746 Method Validation Jobs - Page 12

Candidate must have strong knowledge in Core PHP, Laravel, MYSQL, jQuery, AJAX, HTML and CSS. Must have a work experience of 1-2 years on PHP & Laravel Framework. Web-based software application development and maintenance on PHP

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials

Planned purchase to maintain stock. Having knowledge in IT Hardware & Software Procurement. Creating PO & Buying Activities. Having a good Knowledge in material Follow-up with Vendor & Supplier.

Key Responsibilities: Develop and optimize analytical methods for APIs using techniques such as HPLC, GC, UV-Vis, FTIR, and titration. Perform method validation as per ICH guidelines (specificity, linearity, accuracy, precision, robustness, etc.) Responsible for analytical method development and method transfers to preparative HPLC. Conducted analysis of compounds to determine chemical and physical properties, composition and structure utilizing chromatography, spectroscopy and spectrophotometry techniques including but not limited to HPLC/UPLC. Prepare and review method development and validation protocols and reports. Conduct forced degradation and stability-indicating studies. Support tec...

You will be responsible for bioanalytical sample preparation using different extraction techniques. Additionally, you will conduct method development, method validation, and sample analysis as per regulatory requirements. You are expected to operate laboratory equipment such as Pipettes, centrifuge, evaporator, and extractors. Moreover, handling data generation, compilation, and reporting of results will be part of your detailed responsibilities. Qualifications required for this role include: - B.Pharm / M.Sc. / M.Pharm Preferred skills for this position are: - Good communication and analytical skills - Ability to work as a team player for the timely completion of tasks,

About the Team At Nutanix Cloud Manager, we are trying to build the next generation platform to help enterprises model, develop and manage applications. We want to give them the ability to encapsulate not only infrastructure but even the application its architecture and deployment as code. You will be reporting to the Senior Manager Engineering, QA - NCM Team. Your Role As the gatekeeper of our product quality, you would be required to ensure that product releases adhere to the highest quality norms. You will design and develop a testing framework for our products and be part of a ruthless quality team. You will develop test tools, test cases, maintain test beds, and provide metrics and test...

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 20-09-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to...

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials.

Conduct chemical synthesis of new and existing agrochemical compounds in the lab. Develop and optimize synthetic routes and reaction conditions to improve yield, purity, and cost-effectiveness.

Key Responsibilities Develop and implement quality control systems: Creating procedures and policies to ensure products and services meet defined quality standards. Monitor and analyze quality data: Tracking data to identify trends, defects, and areas for improvement in quality processes. Manage quality teams: Supervising and advising quality assurance personnel and quality inspection teams. Ensure compliance: Making sure the organization adheres to relevant industry standards and regulatory requirements. Implement corrective and preventive actions: Identifying issues and implementing solutions, as well as proactively preventing potential errors. Lead continuous improvement: Driving initiati...

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

B.Sc/M.Sc Chemistry, 1–8 yrs exp in API/Pharma QC. Must handle HPLC/GC/UV/IR, cGMP, stability, and docs. Local preferred Dahej. Only male candidates are required. Only pharma experience required.

1 Perform the testing of Raw Material/Finished goods/Inprocess materials and report the results. 2 Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSAetc 3 Calibration of the Analytical instruments

Plan, setup, monitor, and workup chemical reactions independently 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

Develop, optimize, and validate analytical methods for raw materials, in-process samples, and finished products.Perform analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, dissolution, and others.

Develop, validate, and optimize analytical methods for qualitative and quantitative analysis of raw materials, intermediates,and finished products. Perform instrumental analysis using techniques such as HPLC,GC.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department. Required Candidate profile with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills R&D Research & Development Executive UPLC HPLC GC Analytical Development

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA Calibration of the Analytical instruments as per the master calibration

R & D (Analytical Development) - Agrochemical Industry-Saykha,Gujarat. Capital Placement Services 3 - 8 years Industry Pharma / R&D / Biotech Qualification M.Sc Key Skills R & D Analytical Development LAB Agrochemical UPLC Green Field Projects HPL

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis

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 ...