391 Dissolution Jobs

Analytical Method Development & Validation Develop, optimize, and validate analytical methods (HPLC, UPLC, GC, Dissolution, UV, KF, etc.) for API, intermediates, and finished dosage forms.

Corteva Agri Science (The Agriculture Division Of DowDuPont) is looking for Research Associate (Contract) to join our team Perform plant tissue sampling activities in compliance with established SOPs, ensuring integrity during sampling, storage, and transfer. Support DNA extraction workflows and genotyping assays using production scale and automated liquid handling instruments. Maintain accurate records of lab processes, instrument QC and performance, sample shipping and receiving. Log issues promptly and communicate effectively with team members and the lab leader. Collaborate with the lab leader and team members to complete daily assigned tasks. Ensure adherence to safety protocols and mai...

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...

As a Quality Control Analyst at Zydus Lifesciences Limited, Moriaya, Ahmedabad Unit, your role will involve the following key responsibilities: - Perform analysis using HPLC, GC, IR, UV, Dissolution, and other QC equipment - Conduct QC Method Validation and Transfer Qualifications required for this role include: - Education Qualification: B.Sc / M.Sc / B.Pharma / M.Pharma - Experience: 2 - 8 years Please note that this role is for the Moriaya, Ahmedabad Unit. Walk-in interviews will be conducted on 02nd March 2025 in Indore. As a Quality Control Analyst at Zydus Lifesciences Limited, Moriaya, Ahmedabad Unit, your role will involve the following key responsibilities: - Perform analysis using ...

Job Description: You will be responsible for sampling and testing of raw materials, as well as testing of finished and semi-finished products. Your role will also involve utilizing your knowledge of HPLC/ GC Empower software and operating instruments such as Dissolution, FTIR, HPLC, GC, and Polarimeter. Additionally, you should have an understanding of basic QMS in QC including Incidence and OOS. Handling instrument-related software and being aware of instrument calibration will be part of your key responsibilities. Qualification Required: - M.Sc/B. Pharm/M.Pharm Experience Required: - 3-5 years of experience in pharmaceutical manufacturing machine maintenance Job Description: You will be re...

Education: M.Pharm, M.Sc. (Chemistry), Ph.D. Experience: 5 to 12 years Location: Gurgaon An Analytical R&D Scientist in formulation is responsible for developing and validating analytical methods, conducting complex testing on various formulations, and ensuring product quality and stability. This includes designing and executing experiments, interpreting data, mentoring junior scientists, and collaborating with cross-functional teams to meet project and regulatory goals. Responsibilities Method development and validation: Design, perform, and validate new analytical methods for release and stability testing, ensuring compliance with regulatory guidelines like ICH. Testing and analysis: Indep...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 20-12-2025. 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...

Troubleshoot and identify solutions to resolve system issues. Manage spares ordering and replacement. Handle complaints and ensure timely resolution. Provide pre-sales support and install medical equipment. Achieve service targets through sales of contracts, consumables, and spares. Maintain accurate records of maintenance activities and follow standard operating procedures (SOP) for opening, attending calls, and closing them on time. Escalate unresolved issues to appropriate internal teams. Job Requirements Graduate or Diploma Holder in Biomedical / Electronics / Electrical / Instrumentation / Industrial Electronics. 1-3+ years of customer service in Medical Device/Equipment is preferred. P...

Create and deliver content through various digital marketing activities, including brochures, email newsletters, PowerPoint presentations, video promotions, marketing videos, product videos, and other creative assets. Write, edit, and proofread engaging content for websites, blogs, and social media platforms. Design and develop multimedia materials such as infographics, graphics, and motion content. Collaborate with marketing and design teams to align content with brand strategy and campaign goals. Plan and manage content schedules to ensure timely delivery of marketing materials. Participate in brainstorming sessions to generate innovative ideas for campaigns and promotional materials. Job ...

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...

We are looking for a highly skilled and experienced professional to join our team as an Expert in Science & Technology at Novartis Healthcare Pvt. Ltd. The ideal candidate will have a strong background in science and technology, with excellent analytical and problem-solving skills. Roles and Responsibility Collaborate with cross-functional teams to develop innovative solutions using cutting-edge technologies. Conduct thorough analysis of complex data sets to identify trends and patterns. Develop and implement new methods and techniques to enhance existing processes. Provide expert guidance on scientific and technological matters to junior team members. Stay up-to-date with industry developme...

