326 Dissolution Jobs - Page 2

As a Quality professional at Piramal Pharma Solutions, your role will involve remote support to PPL sites, reviewing analytical data, preparing master build in LIMS, and document preparation. Your key responsibilities will include: - Preparation of Master Build in LIMS. - Overseeing track-wise operations for QMS activities. - Preparation and review of Method Validation, Method Transfer, Method Verification, and Equivalency documents. - Preparation and review of Test Methods, STPs, and Specifications. - Operational knowledge of eDMS and ensure application compliance. - Monitoring compendial changes and preparing evaluation reports. - Reviewing analytical data, raw data, chromatography, and LI...

We are currently seeking a data-driven and detail-oriented Program Intern to join Leap. This role will involve critical thinking, problem-solving, and analytical thinking to drive operational improvements and support strategic initiatives. The charter for this role will include: Work closely with the founder/senior leaders to turn ideas into validated experiments. Dive into industry trends, discover competitor insights while also working on user research. Build a hypothesis to solve the different problem statements, execute, validate and scale the results Align with stakeholders across the org to drive the actionables; be a driving force in cross-functional teams Present findings, recommenda...

Method Validation

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...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improv...

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. (Only Males) Experience : 2 - 6 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. 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 Review of...

Role Overview: As a Chemical Testing Analyst at the company, your primary responsibility will be reviewing and conducting chemical testing of various products, including raw materials, finished products, cosmetics, Ayurveda, Sidha & Unani products. You will play a crucial role in ensuring the accuracy of test results entered into the LIMS software. Furthermore, you will be tasked with handling advanced instruments such as HPLC, GC, FTIR, Dissolution, etc. Another significant aspect of your role will involve preparing technical documentation that adheres to FDA, CDSCO, and Ayush standards for audits. Key Responsibilities: - Review and conduct chemical testing of raw materials, finished produc...

Business Development Professional - Business Excellence 1. Drive SI EP business through assigned Regional Sales & Monitor OI, Revenue, quantity for Regions/ Offices & Coordinate critical customer visits to factories. 2. Monitor and report Top 10*2 BU wise & Office wise. 3. Actively collaborate within BU and Sales to drive BU KPIs. 4. Drive active usage of CRM tools like SieSales to ensuring KPIs i.e. data quality, funnel adequacy, market transparency as per Op-Co guidelines 5. Monitor and drive market transparency improvement objectives thru Siesales. 6. Price Controller to the regions in alignment with the BU. Approve Special Price request from offices. 7. Key role is Business planning and ...

Role & responsibilities Perform routine and non-routine analytical testing of raw materials, intermediates, finished products, and stability samples. Operate and maintain laboratory instruments such as HPLC, GC, UV-Vis, FTIR, Dissolution testers , etc. Prepare standard and sample solutions as per method of analysis and SOPs. Review and interpret analytical data, identify discrepancies, and report out-of-specification (OOS) results. Perform method validation, verification, and transfer activities under supervision. Maintain and calibrate laboratory equipment per schedule. Document all activities accurately and in a timely manner in laboratory notebooks and analytical reports. Ensure complianc...

Concept Pharmaceuticals Ltd. is looking for Quality Control Analyst to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes 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 directly with the employer via their official channels before applying.

Job Description: Knowledge of calibration and operation of LCMS/GC systems with Empower software. Sound knowledge of analytical method development and validation. Handling final compilation of raw data and chromatographic data complying with GLP requirements. Preparing general lab SOPs and instrument SOPs.

4-10 years in HPLC method validation/development Qualification Required: Any graduate/post graduate Location: Manesar, Bahadurgarh Job Description: Calibration and operation of HPLC systems. Analytical method development and validation. Compiling raw data and preparing general lab SOPs. nan

We are looking for a skilled HR professional with strong expertise in Payroll Management, HR Analytics, and Dashboard Reporting, coupled with hands-on experience in Darwinbox HR Core Modules. The ideal candidate will drive operational excellence across payroll processes, ensure compliance, and enable data-driven decision-making through analytics and reporting.

