570 Lcms Jobs - Page 5

calibration &method validation by using LCMSMS/GCMSMS in Food and water samples. Sample preparation for pesticides residue and antibiotics in food samples. Testing of Pesticides Residue, Antibiotics, PAH&PCBs, ETO,PFAS, PA/TA

Research & Development Manager - MNC Agro Chemical in Bharuch,Guj 1.Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation 2.Communicate with synthesis-R&D and lead assist in analytical method remediation/troubleshooting 3.Perform analytical characterization and data interpretation for complex organic compounds 4.Experience in making lab SOPs and study reports 6.Develop analytical methods that are accurate, precise, specific, and robust 7.Calibration of the Analytical instruments as per the master calib...

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.

Walk in interview on Saturday, 8th November 2025 between 9 am to 2 pm at Analytical Solutions (Part of ALS) - Rabale (Navi Mumbai) Details as given below Position: Trainee Analyst / Analyst / Senior Analyst Experience : 0 to 7 yrs Brief Job Role: Carry out routine analysis & Ensure documents pertaining to day-to-day analysis. Calibrate instrument used for analysis as per SOP and maintain its record. Method Transfer Activity Should have experience of handling and calibration of IVRT /LCMS/GC/ GCMS /HPLC/ KF, UV, PH Meter etc and various analytical methods development. Desired profile of the candidate : M.Sc (Chemistry) with minimum 1 Years in LCMS/GC/ HPLC/ ICPMS/ IVRT/IVPT/NG tube Good in co...

Job Description: Looking for a Senior Chemist with hands-on experience in operating advanced analytical instruments such as LC-MS, GC-MS, and GC . The ideal candidate should have a strong background in method development, validation, and routine analysis of samples related to food, textiles, and polymers. Key Responsibilities: Operate and maintain LC-MS, GC-MS, and GC instruments for various analytical tests. Conduct analysis of residual pesticides in food and agricultural commodities . Perform testing of dyes and pigments in textiles and restricted substances such as PFOS, PCAs, REACH compounds, phthalates, and nitrosamines in polymers . Develop, optimize, and validate analytical methods as...

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-09-11-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make healt...

Role & responsibilities: 1. Proper maintenance of LC-MS/MS/HPLCIUPLC and their records of calibration 2. To develop and validate Bio-analytical methods. 3. To process and analyze biological samples for drug/metabolite concentrations 4. To compile raw data and record laboratory note books/logbooks 5. To maintain equipment logbooks 6. To assist Lab Manager in data analysis and compilation of reports 7. Proper operation and routine maintenance of laboratory equipment ill Bioanalytical department 8. Responsible for laboratory instruments like pH meter, analytical balance, micro pipettes, etc. 9. Recording and reviewing of all raw data, method SOPs method validation reports and bioanalytical repo...

About Us Morepen Proprietary Drug Research Pvt Ltd. (MPDRPL) is a leading small-molecule CRDMO providing end-to-end Integrated API Development and Manufacturing solutions to global pharmaceutical and biotech industries. We specialize in APIs, intermediates, and KSMs, combining innovation, scalability, and sustainability. Position Overview We are seeking a motivated scientist to join our API R&D Division. The role focuses on executing synthetic and process chemistry projects with opportunities to learn scale-up, process optimization, and CDMO operations under the guidance of senior scientists. The selected candidate will work on design, optimization, and scale-up of robust, safe, and cost-eff...

Job Description: Job Title: Senior Scientist / Team Leader Process API R&D Department: API R&D Location: Gagillapur, Narsapur road, Near Gandi Maisamma, Hyderabad No. of positions: 4 Experience: 6 - 10 years in API R&D Qualification: Ph.D. in Organic Chemistry About Us Morepen Proprietary Drug Research Pvt Ltd. (MPDRPL) is a leading small-molecule CRDMO providing end-to-end Integrated API Development, and Manufacturing solutions to global pharmaceutical and biotech industries. We specialize in APIs, intermediates, and KSMs, combining innovation, scalability, and sustainability. Position Overview We are seeking an experienced scientific leader to join our API R&D Division. The role combines t...

As a Senior Manager in the R&D department at Gujarat Fluorochemicals Limited, your role will involve the following key responsibilities: - Leading a team of scientists and chemists for new product/process development and enhancing existing products. - Conducting literature surveys and identifying commercially viable and non-infringing routes for fluoro-specialty molecules targeted for commercialization within specified timelines. - Developing and standardizing industrially feasible processes while meeting cost targets. - Identifying and creating new products to meet market demands. - Preparing feasibility reports, cost analysis reports, monthly progress reports, and Technology Development Re...

As an Analytical Chemist, your role will involve developing analytical methods such as Routine Analysis using techniques like HPLC, GC, LCMS, KF, and FTIR. You will be responsible for maintaining analytical documentation including Protocols, specifications, etc. Additionally, you will be involved in the calibration of HPLC and GC instruments. It is essential to have knowledge about data integrity and ALCOA principles. You will also be working on Chiral method development. **Key Responsibilities:** - Performing Routine Analysis using HPLC, GC, LCMS, KF, and FTIR techniques - Maintaining analytical documentation including Protocols, specifications, etc. - Calibrating HPLC and GC instruments - ...

Job description: Related to the analysis of nitrosamine impurities such as NDMA (N-nitrosodimethylamine) and NDPA (N-nitrosodipropylamine) typically focus on analytical method development and validation, LCMS Analyst / Scientist Analytical Method Development & Validation by LCMS. Preparation of Protocols and Reports. Method Development and Validation by LCMS (nitrosamine) Develops and validates reproducible and appropriate analytical methods as needed respecting the GMP practices; Participates in analytical troubleshooting; Writes methods, validation protocols, validation reports and investigation reports; Performs analyses; Participates in drafting SOP/ working instructions. Required Candid...

