quantitative field. 15+ years of experience in data engineering, data architecture and/or data warehousing. 5+ years of experience in a leadership role, managing data engineering teams and driving large-scale data initiatives. Proven track record of successfully leading the stabilization, modernization, and scaling of complex data platforms. Deep expertise in modern data architecture patterns (Data Lakes, Data Warehouses, Lakehouses, Lambda/Kappa architectures). Extensive hands-on experience with cloud data platforms (AWS, Azure, or GCP - specify preferred if applicable) and their associated data services (e.g., S3/ADLS/GCS, Redshift/Synapse/BigQuery, EMR/Dataproc/Databricks, Kinesis/Kafka/Event Hubs, Glue/Data Factory/Dataflow). Strong experience with big data technologies (e.g., Spark, Hadoop ecosystem) and data processing frameworks. Proficiency with data pipeline orchestration tools (e.g., Airflow, Prefect, Dagster). Solid understanding of SQL and NoSQL databases, data modeling techniques, and ETL/ELT development. Experience with programming languages commonly used in data engineering (e.g., Python, Scala, Java). Excellent understanding of data governance, data security, and data privacy principles and best practices. Exceptional leadership, communication, stakeholder management, and strategic thinking skills. Demonstrated ability to translate business requirements into technical solutions.

Job_Description":" About The Company: iLink Digital is a Global Software Solution Provider and Systems Integrator, delivers next-generation technology solutions to help clients solve complex business challenges, improve organizational effectiveness, increase business productivity, realize sustainable enterprise value and transform your business inside-out. iLink integrates software systems and develops custom applications, components, and frameworks on the latest platforms for IT departments, commercial accounts, application services providers (ASP) and independent software vendors (ISV). iLink solutions are used in a broad range of industries and functions, including healthcare, telecom, government, oil and gas, education, and life sciences. iLink expertise includes Cloud Computing & Application Modernization, Data Management & Analytics, Enterprise Mobility, Portal, collaboration & Social Employee Engagement, Embedded Systems and User Experience design etc. . Requirements ETL development to transform data Co-ordinate with Engineering team and Development team to gather their requirement related to Engineering and data. Gather data from various data sources and work with engineering team for any gaps. Meetings with Stake holders for Demo and Data related. Requirements Skill set Expertise in Pentaho ETL Transformation. Expertise in SQL and Oracle. Good knowledge in API. Experience in other Halliburton Products is very good plus Experience in Pentaho Reporting is a plus. Good troubleshooting skills. Benefits Competitive salaries Medical Insurance Employee Referral Bonuses Performance Based Bonuses Flexible Work Options & Fun Culture Robust Learning & Development Programs In-House Technology Training

We are looking for an Account Manager to join our Intellectual Property Sales team for Bangalore. This is an amazing opportunity to champion our line of IP products and services and work with our customers across the innovation ecosystem. If you re experienced in maintaining successful client relationships, with a track record in achieving financial targets, and providing invaluable cross-functional perspective on product and process improvements to the client experience. About You experience, education, skills, and accomplishments Minimum of a bachelor s degree Minimum of 4 years Sales experience in a business-to-business sales environment Business intelligence or SAAS sales experience in the IP industry. Experience with CRM tools (Salesforce.com). Proven track record of account management capability: Developing accounts through proactive account reviews and prospecting. Deep discovery to understand customer workflow and content needs. Adept at cultivating strong customer relationships. Excellent organisational skills and ability to manage multi-stage sales processes. Excellent presentation, communication, negotiation and time management skills. It would be great if you are . . . Understanding of consultative selling and strategic account management. Previous experience in Information Technology and Services, Legal Services, Information Services, or experience in the life sciences industry Experience in Intellectual Property is a plus Flexible and adaptable with a strong desire to learn and develop. What will you be doing in this role? Support and develop sales opportunities both independently and in collaboration with a team to exceed the annual sales target. Utilise domain expertise to conceive and position value-added solutions. Build and develop a pipeline with a clear focus on increasing opportunity size and velocity. Cultivate strong customer relationships creating confidence with senior stakeholders to become a trusted advisor to our customers. Work in alignment with sales team members and solution consultants, to contribute to territory planning and maximise Clarivate s exposure within our customers. Diligent management of opportunities in CRM (Salesforce) ensuring all information is up to date at all times. Contribute to and produce reports, including outlining current and proposed activities, sales forecasts and closing timetables. Work with sales enablement, marketing and other commercial teams to develop and execute sales campaigns and lead generation activities Pro-actively acquire and develop relevant market, industry and product knowledge and skills to support commercial success. Upto 30% travel required

