3433 Hplc Jobs - Page 35

Testing Raw Materials, In-process Samples and Finished Products - Wet analysis HPLC Method Development Quality Audits Record keeping and COA preparation Support troubleshooting of quality deviations Calibrate and maintain laboratory instruments

As XMO Officer, you will support the delivery of experience metrics, contribute to service reviews, and help embed experience thinking into operational workflows. You will work closely with the Digital Hub service desk, and product teams to ensure experience insights drive service excellence. Key Responsibilities Monitor digital experience using Riverbed and other network and application performance tools in conjunction with our delivery partner. Support implementation of XLAs and VLAs and experience dashboards. Assist in preparing reports, reviews, and feedback loops. Coordinate training, Supplier engagement events and awareness sessions in the Digital Hub. Collaborate with service desk and...

Role & responsibilities Implement norms for safety culture and 5S in laboratory Provide support and execute analytical method development and validation Coordinate for analytical testing and reporting Execute calibration of various analytical instruments as per schedule Adhere to ADL department policies and SOPs Comply with statutory and regulatory requirements Experience: MSc : 10 to 15 years PhD : 2 to 4 years Eligibility Individuals who have cleared 10th and 12th in first attempt (50% and above) MSc (50% and above), with no academic gap. Interested candidates can share their CV to juhi_bhavsar@atul.co.in or call on 81605 01583

Dear Candidate, Greetings from SGS India Pvt. Ltd.!!! We are actively looking for Chemist at our Mumbai Location with Min 3 Yrs of Relevant Experience. **Key Responsibilities: Expertise in Analytical method validation, method transfer activity for formulation (Drug product i.e tablets, Capsule, injectables) as per Pharmacopoeia or client approved procedures. Should have expertise in analytical method development or method validation/method transfer. Should have expertise in forced degradation studies of drug product and drug substances as per ICH guidelines. Should have expertise in preparation of analytical method validation/ transfer protocol, report. Should have well verse with ICH guidel...

A QC Chemist in a chemical manufacturing company is responsible for testing and analyzing raw materials and finished products using chemical and instrumental methods such as HPLC, GC, KF and pH Meter to ensure they meet defined specifications. Provident fund

As an Executive/Sr Executive in the Quality Control Department at Ankleshwar QC -U1, you will be responsible for the following: - Must have 2-6 years of experience in GC/HPLC - Hold a full-time MSc in Chemistry As an Executive/Sr Scientific Assistant in the Process Development Lab (ADL) Department, you will be responsible for the following: - Must have 2-5 years of experience in ADL - Hold a full-time MSc in Chemistry As an Executive/Sr Executive in the Quality Assurance (Investigation) Department, you will be responsible for the following: - Must have 2-5 years of experience in PD Lab/R&D/QA - Hold a full-time MSc in Chemistry As an Executive/Sr Executive in the Instrument Engineering Depar...

You will be responsible for testing finished products and analyzing them using instruments such as HPLC, GC, and Dissolution apparatus. Your key responsibilities will include: - Conducting finished product analysis - Performing injectables analysis, focusing on physical parameters using HPLC and GC - Operating instruments like HPLC, GC, Auto titrator, IR, and troubleshooting HPLC/GC issues - Participating in audits by regulatory bodies like USFDA, MHRA, TGA It is essential that you possess good communication and documentation skills, as well as an understanding of data integrity concepts.,

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...

Role Overview: You will be responsible for planning and executing various analytical method development and validation for new products, comprehensive testing of API and finished dosages while ensuring compliance with regulatory and safety requirements. You will review laboratory data, instrument logbooks, and reports when necessary. Additionally, you will initiate departmental change control requests and oversee the progress through the QMS system. Your role will involve preparing Transfer of Analytical Procedures (TAP) protocols and reports for various sites, along with procurement of samples and impurities as required. Key Responsibilities: - Prepare working plans for assigned projects an...

