54 Karl Fischer Jobs - Page 2

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

We are looking for a passionate and skilled M.Sc. Chemistry graduate (Organic/Analytical) to join our R&D or Quality Control team. The candidate will assist in routine chemical and instrumental testing, synthesis, method development.

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, Finished Products & retesting materials in SAP. Stability analysis.

Role & responsibilities Physicochemical characterization, Media preparation, Buffer preparation etc. Preferred candidate profile Experience in working in lab set up and good basic knowledge on physical/chemical techniques. Dilligent and accuracy driven.

Company: Strides Pharma Science Limited Department: Quality Control Profile: Executive Locations: Bangalore Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years Key skills: Analysis of Material / Product by referring current version of specification STP with relevant material code. Responsible for initial set up of Instrument/Equipment before starting the analysis with relevant online entries in usage Log / LIMS. Perform the Assay and RS by LC/UV/Dissolution, content uniformity by LC analysis with simple and complex products Tests as per SOP/STP. Proper handling of chromatographic column used for analysis. Maintain data integrity and appropriate traceability

Role & responsibilities 1. Understands and follows safety requirements within work area to identify and escalate potential hazards and also executes CAPA's for safety observations. 2. Adheres to equipment/ instrument safety procedures and understand associated energies to be isolated and execute LOTO. 3. Understand and follow safety requirements in handling material/glassware. 4. Demonstrates ability to perform physical test/physical parameter verification/ thermal test/ spectroscopy/ Electro-chemical techniques and required non-complex & complex tests and can demonstrate the same for auditors. 5. Understands and executes analytical solution preparation steps as explained in the record of analysis. 6. Recognizes abnormalities and reports malfunctioning of instruments and performs basic maintenance in line with requirements. 7. Plans cleaning of Analytical instruments & calibration and ensures timely completion. 8. Understands and adheres to written procedures. 9. Demonstrates ability to explain/ articulate procedures related to own work areas. 10. Recognizes failures in execution and report incidents, events. 11. To follow safety norms and adhere with company policy. 12. To follow the Quality Policy & Contamination prevention policy of the company. 13. Demonstrates high discipline & orientation to detail while inspecting each sample. 14. Demonstrates complete ownership of end-result of quality check. 15. Analyses raw material/ packaging/ final product, etc. or performs in-process checks Continuously acquires new skills to perform quality check with higher accuracy and prepare for any internal and external audits.

Company: Strides Pharma Science Limited Department: QA/QC Profile: Executive Locations: Alathur/Puducherry Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years

Analysis of Finished Products, Raw Material, In-Process, Solid oral doses form Test, Process Validation, Stability Samples , To Maintain Good Laboratory Practices. Handling Lab Samples &Reports. Required Candidate profile Applicant must be Pharmacy graduate / post graduate with experience of QC functions in Solid Oral dosage form. He must be well versed with instruments like GC, HPLC, UV, Karl Fischer, Dissolution etc

Roles and Responsibilities Conduct chemical testing, analysis, and inspection of raw materials, intermediates, and finished products using various instruments such as Karl Fischer titrator, pH meter, viscometer, etc. Prepare reports on test results and submit them to relevant authorities for review.

Key Responsibilities: 1. Stability Study Design & Planning Define study protocols, including time points, conditions (temperature, humidity, light exposure), and container types. Collaborate with formulation scientists and regulatory affairs teams to ensure studies align with regulatory guidelines (e.g., ICH, FDA). Plan long-term and accelerated stability testing for new and existing products 2. Compliance & Documentation Document study protocols, deviations, results, and reports. Maintain comprehensive stability study records for internal reference and regulatory submissions. Prepare stability data for inclusion in regulatory filings, ensuring compliance with ICH, FDA, or other relevant guidelines. Ensure that all documents are stored according to GMP and are easily retrievable during audits. 3. Equipment & Process Management Well-versed with Chromeleon Software Performing a Dissolution Test Well-versed with QC lab Instruments 4. Cross-functional Coordination Work closely with Production, QA, Engineering, and Warehouse teams to ensure smooth operations. Support QMS activities 5. Safety & Hygiene Compliance Ensure adherence to aseptic techniques and environmental monitoring standards in cleanrooms. Follow safety protocols for handling hazardous chemicals and sterilization processes. Train production staff on GMP, hygiene, and workplace safety standards. Required Qualifications & Skills: Education: B.Pharm / M.Pharm / M.Sc Experience: 2-7 years of experience in QC Stability Section for Formulation (Preferably Injectables) Technical Skills: Well-versed with Chameleon Software Performing a Dissolution Test Familiarity with cGMP, USFDA, EU-GMP, and WHO-GMP guidelines. Soft Skills: Strong problem-solving abilities, teamwork, attention to detail, and adaptability. Preferred Experience: Experience in an injectable/sterile manufacturing in QC Stability Exposure to regulatory inspections and audits. Knowledge of GLP and GDP Benefits: 1. Mediclaim 2. Term Life Plan 3. Accidental insurance 4. Free transportation across city 5. Relocation Allowances If interested, share your updated resume on paresh.meharawat@stmpl.co.in

