35 Method Verification Jobs

Date: 10 Nov 2025 Location: Bangalore, KA, IN, 560099 Division: Dedicated Centre Job Description Job Role : Analytical QA analyst Department : Quality Assurance BGRC Job Location : Bangalore About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation f...

Date: 10 Nov 2025 Location: Bangalore, KA, IN, 560099 Division: Dedicated Centre Job Description Job Role : Analytical QA analyst Department : Quality Assurance BGRC Job Location : Bangalore About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation f...

Required Experience: 03 to 08 years Senior Officer/ Executive Knowledge of Method Suitability Knowledge of Method Verification Testing, Knowledge of Culture Transformation MLT Water Testing

Job Description 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 instrument's / equipment's . 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 instrument's / equipment's. Should have knowledge for the preparation, handling & management of working/reference standards etc. Testing of In-process, Stability and Finished produ...

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...

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...

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...

Key Responsibilities: Sample analysis Maintenance of lab equipment Intermediate checks Calibration all Instrument Sample Allotment Lab Approval Method Verification Chemical verification Sample Disposal Register Logbook Entry : all instrument

Role Overview: As an R&D Executive at PTC Moraiya, your primary responsibility will be to perform analysis of Drug Product and Drug Substances for various test parameters as per the product development requirement. You will also be involved in method development of Drug Product and method verification of raw materials. Additionally, conducting literature search for method development and impurity profile of drug product will be a key part of your role. Your duties will also include compilation of analytical results and preparation of Method Development Report, ensuring adherence to GLP aspects in the analytical laboratory. Key Responsibilities: - Perform analysis of Drug Product and Drug Sub...

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...

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Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company's patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace ...

Title Executive - R&D Quality Business Unit R&D Quality Job Grade G12A Location: Vadodara Key Responsibilities At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Position Summary List of Responsibilities: To Review and approve o...

Role Purpose: This role is responsible for supporting analytical R&D projects related to alcoholic beverages. It includes to support and conduct precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods. The position also to supports senior analysts in innovation and research initiatives. Qualifications & Experience: Education : MSc in Analytical Science / Chemistry / Organic Chemistry Experience : Minimum 1-2 years of experience in chemical and instrumental analysis of food, beverage, alcoholic beverages. Key Technical Responsibilities: Perform chemical analysis on raw materials, intermediates, and finished liquid...

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Biosys Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Dev...

Team Handling , Team Management Analysis as per the procedures/monographs, routine calibration of analytical balance and GC. GC and HPLC Techniques. Method verification Protocols and Reports in urgent basis.

You will be responsible for the execution of analytical method optimization/development, validation/verification of analytical test methods related to Compendia, In-house developed methods, Site transfer methods, Regulatory queries, Method Life Cycle Management (MLCM) studies, Supplier Driven Changes (SDC), and other procedural updations. This includes the preparation of method validation/verification protocols and reports. Your key responsibilities will include: - Executing method optimization/development studies. - Validating/verifying in-house methods, Compendia, SDC, MLCM, and Cleaning Analytical methods while adhering to regulatory procedures. - Preparing Method verification/Method tran...

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Share your Resume to hrd@stedmanpharma.com

Role Overview: You will be responsible for performing chemical and instrumentation analysis on various materials, including in-process, raw materials, packing materials, intermediates, and finished products. Your primary goal will be to ensure compliance with dispatch timelines as per the monthly schedule provided by PPL. Key Responsibilities: - Conduct instrumentation analysis using ICP-MS and LC-MS for various materials to meet dispatch timelines - Participate in analytical method developments, validations, transfers, and verifications using ICP-MS and LC-MS/MS - Prepare and review protocols, worksheets, and reports for method developments, validations, verifications, and transfers - Allot...

As a Quality Control professional at PPL Digwal, your role will involve performing chemical and instrumentation analysis for various stages of production to ensure compliance with GMP and safety standards. You will be responsible for allotting work to the chemists, calibrating instruments, maintaining documentation, managing stock levels of standards and chemicals, and ensuring timely analysis and release of products. Key Responsibilities: - Perform chemical and instrumentation analysis for in-process, raw materials, intermediates, and finished products to meet production schedules. - Allocate work to chemists within the QC department. - Conduct instrument calibrations according to the sched...

You will be responsible for performing microbiological analysis, media inventory, and culture maintenance. This includes executing microbiological method development, method validation, and method verification. In addition, you will be required to perform qualification and calibration of instruments and equipment. It is essential to ensure concurrent documentation of analysis to maintain accurate records. Furthermore, you will be responsible for water sampling and testing to ensure compliance with regulatory standards. Your attention to detail and precision in executing these tasks will be crucial for the successful completion of your responsibilities.,

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary Method verification/validation of compendia/pharmacopeial updations, Method ve...

Role & responsibilities Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Analysis of raw material / finished products / stability samples / Dissolution profiling for R&D/ Plant support. Analytical Method Development /Verification Assay, Related substances, Dissolution etc . Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hot Air Oven, Refrigerator temperature monitoring. Develop/ optimize the analytical methods by Chemical/ instrument analysis Verify/ validate the analytical methods by Chemical/ instrument analysis Preparation / Revision of Specification and Method of analysis for Ra...

1. Execute validation of analytical methods as per ICH guidelines 2. Method Verification 3. Method Transfer 4. Instrument Handling (HPLC,UV-Visible Spectrophotometer) 5. Documentation & Compliance 6. Audit Readiness & Regulatory Support Perks and benefits Bachelor's Accommodation and Travelling facility

As an R&D Executive at PTC - MORAIYA, your primary responsibility will be to perform analysis of Drug Product and Drug Substances for various test parameters according to the product development requirements. You will be involved in the method development of Drug Product and method verification of Raw Materials. Conducting literature searches for method development and impurity profile of drug products will also be a key part of your role. Additionally, you will be responsible for compiling analytical results and preparing Method Development Reports. Ensuring adherence to Good Laboratory Practices (GLP) in the analytical laboratory is crucial to maintain quality standards. Your contributions...