3439 Hplc Jobs - Page 49

Responsibilities: * Collaborate with production team on quality control measures. * Conduct HPLC, GC, Gas Chromatography tests on products. * Ensure compliance with industry standards and regulations. Free meal Accidental insurance

About The Role : Job TitleSenior Engineer, AVP LocationPune, India Corporate TitleAVP Role Description Technology underpins our entire business. Our Technology, Data and Innovation (TDI) strategy is focused on strengthening engineering expertise, introducing an agile delivery model, as well as modernising the bank's IT infrastructure. We continue to invest and build a team of visionary tech talent, providing you with the training, freedom and opportunity to do pioneering work. As an [Engineer] you will develop and deliver significant components of engineering solutions to satisfy complex and diverse business goals. You will engage and partner with the business whilst working within a broader...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application requirements are met, overseeing the development process, and providing guidance to team members. You will also engage...

Opportunity for ADL Officer at Pharmaceuticals Manufacturing Company in Vapi, Gujarat. Minimum 3 years of experience required Qualification - B.Sc. / M.Sc. degree preferred Attractive Salary Required Candidate profile Interested candidates can share their updated CV at hire@hireindians.com OR Call/ WhatsApp on +918882212450.

Walk In drive for Formulation Analytical Research & Development - Department (FAR&D) - ASQA & ASRD : MSN Laboratories, R&D Center on Friday 26-09-2025. Roles & Responsibilities : ASRD Responsibilities : 1) Execution of Analytical Method validations for drug products for various markets. 2) Execution of DPDM Method validations for drug products. 3) Analytical method transfers to the Quality control labs. 4) Performing the calibrations of the analytical instruments. 5) Preparation & review of Analytical Method validations protocols and reports. 6) Responsible for cGLP, documentation and implementation of departmental quality systems. AQA Responsibilities : 1. Preparation and Review of AQA SOPs...

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. Experience : 2 - 6 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Review of Tentative me...

As an Executive or Senior Executive at Syngene, your primary responsibility will be method development, validation, and stability testing of drug substance/drug product. You should have strong hands-on experience in developing and validating Assay & related substances methods for drug substance/drug product. Additionally, you should be willing to work with complex injectables and be open to working in shifts. - Handle instruments such as HPLC, UPLC, GC, UV Visible spectrophotometer, balances, Potentiometer, and stability chambers. - Well-versed in Good documentation/laboratory practices like ALCOA+. - Experience in calibration and qualification of laboratory instruments. - Prepare and review...

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Job Description About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient hea...

As a Fill and Finish QC at our company, you will play a crucial role in ensuring the quality of our pharmaceutical products. Your responsibilities will include: - Performing quality control tests using equipment such as HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. - Conducting weight analysis and stability studies for Injectable dosage forms. To excel in this role, you should possess the following qualifications: - B.Pharm/B.Sc/M.Sc. degree. - 2 to 6 years of hands-on experience in a similar role. - Proficiency in using HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. Join our team and contribute to the production of high-quality pharmaceutical products.,

As a Pharmaceutical Documents Associate at our company, you will play a crucial role in ensuring the quality and compliance of our pharmaceutical products. Your responsibilities will include: - Having experience or sound knowledge in Active Pharmaceutical Ingredients, Finish Product, Packaging Material Standards, Quality Management, and Quality Control. - Demonstrating knowledge or experience in Quality control tests for various formulations and APIs such as Assay, Dissolution, Disintegration, Uniformity of Weight/dosage, Impurity testing, Water content, etc using methods like HPLC, GC, TLC, IR/UV, Disso, etc. - Understanding pharmacopoeia applications and all documentation relevant to QA/QC...

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will play a crucial role in leading method development, validation, stability studies, and technology transfer activities. Your meticulous nature and extensive experience will be essential in collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. You should possess strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement. - Developing, optimizing, and validating analytical methods such as HPLC, GC, UV-Vis, and Dissolution according to ICH and regulatory guidelines....

Company Name Gangwal healthcare Job Title Quality Control Manager Job Location: Maharashtra Description Job Summary: We are seeking an experienced and detail-oriented Quality Control professional with strong expertise in Nutraceutical products testing, nutritional profiling, and regulatory compliance. The ideal candidate will ensure all raw materials, in-process samples, and finished goods meet internal quality standards, statutory requirements, and international regulations. Key Responsibilities Testing & Analysis Perform qualitative and quantitative analysis of nutraceutical and food products. Conduct nutritional profile testing including macronutrients, micronutrients, vitamins, and miner...

