570 Lcms Jobs - Page 2

Role & responsibilities Job Responsibilities: 1. Handling of stability section independently. 2. Handling of additional stability studies, such as, Photo stability, In-use studies, freeze thaw studies. Split studies etc. 3. Preparation of stability protocols, reports and stability compilation. 4. Responsible for timely initiation, closure of QMS documents related Quality Control and implementation respective corrective and preventive action. (i.e. Change controls, Laboratory Incidents, OOS, OOT & CAPA) 5. Responsible to follow ALCOA + principle while doing the data recording. 6. Review of In-process, finished, stability, process validation, in-process, Raw material, Excipients, packing mater...

Role Overview: You will be working as a Sr. Scientist I in the India Biologics department at USP, in a hands-on, non-supervisory role. Your main responsibility will be to collaborate in the development of reference standards for biotechnology pharmaceutical products. You will also be involved in supporting the suitability program by preparing and reviewing testing protocols, providing technical assistance to testing labs, and reviewing analytical data to confirm the continued suitability of USP Reference Standards. Key Responsibilities: - Maintain smooth collaboration with key stakeholders to develop reference standards for biotechnology pharmaceutical products - Draft protocols, reports, an...

Experience in Quality Control Experience with HPLC and GC analysis Familiarity with laboratory equipment and instruments Ability to work independently and in a team Excellent organizational and time management skills AMV, AMD

NATCO Pharma is hiring! Join us for a walk-in interview on 06th December 2025 in Chennai across key functions: Maintenance, Production, EHS, QA, QC & Microbiology. Be part of a team that is committed to quality, innovation, and excellence in API manufacturing. Job Requirements Maintenance - Utilities / Mechanical / Electrical / Instrumentation Qualification: DME / B.E (Mechanical / Electrical / Instrumentation ) Operator: 3 to 5 yrs (Utilities Water Systems, AHUs, Compressors, Chillers, Boilers) Supervisor: 7 to 10 yrs (Process & Utility Equipment Maintenance, GMP Documentation) Instrumentation Operator: 2 to 3 yrs (Calibration, Automation) Electrical Operator: 3 to 5 yrs (HT/LT Operation, G...

Role & responsibilities Managing the projects/ studies for timely start and completion of the projects in conformance to GLP guidelines. 2. Allocate personnel for conducting bio analytical study and maintain list of persons to whom trial related activities are delegated. 3. Ensure that the study personnel are qualifies by appropriate education, training and experience to accept the responsibility for the delegated study related activities. 4. Method Development and Method Validation, executing methods for analysis of drugs using Solid Phase extraction, Liquid-Liquid extraction and Precipitation techniques for BA/BE studies are as per applicable regulatory requirements. 5. Ensure compliance t...

Walk In Drive For Quality Control Department In Formulation Division @ Jadcherla Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). About Company:- MSN Group is the fastest ...

Analytical Method Development for ointments, gels, injectables, BFS & lyophilized products. Hands-on with HPLC/UPLC, LCMS/GCMS, dissolution, stability & impurity profiling. Experience: 510 yrs. Location: Bangalore Food allowance Annual bonus Office cab/shuttle Provident fund Health insurance

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. Additionally, you will participate in investigations, address Out of Specifications (OOS), resolve deviations, and implement Corrective a...

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, validation, impurity profiling, and instrumental analysis to support Synthesis R&D and quality operations. Your primary responsibilities will include: 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, identifying and characterizing impurities using advanced techniques like mass spectrometry. - Ensure all analytical instruments are ...

This job is with Danaher, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. In this role, you will have the opportunity to : Perform Multi step Organic Synthesis. Purify different Organic compounds by various chromatography/other separation techniques such as column/flash/HPLC. Work on various analytical techniques such as HPLC, UPLC, GPC, UV-Vis, Fluorescence. The Essential Requirements Of The Job Include M.Sc. in Organic Chemistry/Chemistry with minimum 1-2 years of work experience preferably in Organic Synthesis either in Chemical Industries/CROs/APIs or in academic research institutio...

This job is with Danaher, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. In this role, you will have the opportunity to : Perform Multi step Organic Synthesis. Purify different Organic compounds by various chromatography/other separation techniques such as column/flash/HPLC. Work on various analytical techniques such as HPLC, UPLC, GPC, UV-Vis, Fluorescence. The Essential Requirements Of The Job Include M.Sc. in Organic Chemistry/Chemistry with minimum 1-2 years of work experience preferably in Organic Synthesis either in Chemical Industries/CROs/APIs or in academic research institutio...

Role & responsibilities Assist in routine inspections, calibration, and preventive maintenance of laboratory instruments and equipment. Support troubleshooting activities and ensure timely repairs to minimize equipment downtime. Maintain accurate documentation of maintenance activities, equipment history, and service schedules. Ensure compliance with laboratory safety protocols, quality standards, and regulatory requirements. Coordinate with external vendors and service partners for specialized maintenance, calibration, and technical support. Monitor critical laboratory utilities including HVAC systems, water supply, and power backup to ensure smooth operations. Assist in managing inventory ...

Follow Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Review scientific literature and patents to identify new product development opportunities. Design & execute laboratory experiments for specialty chemicals or excipients. Required Candidate profile Up to 5 years in Specialty Chemicals / Excipients / Pharmaceutical Field

Role & responsibilities Key Responsibilities Sales Target Achievement : Drive sales and adoption of LCMS columns portfolio across target institutes and pharma companies on PAN India Technical Consultation : Provide expert-level technical guidance on LC-MS/MS proteomics workflows and column compatibility with major platforms (e.g., SCIEX, Agilent, Thermo). Competitive Strategy : Conduct competitive analysis and demonstrate superior Total Cost of Ownership (TCO) and column longevity against incumbent products. Trial Management : Plan, execute, and manage customer column trials, providing technical support and performance benchmarking (resolution, reproducibility). Required Skills & Qualificati...

