2506 Lims Jobs - Page 13

Job Location: Mumbai Experience: 3-4 Years Requirements: Labware Experience Package Creation Subordinate Creation Parsing Script Troubleshooting for Labware Application Interested Candidates please share your CV at careers@ecotech.ai

1. Greet customers and visitors in person or by phone, answer inquiries, and provide assistance and directions. 2. Schedule, confirm, and reschedule appointments, and help keep the schedule on track by notifying staff of customer or third party witnesses arrivals. 3. Answer and direct phone calls, manage the front desk, and maintain a clean and organized reception area 4. Verify and update sample information in LIMS software with filling out forms, and maintain customer confidentiality. Job Type: Full-time Pay: ₹14,000.00 - ₹16,000.00 per month Work Location: In person

Job description we are hiring for Sample manager for Bhubaneswar Location for cognizant. If interested please share your updated resume to [HIDDEN TEXT] Job Description: Job experience : 3 to 9 years Notice period : Immediate to 90 Days Job Location : Bhubaneswar Job Description: We are seeking a Sr Analyst with 3 to 8 years of experience to join our team. The ideal candidate should possess deep technical knowledge in SampleManager LIMS applications to effectively guide the team and troubleshoot complex issues. Analyzes and resolves intricate technical problems often collaborating with onshore teams for guidance or escalation. Coaches and mentors team members fostering a culture of continuou...

we are hiring for Labvantage developer for Bhubaneswar Location for cognizant. If interested please share your updated resume to [HIDDEN TEXT] Job Description: Job experience : 3 to 9 years Notice period : Immediate to 90 Days Job Location : Bhubaneswar Job Description: 2-10 years experience in LabVantage LIMS implementation experience of LV8.x projects Must have experience in requirement analysis and system designing. Must have hands on experience in configuration and/or coding in LabVantage. Strong understanding of SDLC & CSV methodologies Must have good communication skills and have experience in customer communication. Strong understanding of Oracle, PL/SQL Workable experience in Jasper ...

We are hiring for CDS for Bhubaneswar location for cognizant . If interested please share your updated resume to [HIDDEN TEXT] Job Description : Notice period : Immediate to 90 days Job location : Bhubaneswar Job Experience : 4 to 9 years 2+ years of experience and hands-on experience with Empower CDS / Chromeleon CDS / OpenLab / Agilent & Waters Instruments Knowledge of any CDS applications, with Sample set acquisition, processing chromatographic data & reporting Working knowledge in Empower/Chromeleon Enterprise architecture and Installation of Empower/Chromeleon application Hands on experience on different type of CDS functional related issues. Hands on experience on different type of ins...

Job description We are hiring for the Labware developer for Bhubaneswar location for cognizant . If interested please share your updated resume to [HIDDEN TEXT] Job Description : Notice period : Immediate to 90 Days Job Location : Bhubaneswar. Experience : 3 to 9 years LabWare Developer with work experience of at least 2 years and responsibilities that include: Gathering user requirements to understand the needs of the laboratory and stakeholders. Configuring LabWare LIMS and providing technical assistance to the team and troubleshooting when needed. Configuration and creation of Master Data including but not limited to Products, Projects, Analysis, Calculations, Automation Scripts, Message ...

As a Quality professional at Piramal Pharma Solutions, your role will involve remote support to PPL sites, reviewing analytical data, preparing master build in LIMS, and document preparation. Your key responsibilities will include: - Preparation of Master Build in LIMS. - Overseeing track-wise operations for QMS activities. - Preparation and review of Method Validation, Method Transfer, Method Verification, and Equivalency documents. - Preparation and review of Test Methods, STPs, and Specifications. - Operational knowledge of eDMS and ensure application compliance. - Monitoring compendial changes and preparing evaluation reports. - Reviewing analytical data, raw data, chromatography, and LI...

