28 Chromatographic Techniques Jobs

Role Overview: As a Scientist at U.S. Pharmacopeial Convention (USP), you will be a vital part of the team responsible for the oversight and successful implementation of activities related to a portfolio of Reference Standards (RS)/Analytical Reference Materials (ARMs). Your role will involve tasks such as preparing procurement specifications, testing protocols, and summary reports, providing technical assistance to collaborating labs, and ensuring the availability of high-quality reference standards. Additionally, you will play a key role in supporting the public health mission of USP by contributing to the development of quality standards for medicines and supplements. Key Responsibilities...

Role Overview: As a Manager - Research Scientist at our Supply Chain and Manufacturing team, you will be a vital part of the analytical research focused on flavor chemistry for process research initiatives. Your role will involve utilizing advanced analytical techniques to identify, quantify, and understand the flavor compounds in our ingredients, process intermediates, and products. You will contribute significantly to process projects from concept to completion while gaining experience in different disciplines and research programs. Key Responsibilities: - Design studies and solve complex analytical objectives related to flavor development during fermentation, distillation, maturation, and...

As an Analytical / Conjugation specialist, your role involves: - Developing assays for Protein and Carbohydrate characterization. - Standardizing and optimizing various Biochemical assays. - Utilizing immunochemical methods such as ELISA, SDS-PAGE, slot blotting, and Western blotting. - Implementing instrumental methods like LC-MS, Protein sequencing, HPLC, ELISA reader, AKTA, Spectrophotometer, and RT-PCR. - Applying different need-based chromatographic techniques in the lab. - Developing analytical methods for physicochemical characterization of Protein and Polysaccharide based vaccines. In the area of Conjugation/DSP Process Development, your responsibilities include: - Conducting chemica...

Roles and Responsibility: Analytical /Conjugation Analytical Characterization Development of assays for Protein and Carbohydrate characterization. Standardization and optimization of various Biochemical assays. Immunochemical methods of analyses such as ELISA, SDS-PAGE, slot blotting and Western blotting. Instrumental methods of analyses such as LC-MS, Protein sequencing, HPLC, ELISA reader, AKTA, Spectrophotometer and RT-PCR. Knowledge and implementation of different need based chromatographic techniques in lab. Analytical method development for physicochemical characterization of Protein and Polysaccharide based vaccines. Conjugation/DSP Process Development Execute chemical conjugation exp...

Technical/functional skills : Experience in Downstream unit operations such as Chromatography (AKTA Avant, AKTA Pure or similar) Filtration and TFF systems and a thorough understanding of the theory and techniques Experience in recombinant protein purification from mammalian cells Ability to design, troubleshoot and execute experiments with minimal supervision Experience analysing data, interpreting results and reporting data Good documentation practice is essential and experience with electronic laboratory notebook is preferred Ability to communicate ideas, concepts and presentation skills. Protein biochemistry and downstream process development Process characterization for late stage biolo...

Role Overview: As a Research Scientist - Analytical at CreAgro in Udaipur, your primary responsibility will be to support the Process Research team by assisting in reaction monitoring, characterization, data generation of submitted compounds, and final product assay method development. You will also be responsible for the analysis of impurities, physical characterizations, residue content, stability studies, and more. Your contribution will play a crucial role in the success of the Analytical Chemistry department by adhering to objectives and targets set by the leadership team. Key Responsibilities: - Perform experimental determination of physico-chemical parameters such as Small molecules A...

Role Overview: As an LCMS Analyst, you will be part of our laboratory team, where your primary responsibility will be to operate, maintain, and troubleshoot LCMS instruments. Your expertise in analytical chemistry will be crucial in conducting advanced testing and ensuring compliance with ISO 17025:2017 standards. Additionally, you will play a key role in method development, validation, and maintaining accurate laboratory documentation. Key Responsibilities: - Independently operate, calibrate, and troubleshoot LCMS instruments. - Perform routine preventive maintenance following standard operating procedures (SOPs). - Monitor system performance, control charts, and maintain updated instrument...

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

To own YBL Vision and Values. In depth knowledge and technical understanding of protein purification, protein analysis and its characterization. Hands on experience on Chromatographic purification, FPLC/AKTA system, UFDF, TFF. Completion of allotted projects in time bound manner. Solving the customer complaints of projects. Execution of policies and strategies implemented as and when for reducing the timeline for product/process development. On time calibration and validation of equipments. Documentation related of ISO, OHSAS, customer related or any other kind of audits. Interpretation and documentation of daily project activities in electronic lab notebook. Technology transfer document pre...

As an Analytical Specialist at our Contract Development and Manufacturing Organization (CDMO), you will play a crucial role in supporting analytical development and testing activities. Your expertise in analytical method development, validation, structural characterization, impurity profiling, and troubleshooting for drug substances and its intermediates will be essential in managing multiple client projects effectively. Additionally, you will serve as a mentor to junior team members and make informed decisions based on analytical data. Key Responsibilities: - Develop, optimize, validate, and transfer analytical methods in compliance with ICH and client-specific requirements. - Support the c...

