645 Method Development Jobs

Role & responsibilities - Analyst Perform bioanalytical analysis of biological samples (plasma, serum, urine, tissue, etc.) using techniques such as LC-MS/MS & HPLC. Support method development, optimization, and validation as per regulatory guidelines (US FDA, EMA, GLP). Conduct routine sample preparation, extraction, and data acquisition. Maintain accurate documentation including raw data, analytical reports, and laboratory notebooks. Role & responsibilities - BQM Perform quality review of bioanalytical data, including chromatograms, calibration curves, QC samples, and final reports. Review bioanalytical method validation (BMV), partial validation, and cross-validation reports for complianc...

As a Senior Microbiologist, you will lead and perform microbiological testing to ensure quality control and compliance in various settings such as research, manufacturing, and clinical environments. Your responsibilities will include designing, executing, and analyzing experiments, as well as developing and validating methods. Additionally, you will be required to train and supervise junior staff, manage laboratory operations, and ensure adherence to quality standards and regulatory requirements. Key Responsibilities: - Lead and perform microbiological testing in research, manufacturing, and clinical environments - Design, execute, and analyze experiments - Develop and validate methods - Tra...

Role Overview: As an ADL - Analytical Development Laboratory Executive/Senior Executive at Zydus, you will be responsible for method development, verification, and validation to ensure compliance with Pharmacopeial standards and support various analytical activities within the department. Key Responsibilities: - Method development, verification, and validation for Pharmacopeial, DMF updations & others required in department - Conduct all Calibration and Analytical activities of the department (Engg. Batch, F&D Batch etc.) - Provide On-Site or Off-Site Support to Site-QCs in investigations or analysis - Perform evaluation and analysis on Elemental Impurities and Nitrosamine Impurities Complia...

In this role, you will be responsible for following the standard practices cGLP during lab experiments. Your key responsibilities will include: - Cleaning verification method development - API method evaluation and verification - API solubility study assessment - Working standard qualification - Method Development and verification of drug product formulation - ARF release of raw material and packaging material - Preparation of test procedures for routine development analysis - Column Management - TOC sample analysis - Ensuring the use of Personal Protective Equipment & attending EHS training & sending waste to the concerned person & complying with EHS requirements - Following GxP (GMP, GDP, ...

The successful candidate will be responsible for designing, developing, and optimizing OSD formulations, ensuring product quality, stability, and performance. Interested candidates please sent your resumes to email id: jones.naveen@insta-pill.com Food allowance Health insurance Office cab/shuttle Provident fund

As a Quality Control Analyst in the chemical industry at Gait Naurish (I) Ltd., located in Sector 155, Noida, Uttar Pradesh, you will play a crucial role in ensuring the quality and regulatory compliance of our fine chemicals and flavour intermediate synthesis products for the food, fragrance, and nutraceutical industries. **Key Responsibilities:** - Conduct and interpret chromatographic analyses using GC (Gas Chromatography) and HPLC (High-Performance Liquid Chromatography). - Perform moisture determination via Karl Fischer titration. - Execute TLC (Thin-Layer Chromatography) for rapid qualitative assessments. - Assist in developing, optimizing, and validating new analytical methods in acco...

Job Purpose: To design, develop, and validate HPLC, GC, and other analytical test methods that support the scale-up and manufacturing of new products, ensuring all project activities are completed within defined timelines and quality standards. Key Responsibilities: Operate analytical instrumentation including GC, HPLC/UPLC, UV/VIS, and other relevant laboratory equipment. Develop and validate analytical methods for new and existing products, including in-process samples for product development. Develop and validate test methods for use in cleaning validation studies. Prepare comprehensive method development, validation, and analytical test reports. Perform routine calibration and verificati...

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...

Role & responsibilities 1) Maintain GLP in the laboratory as per regulatory requirement. 2) Issuance and Maintain the records of reference standards, working standards and impurities standards 3) Issuance and Maintain the records of HPLC columns 4) Calibration of all laboratory instrument/Equipment likewise HPLC/Dissolution/UV/FTIR/GC/LCMS MS/Auto titrator/Analytical Balance 5) To perform daily calibration of Instruments/Equipment likewise Analytical Balance, pH meter, Temperature record for Refrigerator and thermometer etc. 6) Preparation and revision of Analytical laboratory's SOP. 7) Issuance and Maintain the records of LNB for validation group, development groups. 8) Issuance and Maintai...