We are looking for a skilled Senior Data Engineer with 4 to 7 years of experience to join our team, focusing on PowerBI development. The ideal candidate will have a strong background in data engineering and excellent technical skills. Roles and Responsibility Design, develop, and implement data models and architectures to support business intelligence solutions. Develop and maintain complex data visualizations using PowerBI. Collaborate with cross-functional teams to identify and prioritize project requirements. Ensure data quality, integrity, and security by implementing robust data governance policies. Optimize data performance and scalability through advanced analytics techniques. Provide...

Read and understand various in vivo study protocols Good knowledge of various in vivo animal models employed in DMPK arena Handling of laboratory animals (mice, rats, guinea pigs, rabbits, hamsters etc.) Conduct various in vivo ADME studies (IV and PO studies, excretion studies etc.) Ability to administer compound via various routes in rodents (IV, PO, IP, SC, tropical, intravitreal etc.). Should be adept at conducting IV studies employing infusion pumps Should be able good at rodent cannulations (jugular, carotid, femoral) and conduct studies in these animals Maintain required documentation for animal ethics committee purpose Conducting simple pre-formulation work for day-to-day PK studies....

JOB DETAILS Proven hands-on experience with HPLC and LC-MS techniques. Strong background in method development and validation processes. Ability to plan, coordinate, and execute projects from initiation to completion, ensuring timelines, budgets, and quality standards are met. Track and report progress on ongoing projects to Management Minimum 3+ years of hands-on experience in supervising, mentoring, and guiding both junior and senior research associates. Ensure accurate documentation and maintenance of research and experimental data in alignment with company policies and regulatory standards. Should take care of maintenance and preventive maintenance of instruments. Ability to identify and...

Role & responsibilities Manager technical is the In-charge of Analytical Division. He/She shall report to the SBU-head about all the activities in the Analytical Division. He/She shall look after all the operations of the Division under the guidance/ supervision of SBU-Head. He/She shall be responsible for the standardization and validation of the test methods. He/She shall be responsible for ensuring the availability of the reference material / working reference standard. He/She shall be responsible for assigning the jobs to the analyst as per their calibre. He/She shall be responsible for checking the calculation part and reporting of the results before sending for authorized signatory. He...

Position: Analyst Quality Control LCMS (Liquid ChromatographyMass Spectrometry) Qualification: M.Sc. in Analytical Chemistry or related field Experience: 1 to 2 years Key Responsibilities: Perform LCMS analysis for routine, stability, and validation samples. Support method development and transfer activities. Maintain instrument calibration logs and documentation. Ensure cGMP, data integrity, and safety compliance. Work in shifts as per laboratory requirements. Skills Required: Hands-on experience in LCMS operation. Attention to detail and accuracy in documentation. Basic understanding of analytical method validation.

Position: Manager Quality Control -LCMS (Liquid ChromatographyMass Spectrometry) Qualification: M.Sc. in Analytical Chemistry or related field Experience: 10-15 years Key Responsibilities: Lead installation and qualification of LCMS instruments. Manage method development, validation, and transfer activities. Supervise routine and non-routine sample analysis using LCMS. Ensure data integrity, cGMP compliance, and documentation accuracy. Review analytical reports, protocols, and SOPs. Coordinate with QA, R&D, and Production for analytical support. Train and guide the team; manage activities across shifts. Participate in internal and external audits and ensure timely closure of observations. Sk...

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department Masters degree level in Chemistry,M pharmacy & B pharmacy 2023,24,25 passed outs. 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Bio-analytical: Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the con...

Regular Batch Analysis by using LCMS. Preparation and analysis of method validation, method transfer, method verification and method development protocols and reports. Experience in GTI & NDSRI by LCMS

Developing analytical methods and validating for NCEs and generic compounds by HPLC-UV, GC, LC-MSMS, ICP-MS Dose verification analysis in preclinical dose formulation samples by HPLC-UV, GC, LC-MSMS Generating COA for IND’s Calibration of lab equipment’s like HPLC, pH meter, balances, and pipettes Safe maintenance of raw data Work experience in GLP/GMP lab Preparation of study protocols and SOP’s Maintaining the lab as per GLP

As an Assistant General Manager in Research & Development at an Indian Pharmaceutical MNC based in Thane, you will play a crucial role in leading the Analytical Method Validation team. Your responsibilities will include overseeing validation activities, ensuring regulatory compliance, driving quality and efficiency, and fostering collaboration with R&D, Regulatory, and Plant QA/QC teams. Key Responsibilities: - Provide leadership for analytical method validation (AMV) across multiple dosage forms. - Oversee RM and PM characterization in compliance with regulatory requirements. - Plan and manage validation projects adhering to international regulatory guidelines. - Act as an SME for analytica...

Role Overview Position Title: Team Leader - Process R&D Role Band : L1 Location : Hyderabad Purpose: Lead the design, development, and scale-up of safe, robust, and cost-efficient chemical processes that meet client specifications for quality, yield, and timelines. Objective: Ensure on-time delivery with scientific rigor, data-driven decision-making, and measurable value addition across route selection, optimization, and tech transfer. Minimum Requirements Education: PhD in Organic Chemistry with 10 + years of experience (Mandatory) Business/Domain Understanding: Strong grasp of CDMO workflows, client expectations, IP awareness, and drug discovery/development interfaces (non-GMP to GMP hando...

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Ingrevia Limited JubilantIngrevia...

Responsible for synthesis, purification, and identification of organic compounds. Perform reactions, analyze using HPLC/NMR, maintain documentation, ensure lab safety, and support R&D through literature review and process optimization.