3433 Hplc Jobs - Page 26

,in-processthe ,for leading,for leading,problem-solvingResponsibilities We are looking for a senior professional AGM with a range of 15 to 20 years of experience in Analytical Method Validation for regulated markets. The role involves leading API and excipient method validation across multiple dosage forms and managing a team of 30, including three senior managers. The ideal candidate must be technically strong, experienced in US/EU compliance, and hold an M. Pharm, M.Sc., or Ph.D. Role & responsibilities: Accountable to lead the team for AMV of OSD, Nasal, Injectables, Ophthalmic and Topical dosage formulations. Responsible for RM & PM characterization and documentation. Generate qualificat...

Job Track Description: Requires relevant expertise in a professional, sales, or technical area through formal education. Performs technical-based activities. Contributes to and manages projects. Uses deductive reasoning to solve problems and make recommendations. Interfaces with and influences key stakeholders. Leverages previous knowledge and expertise to achieve results with teams and can complete work self-guided. College or university degree required. General Profile Requires knowledge and experience in own field. Will acquire on-the-job knowledge and skills. Develops an understanding of the company, processes, and customers. Uses existing procedures to solve routine or standard problems...

Preferred candidate profile Expert in independently handling HPLC along-with experience in handling other instruments Interested candidates can share their CV/Resumes on - noor.m.judge@zyduslife.com

STEVIA DELIGHTS is looking for lab analysts to join our dynamic team and embark on a rewarding career journey. Analyst For Laboratory is responsible for various tasks including planning, execution, and management of related duties. They should possess relevant skills and experience to excel in this role. Duties include teamwork, problem-solving, and achieving organizational goals. Candidates must have strong communication and technical abilities. Responsibilities include project management, strategy execution, and performance optimization. (More details as per role requirements.) Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com t...

JD: 1) Working as per company / management policy & reporting to Quality Control Head. 2) To conduct analysis and testing of Raw Material, Packing Material, In-Process sample, Finished goods, Stability samples etc. with the help of analytical instruments and techniques. 3) To calibrate / verifies analytical instruments i.e. ICP-OES, Ion Chromatography etc..and balances. 4) To trouble shoot analytical instruments. 5) Preparation and standardization of Volumetric Solution. 6) Preparation and maintenance of records for stock / reagents. 7) Analysis of samples for qualitative and quantitative test parameters as per specification. 8) To maintain record of analysis and supporting logbooks as per G...

Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up. Perform method validation and verification to roll out new testing method in the lab. Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system. Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports. Mainta...

JOB OVERVIEW Executes complex simulations in CFD and Thermal to optimize design and manufacturing. Develops complex Multiphysics simulation methods that meets design requirements in thermal management of Electronic Systems, especially in high-speed transceivers, connectors, and their assemblies. KEY RESPOSBILITIES: 5 to 8 years of industry experience. Expertise in Ansys Workbench. Experience on connector products (Plastic and Sheet Metal parts). Knowledge on material science (Metals, Resins & hyper elastic material) and implement for simulation. Expertise on CAE tools, Optimization techniques, and testing methods. Development & execution of complex Thermal simulation models to optimize manuf...

Walk In drive for Formulation Analytical Research & Development - department (FAR&D) - Quality Inn Ramachandra, Ward No- 58, 31-41/10/1, Duvvada, Revenue, Visakhapatnam, Andhra Pradesh on 25.10.2025 (Saturday ) Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Roles & Responsibilities : 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,...

Job Description We are looking for a motivated and detail-oriented Research Associate to join our Analytical R&D team within the Peptide Synthesis division. The selected candidate will support the development and execution of analytical methods for peptide characterization, working closely with cross-functional teams in R&D and Quality. Key Responsibilities Assist in developing and performing analytical methods (e.g., HPLC, UPLC, UV, FTIR, KF, LC-MS) for the characterization and quality assessment of peptides Conduct routine testing of raw materials, intermediates, and final peptide products Support method validation, transfer, and troubleshooting under the guidance of senior scientists Docu...

