47 Lcmsms Jobs - Page 2

As a Scientist C in the GCMSMS & LCMSMS section at our laboratory located in Gurugram, Haryana, you will be responsible for creating a conducive working environment and ensuring harmonious inter-laboratory working conditions. Your primary duties will include working in compliance with ISO17025 documentation, conducting environment monitoring of Food & chemical laboratories, maintaining log books, and standardizing titrimetric solutions. You will play a crucial role in facing technical audits conducted by regulatory bodies such as NABL, BIS, APEDA, AGMARK, FSSAI, MOEF, EIC, and CPCB, as well as customers. Your responsibilities will also involve calibration, uncertainty calculation, preparing ...

As an Analytical Chemist at our leading Contract Research Organization (CRO), you will have the opportunity to assist in conducting analytical testing of samples using instruments such as HPLC, GC, LC-MS/MS, and UV Spectrophotometer under supervision. You will play a crucial role in preparing reagents, solutions, and standards following Standard Operating Procedures (SOPs) with precision and attention to detail. Your responsibility will include accurately recording and maintaining raw data, logs, and reports in compliance with GLP/GMP standards. By ensuring proper documentation, you will play a pivotal role in meeting regulatory and internal audit requirements. You will provide essential sup...

As a Laboratory Analyst, you will be responsible for conducting day-to-day sample extractions and sequencing using instruments such as LCMS/MS and GCMS/MS. Your duties will include testing various agriculture and food products for chemical and nutritional properties using standard and in-house methods. You should have hands-on experience in Proximate Analysis and be proficient in operating lab instruments such as pH meter, weighing balance, incubator, GCMS/MS, LCMS/MS, and UPLC. Additionally, you will be required to prepare standard solutions, perform daily maintenance of lab equipment, and adhere to good laboratory practices. You will also be responsible for following the disposal process f...

You will be responsible for performing chemical and instrumentation analysis for various materials such as in-process, raw materials, intermediates, and finished products according to the monthly schedule provided by PPL. This includes utilizing instruments like ICP-MS and LC-MS to ensure analysis is completed within the dispatch timeline. Additionally, you will be involved in developing, validating, transferring, and verifying analytical methods using ICP-MS and LC-MS/MS. Your role will also entail preparing and reviewing protocols, worksheets, and reports related to method developments, validations, verifications, and transfers. Allocating work to chemists, performing instrument calibratio...

As the Manager of Analytical Method Development, you will be responsible for the overall development and validation of analytical methods for R&D projects, specifically focusing on oral controlled release dosage forms. Your key responsibilities will include leading the scientific development of new analytical methods, identifying areas for improvement in existing methods, and staying updated on evolving technologies and Regulatory requirements. You will play a crucial role as a member of the new product development team, contributing to the preparation of development proposals, project plans, timelines, and project activity reviews. Your expertise in analytical methods development using tech...

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...

LC-MS/MS expert for a NABL-accredited lab to perform high-precision analysis of pesticide, mycotoxin, antibiotic residues in food and water samples. Expertise in method development, validation, troubleshooting ability, data accuracy are essential. Required Candidate profile Must have thorough expertise in LC-MS/MS and complete understanding of NABL/ISO 17025 regulations. Candidate is expected to independently handle, operate, and maintain LC-MS/MS instrumentation. Perks and benefits Best in the industry.

As an in-vitro Bioanalytical Scientist at Syngene, your core purpose will be to provide expert DMPK support to multidisciplinary integrated Drug Discovery projects. Your responsibilities will include defining and implementing the DMPK strategy to expedite project progression, participating in capability building projects as per business requirements, and providing input into the design of experimental protocols and Bioanalytical procedures for the analysis of drug candidates in biological samples. Additionally, you will be expected to deliver scientific presentations in departmental journal clubs and write official project reports. Your role accountabilities will involve planning and supervi...

You should possess a DMPK background with hands-on experience in DMPK-ADME assays and bioanalysis using LCMS/MS & HPLC techniques. Your strong scientific knowledge and excellent communication skills will be key in this role. As part of the team, you will work in the lab under supervision, ensuring the generation of quality data consistently and maintaining high individual productivity levels. Your responsibilities will include running ADME assays and taking charge of the archival of documents and data. Additionally, your ability to learn new techniques, experiments, and instruments will be crucial for success in this position.,

As a candidate for the position, you should possess a M. Pharm (Pharmacology/ Pharmaceutical Analysis) or M.Sc. (Biochemistry/ Pharmaceutical Chemistry) degree with 11-14 years of experience or a Ph.D. with 2-5 years of experience in the fields of large molecule/ADC PK and bioanalysis. Your expertise should include Antibody Drug Conjugate characterization and bioanalysis, mass spectrometry-HRMS, Q-TOF, and Triple quad. Your role will involve being an expert in designing and executing DMPK studies to support antibody-drug conjugate (ADC) and monoclonal antibody (mAb) programs, ranging from discovery to IND-enabling stages. You should have extensive experience in quantifying biologics such as ...

As a Quality Analyst I at Teva Pharmaceuticals, you will be responsible for auditing each BA/BE study to ensure that facilities, personnel, equipment, instruments, protocols, methods, practice, records, and controls comply with relevant GCP/GLP guidelines, protocols, and SOPs. Your day will involve reviewing SOPs, forms, logbooks of departments, providing feedback, reviewing change control and deviations, and preparing audit reports in accordance with guidelines and regulatory inspections. You will also conduct in-process study audits to ensure compliance with GCP/GLP, protocols, SOPs, and regulatory requirements. Additionally, you will audit raw data, validation reports, bioanalytical repor...