Responsible for handling Analytical activities for the R&D campus, including method development, validation, and supporting tech transfer for API projects. Key Responsibilities: Understand project scope and manage scope changes effectively. Plan and conduct analysis using advanced analytical skills. Develop suitable analytical methods based on project requirements. Guide analysts on: Analytical method development approach Analysis planning and data generation Compliance with GMP/GLP and safety standards Drawing inferences from analytical results Compile data and prepare technical reports, AMD reports, and weekly project updates. Interact with PE, PM, and PR&D teams; participate in customer c...

K ey Responsibilities: Develop and validate analytical methods for LC-MS/MS and GC-MS/MS systems. Troubleshoot instrument and method-related issues on Agilent, Waters, and AB Sciex platforms. Ensure compliance with regulatory guidelines (ICH, FDA, EMA) for impurity profiling. Prepare and review validation protocols, reports, and SOPs. Required Skills & Experience: Hands-on experience with LC-MS/MS and GC-MS/MS instrumentation (Agilent, Waters, AB Sciex). Strong knowledge of GTI and Nitrosamine analysis in pharmaceutical matrices. Expertise in method development, optimization, and troubleshooting. Familiarity with regulatory requirements for impurity testing. Minimum 5-6 years of experience i...

Job title ADL executive Division phrama Function Analytical method validation Location dombivali Designation ADL executive Job Grade Reporting to (position) ADL Head Direct Reportees (Nos) Company Name Aart industries limited Key Role & Responsibilities 1)Able to performed method validation on GC HS 2)analytical method transfer 3) Able to performed method validation on GCMS 4)method development on GC 5)Handling incident and deviation 6) online review of system,log books 7)Aware of 21 CFR part 11 guidlines ICH and Anvisa Guidlines 8) GC MS and LCMS Linkages within / outside the organisation Internal External Job specification Experience min 9 years Qualification MSc CTC Range as per company b...

Required Skills & Competencies Strong knowledge of GMP, GLP, OOS/OOT guidelines. Hands-on experience with HPLC/GC/UV instruments.

1. Should have performed instrumental analysis of stability samples, Intermediate and finished products by HPLC, UV Spectroscopy, Dissolution Test apparatus, LCMS, Particle Size Analyser and FTIR as per controlled specification and method of analysis. 2. Should able to calibrate and maintain instruments like HPLC, GC, LCMS, Dissolution apparatus UV and FTIR. 3. Should be able to performed method development and method validation on HPLC, GC and LCMS. 4. Should have well versed with ICH guideline of Stability and Method Validation. 5. Should have knowledge of Data integrity and QMS. 6. Should able to maintain cGMP throughout the activities done in the laboratory

Education: Masters degree in Chemistry, Analytical Chemistry, Biochemistry, Biotechnology, or a related field. Experience: For Analytical Chemist: Minimum 1 to 3 years of hands-on experience in analytical testing. For Senior Analytical Chemist: Minimum 4 to 7 years of experience in analytical method development, validation, or routine analysis. Perform analysis of: Residues and contaminants by LC-MS/MS and GC-MS/MS Nutritional profiling, mycotoxins, amino acids, vitamins, antioxidants and synthetic colours by HPLC across various sample matrices Operate, maintain, and calibrate analytical instruments such as HPLC, LC-MS/MS, UV-Vis spectrophotometer, GC-MS/MS, etc. Prepare and maintain standar...

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...

Dear Candidate, We are seeking a skilled and detail-oriented LCMS Scientist to join our Analytical Characterization Team, focusing on peptide-based products as well as other technology-driven formulations. Position: Assistant Manager Department: Analytical Characterization Required Exp : 3-10years Qualification: Ph.D/M.Sc/M.Pharmacy Role & Responsibilities: Perform intact mass analysis and primary structure characterization of peptides. Conduct advanced studies including: - Disulfide bond mapping - Sequence confirmation - D/L isomer differentiation Develop and validate LCMS/MS methods for peptide analysis. Conduct impurity profiling for peptide-related impurities using LC-HRMS. Identify unkn...

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Skills : HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals | GC | GLP & QMS Activities | Method Transfer & Method Verification | LIMS | Audit Handling | Empower 3 Software | Wet Analysis | Documentation | Raw Material | Material Analysis Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Division :- Formulation Interview Date:-29-11-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF Unit-V, Chinna Chilkamarri Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbu...

Testing and Analysis as per documented procedure Complication and reporting of analysis results. Calibration of equipment's and instruments as per SOP. Maintaining housekeeping practices as per the requirements of GLP. Conduct quality control tests. Maintain laboratory instruments to ensure proper working order and troubleshoot malfunctions when needed. Technical reports or prepare standards and specifications for processes facilities, or analytical methods. Handling, calibration & maintained of weighing balance, palarimeter, refractometer, UV-spectrometer, ICP-MS, AAS, LCMSMS, GC, GCMSMS, Microwave Digester and ICP-OES. Analytical Method development, validation and verification of metals on...

As a Research Associate specializing in Custom Synthesis at SynSmart, your role will involve planning, executing, and optimizing chemical synthesis projects for global clients. Your key responsibilities will include: - Conducting complex organic synthesis - Developing innovative methodologies - Optimizing reaction conditions - Documenting experimental results - Collaborating with cross-functional teams to meet project deadlines and objectives To excel in this role, you should have the following qualifications: - Proficiency in Organic Chemistry, Synthetic Chemistry, and related experimental techniques - Experience with custom synthesis, reaction optimization, and process chemistry - Strong a...