455 Lcms Jobs - Page 9

Understand the project requirements & deliverables from supervisor/manager Carry out literature search by using SciFinder, Reaxys and other search engines Comprehend and discuss the MSDS with supervisor/ team members Plan, setup, monitor, and workup chemical reactions independently Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc.) Isolate product and Optimize reaction conditions for improved yields and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Scale up of R&D developed compounds to k...

As a Quality Assurance & Analytical Chemist at FMC, you will be part of a team dedicated to providing innovative solutions for agriculture, contributing to the productivity and resilience of farmers" land. With a focus on science and technology, you will play a vital role in developing new herbicide, insecticide, and fungicide active ingredients, product formulations, and pioneering technologies that benefit both farmers and the environment. Your responsibilities will include: - Ensuring laboratory safety and industrial hygiene protocols are followed at all times. - Developing, validating, and implementing qualitative and quantitative analysis methods to meet business needs. - Conducting rou...

The Chemist role involves performing standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. As a Chemist, you will contribute by conducting laboratory testing, including qualitative and quantitative chemical and physical analysis of raw materials, finished products, and stability samples. You will be responsible for preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation such as HPLC, FTIR, UV-Visible spectrophotometer, and reviewing product certificates of analysis for accuracy and conformance. Additionally, you will perform routine calib...

As the General Manager - R&D at Gujarat Fluorochemicals Limited, you will play a crucial role in leading a team to drive the research and development efforts of the organization. Your primary responsibilities will include conducting literature surveys, identifying innovative and cost-effective processes for fluoro-specialty molecules, developing new products, and ensuring the scalability of lab processes to commercial levels. You will be tasked with managing a team of scientists and chemists to facilitate new product and process development while enhancing existing products. A deep understanding of synthetic and analytical methods, along with proficiency in interpreting data from various ana...

Responsibilities Collaborate with clients to understand their business requirements and translate them into cloud-based solutions, Design and architect scalable, reliable, and secure cloud solutions on platforms such as Amazon Web Services (AWS), Microsoft Azure, or Google Cloud Platform (GCP), Conduct cloud assessments and provide recommendations on cloud migration strategies, including lift-and-shift, re-platforming, or refactoring, Develop architecture blueprints, diagrams, and documentation that clearly articulate the proposed solutions, Work closely with development teams to ensure cloud architecture best practices are followed throughout the software development lifecycle, Assist in th...

It has been more than 60 years since SYSTRA has garnered expertise that spans the entire spectrum of Mass Rapid Transit System SYSTRA Indias valuable presence in India roots back to 1957, where SYSTRA worked on the electrification of Indian Railways Our technical excellence, holistic approach and the tremendous talent provides a career that puts people who join us at the heart of improving transportation and urban infrastructure efficiency, Understand better who we are by visiting systra in Context BIM Modeller Missions/Main Duties Support the Discipline Lead, BIM Manager and Production Team(s) in day to day BIM implementation activities, Provide progress and performance updates to Disciplin...

Experience in section LCMS/ PSD/ HPLC/ GC/ Method Validation. Interview will be held in Pune location. Required Candidate profile 2 to 5 years of experience in section LCMS/ PSD/ HPLC/ GC/ Method Validation.

Roles and Responsibilities Conduct analytical method validation, including preparing methods, running samples, and reporting results. Perform routine maintenance of laboratory equipment such as GC-MS, HPLC, LCMS, and other chromatography systems. Develop and maintain calibration protocols for instrument qualification and preventive maintenance schedules. Collaborate with cross-functional teams to resolve issues related to analytical testing and method development. Ensure compliance with regulatory requirements by maintaining accurate records of test data and reports.

!! Greetings from Natco Pharma Limited..!! We are conducting Walk-in Interview for Formulation Analytical Research & Development Department for our Pharma Division located at Kothur (Near to Shamshabad) Roles: Trainee /Officer / Executive / Sr. Executive / Asst. Manager Qualification: B. Pharmacy / M. Pharmacy (Pharmaceutical Analysis) / M. Sc (Analytical Chemistry) / B.Sc (Chemistry) Experience: 0 to 15 Years (Only freshers who graduated in 2024 or 2025 are eligible to attend) Skills Required: Analytical method development & validation Complex Injectable, Peptide chemistry knowledge preferred Analysis of raw materials, finished products, stability samples, Discriminatory dissolution studies...

Walk In Drive For Quality Control In Formulation Division @ MSN Formulation Unit -II , Kothur . Department :- Quality Control Formulations Experience:- 2 to 8 Years Skills :- Formulation QC - HPLC | GC | GC MS | LIMS | LCMS | ICPMS | Dissolution | IP/FP | Stability | Method Validation | Method Development | Method Transfer | E&L | | Proficiency with Equipment | Method Development & Optimization | Understanding of Regulations | Data Analysis | Testing and Inspection | Process Improvement | Regulatory Compliance | Equipment Maintenance | Training and Support | Root-cause analysis | Method development and validation | (OSD & Injectables) | USFDA | Regulatory Approvals Division :- Formulation In...

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role To Prepare sample for the determination of heavy metals, micro minerals and minerals in Food and Agriculture samples as per ISO, IS and Customer specific requirements adopting test methods ISO, AOAC and IS methods...

