395 Dissolution Jobs - Page 3

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...

Jubilant Biosys is looking for Research Associate II - In Vitro, ADME - for Bengaluru location Qualification : M.Pharmacy Experience : 3- 5 Years Responsibilities : Read and understand various in vitro ADME protocols Conduct in vitro stability (liver microsomes, plasma and in any other relevant matrix, chemical stability) experiments for new chemical entities Conduct the following in vitro ADME experiments logP, logD, pKa measurements CYP induction and inhibition assays Permeability determinations (Caco-2, MDCK etc) in relevant cell lines CYP phenotyping in purified enzyme systems Solubility determinations (kinetic, thermodynamic, simulated fluids) ",

Analytical Testing: Conduct routine quality control tests on raw materials, intermediates, and finished APIs. Utilize techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis spectroscopy, and dissolution testing. Verify compliance with specifications and standards. Validate and verify analytical methods used for API testing. Ensure precision, accuracy, and reliability of results. Stability Studies: Participate in stability studies to assess API shelf life and degradation patterns. Monitor samples under various storage conditions. Documentation and Compliance: Maintain detailed records of all quality control activities. Adhere to Good Laboratory Pract...

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...

Department: Analytical Science Development Qualification: M.Sc / M. Pharm (Analytical Chemistry) Experience: 2 - 5 years in Formulations industry (Analytical Research & Development) Key Skills: Perform RM/FP/IP/Stability sample testing, including instrumental/wet analysis. Develop and validate analytical methods, and manage technology transfer processes using techniques such as HPLC, UPLC, GC, and Dissolution for Assay and RS in OTC, Pharma, and Nutra formulations. Oversee product stability management in accordance with ICH guidelines and customer requirements, including conducting various stability studies (Developmental, Pivotal, Bulk, In-use, Photostability, and Transport studies). Review...

WALK-IN INTERVIEW ON 29TH NOVEMBER FOR ANALYTICAL METHOD DEVELOPMENT AT KANDIVALI (W), MUMBAI. Time: 10 AM to 5 PM Desired profile : Candidates having 4 to 8 years experience in Analytical Method Development in regulated and emerging markets. Experience in technology transfer, QC support and troubleshooting at site Independently handling HPLC , UV spectrophotometer and Dissolution. Well versed with operation of Empower 3.0 and Chromeleon 7.2 software. Should have exposure to Assay, Content uniformity, Blend uniformity, Dissolution and related substances testing. Knowledge and handling of GC , Malvern 3000 is preferred. Job role demands extensive travelling to plants, only candidates willing ...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 29-11-2025. 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...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 21-11-2025. 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...

.Role & responsibilities 1. Analysis of stability sample 2. Incubation of stability samples with Proper labelling & kept into respective chamber, Preparation of stability Protocol. 3. withdrawal of stability samples & maintain the reconciliation of record. 4 .HPLC,UV, Balance calibration. 5. To ensure the GLP all respective log book related requirement to stability are achieved. 6. Maintain all respective log book related to stability. 7. Trouble Shooting of HPLC analysis if any problem occurred planning proper utilization of HPLC System for on the basis of priority. Preferred candidate profile From sterile formation injectable plant. Perks and benefits 1. Pickup and Drop Facility 2. Canteen...

We have opening for Formulation AR&D Department. Job Openings: 6 Nos Position : Jr Research Analyst or Research Analyst Exp 2- 6 Yrs. Job Location: Pashamylaram - Patancheruv (Telangana) Salary : As Per Company Norms Qualification: M.Sc. or M .Pharm Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Re...

Role & responsibilities Should have practical hands on operation of HPLC, GC and Dissolution tester etc. Analysis of stability samples, In-process samples, raw materials and finished products etc. He should able to resolve the day to day analytical issues. Good analytical skill and should have go getter approach. Calibration and maintenance of instruments like HPLC, Dissolution tester, GC etc. as per respective SOP. Timely investigation and resolution of OOT/OOS test results. Follow GLP and ensuring timely documentation as per good documentation practice. Identifying problems in production batches and report to Head-Quality. Practical hands on operation of HPLC, GC and Dissolution system. An...

As a Quality Control Officer, your primary role will involve reviewing stability protocols & reports, preparing Annual Product Quality Reviews, reviewing Master Packing Card & Master Formula Card, preparing and reviewing Process Validation Protocols and reports, reviewing Batch Manufacturing and Batch Packing records, preparing batch release certificates, and ensuring batch release processes are in line with SOPs. You will also be responsible for issuing Formats, Logbooks, Registers, protocols, reports, BMRs, and BPRs as per the respective procedures. Additionally, you will review QC documents such as Specifications and Standard Testing Procedures for raw materials, bulk products, finished p...

