105 Lcms Jobs - Page 2

Responsibilities: * Conduct quality control tests using HPLC, GC, LCMS methods. * Ensure compliance with industry standards and customer requirements. * Collaborate with production team on process improvements. Thanks RIGHTCHOICE Annual bonus Provident fund Health insurance

Walk In Drive For Quality Control Department In Formulation Division @ Vizag Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 08-06-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- Hotel Cygnett Inn Ramachandra , 31-2-4/5, NH16, opp. All India Radio Station, Kurmannapalem, Visakhapatnam, Andhra Pradesh 530046 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 growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

As Temp Field Service Engineer, you are an ambassador of Waters and will bring to the market Waters products and services. The candidate will demonstrates a clear grasp of understanding the customers business and its growth plans and is able to take that knowledge and convert that into a solution and offering from Waters, with a primary aim of bringing customer success”. This position brings a great degree of flexibility working in the field. The role will be designated to either a territory and/or markets. Installation, performance maintenance, troubleshoot and support Waters' product suite (LC, LC/MS, HPLC/UPLC, SFC, Informatics) Establish and maintain effective relationships with external and internal customers ensuring their success Handle customer expectations, by communicating work performed and providing follow up plan if needed Ensure customer compliance regulations are followed Deliver system level training at customer sites Handle service inventory according to Waters policies Issue field service reports daily to document work performed Maintain sound knowledge regarding the technology and customers' application demands Work with Sales team in respect to identifying future business development opportunities and needs for service contract sales Ensure that quality system procedures and Health & Safety standards are adhered to at all times Education: Bachelors in Electronics or Instrumentation, Chemical engineering or other science related field is desired, will also consider applications with equivalent experience, training and education Experience: 1-3 years of experience with installation, performance maintenance, troubleshooting, support and/or end user utilization of scientific instrumentation, preference for previous Waters product suite (LC, LC/MS, HPLC/UPLC, SFC, Informatics) Ability to perform effective system level troubleshooting Understanding of the scientific application workflow along with the scientific software systems (CDS, SDMS, LIM, ELN) Skills: Must possess a strong customer focus Strong communication skills; ability to communicate effectively to a diverse audience with specific customer needs Personal sense of integrity Effective time management skills System level approach to problem solving Analytical approach with a strong aim to resolve open issues Excellent verbal and written communication skills Travel: This is a territory-based position with travelling within your designated territory, and occasional travels to other countries for activities such as governance of department, local business support, meetings and training.

Job Responsibilities Proven experience in leading a team responsible for handling LC-MS systems. In-depth knowledge and hands-on experience in LC-MS method development for NCE molecules on an analytical scale. Should have sound knowledge of LCMS data interpretation/characterization. Expertise in various purification techniques and methodologies. Accountable for troubleshooting and ensuring the proper calibration and maintenance of instruments. Capable of working collaboratively and leading a team of enthusiastic young scientists. Willingness to lead and manage the team across different shifts as required. Job Requirements Have a passion for LC-MS analysis and characterisation techniques Interpersonal skills to interact effectively with people in other departments Creative thinking to spot new techniques and growth opportunities Be highly organised with the ability to work in a fast-paced environment Work collaboratively with others and be able to adapt to various work assignments Must possess a great deal of integrity to maintain confidentiality Fluent oral and written (English) communication skills Apply here - https://o2h.recruitee.com/o/associate-scientist-principal-scientist-adl

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:- 01-06-2025 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 growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Roles and 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 Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Analysis of samples by using HPLC (Open Lab Solutions).Wet Analysis by using IR, UV, pH, etc.Quality Control Documentation. Responsibilities: Conducting Laboratory Experiments: Plan and execute a variety of chemical experiments, including synthesis, analysis, and characterization. Operate and maintain laboratory equipment such as spectrophotometers, chromatographs, and titrators. Collect and record experimental data accurately and meticulously. Data Analysis and Interpretation: Analyze experimental data using statistical and other relevant methods. Interpret results, draw conclusions, and prepare technical reports and presentations. Identify and troubleshoot problems encountered during experiments. Research and Development: Conduct literature reviews and stay abreast of the latest advancements in chemistry and related fields. Contribute to the development of new products, processes, and formulations. Participate in brainstorming sessions and contribute creative ideas. Laboratory Maintenance: Maintain a clean, organized, and safe laboratory environment. Ensure compliance with safety regulations and laboratory protocols. Order and maintain laboratory supplies and equipment.