1) Working as per company / management policy & reporting to Quality Control Head. 2) To sample the incoming Raw materials and packing materials and also Finished Goods. 3) To conduct analysis and testing of Raw Material, Packing Material, In-Process sample, Finished goods, Stability samples etc. with the help of analytical instruments and techniques. 4) To calibrate / verifies analytical instruments like HPLC, GD, ICP-OES Wet lab and balances 5) To trouble shoot analytical instruments. 6) Preparation and standardization of Volumetric Solution. 7) Preparation and maintenance of records for stock / reagents. 8) Analysis of samples for qualitative and quantitative test parameters as per specification. 9) To maintain record of analysis and supporting logbooks as per GLP. 10) To have working experience in shift for supporting production activities by analysis of in-process samples. 11) To participate in laboratory investigation. 12) To checked by the In-Process analysis results.

Job Overview To perform quality control testing of raw materials, intermediates, and finished products as per approved specifications, ensuring compliance with cGMP, regulatory, and company standards. Roles and Responsibilities: Conduct chemical and instrumental analysis of raw materials, intermediates, and peptide APIs using HPLC, GC, UV-Vis, IR, Karl Fischer, and TOC. Execute peptide-specific analytical techniques including reverse-phase and ion-exchange HPLC, amino acid analysis, and peptide mapping where applicable. Perform method validation, verification, and transfer in line with ICH guidelines. Maintain and review analytical documentation such as SOPs, STPs, specifications, and validation protocols. Ensure compliance with cGMP, GLP, and data integrity practices in all laboratory operations. Support OOS/OOT investigations, perform root cause analysis, and assist in CAPA implementation. Monitor calibration, maintenance, and qualification of analytical instruments as per the approved schedule. Prepare samples and documents for regulatory submissions and audits (e.g., DMF support, ANDA filings). Coordinate with QA, RA, Production, and R&D for timely resolution of issues and release of batches. Participate actively in regulatory audits (USFDA, EUGMP, WHO, etc.) and internal quality audits. Experience 14 years of experience in QC in pharmaceutical / chemical / API manufacturing industry Competencies Hands-on experience with instruments like HPLC, GC, UV-Vis, and others. Sound understanding of cGMP, GLP, and regulatory guidelines Strong documentation and communication skills. Ability to work in shifts and under pressure. Team player with problem-solving and analytical skills. Responsibilities Qualifications 2-5 years of experience in the QC department of a USFDA / EUGMP-approved peptide/API manufacturing company

