166 Gas Chromatography Jobs - Page 4

Responsibilities: * Oversee gas chromatography, Karl Fischer titration, GC analysis, report preparation, lab testing, and lab operations * Manage lab operations & distillation processes

Role & responsibilities: The candidate would be required to take on the responsibility of testing of pharma formulations and ensure quality product and production efficiency. Some of the key responsibilities are: 1. Perform QC tests on raw materials, in process samples, and finished products. 2. Conduct analytical testing using instruments like HPLC ,UV , Ph meter, and titration. 3. Maintain proper documentation as per GMP/GLP guidelines. 4. Prepare and review SOPs, quality reports, and calibration records. 5. Ensure compliance with company standards and regulatory guidelines. 6. Report deviations or non-conformances to the QA team. Preferred candidate profile: The candidate should be hardwo...

Role & responsibilities Manager technical is the In-charge of Analytical Division. He/She shall report to the SBU-head about all the activities in the Analytical Division. He/She shall look after all the operations of the Division under the guidance/ supervision of SBU-Head. He/She shall be responsible for the standardization and validation of the test methods. He/She shall be responsible for ensuring the availability of the reference material / working reference standard. He/She shall be responsible for assigning the jobs to the analyst as per their calibre. He/She shall be responsible for checking the calculation part and reporting of the results before sending for authorized signatory. He...

As a Chemical Analyst, your primary responsibility will be to conduct thorough Chemical and Water sample analysis while adhering to precise testing procedures. You should be proficient in performing a wide range of analytical methods and maintaining meticulous laboratory records in accordance with NABL standards. Additionally, you will be expected to troubleshoot technical issues related to laboratory equipment and analysis procedures. Motivation to excel and a willingness to embrace new opportunities and skills are essential qualities for this role. Furthermore, male candidates who are open to working on Air Monitoring and environmental projects are preferred. To qualify for this position, ...

Role & responsibilities Profile: QC Sr. Chemist/ QC Officer to Senior Officer for Active Pharma Ingredients Industry in Samba (Jammu). Distance from Pathankot(Punjab) to Samba (Jammu) Manufacturing Unit is 50Kms away. No. Of Positions - 8(QC Chemist/ QC Officer/ QC Executive/QC Sr. Executive) Mandate Qualification - B.Sc/ M.sc Chemistry Experience - 2-10years Knowledge of Instruments- HPLC, GC (Gas Chromatography), UV Spectrometer, Kal Fischer and Experience of Wet Lab Knowledge of GMP and cGMP and Safety of their concern area. Preferred candidate profile: Candidate required only from API Industry from Pharma Industry. Early Joiner will be preferred for this position

Company Name: Oneiro Lifecare Pvt Ltd Location: Ekalbara Designation: QC Chemist/Officer/Sr Officer Job description (JD): Qualification: Masters (Chemistry) Candidate should have following criteria: 1] Experience of 1-6years in ADL / QC. 2] Handling instruments like HPLC and GC-Headspace. 3] Handling other analytical instruments like KF-Titrator, Auto-Titrator, pH-meter, Polarimeter, UV Spectrophotometer, Balance etc. 4] Analysis of In-process monitoring, Raw material, Intermediates, Stability studies and Drug substances (API). 5] Analytical method development and analytical method validation exposure. 6] Calibration of analytical instruments 7] Should follow GLP practices, Document preparat...

Hi Everyone We Are hiring for Senior Analyst with the below information: Sr.Analyst with 5-6 years exp in food testing labs Good hands on experience in handling either LCMSMS or GCMSMS Antibiotics and pesticides samples preparation Method validations as per SANTE and EU 808/2021 guidelines If Any Interested candidate can Reach out to : lavanya.m@intertek.com/ Whats app 9205065847

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of gene...

Operate & maintain GC & HPLC instruments Analyze pharmaceutical samples using GC & HPLC techniques performing routine maintenance & troubleshooting Assist in developing & validating chromatography methods Record, analyze & report chromatography data Required Candidate profile Qualification required in B.Sc/M.Sc in chemistry Previous experience operating GC and HPLC instruments in a pharmaceutical or related industry Freshers can also apply

QC Testing,HPLC,RP, Stability,GLP

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. Experience in making lab SOPs and study reports 6+ yrs of Agrochemicals/chemicals in Green field/brown field Projects Exp in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD & DSC

> To perform analysis on HPLC and Gas Chromatography as per testing method and as per pharmacopeia monograph > To assist the Head QC in investigation of OOS results > Responsible and experience of 21 CFR of Electronic signature compliances

Responsibilities: * Conduct analytical tests using HPLC, GC, Karl Fischer, spectrophotometer, pH meter, Karl Fischer titrator, viscometer, autotitrator & melting point apparatus.

