1474 Gc Jobs - Page 46

Candidate should be exeprinecd in process development in R&D in API synthesis Candidate with the exeprience of handelling Photo reactor will be prefered . Experience in Vitamin synthesis will be prefered

Job Scope of the role: Responsible for Financial Planning and Analysis (FP&A), including budgeting, budgetary controls, forecasting, variance analysis, and MIS/Analytics to aid/enable decision-making by the leadership team. Preparation of Business modelling scenarios of new business projects. Evaluation of scenarios basis the Capital budgeting tool like NPV/IRR, payback period etc. Preparation of Monthly/ Quarterly/ Half-Yearly and Yearly financial MIS to be presented to the Management. In-depth understanding of the business profitability/ GC realization. Being part of the Finance team, also handle the operational activities efficiently and on time. Co-ordinate with cross-functional departme...

Analyst Analysis of raw material, Drug substance (API), drug products by HPLC, GC, UV-Visible Spectrophotometer, IR, SOR Instruments and chemical analysis (wet lab). Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., and Preparation and maintenance of volumetric solutions, buffers, etc Exposure of GMP / GLP / GDP in laboratory. Designation - Officer / Sr. Officer /Executive Experience : 02 - 07 years Must be having experience in API Reviewer Analytical method development and validation of raw material, in-process and finished products by HPLC, GC, Dissolution apparatus. Review of analytical method validation / verification protocols...

QC Reviewer / Sr. Research Associate: Role & responsibilities Review analytical raw data, calculations, and reports for accuracy, completeness, and compliance with approved specifications and methods. Ensure all laboratory documentation meets regulatory and internal quality standards (e.g., USFDA, EU-GMP, ICH, WHO, etc.). Review chromatographic data (HPLC, GC), wet chemistry reports, and other analytical test results. Verify results for routine analysis, stability studies, and validation reports. Check instrument calibration records and ensure compliance before reviewing analytical results. Identify and report any data discrepancies, deviations, or non-conformities. Review and verify entries...

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.

Position: Research Associate/ Sr. Research Associate, HPLC (API) Note: Candidate should be working in Pharma API industry In ARD Department in HPLC section. Interested one can share updated resume on anuverma@scllifesciences.com or WhatsApp at 9988339860 / 9875994190 Subject matter expert. Through knowledge in theoretical Operational knowledge in handling of Analytical equipment (HPLC, LCMS, Preparative HPLC) Role & responsibilities To perform routine testing of R&D/ PE lab samples in HPLC as per planning. To qualify working standard To maintain and calibrate analytical instruments/ equipment's as per schedule To maintain the good lab practices in ARD Lab To record, process and report data o...

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-28-06-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest gro...

Job Responsibilities - Lead electronic laboratory notebook (ELN) software administration and management. Provide ELN trainings to new joiners. Connect with third party and internal stakeholders on regular basis for implementation and troubleshooting. - Literature survey as per order forms. - Supervision of experimental work in laboratory. - Ensure laboratory safety and compliances - Ensure availability of raw materials and equipment required for the execution of experimental planning - Understand the safety aspects of all reactions and chemicals to be used in laboratory - Play the role of ERT and shift incharge - Perform night duties as per site philosophy -To ensure 100% compliance on ERA a...

- Conduct the experiment as per planning - Calculate reagent quantities, yields, etc. - Enter the experimental observations in Electronic Lab Notebook (ELN) - Conduct chemical reactions in batch and photochemical reactors - Handle the chemistries such as photochemistry, alkylation, oxidation, nitration, diazotization, chlorination, fluorination, vapourphase chemistry, etc - Conduct various purification techiques like fractional distillations, column chromatography and extractions - Prepare reports and documents as per product development element review methodology - Maintain the inventory of the reactors as per the laboratory management element - Interpret the GC, HPLC and wet chemistry resu...

Purpose Statement: Handle high pressure reactions at R&D lab operations, compile data and ensure adherence to safety and incorporate best laboratory housekeeping practices. - Responsible for the availability of raw materials, catalysts and instrument spares as per high pressure lab requirements. -To analyze quality results and discuss the experimentation plan and parameters with Research Incharge. - Understand the safety aspects of all reactions, chemicals and catalysts to be used in high pressure reactions. - Ensure the proper setup ( compatibility of autoclave, high pressure addition pumps, thermostats etc) as planned. - Carry out reaction process as per the provided plan, get the analysis...

"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 ...

Responsibilities: * Develop analytical methods using HPLC & GC techniques * Ensure compliance with regulatory requirements during validation process * Collaborate with cross-functional teams on method implementation Provident fund Health insurance

Role & responsibilities Monitoring the temperature & cleaning in QC area. Daily verifications of balance & pH meter. Preparation & Standardization of Volumetric solutions & there consumption records. Water sampling & analysis. Reagents & Buffer preparation & their records. Sampling & analysis of Raw Material, Packaging material, Semi Finished Products, Finished Products & retesting materials. Their documentation. Preparation & analysis of Working standards. Trace Sampling & analysis. ETP water analysis. Preparation of Specifications & raw data. Calibrations of instruments. Process validation & Hold time study of SFP. Updation of Raw Material, Packaging material, Semi Finished Products, Finis...