Education - MSC Chemistry Educational Requirement :-Diploma Chemical Experience - 2-6 (Agrochemical or Chemical Industry Experience Must) Understand the project requirements & deliverables from supervisor/manager Required Candidate profile If you are interested so please share me your cv at Jyoti Dasoni Contact Person No. - 9315507817 capitalplacement04 @gmail.com

Education - MSC Chemistry Educational Requirement :-Diploma Chemical Experience - 2-6 (Agrochemical or Chemical Industry Experience Must) Understand the project requirements & deliverables from supervisor/manager Required Candidate profile If you are interested so please share me your cv at Jyoti Dasoni Contact Person No. - 9315507817 capitalplacement04 @gmail.com

Bioanalyst who will be responsible for high-quality discovery bioanalysis to support preclinical in vitro ADME and in vivo PK studies. LC-MS/MS based bioanalytical techniques to analyse biological samples in support of Drug Discovery projects. Required Candidate profile Around 5-8 years of experience in discovery bioanalysis to support in vitro ADME and pharmacokinetic studies.

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

GTI & NDSRI by using LCMS. Review of Method Development & Method Validation Data Preparation of Protocols & Validation Reports Handling of Incidents, Deviations & Change Controls.

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures.Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic Required Candidate profile Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods.

Role & responsibilities Responsible for Analysis of Pesticide Residues, Mycotoxins, Antibiotics residue analysis . Preparation and maintenance of Reference standards in Laboratory. Maintain the control of technical records as per requirements; ensure all the tests are performed by correct method and specification in the department. Responsible to implement test methods/process/audit as per regulatory guidelines (NABL, EIC, APEDA, FSSAI Tea Board). Ensure validation data & calibration of all instruments (Intenal and External), chemical, consumable, Glasswares etc.). Thorough Knowledge of SANTE and EC 657 guidelines Should have handling and Troubleshooting Experience of LCMSMS(Should Handles LCMSMS makes like Waters/AB Sciex/Agilent /Thermo/Perkin Elmer) Responsible to maintain Quality Management System in Section (Maintain QC/ILC/PT data) Responsible for calibration of glassware, micropipette, and analytical balance. Ensuring accuracy of calculations, reproducibility of test result. Support in identifying needs for skill development. Perks and benefits -

Role & responsibilities Technically competent & Expertise in Residual analysis & handling of Instrument- LCMS Preparation of the Standard operating procedures and the work instructions. Ensure that the tests are done in accordance with the method Validation of the test methods and establish and standardize the new methods and tests as required by the market To ensure that the national and international standards are available for all tests and are followed while conduct of these test Maintain the Reference Materials in the laboratory and monitor their use Monitor the equipment maintenance and verification plan & calibration schedule & its implementation Calculation of the UOM for the tests in their respective departments and in house calibrations To maintain turnaround time Correctness of the analytical results Validation of Methods and calibration and maintenance of equipment Attributes: Team management abilities. Excellent knowledge of HPLC & GC & trouble shooting Problem-solving and decision-making skills. Strong communication and interpersonal skills. Ability to work in a fast-paced, deadline-driven environment.

