37 Lcmsms Jobs

Role Overview: As a Manager - Research Scientist at our Supply Chain and Manufacturing team, you will be a vital part of the analytical research focused on flavor chemistry for process research initiatives. Your role will involve utilizing advanced analytical techniques to identify, quantify, and understand the flavor compounds in our ingredients, process intermediates, and products. You will contribute significantly to process projects from concept to completion while gaining experience in different disciplines and research programs. Key Responsibilities: - Design studies and solve complex analytical objectives related to flavor development during fermentation, distillation, maturation, and...

You will be responsible for providing drug metabolism and pharmacokinetic support for discovery programs. Your duties will include monitoring Pharmacokinetics studies, supporting bioanalysis, and offering pre-clinical ADME lead optimization support to small molecule Drug Discovery programs. This support will range from Hit Identification to Clinical Candidate Selection in areas such as Inflammation, Neuroscience, Metabolic Disorders, and Anti-infective Research. As a DMPK subject matter lead, you will collaborate in multidisciplinary/cross-functional teams to understand Chemical Structure-ADME relationships and design strategies to enhance Drug like Properties of New Chemical Entities. Key R...

Role Overview: As a Research Analyst at the Contract Research Organization, you will be responsible for performing lab activities following applicable Methods, Plans, SOPs/SWPs, GLP regulatory guidelines, and 21 CFR Part 11 as directed by Group Leader and Sr. Analysts. Your key responsibilities will include conducting Bio-analysis validation and sample analysis independently, performing Pre-Study with minimal supervision, utilizing established techniques to compile and analyze data, documenting work, maintaining study documentation and lab records, providing direction and technical assistance to lesser-skilled team members, assisting with SOP/SWP preparation and other technical-related docum...

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...

As an Analyst / Sr. Analyst - Instrumentation, you will have the following responsibilities: - Expertise in handling Instruments like - ICP-MS/HPLC/LC-MS/MS - Preparation and review of raw data of sample (s) analyzed in respective section - Verification & validation of test methods as per NABL, EIC, APEDA and client requirements - Calculating uncertainty of measurement for different parameters performed in respective sections - Preparation of working reference standard & reagents - Maintenance of records of working reference standards with their logbooks under the supervision of Section In-charge - Maintenance, calibration & intermediate checks of glassware & equipment in respective sections...

Job Description: As a Chemist at Piramal Pharma Solutions (PPS), you will be responsible for performing chemical and instrumentation analysis for in-process, raw materials, packing materials, intermediates, and finished products to meet dispatch timelines. Your role will involve performing analytical method developments, validations, transfers, and verifications using ICP-MS and LC-MS/MS. Additionally, you will be responsible for reviewing protocols, work sheets, and reports, maintaining documentation online, calibrating instruments, and ensuring the cleanliness and upkeep of instruments in the section. Key Responsibilities: - Perform chemical and instrumentation analysis for various materia...

You will be responsible for leading the characterization of peptides and small molecules using Liquid Chromatography and High-resolution mass spectrometry (LC-HRMS, LC-MS/MS) to determine structural elucidation and impurities profiling. As a Team Lead, you will manage a team focused on Peptide / Protein characterization through HRMS. Your duties will include method development, impurity profiling of Peptides/Proteins, and Impurities characterization using HRMS. Additionally, you will utilize spectroscopy (UV-Visible, Circular Dichroism, Spectrofluorometer), Capillary Electrophoresis, and analytical method development for characterization purposes. - Handling LC-HRMS for Characterization of P...

As a Regional HRMS Sales Specialist at SCIEX, a Danaher operating company, you will play a crucial role in driving significant impact within the organization. Located in Hyderabad/Bangalore and working remotely to cover South India, you will be responsible for the following key responsibilities: - Responsible for the LC-MS/MS sale, particularly focusing on the HRMS product line (Order and Revenue) in the assigned region across all market verticals. - Achieve sales targets on a quarterly and annual basis. - Provide the company with reliable business forecasts and relevant market information to assist in developing strategies for products and market growth. - Actively participate in cross-func...

