18 Ion Chromatography Jobs

As a QA/QC team member at GFCL EV Products Limited, your role will involve setting up an analytical facility for testing Battery Materials, raw materials, and in-process samples. Your primary responsibilities will include: - Ensuring all Zero Error testing standards are met to guarantee Zero defect product delivery - Establishing and maintaining Quality Assurance Systems to ensure a world-class product delivery system with zero customer complaints as the ultimate target - Adherence to IMS procedures and documentation To excel in this role, you should have hands-on experience with chemical and instrumental analysis, including handling hygroscopic/hazardous materials such as Glove box operatio...

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...

Job Description : Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Fluctuating Temps hot/cold, Laboratory Setting, Office, Various outside weather conditions Summary Responsible for performing the routine/preventive maintenance, servicing, and breakdown repairs on HPLC /IC instruments in North India. Support the HPLC/IC new installation commissioning, and field solving at customer sites and to provide remote support to the clients as needed. Delivering demonstrations to ensure the customers are educated on safe and effective equipment use. Provide complete detailed service reports on a regular basis as soon as ser...

As a Scientist at USP, your role will involve conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) utilizing suitable methods to enhance the laboratory's scientific proficiency and work ethic. You will offer extensive technical support and knowledge and provide valuable observations and insights into challenging projects. Your responsibilities will include: - Conducting verification projects (Dietary Supplements/Dietary Ingredients) by performing individual analytical tests such as HPLC, GC, Dissolution, ICP-MS, ICP-OES, and wet analysis as assigned - Completing projects within designated timelines and priorities - Demonstrating a robust sci...

Kindly read the below details and then apply Immediate Hiring !!!! Location: Cuddalore, Tamil Nadu Interview Mode: Level1 : Virtual (Mircosoft Teams) Level 2 : Face to Face Role & responsibilities QC Analyst (IC/HPLC) Experience: Minimum 5-8 years in core area (IC/HPLC and wet analysis) Educational qualification: Only Postgraduate in Chemistry/equivalent Work background: Only Pharma (API/Formulation/excipients) Key responsibilities: 1. Hands on experience on Ion Chromatography is most preferable. 2. Responsible for independently handling IC/HPLC analysis. 3. Qualification and troubleshooting of HPLC instruments. 4. Shall have handled software including Chromoleon 5. Shall have good knowledge...

Role Overview: You will be responsible for conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods in a non-supervisory role. As a Scientist at USP, you will enhance the laboratory's scientific proficiency and work ethic by providing extensive technical support and knowledge. Proficient in various common laboratory techniques, you will offer valuable observations and insights into challenging projects, aiding the Verification Program by executing analytical tests and preparing comprehensive summary reports. Key Responsibilities: - Conduct verification projects on Dietary Supplements/Dietary Ingredients by performing indiv...

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...

Perform Feasibility Studies Analysis by using IC. Prepare and execute method validation protocols. Document & Report method development data. Design & optimize IC methods of detection of inorganic anions, cations, counterions residuals&impurities. Required Candidate profile Ion Chromatography

Role & responsibilities Preferred candidate profile

At USP, inclusive scientific collaboration is highly valued as it is believed that diverse expertise enhances the development of trusted public health standards. The organizational culture at USP promotes equitable access to mentorship, professional development, and leadership opportunities to ensure broad participation in scientific leadership for stronger and more impactful outcomes in global health. As an equal employment opportunity employer (EEOE), USP is committed to fair, merit-based selection processes that allow the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Accommodations are provided to individuals with disabiliti...

Job Summary We are seeking a dynamic and experienced Analytical Scientist in Advanced Characterization Structural Elucidation Team (ACT-SEL) for utilizing sophisticated analytical techniques and instruments to investigate the composition, structure, and properties of substances at a molecular and atomic level. To Support Structural Elucidation across all modalities and mechanism elucidation into Research & Development and to study release of drugs substance and structure of unknown Impurities through various method development and validation techniques. Roles & Responsibilities You will be responsible to employ advanced analytical techniques such as Gas Chromatography with Mass Detector( GCM...

You will be responsible for setting up an analytical facility to test Battery Materials, raw materials, and in-process samples as necessary. Ensuring all testing is done to Zero Error standards and guaranteeing defect-free product delivery. You will establish and maintain Quality Assurance Systems to achieve world-class product delivery and zero customer complaints. Adherence to IMS procedures and documentation is crucial for this role. Your essential qualifications should include hands-on experience in chemical and instrumental analysis, with the ability to handle hygroscopic/hazardous materials. Proficiency in Glove box operations, Ion chromatography, GC-MS, ICP-MS, etc. Good analytical sk...

You will be joining the VTC MFG. QC Department as a Probationer-HO Staff, with a primary responsibility of ensuring the quality control of manufacturing processes. The ideal candidate should hold a M.Sc. degree in Biotechnology, Biochemistry, or Microbiology and have at least 3-7 years of hands-on experience in a relevant field, preferably with a background in the pharmaceutical industry. Your role will involve conducting various analytical tests and procedures such as RP-HPLC, SEC-HPLC/SE-HPLC, Dionex, IC/Ion Chromatography, Biochemical analysis, UV spectrophotometer, Protein, O-acetyl. It is essential to have a good understanding of these techniques and equipment to perform accurate qualit...

Location: Rabale, Navi Mumbai Experience: 2 to 7 years Industry: Pharmaceutical / Analytical Research Department: Analytical Research and Development (AR&D) Employment Type: Full-time About Us Fusion Scientific Laboratories is a globally recognized, USFDA and EMA accredited pharmaceutical laboratory located in Rabale, Navi Mumbai. We specialize in Formulation Development , Analytical Solutions , and Integrated Pharmaceutical Services (CDMO) . Our commitment to innovation, quality, and regulatory excellence positions us as a trusted partner to leading pharmaceutical companies around the world. Position Overview We are seeking dynamic and detail-oriented professionals for the role of Senior Re...

Role & responsibilities Preferred candidate profile

"1) Responsible for Laboratory execution of analytical activities on daily basis and ensuring compliance to the Safety and quality system as per cGMP. 2) Responsible for Laboratory execution of instrument calibration, stability analysis, WRS preparation/Qualification and for procurement of reference standard etc. 3) Responsible for maintaining stock of working reference standards and chemicals required routinely for raw material analysis. 4) Review and release of finished product, inprocess, intermediates, raw material, reaction monitoring results. 5) Responsible for Laboratory execution of analytical method validation/Verification and Method Transfer activites. 6) Coordination for reagents ...

Expertise in ICP-OES and ICP-MS techniques. Expertise in Ion Chromatography working knowledge of various chromatography and spectroscopy techniques, including HPLC GC. independently managed development tasks, consistently delivering within timelines. Required Candidate profile Ideal Candidate should Be M.sc With 5 + Years of Experience in ADL Department Must Have Experience in Method Development & Method Validation. Must Have Experience in Ion Chromatography

- Develop analytical methods for OSD products using techniques such as UV, FTIR, Dissolution, HPLC, GC, Ion Chromatography, Wet Analysis etc. - Conduct method validation studies to ensure compliance with regulatory requirements. - Collaborate with cross-functional teams to resolve method-related issues and improve process efficiency. - Ensure timely completion of tasks assigned by supervisors while maintaining high-quality standards.