Preferred candidate profile Expert in independently handling HPLC along-with experience in handling other instruments Interested candidates can share their CV/Resumes on - noor.m.judge@zyduslife.com

Walk In drive for Formulation Analytical Research & Development - department (FAR&D) - Quality Inn Ramachandra, Ward No- 58, 31-41/10/1, Duvvada, Revenue, Visakhapatnam, Andhra Pradesh on 25.10.2025 (Saturday ) Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Roles & Responsibilities : 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,...

Responsibilities: Responsible for performing analysis, corrective action Responsible for maintaining record and documentation eligible for department Responsible for product and process knowledge development of his team/ responsible department members having experience in analysis of Raw material, Stability and Finished Products samples. Must have Knowledge of Handling Lab equipment and related plant equipment ( such as G.C. / H.P.L.C, UV, KF, ICPMS & IR etc.) Required Skills: Knowledge of Basic chemistry Logical thinking. Organizing. Good in communication. Required Qualification: - M.Sc - Chemistry

Responsibilities: Ensure timely and Accurately material testing (RAW/ In Process/Finish/ R&D). Accurate and On-time Reporting and documentation at all stages. Proper Calibration. Understanding of analytical chemistry. Hands-on experience in HPLC /GC Required Skills: Candidate must have good communication skill. Good leadership quality and time management. Ability to work independently and as part of a team. Required Qualification: - B.Sc/M.Sc - Chemistry

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 : NA Minimum 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 comprehe...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improv...

As a Scientist B in the Ayush/Pharma Department at Farelabs Pvt. Ltd., your role will involve conducting analytical procedures in alignment with Ayurveda, Yoga, Siddha, Unani, and Homeopathic pharmacopeia of medicine for the Ayush section. For the Pharma section, you will be responsible for having complete knowledge of different pharmacopeia such as IP, USP, BP, and utilizing analytical procedures accordingly. Additionally, you will need to be knowledgeable about regulatory authorities like NABL, USFDA, TGA, MHRA, WHO, and DCA (drugs and cosmetic act 1940). Key Responsibilities: - Well-versed with analytical procedures for Ayurveda, Yoga, Siddha, Unani, and Homeopathic pharmacopeia - Knowled...

QC planning; GLP/QMS; chemist schedule/qualification Plan/review validation, calibration -AMC/CMC; audits; SOP/STP prep/training; COAs; stability loading/protocols prep Compile batch analysis data Indent materials Internal/External Mail coordination Required Candidate profile QC lead(GMP pharma—oral solids). GLP/QMS docu; ICH method & process validation HPLC/GC/UV, dissolution stability; OOS & CAPA-change control; monthly SOP/STP prep/review-mentoring, working std dev,

QC planning; GLP/QMS; chemist schedule/qualification Plan/review validation, calibration -AMC/CMC; audits; SOP/STP prep/training; COAs; stability loading/protocols prep Compile batch analysis data Indent materials Internal/External Mail coordination Required Candidate profile QC lead(GMP pharma—oral solids). GLP/QMS docu; ICH method & process validation HPLC/GC/UV, dissolution stability; OOS & CAPA-change control; monthly SOP/STP prep/review-mentoring, working std dev,

Responsibilities: * Develop analytical methods using AD techniques. * Prepare analytical reports with accuracy. * Validate methods according to industry standards. * Transfer methods between instruments and locations. Office cab/shuttle Provident fund Health insurance

Key Skills / Knowledge Required The ideal candidate must have hands-on working knowledge and experience in the following areas: Chromatography: Expertise in operating and troubleshooting HPLC (High-Performance Liquid Chromatography) and GC (Gas Chromatography) . Testing: In-depth knowledge of IP/FP (In-Process/Finished Product) testing and analysis. Dissolution: Proven experience in performing and interpreting Dissolution studies for pharmaceutical formulations. Stability Studies: Experience in executing and managing Stability Studies as per regulatory guidelines. Documentation: Strong understanding of Good Laboratory Practices (GLP) and compliance requirements.