Key Role & Responsibilities -To analysed & develop analytical method for the existing and new molecules. -To calibrate and validate the developed method as per the global standards. - To operates and maintains various analytical instruments -To document the developed process along with its calibration and validation data. -To transfer developed method to the quality control with the help of right technology transfer protocol. -To support organization in terms of achieving various quality accreditations. -Prepare COA (certificate of analysis) for finished goods lot as per specifications - Carry out standardization & calibration of LAB reagents and instruments & maintain records as per SOP - Carry out safe and standard operations of instruments/ Lab wares as per SOP - Maintain safe work practices by using applicable PPEs (Personnel protective equipment) w.r.t LAB - Maintain good housekeeping in the laboratory - Segregate the waste as per properties of the material/chemical - To maintain experimental data in ELN and LIMS. -To maintain instruments and equipments of the lab. - To support structural identification of impurities and by-products. -To support waste characterization. - To support synthesis lab, Kilo Lab, Pilot plant in terms of process development and scale up quality needs. - Provides Training and supervision to new executives on analytical methods - Actively searches literature in research publications, patents, etc - Follow BBS (Behavior based safety) to maintain safety culture at workplace - Prepares technical reports and presentations as required related to projects - Supports R&D projects at group level participating in meetings and sharing technical information and "best-practices - Encourages "best-practice" sharing through the participation and promotion of meetings, knowledge sharing tools and all other initiatives liaising on a world-wide basis - Implement Aarti Management System Job Requirements: 2 to 6 Years in industry as a team member. - Experience: a minimum of 2 years experience in analytical managerial roles in chemical companies is needed. - A previous experience in method development is highly appreciated - Knowledge: a good knowledge of analytical tools and organization in chemical companies is needed. - Extensive operation knowledge of GC, HPLC, IR, UV, KF, GCMS, Viscometer is highly recommended. - Knowledge of wet analysis is also required - ETP sample analysis, like COD, BOD, NH3-N, TSS,TDS etc is highly recommended. - Ensure calibration, inspection of measuring & test equipment used for analytical lab - Good knowledge of important IT tools: Scifinder, Chemdraw, and good computer proficiency is needed Qualification: M.Sc Analytical Chemistry or M.Sc (Chemistry with large industrial experience in analytical method development)

Laxmi Organic Industries Limited. We are looking for candidates interested in Technical Associate-Quality for Dahej. Job Title: Technical Associate-Quality Department: Quality Control/ Quality Assurance Location: Dahej. Job Purpose Analysis of Raw material, water sample, Packing material In-process & Finished products Role and Responsibilities Operational: Daily analysis of water, In-process, Daily Finished product sampling and analysis Daily sampling of RM, In-process, Finished product. Dispatch of finished product dispatches of tanker, drum, bags sampling and analysis. Counter samples storage, retrieval, instruments cleaning Detection of abnormalities during analysis and report it to the concerned authority. Raw Material inspection, sampling and analysis. Result recording in SAP. HPLC and GC Data storage Packing material sampling and analysis. Checking of certificate of analysis Report any near miss /incident or any non-compliance To Support Various ISO, Process safety and Responsible Care Initiatives Responsible to compete any other assignment given by the senior. Deviation reporting and recording OOS reporting and recording. Required Knowledge (of any equipment / Tools and techniques / Software) GC, HPLC, UV, Titrimetric, Karl Fischer, Potentiometer, QESH Education Essential: M.Sc in Chemistry Preferred: M.Sc in Chemistry (Analytical, Organic, Inorganic) Experience Essential: 2-4 years in chemical industry If you are interested, kindly share your updated cv on below email id. Email Id: siddhi.pathak@laxmi.com Telephone No: 9125652023

•Education: M.Sc. Chemistry/ Environmental Science •Experience: 3-8years •Skills :Titration Methods, ,Calibration of pH meter, Operation of UV Visible Spectrophotometer, & Karl Fischer ,ISO &5S, SAP Contact NO :6359660041

Kaliberr bioscience pvt ltd is looking for QC Executive to join our dynamic team and embark on a rewarding career journey Develop and implement quality control procedures, standards, and specifications for products or services Conduct regular inspections and tests of raw materials, in-process goods, and finished products to ensure compliance with quality standards Identify and investigate quality issues, determine the root cause, and implement corrective actions Ensure that production processes meet quality requirements and make recommendations for improvements Collaborate with other departments such as R&D, production, and customer service to ensure a seamless quality control process Maintain accurate records of quality control activities and communicate results to management Ensure compliance with regulatory requirements and industry standards Knowledge of quality control procedures, standards, and specifications Strong communication skills and ability to collaborate with other departments Excellent analytical and problem-solving skills

* Instrument Handling of GC, HPLC, Karl Fischer, pH meter, Auto Titrator apparatus, Malvern Partial size analysis etc. * Good understanding of ISO 9001:2015 Quality Management System. * Hands of experience on SAP,COA & Analysis of COD sample. Required Candidate profile * Perform analysis of the raw materials, wet lab analysis, solution preparation, In-process sample. * Preparation of table top SOP’s and detailed manual on Start-up and Shut-down of the equipment

Role & responsibilities

Long 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. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

Testing of RM, intermediates & finished products Operate HPLC, GC, UV, pH meter, KF Follow GMP, QMS & SOPs Sampling, calibration & equipment maintenance Accurate & timely report generation

