136 Karl Fischer Jobs - Page 3

Job description 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,

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis

Responsible for conducting various chemical analyses, ensuring the safety and compliance of waste handling procedures, and contributing to the optimization of waste management processes. Exp: 2 to 5 years Salary : 5-7LPA Location : Baddi/Nalaghare

Job Opportunity at Natco Pharma Limited (Formulation Unit) Department: Quality Control Position: Chemist / Officer / Executive Qualification: B. Pharmacy / M. Pharmacy / M. Sc Experience: 3 to 5 Years Location: Kothur, Telangana Key Responsibilities: Analysis of finished products, raw materials, and in-process samples Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus Testing of Packing Materials Adherence to GLP, GDP, cGMP, and ALCOA+ standards Assay and dissolution testing using HPLC Regulatory exposure in formulation is mandatory Interested candidates may share their CVs at jaganmohan.p@natcopharma.co.in

Test chemical samples for quality control Sample preparation and analysis Perform variety of laboratory testing Analyzing and reporting test result Preparing chemical solutions Writing technical reports of test result Maintain laboratory equipment

Should have 1-2 Years of experience in Quality Control department

Responsible for Analysis of RM/ inprocess/ FP/PM Samples, Instrument Calibration, Instrument Qualification Protocols & perform Qualification activity(OQ/PQ), analytical record, analytical cleaning method validation of the API, Online SAP Activity etc Required Candidate profile M.Sc./B.Sc. with 4 to 8 yrs exp in QC of cGMP, USFDA, MHRA approved Bulk drug/API unit. Sound exp & knowledge of handling GC, HPLC, KF, pH meter, Spectrophotometer, Auto Titrator, MP/BP etc.is must. Perks and benefits Negotiable

Department - Quality Control Experience - 2 to 5 years Qualification - M.Sc chemistry (Full time) Section - HPLC / GC / Wet lab To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. To perform Analysis (Chemical)of raw material/packaging material/in-process samples /intermediate /bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample, PD lab sample etc. To ensure that all tests carried out in the laboratory are documented contemporaneously in an appropriate authorized and controlled worksheet/ bound book. To make entries in the sample inward register ...

Responsibilities: * Conduct quality control tests using HPLC, GC, UV, Karl Fischer, Potentiometer methods * Hands on experience on QC instruments such as GC and HPLC and Titration and potentiometry is must Provident fund Annual bonus

The QC Analyst II position at Piramal Pharma Solutions involves performing analytical chemistry examination testing on raw materials, finished products, or stability samples following approved Standard Operating Procedures (SOPs) and valid methods. This role, which operates during 2nd shift hours, is crucial for ensuring product quality and compliance with regulatory standards. Key responsibilities of the QC Analyst II include conducting chemical or physical testing analysis, documenting and submitting all raw data and results in LIMS, preparing reagents for chemical analysis, and ensuring compliance with compendial (USP/EU) testing requirements as per FDA 21 CFR. Moreover, the incumbent is ...

M.Sc/B.Sc Chemistry Experience - 3 + yrs from Aroma/Chemical/Pharma analytical chemistry, handle lab instruments independently, knowledge of analytical, Must GC,HPLC, karl Fisher,chemistry, handle lab instruments independently, good grasping,

Job Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-7 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ In process / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. HPLC Analyst: Carry out HPLC testing for assay, related substances, dis...

Job Description: 24 7 audit readiness. Participation in internal, external, regulatory audits. Ensure 100% participation in trainings against CAPAs. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA/ other requirement. Determining team priorities in accordance with the plants needs, while coordinating with the team leader /Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as...

Job Summary: We are looking for a skilled QC Chemist to join our QC team. The candidate will be responsible for conducting routine analysis of raw materials,intermediates and finished products,ensuring compliance with internal specifications. Provident fund

As a skilled Analytical Chemist, you will be responsible for various tasks related to method development, validation, and query response for finished products. Your duties will include preparing analytical method development reports, Certificates of Analysis (COA), and performing analysis of in-process samples, finished goods, and stability samples in accordance with cGMP requirements. It will be your responsibility to monitor the general laboratory and ensure its maintenance as needed. Your role will involve routine analysis and stability testing of finished products for parameters such as assay, related substances, dissolution, residual solvent, etc. Additionally, you will be required to r...

Hiring for QC Job Location - Jammu (sambha) Interview Location - Chandigarh Salary Bracket -4LPA to 5.5LPA Industry prefernce - Pharma (API) only Interested one share resume on meenakshikandpal@tdsjobs.com 9815675900

Dear Candidates, Urgent vacancy at Patas, Pune,Maharshtra for the position of QC & QC Officer Experience 3+ years from Chemical /API CTC upto 6 lac Qualification M.Sc/B.Sc Chemistry M.Sc Chemistry Experience (Years) 3 to 6 from Chemical /API Specific Industry Experience Aroma/Chemical/ Pharma Aroma/Chemical Technical Skills Good knowledge of analytical chemistry, competent to handle lab instruments independently, good grasping capacity to adapt processes to complete analysis smartly. Basic chemistry knowledge Behavioral Attributes Positive attitude and sensitive toward own responsibility

Job Description Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. Having analytical knowledge of Nasal/Derma products. 3. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 4. Ensuring data integrity policy, GDP and its effectiveness up to compliance 5. To maintain the stability chamber and tracker. 6. To maintain the stability chamber and tracker. 7. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience...

Job Purpose and Impact The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver im...

Perform analysis using GC, HPLC, UV, KF & wet methods. Ensure GLP, timely reporting, data review, instrument calibration & method validation. Handle OOS, guide juniors & coordinate with QA/production for batch release. Ensure SOP/ISO compliance.

Perform analysis of raw, in-process & finished goods. Operate GC, HPLC, UV, KF, IR. Maintain records, follow GLP & SOPs. Support method validation. Ensure ISO/regulatory compliance & coordinate with QA/production for batch release.

Responsibilities: performing routine testing of raw materials, in-process materials, and finished goods, maintaining and calibrating laboratory equipment, documenting and reporting test results accurately Health insurance Provident fund Annual bonus

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

The responsibilities of this role include performing analysis of raw materials, intermediates, and finished products of Active Pharmaceutical Ingredients (APIs) according to approved specifications and Standard Operating Procedures (SOPs). You will be responsible for operating and maintaining analytical instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, Melting Point Apparatus, etc. Additionally, you will review and verify analytical data, ensuring proper documentation in accordance with cGMP and GLP guidelines. Preparation and standardization of volumetric solutions and reagents, carrying out stability studies as per ICH guidelines, and ensuring timely calibration o...