570 Lcms Jobs - Page 12

Responsibilities : 1. Responsible for robust and efficient implementation 2. Suggest technical solutions for short and long term

job description Monitor progress of the reactions by using standard methods & analytical techniques (TLC,GC,HPLC, LCMS etc).Plan, setup, monitor, and workup chemical reactions independently.Isolate product & Optimize reaction conditions for improved

/>Monitor progress of the reactions by using standard methods & analytical techniques (TLC,GC,HPLC, LCMS etc).Plan, setup, monitor, and workup chemical reactions independently.Isolate product & Optimize reaction conditions

Plan, setup, monitor, and workup chemical reactions independentlyMonitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc)<

Roles & Responsibilities : Perform Analysis: Collect samples for analysis from Custodian. Processing of samples by using various sample extraction technique (to determine the concentration of analyte). Batch sequence preparation and verification in coordination with LIMS Operator. Perform analysis via LCMS/ ICP-OES/ ICP-MS. Follow GxP. Mass Spectrometry operation and ESI, APCI conceptual clarity. Chiral chromatography, polar columns conceptual clarity. Sample extraction process using LLE, SPE, and PPT. Documentation and compliance: Receive controlled forms for various activities. Perform online documentation of development trial in Method Book (Laboratory Record Book), validation experiment ...

Job Description : Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Discover Impactful Work Carry out Installation, maintenance and support of Thermo Fisher Scientific's range of LCMS, HPLC instruments in professional, reliable and customer-orientated manner. Train customers in the operation and maintenance of LCMS and HPLC equipment. Able to demonstrate routine applications of LCMS and HPLC and able to solve primary level application related issues. Have Expertise in Chromatography software and able to demonstrate software features to customers. Responsibility for meeting customer Service KPI's (Key Performance Indicator) and internal critical metr...

Your Role Total Experience of at least 7-8 years of IT experience with 4-8 years of Identity Management and at least 4-5 years of relevant SailPoint IIQ implementation experience. Strong experience in architecting IAM solutions using SailPoint IIQ Experienced in executing the role mining module Strong hands-on development skills in SailPoint and well-versed in creating workflows, rules, custom bean shell, provisioning plan, certifications, LCM, custom connectors, policies, entitlements etc. Experience in integrating with JDBC, Active Directory, Exchange, SAP, ERP etc. Knowledge in web services, XML, SOAP and JMS. Knowledge on the Support life cycle Experience in working on the proposal proce...

Role & responsibilities 1.Responsible for work planning and review of documents related to In process, DS, DP, stability testing, AMV and AMT activities within quality control laboratory. 2. To effectively plan and monitor shift duties of the QC analytical staff members to support 24*7 business operations. 3. Responsible for compliance to internal, external & statutory compliances as per quality policy of Enzene, pharmacopoeia guidelines and other regulated guidelines. 4. Responsible for periodic training management related to quality, GMP, regulatory aspects to quality control laboratory personnels and evaluation of effectiveness. 5. Responsible for the periodic assessments/audits to identi...

You will be responsible for serving as a Service Engineer / Sr. Service Engineer in Kolkata, covering the east territory/region. Your primary expertise should include experience in HPLC, CAD, IC, and LCMS. It is essential that applicants possess relevant experience in the mentioned areas. If you meet these requirements and are interested in the position, please share your CV at ashwani_smash@yahoo.co.in.,

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization collaborating with global health and science experts to develop quality standards for medicines, dietary supplements, and food ingredients. At USP, scientific excellence is driven by fairness, integrity, and global collaboration. With over 1,300 professionals across twenty locations, USP aims to strengthen the supply of safe, high-quality medicines worldwide. USP values inclusive scientific collaboration, recognizing that diverse expertise enhances the development of trusted public health standards. The organizational culture supports equitable access to mentorship, professional development, and leadership oppo...

The role based in Hyderabad, India, within the Chemistry Solutions department involves supporting the chemistry services team in delivering final compounds to clients by ensuring the testing and enhancing of purity levels as per requirements. This is achieved through effective coordination with a team of analysts. The main responsibilities of this role include building lasting internal client relationships by engaging in technical discussions with clients to understand project requirements. It also involves supporting team members in closing identified gaps to enhance client satisfaction. Additionally, ensuring seamless project execution through effective lab support and planning is crucial....

Job Description As an Application Engineer for LCMS, you will play a crucial role in supporting the sales and customer success teams by providing technical expertise and application support for our Liquid Chromatography Mass Spectrometry products. You will work closely with customers to understand their analytical needs, provide demonstrations of our LCMS solutions, and offer guidance on method development and optimization. This role requires a combination of scientific knowledge, technical proficiency, and strong communication skills to ensure customer satisfaction and drive business growth. Key Responsibilities: Customer Engagement: Collaborate with the sales team to engage with customers ...

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 ...

Education Qualification : MSC Chemistry Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc.) Isolate product and Optimize reaction conditions for improved yields and output Required Candidate profile Please Share your Profile capitalplacement04@gmail.com 9315507817

Role & responsibilities Roles and Responsibilities : Independently design, develop, validate, and troubleshoot bioanalytical methods for small and large molecules using LC-MS/MS and HPLC under GLP and non-GLP environments. Thorough understanding of bioanalytical method validation and sample analysis in biological matrices. Ability to lead junior team members, manage multiple projects , and interact with clients/regulatory bodies. Ensure efficient utilization of instruments and laboratory resources. Perform advanced operation, calibration, troubleshooting, and maintenance of LC-MS/MS , HPLC, and allied analytical equipment. Knowledge of international bioanalytical regulatory guidelines (USFDA...