Date: 25 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job role: Research/Senior Research Assistant Location: Bangalore About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety ...

Job Title: Officer -Quality Control At FMC, our employees are guided by our purpose: Innovation for Agriculture, Solutions for the Planet. We provide farmers innovative solutions that increase the productivity and resilience of their land. From our industry-leading pipeline to novel biologicals and precision technologies, we are passionate about the power of science to solve agriculture's biggest challenges. For more than a century, FMC has successfully delivered some of the of the industry's most advanced, innovative solutions that protect farmers crops from destructive pests and disease, while also protecting the environment. We are committed to fulfilling our mission of discovering new he...

As a Quality Control Chemist, you will be responsible for ensuring the quality of products through various testing methods and procedures. You will play a crucial role in maintaining high standards of quality control to meet regulatory requirements and customer expectations. - Perform quality control tests on raw materials, intermediates, and finished products using analytical techniques such as HPLC, GC, UV-Vis, and FTIR. - Record and analyze test results, and report any deviations from specifications to the appropriate personnel. - Maintain accurate documentation of all test results and ensure compliance with standard operating procedures (SOPs) and Good Laboratory Practices (GLP). - Inves...

ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma. Job Summary Perform method verification/validation of compendia/pharmacopeial updations, Method verification of SDC's (Supplier Driven Changes) method. Method validation of cleaning verification, Preparation of method verification and validation protocols and repor...

Job Description Job Title: Senior Executive - Analytical (R&D) About The Function Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo's 30,000+ people work in Supply Chain and Manufacturing. It's an intricate and sophisticated operation that's the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We're committed to realising our Society 2030: Spirit of Progress goals, to protect the environment and suppo...

Role Overview: As a Research Chemist at our specialty chemicals manufacturing company, you will play a crucial role in conducting multi-step organic synthesis for pharma intermediates, APIs, and agro actives. Your responsibilities will include executing and monitoring reactions, purifying products, and characterizing them using various techniques such as TLC, MP, IR, NMR, HPLC, and GC. It will be essential for you to maintain lab notebooks accurately, document experimental procedures, and adhere to lab safety protocols to ensure the safe handling of chemicals and hazardous reagents. Additionally, you will support process optimization and scale-up trials from gram to kilogram scale while stay...

You will be responsible for ensuring the quality control, warehouse operations, engineering, and production activities in the Fill and Finish department. **Quality Control:** - As an Operator, you should have ITI qualification with 1 to 5 years of experience in handling samples, chemicals, reagents, and SAP procurement. - As an Analyst- Chemical, you should hold a B.Pharm/B.Sc/M.Sc. degree with 2 to 8 years of experience in HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. Knowledge of weight analysis and stability studies for Injectable dosage forms is required. **Warehouse:** - The Shift In charge role requires Any Graduate/Postgraduate with 6 to 10 years of experience in wareh...

Overview This role will assist the AMESA Supplier Quality Assurance team by conducting re-approvals annually for low risk designated suppliers located in AMESA that supply ingredients to Pepsico. This role will contact suppliers, request, and review returned pre-requisite data and documents, and re-approve the supplier site (3-year reapproval cycle). The role will update the required database(s) to support the re-approval. The expectation is ~200 supplier sites per year. The role will also support ancillary programs in AMESA SQA such as gathering program evidence from suppliers and brokers related to Food Fraud, Quality and Food safety Certifications and Contaminants programs as well as upda...

Dear All, We are looking for an experienced professional to lead Analytical Method Validation activities for Finished Dosage Formulations (OSD) . The ideal candidate should have extensive experience in analytical development, method validation, and regulatory compliance for both domestic and international markets. Experience: 11-13 Years Location: Hyderabad(Dulapally) Key Responsibilities: Plan, design, and execute Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) activities for formulations as per regulatory guidelines (ICH, USP, EP, WHO, etc.). Review and approve Validation Protocols, Reports, Method Development Reports, and Specifications. Ensure method robustness, a...

