570 Lcms Jobs - Page 9

As a Scientist at USP, your role will involve conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) utilizing suitable methods to enhance the laboratory's scientific proficiency and work ethic. You will offer extensive technical support and knowledge and provide valuable observations and insights into challenging projects. Your responsibilities will include: - Conducting verification projects (Dietary Supplements/Dietary Ingredients) by performing individual analytical tests such as HPLC, GC, Dissolution, ICP-MS, ICP-OES, and wet analysis as assigned - Completing projects within designated timelines and priorities - Demonstrating a robust sci...

As a Senior Scientist I or Scientist IV at U.S. Pharmacopeial Convention (USP), you will have the opportunity to contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. Your role will involve aligning with USP's mission, goals, and objectives, complying with guidelines, and demonstrating laboratory skills in various analytical techniques such as Chromatography, SEC-MALS, LC-MS, HPLC/UPLC, Ion-chromatography, Capillary Electrophoresis, and more. You will be responsible for planning and executing Compendial and R&D projects, including proof of concept studies in Biologics ...

As an Environmental Regulations Specialist, you will be responsible for: - Implementing Li-ion battery recycling and developing efficiency improvements through various sources - Exploring secondary life utilization of EOL batteries and methods to reduce carbon footprint - Managing and controlling Substance of Concern (SOC) through the IMDS platform - Performing RRR & SOC Calculations for vehicles as per standards - Monitoring and circulating information related to upcoming Environmental Regulations - Providing awareness and training to suppliers and internal teams for SOC Management In terms of competencies and skills, you should be: - Well versed with regulations related to Battery Waste Ma...

Experience in Operation and calibration of LCMS /GC Method development and validation of Genotoxic impurities/ nitroso amine impurities/NDSRIs in pharmaceutical products/ substances by LC-MS/MS. Development of MS compatible methods for the HPLC RS methods for the identification of unknown peaks by LC-MS Development of MS compatible methods for the identification of degradation impurities and unknown impurities

- Analytical biochemist with experience in routine protein analysis such as antibodies, bispecific antibodies, Fc fusion proteins. - LC MS, ELISA, SDS PAGE Western blotting Required Candidate profile Complex protein analytical method development, method qualification, analytical method transfer. Antibody Drug Conjugate analysis using HPLC methods, deeper understanding of LC MS-

Sample processing Sample analysis Method Development Method Validation Working experience on LCMS Required Candidate profile Must have worked in Bioanalytical Department with Pharma AND / OR CRO

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. Team management. Desired Candidate Profile : Bachelor's degree in pharmacy (B.Pharma) or Ma...

Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team i...

Job Description Job Title : IT Solution Architect The IT Solution Architect is responsible for driving program-level IT architecture initiatives, facilitating communication and validation of transformational capabilities, guiding project-level IT architecture, providing hands-on support for solution design and implementation within the specified framework, and fostering seamless integration and scalability. Brings rich experience in areas of Services and Education Architecture, including Services Delivery (MS D365), LMS (Totara), LCMS(Xyleme), CMS(Drupal), Development Technologies (MS Power platform), and IT Solution Design. The role develops architecture solutions adhering to standards, ens...

Job Description Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. Broad knowledge of modern organic chemistry and synthetic methods Heterocyclic chemistry, metal catalyzed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. Work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports and other scientific documents, as...

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 Biosys Jubilant Biosys Ltd is a p...

Employment Mode : Contract to Hire Offshore OT Analyst Roles and Responsibilities: Good experience working in the Cyber security domain with a minimum of 5 years in the Industrial automation and controls space Strong understanding of various components in the ICS ecosystem, common security issues faced and best practices to be followed from a security standpoint Strong understanding of Industrial control operations and protocols Sound knowledge of the ICS cybersecurity framework IEC 62443 Good understanding of concepts like Industry 4.0, Cyber Physical Systems, Digital Twin Preferable to have hands-on experience working at a Manufacturing plant Demonstrable credentials in the Industrial cont...

We are seeking an experienced and driven Associate Principle Scientist to join our research team. The ideal candidate will be responsible for conducting cutting-edge research, designing and executing experiments, analyzing results, and contributing to the advancement of projects. This role requires a deep understanding, as well as strong analytical and problem-solving skills. Qualification: Ph.D. With Post Doc in Organic/ Medicinal Chemistry Responsibilities: Understand and manage client expectations Resolve client issues on priority basis Responsible for collaboration growth and retention Ensure increase customer satisfaction scores Enhance scientific capability of team members and establis...

Role Overview: You will be responsible for conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods in a non-supervisory role. As a Scientist at USP, you will enhance the laboratory's scientific proficiency and work ethic by providing extensive technical support and knowledge. Proficient in various common laboratory techniques, you will offer valuable observations and insights into challenging projects, aiding the Verification Program by executing analytical tests and preparing comprehensive summary reports. Key Responsibilities: - Conduct verification projects on Dietary Supplements/Dietary Ingredients by performing indiv...