1. Sampling and routine monitoring of water systems. 2. Environmental Monitoring of Clean rooms. 3. Microbial Limit Test of Finished products, raw materials and water samples as applicable. 4. Bacterial Endotoxin Test of finished products and water samples, BET method validation of products. 5. Maintaining stock of Microbiological media and consumables. 6. Sub-culturing of Microbial Cultures. 7. Growth promotion test of media. 8. Calibration/ Qualification of Microbiology Lab equipment as per schedules. 9. Maintaining Microbiology lab in hygienic condition. 10. Microbiological method Development and validation for Finished products. 11. Preparation SOPs/ STPs, Protocols and other documentati...

Preparation of protocol, raw data sheets, reports, incident reports, excel validation sheets and SOPS. Review of Method validation activities Knowledge and handling of HPLC and GC instrument activities Qualification Groups Post Graduation M.Sc Graduation B.Pharma Graduation D Pharmacy Post Graduation M.Pharma

1. Sampling and routine monitoring of water systems. 2. Environmental Monitoring of Clean rooms. 3. Microbial Limit Test of Finished products, raw materials and water samples as applicable. 4. Bacterial Endotoxin Test of finished products and water samples, BET method validation of products. 5. Maintaining stock of Microbiological media and consumables. 6. Sub-culturing of Microbial Cultures. 7. Growth promotion test of media. 8. Calibration/ Qualification of Microbiology Lab equipment as per schedules. 9. Maintaining Microbiology lab in hygienic condition. 10. Microbiological method Development and validation for Finished products. 11. Preparation SOPs/ STPs, Protocols and other documentati...

Role & responsibilities Managing the day-to-day operation of the concerned department in a complying and in safe manner. Preparing and issuing the job descriptions to the concerned team member. To ensure that only current and authorized documents are being used in the department. Verification of log books and raw data. Verifying the accuracy and validity of technical data, ensuring its proper recording and archiving. Review of method development, verification, validation, protocols, reports and raw data. Supervise and participate in developing, validating, and transferring analytical methods for drug product testing. Ensure all testing procedures comply with established protocols, maintainin...

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...

As a Formulations Specialist at our company based in Hyderabad, India, you will be responsible for the following key tasks: - Designing and executing pre-formulation experiments such as solubility, pKa, log P, dissolution, intrinsic dissolution, bulk density, flow indices, solid-state assessment, excipient compatibility, and more. - Conducting preclinical formulations to support lead identification, lead optimization, and clinical candidate selection, including solutions, suspensions, powders for constitution, compounds in capsules, and basic tablet abilities. - Utilizing solid-state equipment like PXRD, MDSC, TG, DVS, Polarizing and Hot-stage Microscopy, and dynamic image analysis technique...

Title: Executive - Formulation QC Custom Field 2: 2927 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: Formulation Others Travel Description: The candidate should be able to work in shifts and have hands-on experience with HPLC, GC, and formulation-related instrumental techniques (such as dissolution and disintegration) and chemical analysis, along with exposure to QMS. Regulatory experience is an added advantage. Job Segment: Law, QC, Quality, Legal

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.

Role & responsibilities Job Responsibilities: 1. Handling of stability section independently. 2. Handling of additional stability studies, such as, Photo stability, In-use studies, freeze thaw studies. Split studies etc. 3. Preparation of stability protocols, reports and stability compilation. 4. Responsible for timely initiation, closure of QMS documents related Quality Control and implementation respective corrective and preventive action. (i.e. Change controls, Laboratory Incidents, OOS, OOT & CAPA) 5. Responsible to follow ALCOA + principle while doing the data recording. 6. Review of In-process, finished, stability, process validation, in-process, Raw material, Excipients, packing mater...

Core Purpose of the Role: This role involves method development, method validation, method transfer and R&D stability studies by using laboratory instruments like Ultra performance liquid chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, etc. Role Accountabilities: Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Managing the stability studies for individual projects and stability data analysis, knowledge on stability guidelines and maintaining the sample storage. • Must have experience in handling HPLC, UPLC (E...

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will be responsible for leading method development, validation, stability studies, and technology transfer activities. Your role will involve collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. Strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement are crucial for success in this position. **Key Responsibilities:** - Develop, optimize, and validate analytical methods such as HPLC, GC, UV-Vis, and Dissolution in accordance with ICH and regulatory guidelines. - ...

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation AR&D Department . Job Openings: 5 Nos Position : Jr. Research Analyst or Research analyst Job Description: Analytical Method Development. Analytical Method Validation and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity for solid orals and injectables. Instruments Handling (Dissolution, HPLC,UV, GC) Responsible for the documentation. Qualification: M.Sc. or M .Pharm. I nterview Date on 5-12-2025 at 9:30 AM-2:30 PM (Friday) Ref to Friends or colleagues. Please Carry below Documents. 1) Update Resume. 2) Education Qualification Certificates (Xero...

Walk In Drive For Quality Control Department In Formulation Division @ Jadcherla Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). About Company:- MSN Group is the fastest ...