Job_Description":" About The Company: iLink Digital is a Global Software Solution Provider and Systems Integrator, delivers next-generation technology solutions to help clients solve complex business challenges, improve organizational effectiveness, increase business productivity, realize sustainable enterprise value and transform your business inside-out. iLink integrates software systems and develops custom applications, components, and frameworks on the latest platforms for IT departments, commercial accounts, application services providers (ASP) and independent software vendors (ISV). iLink solutions are used in a broad range of industries and functions, including healthcare, telecom, government, oil and gas, education, and life sciences. iLink expertise includes Cloud Computing & Application Modernization, Data Management & Analytics, Enterprise Mobility, Portal, collaboration & Social Employee Engagement, Embedded Systems and User Experience design etc. . Requirements Key Responsibilities: Design, develop, test, and deploy high-quality applications using C# and .NET Core/.NET Framework Build and maintain RESTful APIs and microservices hosted on Azure App Services , Azure Functions , or AKS Integrate with Azure services such as Azure Storage , Azure SQL , Azure Key Vault , Azure Service Bus , and Azure DevOps Collaborate with cross-functional teams including product managers, architects, and QA engineers Participate in code reviews, unit testing, and performance tuning Implement CI/CD pipelines using Azure DevOps Monitor and troubleshoot applications in production using Azure Monitor , Application Insights , and Log Analytics Ensure security, scalability, and performance best practices are followed Required Skills & Qualifications: Bachelor degree in Computer Science, Engineering, or related field 5+ years of experience in C#/.NET development Strong experience with Azure PaaS services (App Services, Functions, Logic Apps, etc.) Proficiency in Azure DevOps , CI/CD pipelines , and Git Experience with SQL Server and Entity Framework Familiarity with containerization (Docker, Kubernetes) is a plus Solid understanding of OOP , design patterns , and software development best practices Excellent problem-solving and communication skills Benefits Competitive salaries Medical Insurance Employee Referral Bonuses Performance Based Bonuses Flexible Work Options & Fun Culture Robust Learning & Development Programs In-House Technology Training

Job_Description":" About The Company: iLink Digital is a Global Software Solution Provider and Systems Integrator, delivers next-generation technology solutions to help clients solve complex business challenges, improve organizational effectiveness, increase business productivity, realize sustainable enterprise value and transform your business inside-out. iLink integrates software systems and develops custom applications, components, and frameworks on the latest platforms for IT departments, commercial accounts, application services providers (ASP) and independent software vendors (ISV). iLink solutions are used in a broad range of industries and functions, including healthcare, telecom, government, oil and gas, education, and life sciences. iLink expertise includes Cloud Computing & Application Modernization, Data Management & Analytics, Enterprise Mobility, Portal, collaboration & Social Employee Engagement, Embedded Systems and User Experience design etc. . Requirements Key Responsibilities Design, develop, and integrate generative AI models into applications to deliver innovative features. Lead the full development lifecycle of AI projects, from requirements gathering and design to testing, deployment, and maintenance. Implement and optimize both frontend and backend components of applications to support AI-driven functionalities. Provide technical guidance and mentorship to junior developers on AI integration and full stack development best practices. Stay current with advancements in generative AI and identify new tools, technologies, and methodologies to enhance application features. Required Skills and Qualifications Education: Bachelors or Master degree in Computer Science, Engineering, or related field. Experience: 5+ years in full stack development. 1+ years working with AI technologies, with hands-on exposure to generative AI projects. Experience in building APIs and microservices for AI integrations. Knowledge of cloud-based AI services (e.g., Azure or AWS AI). Technical Proficiency: Proficiency in JavaScript frameworks (e.g., React, Angular, or Vue.js). Experience with backend technologies (e.g., Node.js, Python, C#) Expertise in Cloud platforms - Azure or AWS. Familiarity with SQL and NoSQL databases. Experience with large language models or generative models (e.g., GPT, BERT). Knowledge of AI frameworks like TensorFlow, PyTorch, or similar Expertise in tools like GitHub, Docker, CI/CD pipelines. Skills: Strong problem-solving skills with an innovative mindset. Ability to translate complex AI concepts into practical solutions. Excellent communication skills and the ability to work in a collaborative environment. Familiarity with data science concepts is a plus. Benefits Competitive salaries Medical Insurance Employee Referral Bonuses Performance Based Bonuses Flexible Work Options & Fun Culture Robust Learning & Development Programs In-House Technology Training