Key Job Responsibilities: Lead Analytical Research and Development (ARD) activities, including method development, validation, stability studies, and method transfers. Review SOPs, STPs, protocols, raw data, and analytical reports. Provide analytical support to formulation development and manufacturing for product development, exhibit, and commercial batches within timelines. Mentor team members, allocate resources, monitor progress, conduct performance reviews, and arrange training. Manage internal and regulatory audits. Ensure compliance with standards, procedures, and data integrity across the department. Coordinate with external laboratories for specialized services and instrument calibr...

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...

You are a detail-oriented Chemist who will be joining the research and development lab at IIT Delhi. Your responsibilities will include conducting chemical experiments, maintaining lab instrumentation, ensuring documentation accuracy, and supporting ongoing research projects related to chemical manufacturing and formulation development. - Conduct routine and advanced chemical experiments as per research protocols. - Prepare, analyze, and interpret sample results using standard laboratory techniques. - Maintain and calibrate laboratory equipment (pH meters, conductivity meters, heating mantles, analytical balances, etc.). - Ensure adherence to lab safety protocols, proper chemical handling, a...

Role & responsibilities To perform the analytical method development and partial validation for Regulatory and Semi-regulatory markets To perform the multimedia dissolution for Advanced & emerging markets Should have hands-on experience in performing the dissolution, assay & RS tests. To perform the calibration of instruments like dissolution apparatus, UV spectrophotometer, Weighing Balances and HPLC Follow the system / operational SOPs. Ensure data integrity and accuracy of data generated. Should have knowledge of ICH and regulatory guidelines. Collaborate with different departments to provide expertise and insight. Preferred candidate profile We are looking for M.Pharm (Pharmaceutical Ana...

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An ADL (Analytical Development Laboratory) role in API job responsibilities includes developing and validating analytical methods for raw materials, intermediates, and finished APIs, performing routine

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) Excellent knowledge in HPLC Method development 2) Excellent knowledge of Good Laboratory Practices (GLP), Quality systems, Standard Operating Procedures. 3) Ability to independently handle HPLC systems Post Graduation M.Sc Graduation B.Sc

Good communication skills. Basic analytical chemistry knowledge. Hands on experience with HPLC/ LCMS / GCMS Method development skills Qualification Groups Post Graduation M.Sc Post Graduation MHRM

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...

As a candidate for this position, your role will involve working in accordance with cGMP guidelines and ensuring compliance with current guidelines and SOPs. You will be responsible for aligning with the organization's goals and carrying out any additional responsibilities assigned by your reporting authority. Your duties will include performing instrument calibration and maintaining instruments/equipment as per SOPs, as well as following safety precautions outlined in laboratory procedures. Key Responsibilities: - Conduct method development studies for Drug Substance, Drug Product & In-process Materials related to Peptides. - Perform method validation studies for Drug Substance, Drug Produc...

In this role at Amneal, you will be responsible for conducting extractables and leachable studies on packaging components, medical devices, and drug products. Your key responsibilities will include: - Performing sample preparation, extraction, and analysis using techniques such as HPLC, GC-MS, LC-MS, ICP MS, ICP OES, and other relevant instrumentation. - Developing and validating analytical methods for E&L testing in compliance with regulatory guidelines (e.g., USP). - Interpreting and reporting analytical data, including the identification and quantification of unknown compounds. - Preparing technical reports, protocols, and documentation for regulatory submissions. - Maintaining laboratory...

You will be responsible for performing analyses of Drug Product and Drug Substances to evaluate various test parameters as per product development requirements. This includes Method Development of Drug Product and Method verification of Raw Materials. Additionally, you will compile analytical results and prepare Method Development Reports. It is essential to ensure adherence to GLP aspects in the analytical laboratory to maintain quality and accuracy in testing processes. - Perform analyses of Drug Product and Drug Substances - Evaluate various test parameters as per product development requirements - Conduct Method Development of Drug Product - Verify Methods of Raw Materials - Compile anal...

Perform HPLC & GC testing for stability & finished products. Conduct HPLC analysis for cleaning samples. Support method validation, data compilation & reporting. Ensure Data Integrity, OOS, 21 CFR compliance, GMP documentation & lab incident handling