We are seeking a dynamic and experienced Quality Control (QC) Manager to lead and manage QC operations, ensuring that products and processes meet stringent quality and regulatory requirements. The ideal candidate will possess deep technical expertise, a strong leadership background, and a commitment to data integrity and continuous improvement within the life sciences industry. A detail-oriented professional with expertise in Nitrosamines/NDSRI method development and validation by LC-MS focused on detecting and quantifying nitrosamine impurities in APIs and Finished Dosage Forms. You will contribute to method development, validation, instrument calibration, and document preparation while ens...

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). ...

Key Responsibilities: Ensure proper installation, calibration, and maintenance of analytical instruments and equipment. Handle and troubleshoot Chromatographic systems (HPLC, GC), Atomic Spectrophotometers, Analytical Balances, pH / Conductivity meters, and Autoclaves. Support validation and qualification of instruments as per regulatory guidelines (USFDA, EU, WHO). Coordinate preventive and corrective maintenance schedules with vendors. Maintain calibration records and ensure compliance with GMP and GLP requirements. Provide technical support to analytical teams for smooth lab operations. Key Skills: Strong technical knowledge of laboratory instrumentation. Familiarity with pharma quality a...

Position Purpose : This position is responsible for daily overall functioning of the R & D laboratory, provide guidance perform experiments and prepare documentation for R & D and Pilot Plant. Role & Responsibilities: To Plan & perform Lab experiments for Process development as per Guideline To modify & optimise lab process for plant scale-up batches To keep record of all experiment taken To prepare & record the documents of R&D & Pilot plant batch work on day to day To execute and assist demo batches to plant chemist To Deliver the project/Product as per committed timeline To provide online support to production dept. for trouble shooting To look after glass wares, lab wares / instruments, ...

The Quality Control (QC) Chemist position requires you to conduct routine and non-routine testing of raw materials, in-process samples, and finished products following relevant specifications and standards. You will need to work in rotational shifts to support 24x7 operations and ensure prompt release of batches. Your responsibilities will include performing chemical, physical, and performance tests on raw materials, intermediates, and finished products using standard test methods. It is crucial to ensure compliance with internal specifications, customer requirements, and regulatory standards. Maintaining accurate documentation of test results, observations, and deviations is essential. Addi...

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. pranathi.p@orbicular.co.in

Production: Execute production batches, ensure GMP, manage documentation QA: Ensure cGMP, Issuance and retrievals and manage records. QC: Analyze biopharma samples & maintain Documentation R&D: Prepare stocks and buffers, extract proteins & analyze.

should Independently be able to perform the development of analytical methods for injectable formulations like suspension, emulsion, peptides, and other simple & complex injectables. Should be able to work on handling chromatographic techniques- HPLC, TLC, SEC-HPLC, IC, GC and other physico-chemical techniques like UV-visible spectrophotometer, coulometer, FTIR, Raman, ATR, etc. Should be able to work on various dissolution techniques applicable for injectable formulations like USP type IV, Bottle rotating apparatus, Type II, selection and use of MWCO membranes, etc. Handling of UPLC, Plate- Assy techniques is desirable. Should be able to perform routine analytical activities independently. ...

Responsibilities: Chromatographic techniques & System Handling Column Packing(BPG & Chromoflow) TFF System Centrifuge System Filtration, Filter Integrity, Buffer Preparation Expertise in Documentation, GMP Compliance

Responsibilities: chromatographic techniques. TFF system. Filtration. Document processes accurately. maintain GMP standards Prepare buffers according to specifications

Responsibilities: * Ensure GMP compliance through documentation & filter integrity checks. * Prepare buffers according to SOPs using chromatography techniques.

Knowledge of Method Validation & verification as per Pharmacopiea requirement. To perform Method Validation & verification of Chromatographic GC / HPLC methods. Preparation of specification in DMS & SAP system. SOP preparation related to AMD work. Required Candidate profile Candidate Must be MSc Regular. AMD protocols & report preparation, non-chromatographic methods. Maintain require stds & Impurities stock, list etc. Operation of instruments like HPLC,GC,UV,IR etc.

Knowledge of Method Validation & verification as per Pharmacopiea requirement. To perform Method Validation & verification of Chromatographic GC / HPLC methods. Preparation of specification in DMS & SAP system. SOP preparation related to AMD work. Required Candidate profile Candidate Must be MSc Regular. AMD protocols & report preparation, non-chromatographic methods. Maintain require stds & Impurities stock, list etc. Operation of instruments like HPLC,GC,UV,IR etc.

Urgent Opening for QC Chemist Knowledge of HPLC, GC, Stability , KF, UV, validation, Documentation etc

Key Responsibilities: The successful candidate will become a member of a team with overall responsibility for purification and analysis of small compound libraries to support lead optimization in medicinal chemistry programs. Individual responsibilities will include analysis and purification of small molecule library compounds (primarily by analytical and preparative LCMS), HPLC and mass spectrometer instrument maintenance, training, and analytical data management. Optimization and/or troubleshooting of analysis conditions will be required to ensure on time delivery of high purity products. Educational Qualification: M.Sc. in Chemistry/Analytical chemistry with 1-3 years of experience in pra...