Job_Description":" About The Company: iLink Digital is a Global Software Solution Provider and Systems Integrator, delivers next-generation technology solutions to help clients solve complex business challenges, improve organizational effectiveness, increase business productivity, realize sustainable enterprise value and transform your business inside-out. iLink integrates software systems and develops custom applications, components, and frameworks on the latest platforms for IT departments, commercial accounts, application services providers (ASP) and independent software vendors (ISV). iLink solutions are used in a broad range of industries and functions, including healthcare, telecom, government, oil and gas, education, and life sciences. iLink expertise includes Cloud Computing & Application Modernization, Data Management & Analytics, Enterprise Mobility, Portal, collaboration & Social Employee Engagement, Embedded Systems and User Experience design etc. . Requirements Requirements Primary Skills- C++, C#, MFC Detailed JD- We are seeking a skilled Senior Software Engineer with around 6 years of overall industry experience. The ideal candidate will have strong expertise in developing desktop applications using MFC, C++, and C#. Proven ability to design, develop, and maintain complex software systems with a focus on performance and scalability. Hands-on experience in debugging, troubleshooting, and optimizing legacy applications. Collaborate closely with cross-functional teams to understand requirements and deliver high-quality solutions. Ability to write clean, efficient, and well-documented code following best practices. Strong analytical, problem-solving, and communication skills are essential. Experience with version control systems like Git is preferred. Prior exposure to the full software development lifecycle is an advantage. Benefits Competitive salaries Medical Insurance Employee Referral Bonuses Performance Based Bonuses Flexible Work Options & Fun Culture Robust Learning & Development Programs In-House Technology Training

Role Summary We re looking for a hands-on AI & Data Platform Architect to design and build a scalable, secure, and modular platform that powers AI research in healthcare. You ll lead the technical architecture for training and deploying models on complex biomedical data, helping shape the future of AI in life sciences. Key Responsibilities Design and build a scalable AI/ML platform to support data pipelines, model training, and deployment. Work with large, diverse biomedical datasets (clinical, genomic, proteomic, chemical). Build secure, cloud-native infrastructure using containers and APIs. Implement and scale foundation models, knowledge graphs, and embeddings. Ensure compliance with security and privacy standards (e.g., HIPAA, SOC2). Collaborate with cross-functional teams (data scientists, clinicians, engineers). Mentor engineers and set best practices for ML platforms and MLOps. Required Skills & Experience Master s or PhD in Computer Science, AI/ML, or related field. 10+ years in AI platform or infrastructure roles. Strong experience with Python, ML frameworks (PyTorch, TensorFlow), and cloud platforms (AWS, GCP, Azure). Experience with distributed systems, MLOps, and tools like MLFlow, Kubeflow, Databricks. Familiar with GPUs, performance optimization, and data security practices. Nice to Have Background in life sciences or biomedical data (genomics, proteomics, EHRs). Familiarity with drug discovery workflows and generative AI tools like LangChain or Hugging Face. Knowledge of bioinformatics databases and ontologies. What We Offer Chance to shape a cutting-edge AI platform in a mission-driven startup. Equity and growth opportunities in a fast-moving team. Budget for learning and experimentation with AI/cloud tools.

