570 Lcms Jobs - Page 3

Role & responsibilities To Operate, loading samples, create, quantify and save the batches as per LCMS/MS SOP. To complete necessary documentation for bio-analysis such as raw data forms and logbook entries. To ensure that Bioanalytical method development and validation activity is progressing smoothly. To ensure that all the equipment and instruments in bioanalytical lab are appropriately qualified, calibrated and validated in line with SOP. To ensure that employees in the department are trained and up to date on all aspects related to bioanalytical systems and procedures and their record are maintained up to date. Ensure that records and data of bioanalytical equipment, processes and syste...

Job Title : Research Associate / Sr Research Associate/ Associate Scientist Department: Biology- DMPK Key Responsibilities: Should expertise in handling the HPLC and LCMS along with sound knowledge on troubleshooting. Well versed with method development, validation knowledge and extraction procedures. Should handle the bioanalysis of different matrices of PK and ADME studies independently. Required good understanding of various column chemistry and its application in method development. Responsible for data integrity and good documentation practices such as recording of data in LNB and completion of studies as per requirement. Operation and maintenance of Laboratory equipment's Ensure all th...

Storyline developer with experience in the eLearning industry. Expertise in authoring tools and working on complex Articulate Storyline 3, 360, Adobe Captivate, Camtasia, etc. and Rapid Authoring Tools with basic HTML skills, and strong debugging skills... Understand functionalities and interactivities from a learning point of view Work closely with Instructional Designers and SMEs to understand the storyboard or concepts Have worked on different LCMS and SCORM compliances or have knowledge of LCMS and LMS. Working knowledge of Multimedia software like Adobe Photoshop, Adobe Flash/Animate and Adobe Illustrator is an advantage. A strong eye for visual composition and ability to develop graphi...

Primary Job Responsibilities: Structural and functional characterization of proteins using LC-MS Expertise in Impurity characterization by LC-MS Data analysis and review for Bio similarity assessment Planning of characterization experiments using LC-MS Drafting and/or review reports and presentations on experimental data and scientific outcomes for CMC / RA for dossier submission. Drafting of scientific study protocols and reports related to method development, method qualification, assessing bio similarity etc. Guiding and mentoring team members sample preparation, LC-MS workflows and data interpretation. Support cross-functional analysis such as charge variant and impurity characterization...

Sample preparation and analysis of food samples for Pesticide residue, Antibiotic residue, Aflatoxins. Method development and validation on LCMSMS and GCMSMS. Sound knowledge of instruments such as HPLC, GCMSMS and LCMSMS. Maintenance of lab records. Knowledge of ISO 17025:2017standard.

As an experienced candidate with 10-15 years of CRO experience, your role will involve strong knowledge and hands-on experience in LC-MS/HPLC/Prep. method development for various chemistry molecules at an analytical scale. You should be proficient in various purification techniques and have a strong understanding of different column chemistries. Your responsibilities will include: - Leading, training, coaching, and mentoring a team of motivated young scientists. - Providing guidance and support across different shifts, including night shifts, to ensure the timely delivery of analytical data to the chemistry team. - Working closely with motivated scientists to foster a collaborative and perfo...

Required Skills & Qualifications Masters degree in Chemistry, Analytical Chemistry, or related field (mandatory). Strong experience in analytical method development . Proficiency in operating and troubleshooting analytical instruments, especially HPLC and GC. Solid understanding of regulatory guidelines (ICH), Pharmacopoeias, and GLP. Key Responsibilities Analytical Method Development: Focus on developing robust analytical methods for related substances, assay, residual solvents, and cleaning procedures. Analytical Support: Provide support to process development teams by analyzing samples using instruments such as: HPLC (High-Performance Liquid Chromatography) GC (Gas Chromatography) IR (Inf...