As a member of the Analytical Development team at Apotex Inc., you will be responsible for planning and executing various analytical method development and validation activities for new products, ensuring compliance with regulatory and safety requirements. You will review laboratory data, instrument logbooks, and reports, and initiate departmental Corrective and Preventive Actions (CCR) to track progress through the Quality Management System (QMS). Your key responsibilities will include: - Preparing working plans and timelines for assigned projects - Developing stability indicative analytical methods for drug substances and finished products - Ensuring compliance with cGLP, documentation, an...

As an Environmental Regulations Specialist, you will be responsible for: - Implementing Li-ion battery recycling and developing efficiency improvements through various sources - Exploring secondary life utilization of EOL batteries and methods to reduce carbon footprint - Managing and controlling Substance of Concern (SOC) through the IMDS platform - Performing RRR & SOC Calculations for vehicles as per standards - Monitoring and circulating information related to upcoming Environmental Regulations - Providing awareness and training to suppliers and internal teams for SOC Management In terms of competencies and skills, you should be: - Well versed with regulations related to Battery Waste Ma...

Position: R&D Executive-API synthesis Company: Titan Pharmaplus Pvt. Ltd Qualification: MSc-Organic Chemistry Experience: 6-10 years Location: Mahad, Raigad And R&d Navi Mumbai Job description: Synthesize APIs/intermediates/impurities Literature search, selection of cost effective synthesis route Good knowledge of Purification & characterization techniques Data evaluation, characterization report preparation & submission in time Expertise to work from gram to kilo scale Roshani Patil/ Vaibhavi Behere: 022-67857000 Share cv on: recruitment@titanpharma.com, roshani.p@titanpharma.com, vaibhavi.b@titanpharma.com

2025 Pass Out Engineers - BSc/MSc Chemistry - Gujarat Location-Fresher Contact Urvi Madam on 9712914207 & Visit Our Office Share with yr friends Golden opportunity to Start yr career We are Best Consultancy in Gujarat to provide Jobs . Required Candidate profile Join My LinkedIN: https://www.linkedin.com/in/urvisdp VISIT OUR BHARUCH OFFICE FOR CALL LETTER SDP HR SOLUTION 610,GOLDEN SQUARE OPP HOTEL REGENTA ABC CIRCLE BHARUCH We Provide Best Jobs in Gujarat

Role Overview: We are looking for an Executive / Sr. Executive Analytical Lab to ensure the quality and consistency of resin production through analytical testing of monomers, raw materials, in-process samples, and finished resins. The role involves wet chemistry and instrumental analysis, method validation, documentation, and compliance with internal and regulatory quality standards. The candidate will support troubleshooting, customer complaint investigations, and continuous improvement in the QC function. Key Responsibilities: Conduct routine QC testing of resin samples (acid value, hydroxyl value, viscosity, solids content, molecular weight, etc.) Perform detailed analyses including puri...

Experience in Operation and calibration of LCMS /GC Method development and validation of Genotoxic impurities/ nitroso amine impurities/NDSRIs in pharmaceutical products/ substances by LC-MS/MS. Development of MS compatible methods for the HPLC RS methods for the identification of unknown peaks by LC-MS Development of MS compatible methods for the identification of degradation impurities and unknown impurities

As an R&D Research Associate at Atomgrid, you will play a core role in our product innovation engine. You will be responsible for conducting lab-scale experiments, optimizing chemical processes, and supporting the scale-up of new specialty molecules. This role is ideal for chemists who love working across diverse chemistries and want to see their lab work rapidly move into commercial production. Key Responsibilities: - Conduct synthesis and process development experiments under the guidance of R&D scientists. - Prepare reagents, carry out reactions, and monitor processes using TLC, HPLC, GC, NMR, and other tools. - Record experimental procedures and results meticulously in lab notebooks and ...