As an experienced individual with a background in M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry) with 11-14 years or Ph.D. with 2-5 years of relevant experience, you will be responsible for the following key roles and responsibilities: - Expertise in designing and executing DMPK studies to support antibody-drug conjugate (ADC) and monoclonal antibody (mAb) programs, covering the entire spectrum from discovery through IND-enabling stages. - Extensive experience in quantifying biologics such as antibodies, therapeutic proteins, ADCs, and peptides using platforms like LC-MS/MS, MSD, and ELISA. - Proficiency in utilizing advanced bioinformatic...

Deputy Technical Manager required for an NABL accredited Food, Water and Environmental testing lab in Kochi. The candidate must have passed both theory and practical of FSSAI 10th Food Analyst Examination (mandatory) and should be anFSSAI Approved Analyst, who is authorized to sign the Chemical and Microbiology test reports. Responsibilities The person will be fully responsible for FSSAI related works and should be well versed in Food analysis including instruments like GCMSMS, LCMSMS, ICPMS, HPLC, UV-Vis Spectrophotometer, wet lab analysis, nutritional factor analysis etc. Qualifications M.Sc. Chemistry / Microbiology / equivalent candidates from Kerala with more than 5 years experience in ...

Key Responsibilities Operation, Maintenance and calibration of GCMSMS and LCMSMS Agilent Instrument. Trouble shooting of Instrument. Maintain all the records in the laboratory for-Calibration, Intermediate checks, Sample Preparation, Standard Consumption, Breakdown, sample logbooks, Environmental conditions etc. Sample preparation and Analysis of Chemical and Nutritional parameters in Food & Agricultural products, AYUSH Products, Marine/Aquaculture, Nutraceuticals & Functional Foods, Animal Food & Feeds, and other matrix at Central lab as per IS, ISO, BSEN, AOAC, FSSAI Manual Methods, customer methods, laboratory developed internal methods, other national and international methods. Analysis ...

JOB SPECIFICATION OF Apurva Bhagat JOB TITLE Team Leader-Material section LOCATION Pune Food Laboratory DEPARTMENT Instrumentation REPORTING TO Atulkumar Rajage EXPERIENCE 5 to10 years OFFERED CTC 4-7 Lacs per year QUALIFICATION MSc Chemistry JOB RESPONSIBILITY 1) Well worse with Extractable and Leachable testing 2) Responsible to identify new requirements and Execute method development and analysis in Material Testing-Packaging Materials such as food packaging. 3) Required good knowledge about food safety and standards packaging regulation 2018 as well as EU regulations. 4) Knowledge required regarding methods and reporting as per regulations IEC,FSSAI,GB China,ASTM,EN,ISO,EC,ICHQ3 guidelin...

Role Overview: As a Chemist in the Instrumentation Laboratory (Residue Lab), you will be responsible for the preparation and analysis of samples using various Instrument techniques while ensuring strict adherence to safety and documentation protocols. Your role will involve receiving, handling, and storing samples and standards, conducting analysis on instruments in compliance with regulations, and contributing to method development and validation. Strong analytical skills and knowledge of NABL and ISO/IEC 17025:2017 standards are essential for this role. Key Responsibilities: - Sample Preparation & Analysis: - Receive, handle, and store samples - Prepare samples, conduct analysis, and gener...

As a Research Associate/ Executive/ Analyst at Syngene International Ltd., you will be a part of the Small Molecule Bioanalytical Laboratory in Bangalore, India. Reporting to the Project Leader / Group Leader, your role will involve conducting BA/BE studies, method development, and validation programs, ensuring technical and regulatory compliance. Key Responsibilities: - Perform bioanalytical work including sample processing, method development, validation, and study sample analysis in compliance with SOPs and STPs. - Prepare STP, MV protocol, and study sample analysis protocol. - Coordinate with the maintenance department for equipment failures. - Document data entries and ensure regulatory...

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.

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 ...