The Process Knowledge Management Specialist acts as a subject matter expert for authoring and updating Emerson DeltaV PKM process templates, Process Recipes and associated Master Data. The primary responsibility is to ensure that Process Recipes within DeltaV PKM are successfully and compliantly designed, developed, deployed, and supported to maximize business benefits and are in line with enterprise business process and technical standards. DeltaV PKM is a new capability being developed by Emerson. In addition to the support and development responsibilities listed below, a successful candidate with have an opportunity to work closely with the Emerson development team to shape the future direction of the product Primary Responsibilities: Support DeltaV PKM training, collaboration, benefit realization, and standardization. The Specialist will follow the standard processes and procedures in performing their duties. These include cGMP regulations, SOPs and global business processes. Identify and implement continuous process improvement opportunities. Assist in the definition and implementation of an SDLC strategy that supports the flexible use of DeltaV PKM capabilities across the development spectrum. Sustain Process recipes and master data, bringing together knowledge of manufacturing processes, and DeltaV PKM capabilities and standards Executes the appropriate change control and life-cycle actions and processes to assure the DeltaV PKM system is in a state of control and compliance. Collaborates and assists with troubleshooting to efficiently resolve user issues. Knowledge of Quality Systems and Regulatory Standards to provide assurance and foster quality decisions with Development teams and their respective Quality units Education Bachelor s Degree and 5+ years of relevant experience with life sciences systems or 7+ years of relevant experience with life sciences systems Required Experience and Skills Proven track record of analytical skills, problem solving and attention to detail High personal integrity, credibility, and energy Excellent communication and influencing skills while working with Global stakeholders (North America). Strong written and verbal communication skills Minimum five (5) years of experience in a production regulated industry. Strong understanding of manufacturing principles/processes (preferably Biologics) and ability to translate manufacturing requirements into Automation/Digital Solutions Preferred Experience and Skills Knowledge of SAP Knowledge of Pharmaceutical Technology Transfer processes Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Automation Systems Design, Change Catalyst, Customer-Oriented, Detail-Oriented, Device Integration, Equipment Calibrations, HMI Programming, HVAC Management, Information Systems Management, Innovation, Knowledge Management, Laboratory Information Management System (LIMS), Management Process, PLC Programming, Production Scheduling, Root Cause Analysis (RCA), Spare Parts Procurement, Technical Support Preferred Skills: Job Posting End Date: 08/15/2025 *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.

Location: Bangalore Experience: 3 5 Years Notice Period: Immediate to 15 Days CTC: 10 20 LPA Role Overview: We are seeking a skilled and innovative LLM Engineer to design, implement, and optimize advanced GenAI solutions across drug discovery, clinical development, and manufacturing. The ideal candidate will have hands-on experience with LLMs, deep learning, MLOps, and agentic frameworks, with a strong focus on building scalable AI infrastructure and production-ready ML pipelines. Key Responsibilities: Design and implement LLM training and fine-tuning pipelines (e.g., using DeepSpeed, PEFT, RLHF). Collaborate with data scientists to customize and deploy LLMs in use cases such as target discovery, clinical trial optimization, and molecule design . Build scalable, reusable backend systems and GenAI agentic frameworks (AutoGen, LangGraph) to power R&D applications. Develop and maintain robust evaluation frameworks , telemetry systems, and performance monitoring tools. Operationalize models on Azure and GCP with MLOps best practices, working closely with the DevSecOps team. Design data pipelines to support rapid ML experimentation and model lifecycle management. Evaluate and integrate third-party GenAI tools and co-develop solutions with external technology partners. Required Qualifications: Bachelor s degree in Computer Science, Engineering, or a related quantitative field. 3-5 years of experience in ML/AI engineering, with a strong focus on LLMs and GenAI . Proficiency in Python and frameworks such as PyTorch or TensorFlow . Experience with LLM technologies , including embedding techniques, RAG, fine-tuning, pre-training , and evaluation benchmarks . Hands-on experience with agentic AI frameworks like AutoGen and LangGraph . Solid experience in MLOps , model deployment, and cloud infrastructure (Azure, GCP). Full-stack engineering mindset with familiarity in CI/CD, testing, code reviews , and scalable software development. Strong problem-solving abilities and communication skills. Preferred: Experience in life sciences, healthcare, or pharma R&D applications is a plus. Familiarity with data governance, model interpretability, and responsible AI practices.

Company: Global calcium Pvt Ltd Location: Hosur, Tamil Nadu Responsibilities Preparing Structural design and drawing for Civil Projects. Cost estimation for Projects. BOQ Preparation for all projects. Ensuring the building Maintenance as per the SOP Executing the Routine civil activities of entire site. Schedule preparation for Projects. Planning and Execution of works as per design and drawing Maintaining quality standards for all civil works Checking quality of incoming materials from vendors and estimation of material required in execution of work Checking and Verification of checklist, test reports, batch reports and Bar Bending schedule. Identifying deviations and providing technical advice and solving problems on site Preparation of daily, weekly, monthly reports on work progress and evaluation as per planned schedules Supervision of working labour to ensure strict conformance to methods, quality and safety. Desired Candidate Profile: Qualification: B.E / B.Tech/Diploma-Civil Engineering Experience: 8 to 10 Years Preferred Industry: Pharmaceutical and Life Sciences