As a Laboratory Operations professional at Piramal Pharma Solutions (PPS) in Morpeth, United Kingdom, your role involves the following critical tasks: - Preparation of samples and associated reagents, performing basic analysis accurately and on time - Gathering, generating, analyzing, and interpreting data - Organizing and planning your work efficiently - Preparing samples, reagents, and equipment required for analysis - Ensuring the laboratory is well stocked and resourced - Performing a variety of analytical testing using wet chemical and instrumental techniques - Conducting routine equipment maintenance and calibration - Writing and reviewing SOPs, sampling and testing procedures, analyti...

Responsible for Analysis of RM/IP/FP/PM Samples, analytical reports & documentation, identifying deviations, stability studies, comply with regulatory requirements, Calibration & trouble shooting of Instruments, Audit, cGMP & GLP, Qualifn Protocols.. Required Candidate profile B.Sc/M.Sc.with 4 to 6 yrs exp in API. Sound exp & knowledge of handling GC,HPLC, KF, IR, UV-VISUAL, Spectrophoto, AT, MP/BP etc.Legal compliance, cGMP, GLP, & regulatory guidelines (eg. ICH, USP, EP).

Deputy Technical Manager required for an NABL accredited Food, Water and Environmental testing lab in Kochi. The candidate must have passed both theory and practical of FSSAI 10th Food Analyst Examination (mandatory) and should be anFSSAI Approved Analyst, who is authorized to sign the Chemical and Microbiology test reports. Responsibilities The person will be fully responsible for FSSAI related works and should be well versed in Food analysis including instruments like GCMSMS, LCMSMS, ICPMS, HPLC, UV-Vis Spectrophotometer, wet lab analysis, nutritional factor analysis etc. Qualifications M.Sc. Chemistry / Microbiology / equivalent candidates from Kerala with more than 5 years experience in ...

Roles and Responsibilities : Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Team management. Desired Candidate Profile : Bachelor's degree in pharmacy (B.Pharma) or Ma...

Learning the operations of Analytical Instruments under the guidance of mentor. Learning the new Analytical Techniques used in Analytical Research Department. Coordination with Synthesis and other cross-functional departments. To ensure Good Laboratory & safety practices in the lab. Participate in ARD SOP trainings and other departmental trainings (Quality Assurance & EHS, HRD etc) as and when required. Basic knowledge of instrumental technique with its application. Analytical chemistry (HPLC/LCMS/NMR or purification) Qualification: - M. Sc (Analytical Chemistry) Experience Any kind of internship or course work done at some Industry or reputed institute

We are looking for a highly motivated and detail-oriented Senior Research Associate to join our research team. This role involves driving experimental research, supporting innovation, and contributing to scientific advancement through data-driven insights. Candidates with a Ph.D. in Organic or Medicinal Chemistry who are early in their careers will thrive in this opportunity to build impactful research experience. Qualification: Ph.D. in Organic or Medicinal Chemistry Experience: 0-2 years Key Responsibilities: Design, execute, and troubleshoot laboratory experiments in alignment with project goals Analyze and interpret data, ensuring scientific accuracy and reproducibility Collaborate with ...

Century Drugs is looking for Quality Control Analyst to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Deloitte is looking for Executive to join our dynamic team and embark on a rewarding career journey Handle operational tasks in the assigned business function Maintain records, follow up on internal processes Coordinate with stakeholders for workflow continuity Support departmental reporting and compliance Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

1. Having adequate knowledge of Sampling, Testing of Raw material, Packing Material, Finish Product, Validation and Stability samples. 2. Having adequate knowledge of Laboratory Instruments and equipment s Calibration, Maintenance/External calibration. 3. Having adequate knowledge of Preparation of laboratory chemicals, Reagents, test solution, and Volumetric solution. 4. Having adequate knowledge of Reference, Chemical and Working standard management i.e., Working Standard qualification and support in working standard management. 5. Having adequate knowledge of Data entry in SAP. 6. Having adequate knowledge of operation and trouble shoot of HPLC/GC/AAS/UV/IR/Dissolution and other QC analyt...