Key Responsibilities: Perform GC (Gas Chromatography), HPLC (High-Performance Liquid Chromatography), and UV-Visible Spectroscopy analysis for quality control of raw materials, intermediates, and finished products. Conduct routine and non-routine analytical testing following standard operating procedures (SOPs). Ensure compliance with Good Laboratory Practices (GLP) and regulatory standards. Maintain and calibrate laboratory instruments to ensure accurate and reliable test results. Document and report test results accurately while ensuring data integrity. Collaborate with production and R&D teams to troubleshoot quality issues and recommend corrective actions. Monitor and maintain laboratory...

Responsibilities: * Conduct quality control tests using GC and HPLC methods * Collaborate with R&D team on product development and optimization * Ensure compliance with industry standards and regulations

Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action. To ensure the analysis activity perform in the laboratory by following approved procedures. To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution. Actively involve and Participate in assessment, investigations, and implementing CAPA effectively. Responsible for Internal & External vendor follow-up and timely completion. Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals...

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials, finished products and/or stability samples Required Candidate profile 6+ yrs of Agrochemicals/chemicals in Green field/brown field Projects Exp in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD & DSC capitalplacement04@gmail.com P- 9315507817

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 27-06-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to i...

* Having an instrumental and wet lab. * Experience of GC -HPLC & all Lab Instruments * Documentary work, SOP preparation activity * ISO, GMP, FDA, WHO Audit Faced. Required Candidate profile * Attention to detail and accuracy * Documentation and report writing skills * Ability to work in a team and under regulated environments

• Having an instrumental and wet lab. • Manpower handling. • Experience of GC -HPLC & all Lab INSTRUMENTS. • Documentary work, SOP preparation activity. • ISO, GMP, FDA, WHO Audit Faced

Role & responsibilities Documentation & Records Maintain and regularly update all Quality Control (QC) registers. Review and ensure accuracy of in-process sample analysis registers. Maintain records for raw materials (RM), packing materials (PM), and finished product QC reports. Document and maintain daily calibration records of laboratory instruments. Maintain and review stability data records and product shelf-life records. Manage retain sample records including expiry and discard documentation. Maintain Food Safety records relevant to QC operations. Sample Analysis Perform and troubleshoot analysis of raw materials, intermediates, and finished products. Ensure accurate analysis control fo...

At Oxford Instruments, we enable the world’s leading industrial companies and scientific research communities to image, analyse and manipulate materials down to the atomic and molecular level. With a sixty-year history, and fourteen Queen’s Awards for Enterprise, our world-class products and technologies are helping our customers to address the greatest challenges of the 21st century.. Primary Purpose:. Support PT’s customers in India on new tool installs, upgrade, warranty support and billable service, and based in Delhi / Mumbai / Chennai.. Key Responsibilities:. New tools install and commissioning: follow QCF300 commissioning guide to install and commissioning the new tools. This will inv...

Role & responsibilities a. Perform routine testing of raw materials, in-process, and finished products as per approved methods. b. Operate analytical instruments like HPLC, GC, UV, FTIR, and dissolution apparatus. c. Maintain and document all test results accurately in compliance with cGMP and GLP guidelines. d. Support stability studies, method validation, and method transfer under supervision. e. Assist in investigation of OOS/OOT results and follow SOPs strictly. f. Ensure proper calibration and maintenance of laboratory instruments. g. Maintain lab safety, cleanliness, and participate in regular training programs. h. Coordinate with other team members to ensure timely completion of lab a...

HIRING FOR FORMULATION UNIT - INJECTABLE/ OSD JOB DESCRIPTION AND EXPERIENCE: WORK LOCATION: Hetero Labs Limited, UNIT V & VI, Polleypally, Jadcherla, Mahabubnagar OSD- PRODUCTION Experience: (02-07Years) Compression, Granulation, Coating, Capsule filling, Inspection INJECTABLE-PRODUCTION Experience: (02-06Years) Autoclave, Compounding, filling, QMS, Vial Washing, Lyophilizer, Visual Inspection INJECTABLE/OSD - PACKING Experience: (01-05Years) Blister Packing, Bottle Packing. QC & QC- Micro Experience: (01-07Years) HPLC, GC, RM,PM, Stability, IP/FP, Microbiology QUALIFICATION : I.T.I, Diploma, B.Com, B.Sc, B.Tech, B. Pharm, M.Sc with relevant experience DESIGNATIONS: Operator, Sr.Operator, J...

Role & responsibilities- Conduct analysis of samples using HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Providing Technical support for internal and external stake holders Being the clear R&D player by working closely with cross-functional teams to drive execution across multiple projects while maintaining and achieving timelines to ensure speed to market. To conduct analysis of samples and provide inputs to R&D/QC teams Required Skill Sets: Hands on experience on HPLC, GC, Spectrometer, and other basi...