Role Overview: As a member of the team, you will be responsible for conducting extractables and leachable studies on packaging components, medical devices, and drug products. Your role will involve performing sample preparation, extraction, and analysis using techniques such as HPLC, GC-MS, LC-MS, ICP MS, ICP OES, and other relevant instrumentation. You will also be developing and validating analytical methods for E&L testing in compliance with regulatory guidelines. Additionally, you will interpret and report analytical data, prepare technical reports, protocols, and documentation for regulatory submissions, and collaborate with cross-functional teams. Key Responsibilities: - Conduct extrac...

Dear Sir, We are hiring Analysts for our IVRT/IVPT team. Please go through below JD, and share your profiles on harisha.p@invitron.co.in or contact us on 9000251866,if JD suits you. Experience Required: 2 to 6 years (pharmaceutical / CRO industry) Location: Plot No.126,ALEAP Industrial Estate, Pragathinagar, Hyderabad - 90. Department: Analytical Research Key Responsibilities Design, plan, and execute in-vitro permeation testing (IVPT) and in-vitro release testing (IVRT) studies for topical, transdermal, and semi-solid dosage forms in line with regulatory guidance (FDA, EMA). Develop, validate, and implement bioanalytical methods for IVPT/IVRT studies using LC-MS/MS (Sciex systems preferred)...

Dear Candidate, We are Conducting Walk -In for the positions in our Analytical Research & Development department. Job Description : Position Name: Research Chemist/Senior Research Chemist/Research Associate Experience: 1 to 5 years Qualification: M.Sc Analytical Chemistry/Organic Chemistry/M.pharm Work location: Uppal/Mallapur Key Skills and Competencies: High-Performance Liquid Chromatography (HPLC) Key Skills and Competencies: Operation and Maintenance : Proficiency in operating HPLC systems (e.g., Agilent, Waters, Shimadzu) and performing routine maintenance, calibration, and troubleshooting of equipment issues like pressure fluctuations or detector errors. Method Development and Validati...

Role & Responsibilities: Perform Analysis: Lead the team along with GL or in absence of GL Design the experiment for development Resource planning skills and shift and manpower planning and coordination Special bioanalytical techniques- Peptide, Liposomal method handling Endogenously present molecule handling and Approach Rare matrix (Aqueous Humour, Skin, tissue etc)handling conceptual clarity failure handling and resolution skills coordinate with SGL for targets alignment and execution target achievement as team LC and LC/MS- calibration Perform analysis via LCMS. Follow GxP Work pressure effective handling skills Documentation and compliance: Preparation of Method SOP, Method validation p...

As a Scientist at Novartis, you will be responsible for planning and performing scientific experiments for the timely delivery of drug substances, drug products, processes, and procedures within a multifunctional project team. Your role will involve collaborating with a Project Leader and contributing to the maintenance of lab instruments and infrastructure. Key Responsibilities: - Meet quality, quantity, and timelines in all assigned projects - Perform and document scientific experiments - Plan and organize scientific experiments with minimal guidance - Provide documentation of raw data and evaluate results - Propose and provide input for the design of next experiments - Generate lab proced...

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. : Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Leadership role to manage team size of 10+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Managing multiple instruments (LC-MSMS, GC-MSMS, ICP-MS, IC etc.) Method development experience in LC-MS...

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Planning/performing and reporting of acute toxicology studies Assist in preparation of SOP"™s, Protocols and Reports Participate in GLP / AAALAC related activities Literature search Maintenance of animal house and relevant documents as per GLP and AAALAC norms. To Assist and work along with SD and TC in Plann...

Note: Walk In Interview at Vadodara. Date: - 28.09.2025 (Sunday) Job Location: Daman & Dahej Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M. Pharma Experience:- 2-6 Years in (API or Solid Oral) Required Candidate profile * 2-6 years of experience into LCMS, HPLC, GC & Wet Chemical sections, Analytical Validation, Finished Goods, Raw Material, Stability & GLP

Exp: 2- 6 yrs • Knowledge in Method Development on Assay, RS, dissolution for formulation complex molecules. • understanding of Q1/Q2 evaluation • PEQ processes and characterization • Instruments: HPLC, GC, KF, UV, IR, etc. kiran.k@orbicular.co.in

Role Overview: You will be responsible for performing chemical and instrumentation analysis on various materials, including in-process, raw materials, packing materials, intermediates, and finished products. Your primary goal will be to ensure compliance with dispatch timelines as per the monthly schedule provided by PPL. Key Responsibilities: - Conduct instrumentation analysis using ICP-MS and LC-MS for various materials to meet dispatch timelines - Participate in analytical method developments, validations, transfers, and verifications using ICP-MS and LC-MS/MS - Prepare and review protocols, worksheets, and reports for method developments, validations, verifications, and transfers - Allot...