2520 Lims Jobs - Page 26

About the job Secure master data (MD) quality and availability at the Sanofi target Support master data quality improvement activities across all sites in the frame of M&S master data playbook Identify any master data quality and availability issues and propose solutions and remediation (continuous improvement spirit) Provide technical analysis on Masterdata and implementation of new scope Key accountabilities MD operational responsibility Site-level data collection to define and set up parameters to ensure the correct scope of Masterdata Preparing the execution of internal assessments / capability reviews by providing relevant data analysis and data situation report Preparing MD deactivatio...

5 - 7 Years 1 Opening Bangalore Role description LabVantage LIMS Specialist Location: Bangalore Seeking a skilled professional with hands-on experience in LabVantage version 8 or higher , including instrument integration , Electronic Lab Notebook (ELN) , and various third-party interfaces . Qualifications: Bachelor’s or Master’s degree in Computer Science , Life Sciences , Engineering , or a related field. In-depth understanding of LabVantage architecture , core modules, configuration, and administrative tools. Proficient in Java , JSP , SQL , and JavaScript . Key Responsibilities: Configure, customize, and maintain the LabVantage LIMS to support laboratory and business requirements. Design ...

Company Description About Eurofins: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is a global leader in food, environmental, pharmaceutical and cosmetic product testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory serv...

Job Description Summary Sr LIMS Programmer – Technical Lead Job Description 1. Setup and Troubleshooting of technical issues related to LabVantage, Instrument Interfaces, Server Environments, Bartender Label Printing Software, and Jasper Reporting. 2. Creation and execution of installation qualification protocols for Quality System’s applications such as LabVantage, LIMS, Empower, and other supporting software. 3. Assistance in the Change Management Tool (CMT) process to moving Master Data between environments. 4. Create and Maintain Jasper Reports and Bartender Labels. 5. Execution of verification protocols to confirm LabVantage reports, labels, and instrument interfaces. 6. Work with busin...

Job Description Summary Sr LIMS Programmer – Empower Lead Job Description 1. Creation of Empower projects, methods and custom fields used for chromatography test methods integrated with LabVantage LIMS. 2. Creation and execution of verification protocols for Empower objects within an Empower validation environment. 3. Promotion of master data (methods, custom fields) between Empower Environments as per defined program. 4. Configuration of LabVantage LIMS master data for chromatography test methods integrated with Empower, including AQC methods, Mixed Consumable Types and Empower policies. 5. Execution of verification protocols to confirm LabVantage master data configuration for LabVantage-Em...

Job Description Summary Sr LIMS Programmer – Change Manager Job Description Manage changes within the Global QC service desk. Assign system-specific impact assessment to required systems owners for proposed changes. Follow-up with system owners as needed for completion of system-specific impact assessments. Complete TrackWise Impact Assessment for all changes based on input from system owners. Lead change management meetings with site change owners to track required timelines for changes. Communicate timelines to LIMS admin team for updating electronic systems. Liaison between LIMS admin team and business owners to ensure business changes and system changes are implemented in parallel. Suppo...

Job Description Job Summary: If you are a Software professional and looking for career opportunity, Emerson has an exciting offer to you! The MES Software Lead Engineer would lead the software development and configuration in Manufacturing Execution System (MES) projects. In this Role, Your Responsibilities Will Be: Lead the detail design, implementation, test of MES solution for MES projects based on Emerson MES platform- Syncade as per best practices. Lead, design, implement, and test a full stack of Syncade MES technologies (using ASP.Net, C#, MVC, SQL, VB Script and VB.Net) on Lifesciences Projects. Engage with the project stakeholders, customer/users, conduct workshops to gather and ana...