Hands on skill and Knowledge of LCMS, HPLC, UHPLC, GC, GCMS, Wet chemical Understanding of analytical chemistry, discussion with synthesis, plant, PE laboratory analysis of samples in time., Ensure that laboratory work is carried out in a safe manner Required Candidate profile Analytical Research & analytical method development for organic molecules. Method validation. Method transfer. Stability studies. GLP. GDP, Building Problem Solving, Customer Centricity, Analysis

Walk-In Drive For API Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Saturday 05-04-2025. Requirement for Executive / Senior Executive - API AR&D - API Analytical Research & Development(AR&D) HPLC,LCMS,GC,GCMS,GCHS High performance liquid chromatography HPLC,LCMS,GCMS HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of drug development. Method Validation of analytical methods as per internal and country specific regulatory guidelines and execution through proper protocols. Compliance of Good Laboratory Practice in the lab Responsible for providing support to technical issues related to R&D to file the Drug Master files. Effective method development ensures that laboratory resources are optimized, while methods meet the objectives required at each stage of drug development. Responsible for ensuring delivery time-lines and adherence to quality and standards and customer Relationship management. Facilitating scientific and technical discussions with team members and external collaborators to resolve issues and communicating conclusions from stability studies. Interview Date : Saturday 05-04-2025 Department : Analytical Research & Development(API AR&D) HPLC AND GC Experience : 2 to 8 Years Qualification : M.Sc Position: Executive / Senior Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details :Venue Details : MSN Laboratories Pvt. Ltd, R&D Centre, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana Saturday 05-04-2025

Job Description: Performing Stability Analysis. Performing Method transfer/ Method Validation Analysis. Calibration and validation of instruments / equipment's Analysis. Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelines Preparation of departmental SOPs in compliance with current guidelines. Preparation of validation protocols in compliance with current guidelines. Entry of stability sample results in LIMS / SAP. Handling of LSCMS Software.

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Division :- Formulation Interview Date:- 05-04-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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 health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Development & Validation of Bioanalytical Method, Analysis of samples PK, BA/BE Studies, Preparation of reports. Should have experience in sensitive assays of drugs from biological matrix, Analysis based on LC-MS/MS Liquid handling system, ICP-MS Required Candidate profile Candidates must have experience in Bioanalytical department. MSc (Analytical, Org, Bioanalytical), M/Pharma, PhD in chemistry or Pharmaceuticals Science. Ready to work in first and second shift Perks and benefits 5 Days week, Bus Facility, Birthday Leave, 28 PL

Walk-In Drive - API- Quality Walk-in Interviews for API - Quality Roles based out of Kurkumbh (Job location) on 06 & 07 April, '2025 (Sunday& Monday), from 1000hrs. to 1600 hrs. at Kurkumbh, Maharashtra We have the below openings: API - Quality Control : M.Sc. (Analytical / Organic Chemistry) with 2-5 years experience with Expertise in handling RM, intermediates & Finished products in API manufacturing. Handling HPLC, GC, LCMS, ICPMS. Knowledge of Particle Size Analyzer/LCMS /GCMS preferred API - Quality Assurance: M.Sc. (Organic Chemistry) BE/B Tech (Chemical Engineering) with 2-5 years of experience with Must have experience only in API. Experience in API Inprocess QA, API line clearance , QMS, APQR, Process & Cleaning validations will be desirable. Experience of API production as well as QA will be preferred.

Job description 1. Candidates will be responsible for Sales of high-tech analytical & Life Science instruments like HPLC, LCMS, GC, GC-MS, UVVis, FTIR, ICPMS, AAS spectrophotometers, Rotary Evaporator, PCR, Digital Droplet PCR, Fermenter, Bioreactor, Liquid handling Systems, Nucleic Acid Extraction etc. 2. Desired candidates profile : The candidate should meet/exceed sales targets, provide accurate sales forecasts, generate leads, deliver timely and accurate reports, and take strategic initiatives to convert inquiries into orders. Products : Analytical Instruments Laboratory Equipments Life Science Instruments Chromatography Columns and Consumables Spectroscopy Accessories and Consumables Required Experience, Skills and Qualifications Qualification: Degree in Science or Engineering. Preferably in Instrumentation, Electronics, Electrical, or Chemical Engineering. An MBA in Marketing can be highly beneficial, along with strong sales skills and a thorough understanding of our products, applications, and support. Additional strengths include proficiency in market research, digital tools, and platforms, as well as strong analytical skills. Location - Hyderabad, Chennai, Bengaluru, Delhi, Chandigarh/Baddi, Haridwar, Ahmedabad About BasilBio BasilBio is a leader in providing innovative laboratory solutions, with a focus on cutting-edge technologies in chemistry, life sciences, and analytical instrumentation. We are looking for a motivated and dynamic professional to join our growing team.

