184 Kf Jobs

Role & responsibilities To ensure implementing agreed quality norms of raw materials and finished goods of the respective Areas of production. To ensure planning and developing quality norms of raw materials and finished goods as per the overall Mfg plan of the unit. To establish system to release the materials as per the timelines provided by ensuring the compliance of the laboratory to meet regulatory bodies. To establish the system and process for releasing or rejecting all finished products. Establishing a system to release or reject raw materials, intermediates, packaging, and labeling materials Reviewing completed batch production and laboratory control records of critical process step...

Greetings from Immacule Lifesciences Pvt. Ltd. We are hiring Quality Control professionals (all sections) for our new Injectable Manufacturing Plant located at Nalagarh . Qualifications: M.Sc. B. Pharma M. Pharma Requirements: 3 to 9 years Strong experience in HPLC analysis Exposure to USFDA-approved facilities is mandatory Job Location: Nalagarh Interested candidates may share their updated resume at: eswar.reddy@immacule.in

Role Overview: As a Quality Control Technician, you will be responsible for testing raw materials, in-process samples, and finished goods. You will perform testing and calibration activities according to standard testing procedures (STP) to ensure compliance with quality standards and specifications. Your role will involve implementing corrective and preventive actions, maintaining good housekeeping in the laboratory, and managing laboratory chemicals including storage, handling, and transportation. Additionally, you will be accountable for ensuring safe working conditions, safety of equipment, and highlighting any inconsistencies in received samples. Key Responsibilities: - Conduct testing ...

Dishman Carbogen Amcis is looking for Executive Formulation QC to join our team Conduct chemical analysis using HPLC, GC, and other relevant techniques. Perform dissolution and disintegration tests according to regulatory requirements. Ensure compliance with QMS standards and regulations. Collaborate with cross-functional teams to resolve quality issues. Develop and implement quality control procedures to enhance product quality. Maintain accurate records of test results and quality control activities. 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...

Job Title: Assistant Manager - Quality Management System (Analytical Assurance) Experience in Analyticaal QA is must to this role. Department: Quality Management System Reports to: Manager Location: Ankleshwar Position Type: Full-time Qualifications And Experience Education: B.Pharm / M.Pharm / M.Sc in Chemistry, Biotechnology, or related field. Experience: Minimum 8 to 10 years of experience in Analytical Assurance within the pharmaceutical industry Job Responsibilities & Accountabilities We are looking for an experienced Analytical Assurance professional to join our team and lead the Out of specification investigation, along with core QMS activities pertaining to QC. Key Responsibilities T...

Walk-in-Interview on dt.13-Dec-2025 from 10:00 AM to 02:00PM Interview Venue Bharat Rasayan Limited 1501, Vikram Tower Rajendra Place Delhi - 110008 Near Rajendra Place Metro Station (Exit Gate No.20 Role & responsibilities Perform routine & non-routine analysis using HPLC, GC, UV, IR, KF, etc. Perform wet analysis- moisture, titrations, Sp.Gr., LOD, COD, MP etc. Support method development, impurity profiling and purity analysis. Prepare and maintain analytical reports, lab documentation and instrument logs. Prepare, archive and retrieve analytical data with accuracy and compliance to GLP. Ensure calibration, routine maintenance and basic troubleshooting of instruments. Coordinate with R&D S...

Job Purpose: We are seeking a candidate to be part of a team focused on innovation in formulation technology including drone applicable, nano technology. The candidate will work with a multidisciplinary team of scientists and be engaged in targeted formulation development and optimization. Responsibilities: Design and implement experiments for the formulation specially for Drone application and characterization of surfactant, polymer, lipid and other delivery chemistry for in drone application. Formulation and characterization of drone ready formulation for platform build and project support Lead and participate in the assessment and development of early-stage formulation development activit...

Role & responsibilities Testing raw materials, in-process samples, and finished products against strict standards (GMP/GLP) to ensure drug safety, efficacy, and compliance, managing documentation (STPs, BPRs), handling deviations, investigating OOS/OOT, and providing batch release certification, requiring strong analytical skills, regulatory knowledge (FDA/ICH), and meticulous record-keeping. Handling Instruments like HPLC, GC.

Role Overview: As a Scientist at USP, you will play a crucial role in conducting analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your expertise will enhance the laboratory's scientific proficiency and work ethic by providing technical support and knowledge. You will be proficient in various laboratory techniques and capable of offering valuable observations and insights into challenging projects. Your responsibilities will include executing analytical tests, preparing summary reports, and contributing to the Verification Program. Key Responsibilities: - Conduct verification projects on Dietary Supplements/Dietary Ingredients by perfo...

Role Overview: As a Scientist at USP, you will be responsible for conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your role will involve enhancing the laboratory's scientific proficiency and work ethic by providing extensive technical support and knowledge. You will be proficient in various common laboratory techniques, offering valuable observations and insights into challenging projects. Your primary responsibility will be to provide technical aid to the Verification Program by executing analytical tests and preparing comprehensive summary reports. Key Responsibilities: - Conduct verification projects on Dietar...