As an In vitro Bioanalytical Scientist at Syngene, based in Hyderabad, you will be responsible for participating in sample processing for PK and ADME assays, as well as handling LCMS/MS. Your role will involve adapting to a dynamic team environment, processing various matrices samples for PK studies, optimizing test compounds manually and automated on LCMS/MS, and independently handling HPLC for UV-based sample analysis. Additionally, you will be expected to develop methods with the team lead, document lab notebooks online, and manage compounds effectively. You will need to demonstrate expertise in column selection, mobile phase selection, solvent preparations, and sample processing techniqu...

As a Research Scientist1 DMPK at the Foundation for Neglected Disease Research in Bengaluru, you will play a crucial role in supporting drug discovery and development projects by performing and analyzing in vitro and in vivo DMPK studies. Your responsibilities will include planning, designing, and executing DMPK experiments, maintaining laboratory instruments, and preparing protocols. Additionally, you will be tasked with writing reports, communicating with the project team, and presenting DMPK data during project meetings. Your technical skills will be put to the test as you set up and conduct physiochemical assays, in vitro DMPK assays, and bioanalytical methods. Your experience in analyzi...

You will be responsible for providing drug metabolism and pharmacokinetic support for discovery programs. Your main duties will include monitoring Pharmacokinetics studies, supporting bioanalysis, and offering pre-clinical ADME lead optimization support to small molecule Drug Discovery programs across various therapeutic areas. You will be working as a DMPK subject matter lead in multidisciplinary/cross-functional teams to understand the Chemical Structure ADME relationships and design appropriate strategies to enhance the Drug like Properties of the New Chemical Entities. To be successful in this role, you should have 2-5 years of experience in GLP with either an M.Sc. or Ph.D. degree. You ...

The key responsibility of the candidate will be to perform and analyze in vitro and in vivo DMPK studies to support drug discovery and development projects. You will be involved in planning, designing, and setting up DMPK experiments, handling instruments, maintaining the laboratory, and preparing and reviewing protocols. Furthermore, you will be responsible for writing reports, communicating with the project team, and presenting DMPK data in project meetings. Required technical skills include the ability to set up and perform physiochemical assays such as solubility and logP, experience in conducting in vitro DMPK assays (microsomal and hepatocyte stability, plasma stability, CYP inhibition...

As a Research Associate/ Executive/ Analyst in the Small Molecule Bioanalytical Research Laboratory at Syngene International Ltd., you will be responsible for conducting BA/BE studies in the laboratory. Your role will involve critical method development and validation programs, ensuring technical and regulatory compliance in all studies. To excel in this position, you should have a strong background in pharmaceutics or related life sciences, along with extensive experience in the bioanalytical field, specifically in small molecule bioanalysis. Your commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecule analysis, will be essential for suc...

Need an Analyst for a laboratory in Aroor. must have experience in handling LCMSMS/GCMSMS/ICPMS instrument at least 2 to 3 years. need to join immediately.

Need an Analyst for a laboratory in Aroor. must have experience in LCMSMS/GCMSMS/ICPMS instrument at least 2 to 3 years. need to join immediately.

Walk-In Drive : Analytical Services Required Qualification & Experience: M.Sc. Chemistry/Analytical/M-Pharmacy, with 0 - 3 Years of experience in the field of pharmaceutical industry/CRO setup. Candidate should have knowledge in method development and validations by GCMS /LC-QTOF. Candidate should have knowledge on GLP/cGMP. Good to have experince in E&L. Job Responsibilities Carries out experimentation in the area of GCMS/LC-QTOF for E&L studies. Records experimental data, ensuring clear and accurate transcription of results and calculations. Completes assigned work with quality and in a timely manner. Assists the group leader in instrument qualifications, implementing laboratory procedures...

Overall technical & operational activities of entire laboratories and coordination with the all Lab HODs related samples & test report reviewing and reporting results of performed analysis and timely deliver with accurate result and provide guidance to the customer if required and also negotiation with chemical & Instrument suppliers. Good Knowledge of latest instruments such as LCMSMS, HPLC, GC, GCMS, GC-HS, ICP-MS, ICP-OES etc. Coordination with QA team for implementing and maintaining the QMS as per ISO/IEC 17025:2017. Documentation for the upcoming audit for the bodies such as NABL, MoEF, CPCB, BIS, FDA, FSSAI, GLP, Ministry of Ayush, CDSCO etc. And proper closure of client complaint & N...

Need an Analyst for a laboratory in Aroor. must have experience in handling LCMSMS/GCMSMS/ICPMS instrument at least 2 to 3 years. need to join immediately.

About the company Meyer Organics was established in the year 1982 & is a part of the worlds No. 1 & fastest growing Nutraceutical Company, Vitabiotics Ltd, headquartered at London and operating in 110 countries across the globe. Vitabiotics is committed for the scientific research in nutrient medicine & has been awarded consequently for three years with UKs prestigious Queens Award for excellence and innovation in vitamin research. Meyer has been manufacturing innovative health care products for over three decades & is committed to excel in human health care and research. www.meyer.co.in Meyer has created a unique portfolio of products in the key segments like Anti-infective, Nutrition Suppl...