Job Overview Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety s involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors. Essential Functions Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product s safety profile Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data Represent safety and clinical data review findings during client meetings Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies Provide medical oversight for label development, review and change Provide medical support and attendance at Data Safety Monitoring Board Meetings Attends and contributes medical safety evaluation on Safety Monitoring Committees Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture. Act as Global Safety Physician or Assistant or Back-up on projects as assigned Attend project meetings, medical safety team meetings, and client meetings as requested Ensure coverage for all medical safety deliverables within regulatory or contracted timelines Provide medical escalation support for medical information projects Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects 24 hour medical support as required on assigned projects Maintain awareness of medical-safety-regulatory industry developments Qualifications Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education Req Three (3) years of clinical practice experience (e.g graduate medical training) with two (2) additional years in the pharmaceutical or associated industry in any role. Or equivalent combination of education, training and experience Req Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice Knowledge of clinical trials and pharmaceutical research process Ability to establish and meet priorities, deadlines, and objectives. Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility Ability to establish and maintain effective working relationships with coworkers, managers and clients A valid medical license, or equivalent, from the country or region in which he/she resides and works Pref

We re seeking a Lead Product Manager to join our Product Management team in Bangalore, focusing on the Life Sciences & Healthcare (LSH) space. This is a fantastic opportunity to work with a diverse, high-performing team and report directly to the Director of Product Management. You ll drive product strategy, lead cross-functional initiatives, and help shape innovative solutions in a fast-evolving domain. We have a great skill set in Product Management and we would love to speak with you if you have similar skills. About You experience, education, skills, and accomplishments Bachelor s degree (B. Pharma/Biotech/B. E) or equivalent At least 10 years of proven experience in product manager role At least 8 years of experience in working with cross functional teams (UI/UX, Sales and marketing, Development team etc.) Strong analytical, communication, and stakeholder management skills It would be great if you also had . . . Experience in SQL, Database Experience in U.S Healthcare or Pharma industry What will you be doing in this role? Directly responsible for delivering business outcomes, ensuring alignment with company goals and objectives. Responsible for product success metrics, adoption and retention. Responsible for a major multi-year product line or functional area, managing all end-to-end aspects of development and delivery. Make independent, informed decisions regarding the product roadmap, balancing innovation with strategic priorities. Deliver strategic insights that impact the company as a whole. Identify unmet needs and emerging markets that the company can strategically pursue for growth and competitive advantage. Mentor and support team members across the organization, fostering a culture of collaboration and continuous improvement. Create and implement frameworks designed to elevate the entire product team s performance and effectiveness. Build and manage key processes that enhance operational efficiency and support product development initiatives. Actively advocate for customer needs and feedback throughout the organization, ensuring that the customer s voice is integrated into all decisions. Lead cross-functional initiatives that drive scalability and enhance the company s overall performance and productivity. Mentor leaders in other teams, sharing insights and best practices to cultivate leadership skills and promote cross-departmental collaboration. Product you will be developing Market Access Intelligence, is a single source of integrated, customizable and comprehensive healthcare data, including formularies, coverage policies, health plan enrollments, current trends and expert insights that help clients develop and execute a comprehensive, analytics-based market access strategy. About the Team We are a global team with team members located across U.S. and India, specialized in providing Product Management Services. We build and manage Market Access Products for Life Sciences & Health, working with stakeholders across the LSH space, globally. Hours of Work Mon- Friday (8.5 hrs. a day), Candidate should be flexible as there will be overlaps with the cross functional global teams located across India, U.S., U.K. and Europe.