Job Title: Operations Analyst (OA)- VDSP, Lalru & VDPP, Baddi Location: Baddi, Himachal Pradesh & Lalru, Punjab Role Summary: To enable data-driven decision-making and support operational excellence across Drug Substance and Drug Product manufacturing by developing performance dashboards, conducting variance analyses, and ensuring strict adherence to WHO-GMP standards in a vaccine production environment. Key Responsibilities: Real-Time Operations Dashboarding: Develop and maintain real-time dashboards covering both DS and DP stages, including Overall Equipment Effectiveness (OEE) , batch yield, deviation trends, downtime analysis, and key quality metrics.Automate daily/weekly/monthly dashboa...

Kenvue is currently recruiting for a: SENIOR SCIENTIST MICROBIOLOGY What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means ha...

Role Overview: As a Quality Assurance Specialist focusing on plant quality, your main responsibility will be ensuring the overall quality parameters of raw milk. Key Responsibilities: - Testing of milk and milk products for physico-chemical parameters. - Preparation of chemicals and standardization. - Monitoring GMP practices and process CCPs. - Maintaining GLP requirements. - Keeping all log sheets as per ISO standards and compiling data. - Coordinating with internal quality, production, and finished goods store teams. - Calibrating and verifying equipment, as well as maintaining records. - Monitoring the weight of finished goods packaging. - Updating and coordinating daily activities. - In...

Primary skills:Technology->Life Sciences->LIMS Experience in developing instrument drivers using SDMS/Talend/Java is to have. At least 5 years of experience in software development life cycle. At least 5 years of experience in Project life cycle activities on development and maintenance projects. At least 5 years of experience in Design and architecture review. Good understanding of sample management domain and exposure to life sciences projects Ability to work in team in diverse/ multiple stakeholder environment Analytical skills Very Good Communication skills At least 4-8 years of experience in LIMS(LV/LW) – Implementation /Configuration/Customization using Java, Java script. integration w...

Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong ...

Seeking a highly skilled developer/analyst to support and enhance the NTM (Notification to Managers) system — a custom-built SharePoint application that automates management notifications across pharmaceutical Manufacturing and Quality Operations . The role involves designing, integrating, and maintaining data workflows powered by Biovia Pipeline Pilot (PPL) for enterprise-scale ETL (Extract, Transform, Load) operations. This position requires a blend of technical development , business analysis , and quality systems understanding , ensuring the NTM application remains compliant. Key Responsibilities Design, develop, and maintain the NTM (Notification to Managers) application, a critical ent...

Hands-on experience on testing tools like HP ALM, Kneat and SNOW - Experience to MES, QMS (Trackwise), Lab solutions i.e. LIMS, Empower CDS, Chromeleon, Business Analytics, Middle wares etc. will be an advantage - OT System Qualification (Radio ligand Therapy or critical dosage forms will be a plus) - PAS/DCS Qualification - ISA95 High level of understanding - OT Security will be a plus. - Standalone Systems Qualifications - PAS/DCS Integrated with Manufacturing Equipment qualification. Key components of the responsibilities are as mentioned below but not limited to:  6+ yrs. of Professional experience and strong knowledge with real time experience in IT Quality & Compliance, Computer Syste...

Responsibilities : A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight. You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise. You will plan the activities of configuration, configure the product as per the design, conduct conference room pilots and will assist in resolving any queries related to requirements and solution design You will conduct solution/product demonstrations, POC/Proof of Technology workshops and pre...

Primary skills:Technology->Life Sciences->LIMS A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight. You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise. You will plan the activities of configuration, configure the product as per the design, conduct conference room pilots and will assist in resolving any queries related to requirements and solution design You will conduct solution/product demonstrations, POC/Proof of ...

Job requisition ID :: 89582 Date: Oct 3, 2025 Location: Bengaluru Designation: Consultant Entity: Deloitte Touche Tohmatsu India LLP What impact will you make? Every day, your work will make an impact that matters, while you thrive in a dynamic culture of inclusion, collaboration and high performance. As the undisputed leader in professional services, Deloitte is where you’ll find unrivaled opportunities to succeed and realize your full potential Deloitte is where you’ll find unrivaled opportunities to succeed and realize your full potential. The Team The team Enterprise technology has to do much more than keep the wheels turning; it is the engine that drives functional excellence and the en...

