3433 Hplc Jobs - Page 24

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy context. Delivering on...

****Only Males Candidate**** Role & responsibilities 1. GC Handling 2. HPLC Handling 3. Finished Goods & Intermediate Testing 4. Raw Material Testing 5. Stability Testing 6. Instrument Calibration 7. Method Validation 8. Hands on Instruments (UV/IR/KF/Potentiometer, Balance) Preferred candidate profile 5 Years into API & Intermediate Pharma Company

Qualification : B. Sc. / M. Sc. Organic Chemistry/Ph.D and currently working as RD Manager. Experience : Minimum 15 years in chemical industry and out of that 10 years of RD experienced is required. We are hiring a proactive and experienced RD Manager to lead our Research and Development team in the chemical industry. The RD Manager will be responsible for new product development, research project supervision, and effective implementation of experiments. This role requires strong technical expertise, project management skills, and the ability to lead a team effectively. Must Have: Product Development: Must have 3 years of experience of product development for Performance Chemicals. Oversee t...

HPLC, GC, UV, Polarimeter, Karl Fisher, Raw Material, Inprocess material and Finished Product Testing. Having good knowledge of GMP and GLP.

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. (Only Males) 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...

Role Overview: As a Chemical Testing Analyst at the company, your primary responsibility will be reviewing and conducting chemical testing of various products, including raw materials, finished products, cosmetics, Ayurveda, Sidha & Unani products. You will play a crucial role in ensuring the accuracy of test results entered into the LIMS software. Furthermore, you will be tasked with handling advanced instruments such as HPLC, GC, FTIR, Dissolution, etc. Another significant aspect of your role will involve preparing technical documentation that adheres to FDA, CDSCO, and Ayush standards for audits. Key Responsibilities: - Review and conduct chemical testing of raw materials, finished produc...

As a 2024 batch MSc. (Chemistry) candidate interested in pursuing a career in Quality Control (QC) within a pharmaceutical Active Pharmaceutical Ingredients (API) manufacturing company situated in the Attibele Industrial Area near Hotel Ramee Guestline in Hosur, Tamil Nadu, you are encouraged to apply for the following opportunity. Role Overview: You will be expected to work in rotational shifts, making male candidates preferred for this role. Your responsibilities will include operating various equipment such as HPLC, GC, TLC, and conducting titrations. Strong English communication skills are a must-have requirement for this position. Key Responsibilities: - Perform quality control tests us...

As a Review Analyst at Piramal Pharma Solutions (PPS) located in Digwal, your role will involve reviewing analytical reports and handling investigation incidents. You will be responsible for the following key responsibilities: - Review in-process analytical data before release - Review intermediates, stability batches, and finished products analytical data - Knowledge on analytical method validations and method transfers - Review system audit trails for all types of instruments in QC - Review calibration data of instruments on a daily basis - Verify SOPs compliance on the shop floor - Conduct audits for laboratory system compliances as required - Investigate incidents, OOS, OOT, and root cau...

We will count on you to Drive the strategy and delivery of the US&CA catastrophe modelling analytics and advisory solutions from India based team. Develop & embed a consistent, curiosity driven and value proposition focused mindset across all our US&CA catastrophe modelling team members who work very closely with multiple onshore teams. Stakeholder Management - ability to govern project deliveries and manage end client expectations through reporting and performance metrics; lead change initiatives with stakeholders; demand gathering and resource planning through stakeholder agreement. Ensure a consistent engagement model between our operations and the onshore teams. Identify best practice wi...

Job Title: Executive – Analytical Development Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Description To work as per cGMP and ensure its...

Hands on experience in HPLC/GC including method development, routine analysis and method validations along with good documentation practices. Responsible to perform the Analytical method validation, method verification and method transfer activities.

We at Smart Infrastructure Division in Siemens Ltd. is one of the top tier global suppliers of products, systems, solutions, and services for the efficient, reliable, and intelligent transmission and distribution of electrical power. As the trusted partner for the development and extension of an efficient and reliable power infrastructure that industry and the portfolio they need. JOIN US! WE MAKE REAL WHAT MATTERS. THIS IS YOUR ROLE. A mechanical / production engineering Bachelor position with 15-20 years experience needed sound knowledge on principles, technologies, SAP QM module and theories; ISO / EHS / IMS certifications in specific fields will be required. Knowledge and hands-on experi...

Business Development Professional - Business Excellence 1. Drive SI EP business through assigned Regional Sales & Monitor OI, Revenue, quantity for Regions/ Offices & Coordinate critical customer visits to factories. 2. Monitor and report Top 10*2 BU wise & Office wise. 3. Actively collaborate within BU and Sales to drive BU KPIs. 4. Drive active usage of CRM tools like SieSales to ensuring KPIs i.e. data quality, funnel adequacy, market transparency as per Op-Co guidelines 5. Monitor and drive market transparency improvement objectives thru Siesales. 6. Price Controller to the regions in alignment with the BU. Approve Special Price request from offices. 7. Key role is Business planning and ...