Job Description: OptraSCAN is seeking a highly detail-oriented and knowledgeable Regulatory Specialist - Technical Writer to create, manage, and maintain regulatory documentation required for product approvals, certifications, and market access in global markets. This role involves a combination of regulatory strategy and high-quality technical writing for medical devices (hardware and software), with a focus on ensuring compliance with international standards such as ISO 13485, FDA 21 CFR Part 820, EU MDR, and others. Key Responsibilities: Regulatory Documentation & Submissions. Prepare and maintain high-quality regulatory documentation including: Technical Files / Design Dossiers Clinical Evaluation Reports (CERs) Risk Management Files Declarations of Conformity FDA submissions (510(k) or pre-submissions, if applicable) Collaborate with cross-functional teams to gather inputs from R&D, QA, Clinical, and Marketing for submission documents. Technical Writing: Write, edit, and proofread SOPs, work instructions, user manuals,labeling, and IFUs to ensure technical accuracy and regulatory compliance. Translate complex technical data into clear, concise, and user-friendly documentation. Compliance & Standards: Stay current with regulatory changes (EU MDR, FDA, etc.) and update internal documentation and processes accordingly. Ensure documentation aligns with applicable standards such as: ISO 13485. ISO 14971 (Risk Management) IEC 62304 (Software Lifecycle) IEC 60601 (Electrical Medical Devices) EU MDR 2017/745 FDA 21 CFR Part 820 Quality System Support: Support internal audits and inspections by maintaining complete and audit-ready documentation. Assist in CAPA documentation and post-market surveillance reports when required. Required Qualifications: Bachelor s or master s degree in Life Sciences, Biomedical Engineering, Pharmacy, or a related field. 3-5 years of experience in regulatory writing or regulatory affairs in a medical device or healthcare product environment. Strong knowledge of global medical device regulatory frameworks (FDA, EU MDR, etc.). Excellent written English and technical writing skills. Strong organizational and project management skills. Preferred Qualifications: Experience preparing 510(k), CE Mark, or similar submissions. Familiarity with digital pathology, imaging devices, or software as a medical device (SaMD). Certification in Regulatory Affairs (e.g., RAPS RAC) is a plus.

Key Responsibilities : Ensure compliance with ISO 13485, FDA 21 CFR Part 820, and other applicable international quality standards. Support design control, risk management, validation, and verification processes for scanners and software. Maintain and improve the Quality Management System (QMS) across departments. Review and approve SOPs, DHRs, DHFs, CAPAs, NCRs, and change controls. Conduct internal audits and support external audits (e.g., customer, notified bodies, FDA). Collaborate with engineering, manufacturing, and regulatory teams to ensure product quality at every stage of the lifecycle. Support software validation and documentation of AI algorithms per FDA/CE/MDR requirements. Participate in supplier qualification and vendor audits. Monitor and report on key quality metrics (e.g., defect rates, complaints, CAPA status). Ensure traceability and document control throughout product development and release. Qualifications: Bachelor s degree in biomedical engineering, Quality, Life Sciences, or related field. 3-6 years experience in a medical device, diagnostics, or regulated health tech environment. Familiarity with digital pathology, AI in healthcare, imaging devices, or SaMD is a plus. Strong knowledge of ISO 13485, ISO 14971, IEC 62304, FDA QSR, and EU MDR/IVDR regulations. Experience with QMS tools, document control systems, and audit practices. Excellent written and verbal communication skills. Detail-oriented, with strong problem-solving and cross-functional collaboration abilities.