Responsible for testing of Raw material,IP/ FP and Stability sample as per method of analysis. Should have knowledge for the Method Verification/validation and Method Transfer analysis. Have an exposure on operation, calibration, Qualification and maintenance of laboratory instruments / equipments . Should have exposure on sophisticated Instruments i.e. HPLC, Dissolution,FTIR,UV, GC, Autotitrator,Karl fischer,PSD etc. Have an exposure for the preparation of calibration & PM schedule of laboratory instruments / equipments. Should have knowledge for the preparation, handling & management of working/reference standards etc. Testing of In-process, Stability and Finished product samples,Raw material. Should have awareness of Caliber LIMS system operation. Having exposure of Method transfer/verification /validation activity.

Responsible for testing of Raw material,IP/ FP and Stability sample as per method of analysis. Should have knowledge for the Method Verification/validation and Method Transfer analysis. Have an exposure on operation, calibration, Qualification and maintenance of laboratory instruments / equipments . Should have exposure on sophisticated Instruments i.e. HPLC, Dissolution,FTIR,UV, GC, Autotitrator,Karl fischer,PSD etc. Have an exposure for the preparation of calibration & PM schedule of laboratory instruments / equipments. Should have knowledge for the preparation, handling & management of working/reference standards etc. Testing of In-process, Stability and Finished product samples,Raw material. Should have awareness of Caliber LIMS system operation. Having exposure of Method transfer/verification /validation activity.

Laxmi Organic Industries Limited. We are looking for candidates interested in Technical Associate-Quality for Chiplun. Job Title: Technical Associate-Quality Department: Quality Control/ Quality Assurance Location: Lote, Chiplun. Job Purpose Analysis of Raw material, water sample, Packing material In-process & Finished products Role and Responsibilities Operational: Daily analysis of water, In-process, Daily Finished product sampling and analysis Daily sampling of RM, In-process, Finished product. Dispatch of finished product dispatches of tanker, drum, bags sampling and analysis. Counter samples storage, retrieval, instruments cleaning Detection of abnormalities during analysis and report it to the concerned authority. Raw Material inspection, sampling and analysis. Result recording in SAP. HPLC and GC Data storage Packing material sampling and analysis. Checking of certificate of analysis Report any near miss /incident or any non-compliance To Support Various ISO, Process safety and Responsible Care Initiatives Responsible to compete any other assignment given by the senior. Deviation reporting and recording OOS reporting and recording. Required Knowledge (of any equipment / Tools and techniques / Software) GC, HPLC, UV, Titrimetric, Karl Fischer, Potentiometer, QESH Education Essential: M.Sc in Chemistry Preferred: M.Sc in Chemistry (Analytical, Organic, Inorganic) Experience Essential: 2-4 years in chemical industry Preferred: Experience in Pharmaceutical Industry If you are interested, kindly share your updated cv on below email id. Email Id: viddhi.kharwa@laxmi.com Telephone No: 91-22-4910444-ext.513

Job Description Job Role: Research Officer Location: Zone-IV Pilot Plant (Analytical), Jhagadia, Gujarat Job Responsibilities: 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 and volumetric solutions preparation, standardization and maintenance. 7) Coordination for maintaining analytical columns of HPLC, GC, IC and spare parts of instruments and Equipments. 8) Coordination of AMC / CMC of analytical laboratory instruments and its calibration. 9) Coordination for disposal of retained analytical samples of raw material, packing material, inprocess and stability samples. 10) Preparation, revision, review and checking of Raw material, inprocess, intermediates, reaction monitoring and finished products specifications and test procedure and departmental SOPs. 11) Planning and execution to review, checking of IQ, OQ and PQ documents of instruments and equipment. 12) Prepare and Review of certificate of analysis (COA) for finished products. 13) Responsible for investigation of incidents and Deviations in coordination with internal and cross functional team 14) Complying EHS promotional activities and complying EHS statutory requirements of the analytical department. 15) Handling of the ICP-MS/ ICP-OES, Ion Chromatography, GC-MS, UPLC,ION Meter and commissioning experience of the product and new Laboratory setup. Job specification Experience: 6-10 Years Qualification: M.Sc Analytical Chemistry or M.Sc (Chemistry with large industrial experience in analytical method development and structure elucidation.)

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-8 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/ Inprocess / 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. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career!!! Regards Team HR Unison Pharmaceuticals Pvt. Ltd.