Job Summary: The Associate Scientist in the Process Analytics lab is responsible for timely analytical support to Upstream Process Development (UPD), Downstream Process Development (DSP), and Cell Line Development (CLD) teams for biotherapeutic projects. The role involves performing various biochemical and analytical techniques to support process characterization and optimization activities. Key Responsibilities: Execute experiments using techniques such as colorimetric/spectrophotometric assays (e.g., BCA, Bradford, OD280), chromatographic methods (HPLC, UPLC SEC, IEX, RP, HIC), and electrophoretic techniques (IEF, SDS-PAGE, Western blotting, Capillary Electrophoresis). Independently plan a...

Job purpose Ecolab is a trusted partner at nearly three million customers locations, and it is the global leader in Water, hygiene and infection prevention solutions and services that protect people and vital resources. Around the world, customer in the food, healthcare, hospitality and industrial markets choose comprehensiveEcolabs solutions, data-driven insights and personalized service to advance food safety, maintain clean and safe environment, operate efficiently and achieve sustainability goals. To support the customers in IMEA market, Ecolab has established a state-of-the-art Research, Development and Engineering (RDE) center in Pune. We are seeking candidate who has strong collaborat...

Job Summary: The ADL Scientist is responsible for delivering high-quality analytical data to support biotherapeutic product development. The role involves hands-on execution of various analytical techniques including chromatography and electrophoresis, with a focus on method development, qualification, and process support, ensuring compliance with regulatory and scientific standards. Key Responsibilities: Timely execution of analytical deliverables for biotherapeutic projects involving QTPP, process support, method development, qualification, and transfer. Perform benchwork using diverse analytical techniques including colorimetric/spectrophotometric assays, chromatographic tests (SEC, IEX, ...

Responsibilities: Assist in performing basic inspection of raw materials, in-process items, and finished products. Learn to read and interpret engineering drawings, quality plans, and technical specifications. Support senior inspectors in conducting visual and dimensional inspections using basic measuring tools (e.g., calipers, rulers, micrometers). Record and report inspection results accurately in logs and inspection sheets. Help identify and segregate non-conforming parts and report issues to supervisors. Follow safety and quality procedures during inspection and testing activities. Participate in on-the-job training and continuous learning sessions related to quality standards (ISO 9001,...

Responsibilities: Responsible for performing analysis, corrective action Responsible for maintaining record and documentation eligible for department Responsible for product and process knowledge development of his team/ responsible department members having experience in analysis of Raw material, Stability and Finished Products samples. Must have Knowledge of Handling Lab equipment and related plant equipment ( such as G.C. / H.P.L.C, UV, KF, ICPMS & IR etc.) Required Skills: Knowledge of Basic chemistry Logical thinking. Organizing. Good in communication. Required Qualification: - M.Sc - Chemistry

Responsibilities: Analytical Operations: Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG). Operate and maintain analytical instruments :- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus Ensure compliance with GLP, 21 CFR Part 11, and data integrity standards. Review and approve analytical reports and LIMS entries , Quality Systems & Compliance Implement and monitor Quality Management Systems (QMS). Lead investigations for OOS, OOT, Deviations, and Laboratory Incidents. Prepare and review SOPs, STPs, and validation protocols. Ensure audit readiness and support regulatory inspections (USFDA, WHO-GMP, etc.) Documentation & Reporting Maintain ac...

Responsibilities: Lead and oversee the entire Quality Control department operations. Ensure compliance with cGMP, regulatory guidelines, and company quality standards. Review and approve analytical methods, specifications, and validation protocols. Supervise raw material, in-process, and finished product testing. Ensure timely release of batches and materials. Manage laboratory investigations, OOS, OOT, deviations, and CAPA. Coordinate with QA, Production, and Regulatory teams for smooth operations. Handle audits (internal, external, and regulatory) and ensure readiness at all times. Provide training, mentoring, and performance evaluation of QC staff. Drive continuous improvement, cost effic...