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud - the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions. OVERVIEW We are seeking a strategic, systems-oriented Manager of Customer Success Operations to lead the backbone of our customer success infrastructure. This position will be instrumental in scaling the operational engine that powers our Top 30 Pharma, Top 10 CRO, and Mid-Market engagement strategies. You will leverage tools like Salesforce, Gainsight, Smartsheet, JIRA, SharePoint, HubSpot, and LinkedIn Sales Navigator to deliver actionable insights, enable customer-facing teams, and drive measurable impact. This role will be a critical partner to the VP of Customer Strategy & Success and a key contributor to our transformation into an AI-native, customer-obsessed organization. KEY TASKS & RESPONSIBILITIES Customer Success Systems Ownership Serve as the product owner for Gainsight and Salesforce within the CSS function owning configuration, process optimization, and reporting. Integrate data from platforms like HubSpot, Consensus, LinkedIn Sales Navigator, and SharePoint to build a unified customer view. Administer and continuously improve Smartsheet trackers and dashboards used for customer journey and lifecycle management. Data, Reporting & Insights Build and manage dashboards and reports in Salesforce, Gainsight, and Smartsheet to track CSAT, NPS, adoption, renewal risk, and lifecycle progress. Develop segmentation-driven insights to support the differentiated management of strategic, enterprise, and mid-market accounts. Collaborate with the Data & Analytics team to develop predictive health score models and success metrics. Process Optimization & Program Enablement Standardize and document customer success processes including onboarding, renewals, expansion, and risk mitigation using SharePoint and Smartsheet. Help operationalize and automate CS playbooks and processes Support one-to-many outreach with customers Use JIRA to manage CSS project backlogs, feature feedback loops, and cross-functional initiatives. Operationalize strategic programs such as QBRs, Voice of Customer, and Adoption Accelerators in partnership with Product, Marketing, and Sales. Cross-Functional Alignment Partner with Revenue Operations to sync Salesforce pipeline and renewal workflows with CSS engagement models. Coordinate with Product and Engineering teams through JIRA for feature tracking and issue resolution visibility. Collaborate with Enablement to train the CSS team on tooling (Gainsight, Salesforce) and share best practices through SharePoint playbooks. Governance & Transformation Support Support the VP of Customer Strategy & Success in OKR execution, strategic initiative tracking, and leadership reviews. Lead readiness efforts for new rollouts, platform enhancements, or strategic account programs tied to Operational Excellence 2.0. QUALIFICATIONS 6-10 years of experience in Customer Success, Revenue, or Business Operations in a SaaS or Life Sciences technology firm. Salesforce & Gainsight (administration, reporting, workflow management) SharePoint and Office 365 suite JIRA (project intake, prioritization workflows) HubSpot, LinkedIn Sales Navigator, Consensus (engagement and insights tools) Project management systems like Smartsheets preferred (project tracking, dashboards) TECHNICAL SKILLS Strong analytical skills with experience in lifecycle metrics, cohort analysis, and revenue attribution. Excellent communicator who can influence cross-functional stakeholders and drive accountability. A customer-first mindset with deep empathy for internal teams and client value realization. Agile, proactive, and comfortable navigating transformation and scale. Accelerate your skills and career within a fast-growing company while impacting the future of healthcare. We have shared our story, now we look forward to learning yours! eClinical Solutions is a people first organization. Our inclusive culture values the contribution that diversity brings to our business. We celebrate individual experiences that connect us and that inspire innovation in our community. Our team seeks out opportunities to learn, grow and continuously improve. Bring your authentic self, you are welcome here! We are proud to be an equal opportunity employer that values diversity. Our management team is committed to the principle that employment decisions are based on qualifications, merit, culture fit and business need.

Working in an Agile software development framework, POs collaborate with customer/market facing Product Managers (PM) who are responsible for the product strategy and own the product roadmap. As a PO, you will discuss the product strategy, roadmap, and business requirements in detail with the PM, convert them into functional / non-functional requirements for the development team and help prioritize these requirements. You will also lead Sprint review meetings, guide developers and testers on meeting product requirements, and oversee the release and deployment of high-quality products. Qualifications, Skills, and Experience: Bachelor s / Master s degree in Computer Science & Engineering (CSE) or equivalent STEM degree 4+ years of experience working in the software industry, with at least 3 years working as a Product Owner, Business Analyst or Systems Analyst, ideally for customers in the Life Sciences industry. Proven experience of writing meaningful and clear stories and guiding Agile teams on product development Experience of guiding teams developing rich, dynamic, and interactive multitenant web applications Strong mathematical and logical aptitude, and analytical mindset Strong verbal and written communication skills Good documentation skills Hands-on experience of working with Atlassian Jira and Confluence Optional Skills and Experience (preferred but not mandatory): Prior hands-on software testing experience Familiarity with web technologies, service-oriented architecture (SOA), cloud technology, and cloud security Knowledge of government regulations like GxP SEQ, GDPR, and 21 CFR Part 11 or EU GMP Annex 11 Summary of Job Responsibilities: Discuss the product strategy and roadmap with the Product Manager (PM) and help determine the release schedule Work with the PM, SMEs, and other stakeholders (architects, DevOps, etc.) to develop strong understanding of high-level functional and non-functional requirements and help in estimating the overall effort required to develop and test them Assist the PM in reviewing and prioritizing the epics for a specific release cycle and create a release backlog Perform backlog grooming periodically and define finer stories that can be implemented in sprints Work with the team to analyze and elaborate stories, define clear acceptance criteria covering relevant functional / non-functional requirements, and assist the team in story estimation and sequencing Review reported bugs and participate in their analysis, triaging, and prioritization Review test strategy for feature testing and guide testers on ensuring high testing coverage Perform hands-on testing of the product regularly, especially from user acceptance point of view and provide feedback to the team Review and approve implemented features as they are completed by the team Produce and maintain necessary project documentation as required by Cytel s SDLC processes (e.g., requirements). Participate in internal / external process audits.