Roles and Responsibilities : Responsible for drug metabolism and pharmacokinetic support for drug discovery programs. Develop and validate Bioanalytical method using LC-MSMS and other sophisticated instruments. Have a thorough knowledge of LC-MSMS, HPLC. Have knowledge of USFDA, MHRA, and M10 guidelines. Have excellent communication skills and the ability to co-ordinate with team members. Process good interpersonal and management skills. Strong basic knowledge of Operation, Calibration, and maintenance of laboratory equipment viz. Analytical balance, pH meter, centrifuge, Solid phase extraction unit and evaporator, and pipettes. Active involvement in method development of drug in In-vitro/In...

The ADL Research Associate role at our organization in Vadodara requires 1-3 years of experience and a qualification of BSc/MSc Chemistry. As an ADL Research Associate, you will be responsible for developing, validating, and implementing analytical methods to support pharmaceutical product development. Your expertise in analytical instrumentation and regulatory guidelines will ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Collaborating closely with R&D, Quality Assurance (QA), and Regulatory Affairs teams, you will contribute to formulation development, stability studies, and technology transfers. Your key responsibilities will include develop...

Role & responsibilities : Person would be team leader. Person would be responsible for managing 6-10 people from sr. scientist to interns. Candidate would be responsible for planning of work for direct reportees, reviewing of their timesheets. Candidate would be responsible for coordination with cross functional team and AAT team. Person would be responsible for representing AAT in internal meetings Person should be experienced for HPLC, CE, SoloVPE related techniques, trouble shooting , data review and data interpretation Knowledge in characterization methods such as Mass analysis, CD, Flr, DSC, MALS would be an additional advantage. Person should know method qualification for HPLC, CE, Sol...

Job Summary: We are seeking a motivated and detail-oriented fresher to join our Analytical Chemistry team focused on small molecule analysis. The role involves working with advanced analytical instruments and supporting the development, validation, and quality testing of small molecule compounds in a pharmaceutical or chemical environment. Key Responsibilities: Assist in the analysis of small molecules using techniques such as NMR, HPLC, GC, UV, IR, and dissolution testing Prepare analytical test reports and maintain laboratory documentation in compliance with GLP/GMP guidelines Support method development and routine analysis under supervision Calibrate and maintain analytical instruments ac...

We are looking for skilled Analysts with expertise in HPLC and GC techniques for immediate joining. The candidate will conduct analytical testing to ensure pharmaceutical product quality, develop and validate analytical methods, and contribute to continuous laboratory improvement initiatives. Key Responsibilities: Perform analytical testing using HPLC, GC, UV-Vis, ICP-MS, and LC-MS techniques to assess product quality and purity. Develop, validate, and optimize analytical methods in compliance with cGMP guidelines. Collaborate with cross-functional teams to troubleshoot and resolve method validation and analytical issues. Maintain detailed and accurate records of test results, instrument cal...

Job Summary: The Lab Technician is responsible for performing routine and specialized laboratory tests, preparing samples, maintaining lab equipment, and ensuring the accuracy and reliability of test results. This role supports research, development, quality control, or clinical analysis activities within the laboratory. Key Responsibilities: Collect, prepare, and analyze samples according to standard operating procedures (SOPs). Perform routine laboratory tests and record results accurately. Calibrate, maintain, and clean laboratory equipment and instruments. Maintain laboratory inventory, including reagents, supplies, and equipment. Ensure adherence to safety protocols and maintain a clean...

Roles and Responsibilities: Develop analytical methods for biochemistry samples using GC-MS, LCMS, and other relevant techniques. Conduct method validation, optimization, and transfer to ensure accuracy and reliability of results. Collaborate with cross-functional teams to resolve method-related issues and improve overall efficiency. Maintain accurate records of experiments, data analysis, and reporting in accordance with regulatory requirements. Stay up-to-date with industry developments in mass spectrometry technologies and apply this knowledge to improve laboratory operations. Desired Candidate Profile: 2-7 years of experience in Analytical Method Development & Validation (GC-MS & LCMS). ...

Need to have strong theoretical knowledge (Chiral HPLC/LCMS /Prep HPLC/SFC) Plan and conduct the analysis with required skills. Record the observations meticulously and update to the TL/SME. Share and discuss the observations with supervisor. Structure based method development and purification skills Expected to be aware of basics in analytical chemistry (basic analytical techniques Theory and application) as well as handling of laboratory equipment / instruments with basic understanding. Scientific and instrumental troubleshooting skills

Dear Candidate, We are Inviting Applications 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 Valida...

Roles and Responsibilities Develop analytical methods for biochemistry samples using GC-MS, LCMS, and other relevant techniques. Conduct method validation, optimization, and transfer to ensure accuracy and reliability of results. Collaborate with cross-functional teams to resolve method-related issues and improve overall efficiency. Maintain accurate records of experiments, data analysis, and reporting in accordance with regulatory requirements. Stay up-to-date with industry developments in mass spectrometry technologies and apply this knowledge to improve laboratory operations. Desired Candidate Profile 2-7 years of experience in Analytical Method Development & Validation (GC-MS & LCMS). MS...