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

Division Department Employment Type Job Purpose Develop and finalize budget and monitor actual performance on key KPIs and support business by providing actionable insights to team to deliver long term sustainable & profitable growth To develop and implement systems for collecting, analysing, verifying, and accurate reporting financial information on a regular basis. To have an understanding of the business and prepare a rolling forecast to estimate the future performance of division. To create a robust MIS infrastructure to support decision making process. Accountabilities I. P&L Forecasting/ Budgeting ¢ Lead annual/quarterly forecasting/budgeting activity for business with help of marketin...

* Handling of hazardous chemical reaction * Good Lab Practices * Laboratory Documentation preparation * Interpretation of Analysis (IR, NMR) * Handling & Operation of GC, HPLC, KF, Melting Point

Role & responsibilities Graduate/Post Graduate in Chemistry with 3 to 5 years of experience in QC, familiar with HPLC/GC/FTIR/UV Preferred candidate profile Graduate/Post Graduate in Chemistry with 3 to 5 years of experience in QC, familiar with HPLC/GC/FTIR/UV Job Location : Sikkim Interested candidates may apply at hr.plant@zuventus.com

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Skills : HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals | GC | GLP & QMS Activities | Method Transfer & Method Verification | LIMS | Audit Handling | Empower 3 Software | Wet Analysis | Documentation | Raw Material | Material Analysis Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Division :- Formulation Interview Date:-29-11-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF Unit-V, Chinna Chilkamarri Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbu...

Responsibilities: Perform routine and non-routine analysis of Finished Goods (FG), In-Process samples, Stability samples, and Raw Materials (RM) using sophisticated analytical instruments, primarily HPLC and GC . Health insurance Annual bonus Provident fund

Interview for QC Exe & AM in Bharuch on 25-11,Tuesday Qualification: MSC Chemistry Experience Executive : 5 to 10 AM : 10 -20 CTC: Up to 12.0 Executive : 7.0 AM : 12.0 Job Location : Dahej Apply on: sdpbharuch@gamil.com sub with QC Bharuch Required Candidate profile Interview on : 25 Nov 2025, Thursday Interview Venue : SDP HR SOLUTION, 611, Golden Square, Beside DMart Near ABC Circle, Bholav, Bharuch

As the Quality Control Head at Celogen Pharma Pvt. Ltd., you will be responsible for directing all laboratory operations related to testing of raw materials, packaging materials, in-process materials, and finished pharmaceutical products. Your role will involve ensuring strict compliance with current Good Laboratory Practices (GLP) and all applicable national and international regulatory standards to provide high-quality, timely analytical support for manufacturing and product release. **Key Responsibilities:** - **Analytical Testing:** - Perform routine and non-routine analytical testing using various techniques such as HPLC, KF, Dissolution, Titration, and Physical testing. - Ensure testin...

Date: 10 Nov 2025 Location: Bangalore, KA, IN, 560099 Division: Development Services Job Description Designation: QC Senior Executive RSQ AND MV&SI (9-II) Job Location: Bangalore Department: QC About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene's clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its more than 4000- ...

As an Analyst with knowledge of Instrument HPLC, UV, FTIR, GC, Polarimeter, KF, Autotitratior etc., your role involves the following responsibilities: - Sampling, testing, and release of Raw material, packing material, and miscellaneous material samples - Maintenance of reserve samples as per SOP - Review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products, and water analysis Qualifications required for this role include: - Bachelor or Master's degree in science - Minimum 4 to 6 years of relevant experience in the QCC Department Please note that candidates applying for internal job postings must have completed at least...

Job Title: Research Associate Analytical Development Laboratory (ADL) Department: Research & Development (API Manufacturing) Location: Dholka, Ahmedabad, Gujarat Position Summary: We are seeking a highly skilled and detail-oriented Research Associate ADL to join our API R&D team. The selected candidate will be responsible for the development, validation, and transfer of analytical methods for Active Pharmaceutical Ingredients (APIs). The role plays a critical part in ensuring product quality, supporting process development, and facilitating regulatory compliance across the API lifecycle. Key Responsibilities: Develop and validate analytical methods for raw materials, intermediates, and APIs ...

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 maintece of laboratory instruments / equipments Should have exposure on sophisticated Instruments ie 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 h...

Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensure safe operations and compliance to company s integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team inclu...

Method development like Related compound, Assay, Dissolution and Residual solvents etc. for development projects using instruments like HPLC, IC, GC, Particle size analyzer etc. Prepare method development report along with tentative analytical method. Attain method transfer activity. Method validation like Dissolution, Assay, Related compound and Residual solvents etc. Preparation TT report To keep neat and cleanliness at workplace and follow the Good Laboratory Practices in the Laboratory. Preparation of study protocols with respect to Laboratory. Development batch stability analysis as per stability protocols To attain and complete self-training through QMS. Responsible for COA preparation...

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 maintece 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...