Project Research Scientist -II (Non-Medical)-ICMR - CAR -MEDTECH Project Division Non Division User Contact Person Ms. Lincy Thomas Job Details Brief Description about the Project CAR : Center for Advance Research (CAR) on Medical Devices Development, Characterization and Validation : A clinical trials approach: Aims to provide a comprehensive platform for the end-to-end development, testing, and validation of medical devices. Project Research Scientist -II (Non-Medical) No.of Vacancy:One Prefered Qualifications: Post graduate Degree or PhD in Lifesciences, Pharmacology and Biomedical engineering with experience (three years) in conducting large scale intervention studies. Experience:Minimum of 3 years Language: English, Kannada, Telugu, Tamil, Hindi Salary:Rs.85,090/- per month Roles and Responsibilities: Experience and proficiency in designing and executing clinical and pharmaceutical/medical device trials. Experience in conducting large-scale intervention efficiency and effectiveness studies or Phase III trials. Responsible for managing the daily operations of all aspects of the research project. Contribute to the planning and execution of clinical trials within the research projects. Utilize scientific expertise to design and implement non-medical aspects of clinical trial protocols. Analyze and interpret data generated from clinical trials, providing valuable insights. Collaborate with the clinical research team to ensure adherence to study protocols and regulatory standards. Contribute to the publication of research findings in scientific journals and present results at conferences. Contribute to the publication of research findings in scientific journals and present results at conferences. Interested candidates may send their Resume to: The Principal Investigatior

We are looking for a Patent Drafting Sr. Analyst or Lead to join our Patent Preparation and prosecution team in Noida, India. This is an amazing opportunity to work on drafting and prosecuting work and also managing one or more clients. The team includes 18 people and is reporting to Director. We have a great skill set in preparations and prosecution and we would love to speak with you if you have skills in patent drafting, patent prosecution and client management experience. About You experience, education, skills, and accomplishments Strong Technical knowledge in the fields of Mechanical / Electronics / Chemistry and/or Life sciences domains and proficiency in drafting projects related to other technology domains Excellent communication skills, both verbal and written. Good understanding of Intellectual property laws and particularly patent laws At least Masters degree in Mechanical / Electronics / Chemistry/Life sciences/Biotechnology/Pharma or other relevant disciplines. Ability to work on multiple projects and with multiple teams under strict timelines Self-starter, meticulous with strong analytical and problem-solving skills. Proficiency in MS Excel, MS Word, MS PowerPoint and other MS office applications Good interpersonal and client management skills. It would be great if you also had Prosecution experience Working knowledge of AutoCAD, ChemDraw, Visio or other drawing tools is an advantage Masters degree or PhD Knowledge and experience on patent prosecution, patent search or patent analytics projects Prior knowledge of different patent and non-patent databases What will you be doing in this role? Preparation of patent application drafts in compliance with USPTO, EPO and PCT rules and requirements Analyzing prior art and invention disclosure documents to evaluate patentability of the invention Conducting inventor interviews and/or technical discussions with client IP counsel Independently preparing and delivering multiple projects in compliance with internal policies and processes Willingness to work extended hours to meet client requirements Effectively collaborating with cross-skilled and cross-functional internal and external teams to complete and deliver assigned projects on time Effectively working with reporting managers or project managers to scope multiple projects and deliver them with a high level of accuracy and attention to detail About the Team The team supports various corporates and law firms across the world in drafting and prosecution services. The team has dedicated professions with strong passion in technology. Hours of Work 8 hours of work for 5 days a week in IST.

Sr Project Spprt Team Coord at IQVIA Job Description Sr Project Spprt Team Coord Job available in additional locations Bengaluru, India| India Save this job Job Description Job Overview Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions. Assists in the development of detailed documentation and specifications. Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions. Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience. Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities. Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications Bachelors Degree Req 1-3 years of related experience Req Works willingly and effectively with others in and across the organization to accomplish team goals. Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline. Knowledge of consulting methods, tools and techniques, related to one s functional area. Knowledge of current events and developments within an industry and major competitors. Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies. Effective time management skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at Save this job LEARN ABOUT HOW WE WORK Join our Global Talent Network Let s stay connected. Sign up to receive alerts when new opportunities become available that match your career ambitions.