Job Summary: As a Medicinal Chemist, you will play a pivotal role in the design, synthesis, and optimization of novel drug candidates. This role requires scientific expertise, problem-solving skills, and hands-on laboratory experience to drive drug discovery projects from hit identification to lead optimization and preclinical development. You will work closely with cross-functional teams to develop innovative therapeutics that address unmet medical needs. Responsibilities: Design and synthesize novel small molecules to target specific disease indications. Planning and implementation of novel approach to drug discovery and development independently or in collaboration. Apply Structure-Activity Relationships (SAR) and Structure-Property Relationships (SPR) to optimize potency, selectivity, and pharmacokinetic properties. Collaborate with computational chemists, biologists, and pharmacologists to design and prioritize new chemical entities for synthesis and biological evaluation. Perform literature searches and analyze scientific literature to identify and implement new synthetic methodologies and technologies. Contribute to the preparation of patent applications, technical reports, and scientific publications. Use computational models and simulations to predict the behavior of new drugs and to guide the design of new compounds. Stay updated with emerging trends in AI-driven drug discovery and medicinal chemistry innovations. Understand Structure Activity Relationships and Structure Property Relationships of various projects. Qualifications and Skills: Ph.D. in Organic Chemistry, or related field. 10-13 years of industry experience in Life Sciences, R&D, CRO, biotech, or pharmaceutical settings. Strong background in synthetic organic chemistry, medicinal chemistry, and chemical biology. Proficiency in modern synthetic methods, purification techniques, and analytical instrumentation (e.g., NMR, LC-MS, HPLC). Demonstrated success in lead optimization and preclinical drug discovery. Familiarity with pharmaceutical industry practices and regulatory frameworks. Knowledge of AI-driven drug discovery methodologies is an advantage. Excellent problem-solving skills, scientific creativity, and a passion for innovation. Strong communication and interpersonal skills, with the ability to collaborate in a multidisciplinary environment.

Qualifications required: Bachelors /Masters (2-5 Years of experience in Bioanalytical Department Role and responsibility: 1. To work on the method development / validation / study sample analysis using HPLC, LC/MS/MS techniques as per principles of GLP, SOPs and approved protocols. 2. To plan and monitor the laboratory work involving the various processing techniques, analytical methods and standard operating procedures (SOPs) and complying with the principles of Good Laboratory Practices (GLP) as well as approved protocols to ensure the quality, integrity and reliability of the results. 3. To establish quality control program and safety of the staff and to establish corresponding corrective actions. 4. To review the raw data forms and chromatographic data sheets 5. To electronically transfer the data duly checked with the raw data and chromatograms to Pharmacokinetics department for PK analysis. 6. Review of Method SOPs, bio-analytical reports of Method Validation and Studies. 7. Review and/or approval of operational SOPS and Method SOPs. 8. Training of personnel. 9. Responding to queries from Sponsor and/or regulatory authorities.

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Qualifications required: Bachelors / Masters (0-4 yrs. experience) degree level in biological/ life science, pharmacy qualification. 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 concentration data of subject samples before releasing to PK department. Generation, control and distribution of method SOPs. Logbook handling and archival of the completed logbooks. Performing the routine glassware validations and monitoring of the temperature and humidity in the Bio-analytical lab. Calibration of pipettes and multipedes. Coordinating for training programs on SOPs. Ensure cleanliness of laboratory and disposal of non-bio-waste & Bio-waste.