Key Responsibilities: A day in the life of an Infoscion As part of the Infosys consulting team your primary role would be to get to the heart of customer issues diagnose problem areas design innovative solutions and facilitate deployment resulting in client delight You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise You will plan the activities of configuration configure the product as per the design conduct conference room pilots and will assist in resolving any queries related to requirements and solution design You will conduct solution product demonstrations POC Proof of Technology workshops and prepare ...

Job Title IT- Manager(Trackwise) Job Grade (refer to JE) G10A Function IT Location: Tandalja(Baroda) Areas Of Responsibility At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Job Summary To lead the end-to-end implementation of...

Prepare, collect, and label biological or chemical samples. Conduct routine and specialized laboratory tests according to protocols. Record, analyze, and interpret data accurately. Maintain and calibrate laboratory instruments and equipment. Ensure proper storage and disposal of samples and hazardous materials. Follow safety and quality assurance procedures (GLP, ISO, NABL standards, etc.). Maintain detailed laboratory records, logs, and reports. Assist senior staff or researchers in experiments or diagnostic work. Monitor inventory and order lab supplies as needed. Maintain cleanliness and organization of the laboratory. Qualifications & SkillsEducation: Diploma / B.Sc. / M.Sc. in Medical L...

Overview Position summary statement: This position will serve as an Analyst and will be responsible for extracting, analyzing and interpreting data and developing strategies for Quality, Technical Services and Operations team, developing reports and dashboards to translate data analysis to business insights; this is to enable management to take action on findings and recommendations and Regularly report on benchmarks and scorecards for sharing with all parties to monitor performance. Detailed Responsibilities/duties Generate reports and manage information stored from Quality systems and ERP/PLM systems to statistically analyze, interpret data and investigate causes for solutions. Establish d...

Position Title: Executive : Manufacturing Science and Technology (MST) Qualification And Experience POST GRADUATE IN CHEMISTRY/PHARMACY Experience: 0-7 years of Experience as an analyst/Development technologist in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Providing analytical support for Chemistry activities ensuring compliance to regulatory, group directives, quality requirements, safety standards to fulfill the organization's objective, living Group's Values and Code of Ethics Responsibilities Responsibilities: Analytical method validation: Analytical method Development Analytical method transfer, Analytical method validation CMC Activity Sampling & testing of Pr...

Our client, a global healthcare company, is looking for a highly skilled SAP PP/QM Consultant with extensive hands-on experience in SAP Quality Management (QM) module, preferably within S/4HANA environments. The consultant will be responsible for leading design, configuration, implementation, and support activities for PP and QM processes, while ensuring seamless integration with related SAP modules. This role demands both technical depth and functional expertise, including strong capabilities in configuration, business process analysis, system integration, and stakeholder management. This is a contractual position, working in the client’s preferred EU time-zone (Offshore). The initial contr...

Job Description Roles and Responsibilities Operate as part of the QC team according to Company safety policies and cGMP to drive compliance with our company's Global policies, procedures, guidelines and regulatory requirements in the performance of all applicable job functions. Complete all documentation in compliance with cGMP and GxP standards. Perform receipt and release of all materials ensuring QC Right First Time and turnaround time KPIs are achieved. Review of all vendor and external laboratory documentation associated with receipt and release of materials to ensure compliance with internal specifications and Pharmacopeia. Maintain clear, accurate records associated with all day to da...

Designation: Assistant Manager Environment Services Department: Biosciences / Environment Division Reports to: Head Environment Services Qualification M.Sc. in Environmental Science (mandatory). Additional qualifications in Environmental Management / Industrial Safety ISO/IEC 17025 Internal Auditor / Lead Auditor training is desirable. Experience 810 years of progressive experience in environmental laboratory testing and management. Demonstrated expertise in NABL/ISO 17025 accredited environments, with experience in report signing authority preferred. Strong technical exposure across biodegradation, microplastics, water/wastewater, soil, hazardous waste, and air monitoring studies. Key Respo...