Dear Candidate, Greetings from SGS India Pvt. Ltd.! We are actively looking for Chemist Role at our Kopar Khairane Lab. We are conducting a Walk-IN Interviews on 29th November 2025 (Saturday) between 10AM to 4PM. Brief Job Description : To perform E&L and nitrosamine testing and other analytical activities like method development and method validation on instruments like LCMS, HRMS, IC and GCMS. Documentation as per GMP requirement. Adhere to SOPs of SGS while performing the activities. Deliver the projects as per commitment to the clients. Interested Candidate can share updated CV on fleur.dsouza@sgs.com Venue Details: Address - Plot No. A-772/ A-773, MIDC, TTC Industrial Area, Kopar Khaira...

Understand the project requirements as specified by the client, the synthetic route Understand and discuss the MSDS (Material Safety Data Sheet) with team members Identify and mitigate any potential safety risk with the help of supervisor Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage and minimum wastage Ensure parallel execution of multiple reactions Monitor the reaction by observing progress by using analytical techniques Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality Anal...

Job description Roles and Responsibilities Conduct analytical testing using HPLC, GC, UV-Vis, ICP-MS, LCMS techniques to ensure product quality and purity. Develop and validate methods for analysis of pharmaceutical products according to cGMP guidelines. Collaborate with cross-functional teams to resolve method validation issues and implement changes as needed. Maintain accurate records of test results, instrument calibration, and maintenance schedules. Participate in continuous improvement initiatives to optimize laboratory processes and procedures.

Role & Responsibilities: : Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Desired Candidate Profile - Strong understanding of analytical instruments such as HPLC/UPLC/...

As a Sr. Analytical Chemist, you will be responsible for the following key responsibilities: - Analysis of compounds for various projects from medicinal chemistry team and lead NCEs to ensure quality output within set targets by Group leader (60% of time spent) - Analytical method development for new NCEs using different instrumental techniques like HPLC, LCMS, NMR, IR, and SFC along with other wet analysis methods to ensure quality output within set targets by Group leader (20% of time spent) - Demonstrating good analytical skills and possessing basic knowledge of HPLC, LCMS, NMR, and SFC instruments to ensure quality output within set targets by Group leader (20% of time spent) Qualificati...

We are thrilled to announce a walk-in drive for the role of Scientist in Medicinal Chemistry at our cutting-edge R & D facility. If you have 2 to 5 years of experience with synthetic skills in performing various kinds of reactions and purifications skills and has passion for drug discovery, we want to meet you, experience on IDD project will added advantage for these roles. What you will do: - Planning & Synthesis: Execute multi-step synthesis of target compounds, conduct literature searches, and troubleshoot experimental bottlenecks. - Data Interpretation: Interpret complex analytical data (NMR, LCMS, HPLC) to characterize synthesized targets and key intermediates. - Documentation: Meticulo...

Analytical method validation and Stability studies. Day to day trouble shooting QC sophisticated Equipment's like GC-MS, UPLC, HPLC, GC, GC-HS, Dissolution etc. Designation - Executive/Senior Executive/Deputy Manager/Manager

LCMS Data Interpretation Analyst Location: Bengaluru Mode: WFO, Full time JD: Key Responsibilities: Analyze and interpret LC-MS data (primarily QTOF) for qualitative and semi-quantitative chemical characterization studies. Evaluate mass spectral data using a weight-of-evidence approach, including critical assessment of database matches, fragmentation patterns, isotopic distributions, and chromatographic behavior. Collaborate with technical analysts, chemists, and project managers to communicate findings, resolve discrepancies, and meet client expectations. Ensure data integrity and compliance with regulatory and accreditation standards (e.g., ISO 10993, ISO 17025, GLP). Document findings in ...

Chemist (HPLC & GC-MS) Core Responsibilities Instrument Operation & Maintenance Calibrate, operate, and maintain HPLC, GC, GC-MS, UV, FTIR, and Karl Fischer titration instruments . Troubleshoot technical issues and ensure instruments are in optimal condition. Analytical Testing Perform qualitative and quantitative analysis of raw materials, intermediates, and finished products using HPLC and GC-MS. Conduct method development and validation for new compounds or formulations. Ensure precise analyses within specified turnaround times (TAT) . Quality Control Verify the identity, purity, and potency of pharmaceutical drugs and chemicals. Document and review analytical data to comply with GLP (Goo...