Role & responsibilities 1.HPLC,UPLC and GC analysis of raw material, intermediate, finish product, stability sample, equipment cleaning and distilled solvent, Analytical Method development and validation 2.HPLC,GC, UPLC calibration HPLC and GC Analysis of all in-process,Intermediate, Finish Product,Stabiltity Analysis Equipment cleaning, Distilled Solvent and Raw materials. If required then sampling of finished product. Working Standard Qualification. Calibration of HPLC and GC. GCHS. R&D Analytical Metliod Development of new molecule. Analytical Method Validation. lnstnmrent Troubleshooting

Daily Analysis of Finish Goods , Raw material. In - process batch testing for R &D. Result and data entry in SAP COA / Report preparation offinifh and raw material soft copies Say to day instrument calibration and handling Co -ordinating with dispatch department for finish product and raw material store for daily raw material updates and reports. Keeping inward and outward recordd of samples. Maitaining 5s cluture

Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M.Pharma Experience:- 2-7 Years in API plant (HPLC/ GC/ LCMS/ HPI / method valication knowledge must)

Pharmaceutical Industry Raise laboratory Change control, incidents, deviations & LI wherever applicable. Review of Instrument qualification & scheduled calibration planner. Ensure proper laboratory analysis as per MOA & product specification. Required Candidate profile Mandatory - Operation & calibration of GC , HPLC, Good to have - GC-HS, FTIR, UV, AAS, KF, AUTO TITRATOR, BALANCE To maintain all record viz, consumption, Column, humidity, all instrument logbooks

Key Responsibilities: Develop and validate robust analytical methods (e.g., HPLC, GC, LC-MS, UV, FTIR) for drug substances, drug products, raw materials, and intermediates. Conduct routine and non-routine testing to support formulation development, stability studies, and process optimization. Maintain and troubleshoot analytical instrumentation and software. Prepare and review analytical documents such as protocols, reports, SOPs, and method transfer documentation. Ensure compliance with GMP/GLP, company SOPs, and regulatory requirements. Collaborate with formulation scientists, QA/QC, regulatory, and production teams to ensure seamless project progression. Analyze, interpret, and present da...

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...

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...

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...

Sr.Exceutive PPC/-/1325239 Accounts Madhavaram Posted On 16 Apr 2025 End Date 31 May 2025 Required Experience 5 - 6 years ShareApply Basic Section No. Of Openings 1 Designation Grade Assistant Manager - M3 Freshers/Experience Experience Employee Bonus One Month Organisational GPCOMP Pon Pure Chemicals Group Company Name Pon Pure Chemical India Private Limited Department Accounts Country India State Tamil Nadu Region Madhavaram Branch Madhavaram Skills Skill Minimum Qualification No data available CERTIFICATION No data available Working Language English Hindi Tamil About The Role LR Updation - for all transaction for the previous day for all Contract Vehicle Effective Usage Monitering Contrac...

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt. Ltd.! We're hiring a Quality Control Head for our client. Qualification: MSc in Chemistry, Biochemistry, or a related field Location: Vikarabad District, Telangana Experience: 5 to 8 Years Salary: 3.5 lakhs to 4 lakhs per annum Required: Male Note: Preferably with strong experience in the pharmaceutical or ethanol industry. Job Summary: We are seeking an experienced Quality Control Head to lead the QC team at our client's facility. The ideal candidate will have a strong background in analytical techniques, including Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC), and will be responsible for ens...

Analysis of different in process samples for Drying study Reaction monitoring by HPLC and other samples on GC Impurity profile and hold time study of process validation samples calibration activities reputed API industry having regulatory approvals

Were Hiring: Service Engineer – TechnoValue Solutions Pvt Ltd Location: Navi-Mumbai / Hyderabad | Full-Time | Experience: 1–3 Years (Freshers with strong technical background can also apply) TechnoValue Solutions Pvt Ltd is looking for a dynamic and technically skilled Service Engineer to support our pharma clients with the installation, servicing, and maintenance of high-end laboratory and pharmaceutical instruments. Key Responsibilities: Installation, calibration, and servicing of pharma lab instruments at client locations Provide preventive maintenance and on-call technical support Troubleshoot and resolve issues related to hardware/software Maintain service records and submit reports reg...