455 Lcms Jobs - Page 5

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...

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...

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

Role & responsibilities Analytical testing of chemicals, Reagents, Raw materials and other Pharmaceutical products. Preparation, Standardization and stability evaluation of volumetric solutions/Reagents/Indicators. Performing computerized system validation (CSV) as per current regulatory requirements. Testing of Raw materials, In-process, Intermediates and APIs using Chromatographic Data system. Analytical Testing of Related substances/Content/Assay/Purity testing and Calculation by HPLC Using Empower/Lab Solutions. Data generation, Integration and Review of Chromatographic data generated by Chromatographic data system. Method Transfers & Holding time Studies. Testing of Raw materials, In-pr...

Job Title: AQA Quality Assurance (LCMS, GCMS, ICPMS) Company: Energon Labs Location: Hyderabad Experience Required: 2 - 6 years Employment Type: Full Time, Permanent Role Overview We are seeking experienced professionals in Analytical Quality Assurance (AQA) to review and ensure compliance in analytical data generated through LCMS, GCMS, and ICPMS techniques. The role requires a keen eye for detail, strong knowledge of analytical methods, and the ability to uphold the highest quality standards. Key Responsibilities Review analytical data for LCMS, GCMS, and ICPMS techniques. Conduct electronic audit trail reviews for analytical instruments and ensure compliance. Review Analytical Method Vali...

Role & responsibilities Preferred candidate profile

Home The University Job Opportunities and Working At Swansea Current Vacancies Research Officer in Antihydrogen Physics Back to list Research Officer in Antihydrogen Physics Related pages Current Vacancies Benefits & Rewards Equality Diversity & Inclusion Information for Applicants Information for for colleagues from around the world Our reward and benefits, and ways of working enable those who join us to have enriching careers, matched by an excellent work-life balance, About The Role The group is a leading member of the ALPHA collaboration with responsibility for positrons, antihydrogen synthesis, laser-spectroscopy and frequency metrology Recent research highlights include the first laser...

Understand the project requirements and deliverables from manager as specified by the client Understand the reaction protocol and search literature as required Efficiently delegate work and monitor team members for effective planning, execution and delivery Understand and discuss the MSDS (Material Safety Data Sheet) with team members Identify and mitigate any potential safety risk with the help of supervisor Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage and minimum wastage Ensure parallel execution of multiple reactions Monitor the reaction by observing ...

The HRMS and Omics/Biologics Market Development Manager is responsible for developing business, drive market development initiatives, promote newer technologies and create growth opportunities. This role combines strategic marketing with technical proficiency, deep and advance knowledge to shape business performance and is required to understand the challenges of High Resolution Mass Spectrometers (HRMS) products applications to diverse segment customers. Responsibilities: Promote newer HRMS technology products, providing guidance, training, and mentorship to ensure alignment with organizational goals and continuous team growth. Analyze HRMS market trends and competitive information to ident...

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 exper...

Role Overview: As a Chemist in this role, you will be responsible for performing standard chemical and physical analysis of inner and outer nutritional products in the quality control lab. Your tasks will involve using wet chemistry techniques and instrumental analyses to ensure the quality of the products. You will play a vital role in conducting laboratory testing, preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation, reviewing product certificates of analysis, and maintaining Certificates of Analysis (C of A) files. Additionally, you will provide input on Standard Operating Procedures (SOPs), Test Methods, and laboratory documents while stri...

As an ARD Chemist / Scientist at the Udaipur location, you will be a key member of the ARD team, responsible for method development and validation, impurity profiling, and instrumental analysis to support Synthesis R&D and quality operations. - Developing and validating HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples. - Developing HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC. - Performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry. - Ensuring that all analytical instruments are maintained in optimal working condition through regula...

Role Overview: You will be responsible for analyzing compounds for various projects from the medicinal chemistry team and lead New Chemical Entities (NCEs). Your main focus will be on ensuring quality output within the set target by the Group leader. Key Responsibilities: - Analyze compounds for various projects from the medicinal chemistry team and lead NCEs - Develop analytical methods for new NCEs using instrumental techniques such as HPLC, LCMS, NMR, IR, SFC, and other wet analysis - Demonstrate good analytical skills and possess basic knowledge of HPLC, LCMS, NMR, and SFC instruments Qualifications Required: - Proficiency in analytical techniques such as HPLC, LCMS, NMR, IR, and SFC - A...

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:-1 to 5 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-20-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF-IV, Mekaguda | MSNF-V, RK Puram Venue Location :- 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 Car...

GC, HPLC, UV, Malvern, LCMS | SOPs, MSDS, COA | 5S, NABL, GLP, IMS | Reports | Impurity Profiling Inventory, AMC, CMC & LIMS management. Monthly/Yearly report preparation. Audit exposure

About The Role About The Role Job Title - Organizational Analytics- LMS- Specialist - T&O- (S&C GN) Management Level:09 - Specialist Location:Gurgaon, Mumbai, Bangalore, Kolkata, Pune, Hyderabad, Chennai Must have skills- LMS integration Good to have skills:Cornerstone OnDemand, Saba, SuccessFactors Learning, SumTotal, Docebo Job Summary : Collaborate with leadership to determine the programming objectives. Develop or write codes that support the overall business objectives and strengthen the quality and functionality of business-critical applications to provide optimal functionality. Roles & Responsibilities: Design new programs and applications that meet the business requirements. Formulat...