Job Description: - Possess a minimum of 2 years to a maximum of 6 years of experience in handling Analytical instruments such as HPLC and GC. - Conduct routine analysis using these instruments and participating in method development processes. - Expertise in analytical techniques will be essential in ensuring accurate and reliable results.,

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...

Date: 15 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Location: Bangalore Department: Analytical Development Drug Product About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work ...

Sales reporting and Analytics We are seeking a detail-oriented and proactive professional to join our Sales Operations team as a Sales Reporting and Analytics Analyst. This role will be responsible for delivering strategic and operational sales insights through regular and ad-hoc reporting, dashboard creation, and data quality management. The ideal candidate will support business units (BU/SBU) with performance tracking, forecasting, and executive-level analytics. Your role Provide timely and accurate sales data for BU/SBU and management reviews. Develop and maintain BAU (Business As Usual) strategic reports on BU sales performance. Conduct on-demand ad-hoc analysis on bookings, pipeline, fo...

Note: Walk In Interview at Vadodara. Date: - 28.09.2025 (Sunday) Job Location: Daman & Dahej Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M. Pharma Experience:- 2-6 Years in (API or Solid Oral) Required Candidate profile * 2-6 years of experience into LCMS, HPLC, GC & Wet Chemical sections, Analytical Validation, Finished Goods, Raw Material, Stability & GLP

Role & responsibilities Analytical testing of chemicals, Reagents, Raw materials and other Pharmaceutical products. Preparation, Standardization and stability evaluation of volumetric solutions/Reagents/Indicators. Performing computerized system validation (CSV) as per current regulatory requirements. Testing of Raw materials, In-process, Intermediates and APIs using Chromatographic Data system. Analytical Testing of Related substances/Content/Assay/Purity testing and Calculation by HPLC Using Empower/Lab Solutions. Data generation, Integration and Review of Chromatographic data generated by Chromatographic data system. Method Transfers & Holding time Studies. Testing of Raw materials, In-pr...

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their labora...

Formulate, analyze, and implement algorithms that power real-time auctions, dynamic pricing, bid shaping, pacing, and traffic allocation across a massive-scale ad marketplace. Design and experiment with methods in online learning, reinforcement learning, multi-armed bandits, forecasting, game theory, and Bayesian modeling in non-stationary, adversarial environments. Collaborate with product and engineering teams to deploy your models in production and run real-world experiments with rapid feedback loops (measured in hours, not weeks). Provide technical leadership by reviewing scientific approaches, mentoring junior scientists, and guiding the team toward robust methodologies. Contribute to t...

Analysis of routine samples (product development batches, stability study samples, raw materials etc.). Operation and Calibration of analytical instruments/equipment s. Analytical activities related to Quality control department. Qualification of working standards. Documentation of analytical activities as per good documentation practices. Work in laboratory as per good laboratory practices. To use PPEs and follow safe practices in lab. Any other task assigned by management. Sampling of raw materials from pilot plant dispensing area. Analysis of samples in quality control laboratory. Operation and Calibration of instruments in quality control laboratory

Leading contributor providing guidance and mentorship to define, design and deliver product quality improvements from ideation stage to shipping to the customer Write high quality code to power experiments and build models Contributes to writing production model code Work closely with product management and engineering to deliver products which solves the needs of our customers by building relevant, innovative results which strategically differentiates Oracle in the market Set up environment needed to run experiments for all projects Set up distributed environments Engage with customers and help solve complex problems with the customer/partner Directly impact our customers via innovation in ...

Leading contributor providing guidance and mentorship to define, design and deliver product quality improvements from ideation stage to shipping to the customer Write high quality code to power experiments and build models Contributes to writing production model code Work closely with product management and engineering to deliver products which solves the needs of our customers by building relevant, innovative results which strategically differentiates Oracle in the market Set up environment needed to run experiments for all projects Set up distributed environments Engage with customers and help solve complex problems with the customer/partner Directly impact our customers via innovation in ...

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

To ensure and carry out the analysis of sample and all other activities as per Standard Operating Procedure (SOP). To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside lab. To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule. To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same. To work for lab readiness for audit and ensure compliance in Laboratory.