Role Overview: As an ARD Chemist / Scientist at the Udaipur location, you will be a key member of the ARD team, focusing on method development, impurity profiling, and instrumental analysis to support Synthesis R&D and quality operations. Your primary responsibilities will include developing and validating analytical methods, performing impurity profiling, and maintaining analytical instruments. Key Responsibilities: - Develop and validate HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples - Develop HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC - Perform impurity profiling of APIs and intermediates using advanced techniques lik...

As a Chemist, your 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. You will contribute by conducting laboratory testing, preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation, reviewing product certificates of analysis, maintaining Certificates of Analysis (C of A) files, and providing input on Standard Operating Procedures (SOPs), Test Methods, and laboratory documents. You will also participate in investigations, address Out of Specifications (OOS), resolve deviations, and implement Corrective and Preven...

As a Leachables & Extractables (L&E) Analyst at Anazeal Analytical & Research Pvt. Ltd., located in Navi Mumbai, Maharashtra, you will be responsible for performing analytical testing and characterization of extractables and leachables in pharmaceutical containers, closures, and medical devices. Your role will involve method development, validation, and data interpretation in compliance with regulatory guidelines such as USP, ISO, and ICH. Key Responsibilities: - Perform Extractables and Leachables studies for pharmaceutical packaging materials, process equipment, and medical devices. - Conduct sample preparation, extraction, and analysis using analytical instruments such as GC-MS, LC-MS, IC...

Urgent openings in Quality Control In Hyderabad Location Urgent openings in Quality Assurance In Hyderabad Location Urgent Openings in ARD for Vizag Location Please Schare Your Update CV to info@pulsehr.org Vijay Kumar

• Java, Bean Shell, JDBC, XML and Web services • Excellent Knowledge on Sailpoint IIQ Fundamentals: o Installation and Configuration o Application Onboarding o Entitlement Catalog o Roles, Reports and Rules o Tasks (Aggregation/Refresh/Perform Maintenance) • Highly skilled on Sailpoint IIQ Provisioning concepts: o Provisioning Object Model o Custom Connectors o Connector/Integration Architecture o Workflow and Dashboard QuickLinks o Generating Workitems/Approvals o Lifecycle Manager (LCM) Configuration, Events. workflows etc. • UNIX/Linux experience, and scripting skills (shell, Perl, Python, etc.) • Strong database skills (SQL, MySQL, ORACLE) • Very good understanding of Identity and Access...

As a Chemist at the Water Technology Center in Kanchipuram, you will play a crucial role in leading research, development, and innovation efforts in the field of water treatment. Your technical expertise, project leadership, and economic analysis skills will contribute to advancements in water technologies and enhance process efficiency. Here is what will be expected from you: - Lead and manage projects related to water chemistry for water treatment technologies, ensuring alignment with business objectives and delivering tangible results - Propose and implement innovative ideas to improve existing processes and products, fostering innovation within the organization - Mentor and guide project...

Responsible for LC-MS/MS operations, method development, validation, GLP documentation, equipment calibration, and overall lab supervision, ensuring trained staff, smooth workflows, and timely, compliant bioanalytical project execution. Life insurance Job/soft skill training

Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensure safe operations and compliance to company s integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team inclu...

Method development like Related compound, Assay, Dissolution and Residual solvents etc. for development projects using instruments like HPLC, IC, GC, Particle size analyzer etc. Prepare method development report along with tentative analytical method. Attain method transfer activity. Method validation like Dissolution, Assay, Related compound and Residual solvents etc. Preparation TT report To keep neat and cleanliness at workplace and follow the Good Laboratory Practices in the Laboratory. Preparation of study protocols with respect to Laboratory. Development batch stability analysis as per stability protocols To attain and complete self-training through QMS. Responsible for COA preparation...