JOB OVERVIEW Executes complex simulations in CFD and Thermal to optimize design and manufacturing. Develops complex Multiphysics simulation methods that meets design requirements in thermal management of Electronic Systems, especially in high-speed transceivers, connectors, and their assemblies. KEY RESPOSBILITIES: 5 to 8 years of industry experience. Expertise in Ansys Workbench. Experience on connector products (Plastic and Sheet Metal parts). Knowledge on material science (Metals, Resins & hyper elastic material) and implement for simulation. Expertise on CAE tools, Optimization techniques, and testing methods. Development & execution of complex Thermal simulation models to optimize manuf...

Job Description Provides Technical & application services & support to external customers and Agilent customer engineers. This includes reactive and pro-active actions that result in a timely and cost-effective problem resolution with the objective to meet contractual agreements. May support third party products and occasionally visit customer sites. Acts as part of CSO Field Service staff Serves as an internal resource on technical issues and manages product escalations Collaborates with Agilent teams such as Support, Sales, Marketing and R&D to provide solutions to customers. Responsibilities of this position include but are not limited to; Responsible for providing technical & application...

Role & responsibilities Collect samples for analysis from custodian. Processing of sample by using various sample extraction technique (to determine the concentration of analyte). Perform analysis via LCMS. Follow GXP. Sample extraction process using LLE, SPE, PPT. Stability issue handling, derivatization, etc. approach. Receive controlled forms for various activities. Document all linked activities and forms as per SOP. To check documents done by Jr. Analyst/ Fresher. Method development skills Trouble shooting of method Excel and MS Word.

Role & responsibilities Perform quality control testing of oncology products (raw materials, intermediates, and finished products) using validated analytical methods. Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, Dissolution Apparatus, FTIR, and other relevant equipment. Conduct stability testing as per ICH guidelines and prepare stability reports. Review and document analytical results in compliance with GDP and cGMP requirements. Identify and investigate deviations, OOS (Out of Specification) and OOT (Out of Trend) results, and implement corrective and preventive actions (CAPA). Support method validation, method transfer, and analytical troubleshoo...

Role & responsibilities Perform quality control testing of oncology products (raw materials, intermediates, and finished products) using validated analytical methods. Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, Dissolution Apparatus, FTIR, and other relevant equipment. Conduct stability testing as per ICH guidelines and prepare stability reports. Review and document analytical results in compliance with GDP and cGMP requirements. Identify and investigate deviations, OOS (Out of Specification) and OOT (Out of Trend) results, and implement corrective and preventive actions (CAPA). Support method validation, method transfer, and analytical troubleshoo...

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Planning/performing and reporting of acute toxicology studies Assist in preparation of SOP"™s, Protocols and Reports Participate in GLP / AAALAC related activities Literature search Maintenance of animal house and relevant documents as per GLP and AAALAC norms. To Assist and work along with SD and TC in Plann...

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Leadership role to manage team size of 10+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Managing multiple instruments (LC-MSMS, GC-MSMS, ICP-MS, IC etc.) Method development experience in LC-MS...

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. : Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.

Urgent opening for QC Officer-Sr. Officer in Dahej, Bharuch. Note: Walk In Interview at Bharuch Date & Time: 24th August, 2025 at 09:00 AM Onwards Job Location: Dahej, Bharuch Experience: 2 to 7 years in API Qualification: M.Sc./B.Pharm/M. Pharm Required Candidate profile Roles and Responsibilities: -Experience in Section LCMS / PSD / HPLC / GC /Method Validation -Candidate preferred from Pharma API (Active Pharmaceutical Ingredient).

Role & responsibilities Should perform sample processing smoothly as well as project execution with in assign time. Should handle instrument as well as QA observation. Should coordinate with Group members/ Group leader/ Lab manager Should be able to inspect raw data as per defined procedure. Should report inspection result properly. Should verify calibration record. Should maintain GLP in Lab. Preferred candidate profile 5-6 Years of Experience in Clinical Research Organizations only (Bio-Analytical Department) Qualification: MSC Immediate to 20 days joiners are preferred. You can also share your resumes on: pradnya.raut@accutestglobal.com for quicker callback

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At USP, inclusive scientific collaboration is highly valued, recognizing the importance of diverse expertise in strengthening the development of trusted public health standards. The organizational culture at USP supports equitable access to mentorship, professional development, and leadership opportunities, reflecting the belief that broad participation in scientific leadership leads to more impactful global health outcomes. As an equal employment opportunity employer, USP is committed to fair, merit-based selection processes that enable the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Reasonable accommodations are provided to...

At USP, we highly value inclusive scientific collaboration and acknowledge that attracting diverse expertise strengthens our ability to develop trusted public health standards. We cultivate an organizational culture that supports fair access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research embody our belief that ensuring broad participation in scientific leadership leads to stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is dedicated to ensuring fair, merit-based selection processes that enable the best scientific minds - regardless of background - to co...

We are seeking a proactive Sr. Research Associate I- Analytical to independently handle analytical chemistry tasks. You will be responsible for method development and purification of samples using various chromatographic instruments. This role requires the ability to troubleshoot instruments and apply a strong knowledge of instrumental techniques to support drug discovery and development services. Roles & Responsibilities: Independently handle routine analysis on respective instruments. Conduct method development and purification of samples on chromatographic instruments such as HPLC, Prep-HPLC, SFC, and Prep-SFC . Troubleshoot analytical instruments to ensure their reliable operation. Apply...