Greetings from Themesoft! We're looking for experienced MES Support Consultants-Pharmaceutical/Life Sciences to join our team in Chennai. In this role, you'll provide L2/L3 functional and technical support for enterprise-grade Manufacturing Execution Systems (MES) , especially Werum PAS-X and FTPS , ensuring seamless operations in a highly regulated, high-impact environment. Location: Chennai, India Experience: 610 Years Notice Period: Immediate to 10 days joiners Schedule: Must be flexible to work in shifts (rotational or fixed, based on business needs) Key Responsibilities Application Support: Deliver expert L2/L3 support for MES systems like PAS-X and FTPS. Troubleshooting: Analyze logs, ...

Role: Siemens Opcenter Administrator / Specialist Overview We are seeking a highly skilled Siemens Opcenter Specialist to lead the implementation, configuration, and integration of Opcenter MES solutions with Teamcenter and SAP PLM. The ideal candidate will have deep expertise in manufacturing operations, quality management, and enterprise system integration. Key Responsibilities Implement, configure, and maintain Siemens Opcenter MES solutions. Integrate Opcenter with PLM systems (Teamcenter) and ERP platforms (SAP PLM). Collaborate with cross-functional teams to ensure efficient data flow and streamlined operations. Support decision-making through integrated manufacturing intelligence and ...

Job Title: Executive Department: Quality Control - Microbiology Location: Dahej, Gujarat Company: Cadila Pharmaceuticals Limited Job Responsibilities: Ensure timely validation and calibration of all instruments in the Quality Control laboratory. Maintain all Regulatory Compliance documents as per cGMP and internal quality standards. Report any OOS (Out of Specification), incidents, deviations, or discrepancies observed during laboratory activities to the Section In-charge / QC In-charge. Ensure preparation and review of analytical documents such as Specifications, Protocols, and Standard Testing Procedures (STPs) as per approved SOPs. Maintain and update instrument logbooks as per analysis r...

Job Description Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC ,Polarimeter , KF, Auto titrator e.t.c. Responsible for sIn-process Sample . Miscellaneous Samples, Finish Product and Stability Sample testings and maintain sample as per SOP. Responsible for review of instruments logbooks, miscellaneous materials, in-process, finished products and water analysis. Analysis related to qualification of Instrument/Equipment and Standards Qualification of Standards and Instruments Knowledge and Skill on Sophisticated instruments like UV, HPLC, GC, UPLC, FTIR, Polarimeter and KFtitrator. Knowledge of Chemical analysis. Knowledge of LIMS/QMS Knowledge of current pharmaceuticals gui...

About Sun Pharma: Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5.4 billion. Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Job Summary LIMS Testing & Documentation Specialist will be responsible for the thorough testing of LIMS application before deployment or patch deployment. This role requires a deep understanding of laboratory workflows, strong technical & testing skills, and the ability to work closely with cross-functional teams to ensure the LIM...

About Sun Pharma: Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5.4 billion. Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Job Summary Integration Specialist – LIMS, will be responsible for the integrating various lab instruments/software with LIMS application for successfully establishing paperless environment in QC/R&D Labs. This role requires a deep understanding of laboratory workflows, Instrument connectivity techniques, strong technical skills, a...

Hands-on experience in LIMS administration, access/configuration management. Basic knowledge of Crystal Reports and report modifications. Familiarity with data migration processes. Understanding of CSV (Computer System Validation)

Why Quark Software: At Quark, we've been revolutionizing graphic design, digital publishing, and content automation since 1981. With over four decades of expertise, we empower organizations to master their content lifecycle through cutting-edge design, automation, and intelligence. Our software solutions enable customers to create, manage, publish, and analyse their content with unrivalled effectiveness. As we embark on an exciting new era of growth, we're on the lookout for exceptional individuals to join our Global team. Why Choose Quark: Quark is entering a transformative phase of growth, driven by visionary leadership focused on research and development and customer success. Our culture ...

Designation : Report Executive OR Chemist Qualification: Postgraduate in Chemistry (preferred) Experience: Fresher Job Description: We are looking for a Fresher . The ideal candidate should have strong Knowledge in data entry, report preparation , and maintaining accurate laboratory records. Key Responsibilities: · Prepare and format laboratory test reports accurately and efficiently. · Enter data into LIMS or lab management software systems. · Ensure quality control and consistency in report documentation. · Coordinate with lab staff for timely submission of test data. · Maintain records in compliance with standards. Required Skills: · Proficient in MS Office (Word, Excel) and data entry so...

Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC ,Polarimeter , KF, Auto titrator e.t.c. Responsible for sIn-process Sample . Miscellaneous Samples, Finish Product and Stability Sample testings and maintain sample as per SOP. Responsible for review of instruments logbooks, miscellaneous materials, in-process, finished products and water analysis. Analysis related to qualification of Instrument/Equipment and Standards Qualification of Standards and Instruments Knowledge and Skill on Sophisticated instruments like UV, HPLC, GC, UPLC, FTIR, Polarimeter and KFtitrator. Knowledge of Chemical analysis. Knowledge of LIMS/QMS Knowledge of current pharmaceuticals guidelines (eg. ICH...

Essential Functions: Responsible for cGMP compliance review in QC laboratory Responsible tenure the completeness of the analytical documents and approval of CoA of Raw materials, packaging materials, In-process, finished products, stability study intended for submission, validation & commercial batches. Responsible to perform / review of the investigation for Quality issues like OOS, Deviations, Incidents, CSIR of QC laboratory Responsible to ensure the implementation of CAPAs recommended in OOS, OOAL, Incidents and deviations related laboratory. Responsible for the review of Change controls related to QC laboratory. Responsible for the review of chromatographic and non-chromatographic data ...

Job Summary The Front Desk and Accessioning Executive is responsible for managing client interactions, handling sample accessioning, maintaining accurate documentation, and ensuring smooth coordination between the reception and laboratory teams. This role requires strong organizational skills, attention to detail, and familiarity with laboratory operations and sample handling protocols. Key Responsibilities Front Desk Operations Greet and assist clients, patients, and visitors in a professional and courteous manner. Handle inquiries (in-person, phone, or email) regarding lab services, tests, and reports. Schedule appointments and manage the daily workflow of sample collection and dispatch. C...

Company Description Entiovi Technologies is a technology solutions and services provider that helps customers grow their businesses and cut costs using the latest technology. Our consultative approach focuses on designing, developing, training, and supporting customer solutions for easy adaptation. We continually adopt and learn new technologies and skills to stay market-ready and ensure customer satisfaction. Our mission is to improve the competitiveness of organizations worldwide by providing comprehensive, cost-effective IT solutions and services. Role Description 𝗪𝗲'𝗿𝗲 𝗛𝗶𝗿𝗶𝗻𝗴 – 𝗟𝗮𝗯𝗩𝗮𝗻𝘁𝗮𝗴𝗲 𝗟𝗜𝗠𝗦 𝗣𝗿𝗼𝗳𝗲𝘀𝘀𝗶𝗼𝗻𝗮𝗹 We are looking for an experienced professional to join our team. Please find the J...

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 services for genomics, discovery pharmac...

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 services for genomics, discovery pharmac...

Company Description 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 services for genomic...

Why Quark Software: At Quark, we've been revolutionizing graphic design, digital publishing, and content automation since 1981. With over four decades of expertise, we empower organizations to master their content lifecycle through cutting-edge design, automation, and intelligence. Our software solutions enable customers to create, manage, publish, and analyse their content with unrivalled effectiveness. As we embark on an exciting new era of growth, we're on the lookout for exceptional individuals to join our Global team. Why Choose Quark: Quark is entering a transformative phase of growth, driven by visionary leadership focused on research and development and customer success. Our culture ...

As the Lead of the Residue Analysis & Instrumentation section in the laboratory, your role involves overseeing and managing the analysis of pesticides, antibiotics, veterinary drugs, mycotoxins, heavy metals, and other contaminants in food samples. You will be responsible for operating, supervising, and maintaining advanced analytical instruments such as LC-MS/MS, GC-MS/MS, ICP-MS / ICP-OES, HPLC, GC, AAS, UV-Vis, and FTIR. Your duties include ensuring compliance with NABL (ISO/IEC 17025:2017), FSSAI guidelines, Codex, and BIS standards. You will also be involved in method validation, verification, calibration, and measurement of uncertainty. Reviewing and authorizing test reports as an Auth...