Roles and Responsibilities Perform KF titration, pH meter calibration, and GC testing as required. Perform analysis of raw materials and finished products using Uv,IR,HPLC,UPLC,GC etc. Ensure adherence to SOP's,GMP,ALCOA principals during shift operations. Ensure accurate results by following standard operating procedures (SOPs). Collaborate with cross-functional teams to resolve analytical issues. Maintain laboratory equipment and perform preventive maintenance tasks. Conduct HPLC analysis using UPLC and Dissolution techniques. Instruments Handling:- HPLC , FTIR , Karl Fischer , Autotitrator , Coulometer , UV , Polarimeter , Melting point, pH meter , Balance

Responsible for analytical method development, validation & transfer, ensuring cGMP & regulatory compliance. Supports R&D projects, stability studies, and dossier preparation for global submissions. Required Candidate profile M.Pharm or M.Sc with 10–15 years in AR&D for formulations. Hands-on with HPLC/GC, stability studies & regulatory documentation.

Role & responsibilities Preparation and review of analytical method validation and method verification protocols and reports. Execution of analytical methods as per approved protocols. Coordination with cross-functional departments (QA, ADL, Production, etc.) for analytical method validation activities. Ensure compliance with Good Laboratory Practices (GLP) and Safety Guidelines in all laboratory operations. Ensure all laboratory activities are performed as per existing Standard Operating Procedures (SOPs) . Provide technical guidance and training to team members on SOPs and analytical techniques. Support the QA team by ensuring timely availability of audited and reviewed validation document...

Job Description: API analytical job in the pharmaceutical industry involves developing and validating analytical methods for active pharmaceutical ingredients (API), analyzing impurities, Method Validation transfers, and ensuring regulatory compliance. Key responsibilities include using techniques like HPLC, GC, and LC-MS, documenting results, troubleshooting issues, and collaborating with R&D, quality, and regulatory teams. Key responsibilities: Method development and validation: Develop, optimize, and validate analytical test methods for raw materials, intermediates, and APIs, ensuring they comply with regulatory guidelines. Analytical testing: Perform testing and analysis using techniques...

About The Role Project Role : VIS & BI Strategy Practitioner Project Role Description : Develop a VIS/BI vision, business case, and modernization strategy; discover and assess VIS/BI opportunities; identify industry- and function-centered VIS/BI use cases; guide clients on industry and function relevant measures and metrics; develop a VIS/BI roadmap and operating model; help drive adoption, decision making and behavior change; measure VIS/BI value. Must have skills : Kinaxis Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a VIS & BI Strategy Practitioner, you will engage in the development of a comprehen...

Every day, we get opportunities to make a positive impact on our colleagues, partners, customers and society. Together, we re pioneering the solutions of the future and unlocking the full potential of precious resources. Trusted to act on initiative, we challenge conventional thinking to develop world-leading technologies that inspire progress in vital areas, including energy, food, water and shipping. As we push forward, the innovative, open spirit that fuels our 140-year-old start-up culture and rapid growth also drives our personal growth. So, as we shape a more resourceful, less wasteful world, we build our careers too.

We are expanding!! You are invited to join one of the fastest growing pharma companies in India!! About us : Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. Department: Quality Control Section: HPLC Analysis of OSD products Experience: 2-7 years Design...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories Private Limited MSN House, D.No: 2-91/10 & 11, White Fields,Kondapur, Hyderabad on Sunday 16-11-2025 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 suc...

.Quality Control officer/Executive Formulation, dissolution, stability studies Raw material, Stability, HPLC,GC experience required. (Preferably from Bangalore candidates who can join in 30 days)

Key responsibilities Inspection and testing : Examine incoming raw materials, in-process materials, and finished products to ensure they meet specifications. Process monitoring : Monitor production processes and quality control activities to identify deviations and opportunities for improvement. Data analysis and reporting : Collect and analyze data to identify quality issues, produce statistical reports, and track quality trends. Documentation : Create and maintain accurate documentation of procedures, inspections, and test results. Collaboration : Work with production teams to implement corrective actions and improvements. Compliance : Ensure compliance with company, national, and internat...

Vibonum Technologies Private Limited, Mysore, (Althera Group), is conducting a Walk-in Interview on Nov 09th, 2025 to hire Quality Control professionals for its state-of-the-art OSD manufacturing facility in Nanjangud, Mysore . Department: Quality Control Work Location: OSD Plant, Nanjangud, Mysore Interview Date: Nov 09th, 2025 (Sunday) Time: 09.00 am to 05.00 pm Venue: Althera Laboratories India Pvt Ltd, Bangalore (https://maps.app.goo.gl/ozdZFQh9pN3YkYAb) Althera Laboratories India Pvt Ltd No S26, Yarandahalli, Bommasandra-Jigani link road, Hebbagodi post, Bengaluru 560099 Bengaluru, Karnataka 560099 Open Positions in Quality Control- 50 Nos Officer / Sr. Officer -QC / Executive and Fresh...

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...