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). Job Description GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy contex...

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...

Role & responsibilities: We are looking for an energetic and Analytical R&D experienced candidate with good skills in handling HPLC, HPTLC, GC Etc. GLP experience will be an added advantage.

Role & responsibilities Perform daily monitoring of laboratory activities as per defined SOPs. Experience in handling GMP documentation and regulatory audits preferred. Carry out calibration of instruments such as the pH meter and weighing balance. Conduct Environmental Monitoring (EM) through microbial methods. Perform water sampling and microbiological analysis of purified and process water. Conduct sterility and bacterial endotoxin tests (BET) as per standard methods. Perform Liquid Particle Count (LPC) testing and maintain trend data. Maintain all laboratory documentation and records in compliance with GMP and regulatory requirements.

Opportunity Details Start Date event Please select start date, End Date event Please select end date, Please select valid Start Date and End Date Start Date is older than Current Date Please enter start date or end date in dd-mm-yyyy format, Center Please enter city Special character (% and ) are not allowed Special character and digit not allowed, of volunteers required (Approved Volunteers:) Please enter No of volunteers required Special character (% and ) are not allowed Please enter number in No of volunteers required No of volunteers required should be greater than apporved volunteers, PENAVMOTA FOUNDATION Posted on PENAVMOTA FOUNDATION Posted on 04 Aug, 2025 07 Feb, 2026 Thane 2 Volunt...

Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams. Devising ways to improve the manufacturing process to ensure higher-quality goods. Required Candidate profile Strong attention to detail, observation, organizational, and leadership skills. Knowledge of quality control procedures and legal standards. Good technical and IT skills. Perks and benefits Bonuses Flexible Work Arrangements Paid Time Off

Role & responsibilities Perform routine and non-routine analytical testing of raw materials, intermediates, finished products, and stability samples. Operate and maintain laboratory instruments such as HPLC, GC, UV-Vis, FTIR, Dissolution testers , etc. Prepare standard and sample solutions as per method of analysis and SOPs. Review and interpret analytical data, identify discrepancies, and report out-of-specification (OOS) results. Perform method validation, verification, and transfer activities under supervision. Maintain and calibrate laboratory equipment per schedule. Document all activities accurately and in a timely manner in laboratory notebooks and analytical reports. Ensure complianc...

Job Title Junior Research Fellow Required Number 1 Qualification MSc Chemistry, Nanoscience with NET or GATE or MTech Chemical Engineering Desired Skills Experience in nanomaterials synthesis and characterization, development of biosensors, spectroscopy, water quality analysis, paper microfluidic devices Workplace Amrita Biosensor Research Lab, Amrita Vishwa Vidyapeetham, Coimbatore Job Category Project Last Date to Apply August 28, 2025

Your Responsibilities Provide support at BR India within Discovery Sciences (DSc), focusing on small molecule lead identification and optimization in close collaboration with Novartis colleagues in the US and Switzerland, as well as Indian CROs, to discover and advance innovative therapies addressing areas of high unmet medical need, Make significant contributions to multidisciplinary project teams by developing and implementing in vitro activity assays, including biochemical, cell-based, and biophysical assays, Establish advanced assay protocols at CROs, adapting from internal Novartis SOPs or relevant literature sources, Oversee the transfer and troubleshooting of all assay protocols betwe...

Opportunity Details Start Date event Please select start date, End Date event Please select end date, Please select valid Start Date and End Date Start Date is older than Current Date Please enter start date or end date in dd-mm-yyyy format, Center Please enter city Special character (% and ) are not allowed Special character and digit not allowed, of volunteers required (Approved Volunteers:) Please enter No of volunteers required Special character (% and ) are not allowed Please enter number in No of volunteers required No of volunteers required should be greater than apporved volunteers, PENAVMOTA FOUNDATION Posted on PENAVMOTA FOUNDATION Posted on 04 Aug, 2025 07 Feb, 2026 Thane 2 Volunt...

As a Senior Executive QC in the Pharma and Herbal industry, you will be responsible for managing the QC laboratory and ensuring compliance with cGMP and GLP requirements. Your role will involve supervising QC analysts to maintain seamless laboratory operations and overseeing the testing of incoming raw materials, bulk, semi-finished, and finished products. You must have a minimum of 5-8 years of experience and demonstrate proficiency in operating HPLC, GC, UV, and other instruments used in QC analysis. Key Responsibilities: - Manage the QC laboratory in compliance with cGMP and GLP requirements - Supervise QC analysts to ensure seamless laboratory operations - Oversee regular testing of inco...