341 Method Development Jobs

As a Formulation Development Scientist, you will be responsible for the following: - Conducting formulation development for oral solid dosage forms such as tablets and capsules. - Executing method development, method validation, and technology transfer activities. - Compiling and reviewing development protocols, reports, and other technical documents. - Coordinating with cross-functional teams (QA, QC, RA, Production) to ensure successful project execution. - Ensuring compliance with regulatory guidelines from ICH, WHO, USFDA, etc. - Maintaining accurate records and documentation as per cGMP requirements. Key Skills Required: - Sound knowledge of pre-formulation and formulation techniques. - Expertise in method development and validation. - Hands-on experience with Quality by Design (QbD), Design of Experiments (DoE), and scale-up activities. - Strong analytical and problem-solving skills. - Proficiency in compiling and reviewing technical documents. Additionally, the company operates on a Full-time basis with a Day shift schedule and requires a minimum of 2 years of experience in Formulation & Development, Pharma Industry, tablets, capsules, pre-formulation, formulation techniques, and QbD, DoE, and scale-up activities. The work location is in person.,

Role Overview: As an experienced analytical development scientist at Dr. Reddys Laboratories Ltd., your main responsibility will be to execute analytical activities based on priorities and established timelines. You will be required to provide timely analytical delivery for stability testing, test method development/validation, method transfers, and other related requests from Research & Development (R&D) or formulation development. Key Responsibilities: - Conduct Literature survey and prepare analytical strategy for assigned projects. Should have a minimum understanding of DMF and test methods of drug substance, etc. - Perform analytical method development of Viscosity, PSD, GSD, Assay, RS, preservative content, residual solvents, rheology, IVRT etc. - Conduct method validation and method development. Prepare new specifications/STPs and COAs. Integrate inputs from QA, QC, and RA members. - Execute method feasibility studies for compendia procedures of excipients/API/FP. - Ensure analytical methods and process compliance as per quality assurance requirements. - Perform calibration or performance verification of analytical equipment. Maintain and standardize reference or working standards. Check for the availability and validity of the Impurities. - Execute assigned day-to-day routine analysis of development, stability samples, scale-up, PE batches. - Coordinate with other departments (CFTs) for procurement, analytical method transfer activities, specification finalization, etc. - Perform method transfers to plant QC, customers, or Third-party labs for projects and support at the time of exhibit/submission batch execution. - Adhere to safety guidelines, applicable ISMS guidelines, SOPs, equipment usage, and maintenance procedures. - Conduct studies at external CRO labs to manage peak workloads or when internal capabilities are not available. Provide technical support to CRO labs for smooth execution of studies. Qualification Required: - Education Qualification: MSc Chemistry, M Pharm Chemistry - Minimum experience required: 8-12 years of experience in analytical development department and must have worked on the nutritional product portfolio. Additional Details: Dr. Reddys Laboratories Ltd. is a leading multinational pharmaceutical company with a commitment to access, affordability, and innovation. With a focus on sustainability and reaching over 1.5 Bn+ patients by 2030, the company aims to be purpose-driven, future-ready, and sustainable. The company's work culture fosters empathy, dynamism, and teamwork, where individual abilities are supported in a shared success environment. Visit the career website at https://careers.drreddys.com/#!/ for more information.,

As an Analytical Specialist at our Contract Development and Manufacturing Organization (CDMO), you will play a crucial role in supporting analytical development and testing activities. Your expertise in analytical method development, validation, structural characterization, impurity profiling, and troubleshooting for drug substances and its intermediates will be essential in managing multiple client projects effectively. Additionally, you will serve as a mentor to junior team members and make informed decisions based on analytical data. Key Responsibilities: - Develop, optimize, validate, and transfer analytical methods in compliance with ICH and client-specific requirements. - Support the characterization of raw materials, intermediates, and APIs. - Establish impurity profiles, assay methods, and residual solvent analyses. - Review ELN experiments, release analytical reports timely, and prepare technical and quality reports. - Calibrate instruments, qualify standards, and maintain equipment. - Experience in structural elucidation, impurity identification, and profiling is necessary. - Act as the technical point of contact for client analytical needs and coordinate analytical activities to meet project timelines. - Operate and maintain various analytical equipment, resolving technical and analytical challenges promptly. - Prepare method validation protocols, reports, and SOPs, ensuring adherence to internal procedures and data integrity principles. - Support client and regulatory audits and prepare structural characterization reports using various analytical techniques. Education & Experience: - M.Sc or M.Pharm with 10+ years of experience in Analytical R&D 4-5 years of experience with a PhD. - Flexibility to travel to other cities such as Vizag, Miryalaguda, and CTO locations as required. Technical Skills: - Strong command of chromatographic, spectroscopic, and other analytical techniques. - Proficiency in chromatography data systems such as Empower and Chromeleon. - Regulatory Knowledge: ICH Q2, Q3, GMP, GLP, USP, EP, JP guidelines. Preferred Qualifications: - Direct experience working in a CDMO. - Knowledge of early and late phase molecules. - Experience in managing analytical work across multiple projects simultaneously. Key Attributes: - Strong client-facing communication skills. - Ability to work in a fast-paced, deadline-driven environment. - High attention to detail and scientific rigor. - Effective multi-tasking and prioritization skills. Join us in our mission and contribute your expertise to drive analytical development and testing activities in a dynamic CDMO environment.,

Responsibilities: (1) To conduct analysis such as GC, HPLC, Wet Chemistry, GC-MS, LC-MS, FTIR, UV-Vis, DSC, Particle Size Analyzer, Viscosity, Density etc.(2) To maintain Analytical Lab note books, procedures, documents and records(3) To maintain laboratory and work place as per norms(4) To maintain ISO 17025 and ISO 9001 management systems(5) To work safely and maintain housekeeping of the lab(6) To work in shifts as per requirement of the job(7) Implement SOP for the storage of analytical standards and reference samples at Thane under required conditions and maintain a database

Product Development: Assist in the design, formulation, and testing of new products or services, ensuring they meet quality and performance standards.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Planned purchase to maintain stock. Having knowledge in IT Hardware & Software Procurement. Creating PO & Buying Activities. Having a good Knowledge in material Follow-up with Vendor & Supplier.

Key Responsibilities: Prepare and review heavy lift erection schemes for major equipment. Experience in understanding and preparing the method statement for critical lifts and provide support to site team during execution Coordinate with engineering, safety, and execution teams for constructability review Planning and execution of lifts using different types of cranes, strand jacks Hands-on knowledge of cranes, strand jack systems, and rigging equipment Ensure safe and efficient handling of critical lifts at site Manage lifting equipment mobilization & demobilization Strong understanding of lifting safety standards and procedures Proven experience in thermal power plant construction and heavy lift operation for Boiler Strcuture,Pressure parts, Ceiling Girder jack up, Stator, critical piping etc.

You will be responsible for bioanalytical sample preparation using different extraction techniques. Additionally, you will conduct method development, method validation, and sample analysis as per regulatory requirements. You are expected to operate laboratory equipment such as Pipettes, centrifuge, evaporator, and extractors. Moreover, handling data generation, compilation, and reporting of results will be part of your detailed responsibilities. Qualifications required for this role include: - B.Pharm / M.Sc. / M.Pharm Preferred skills for this position are: - Good communication and analytical skills - Ability to work as a team player for the timely completion of tasks,

Role Overview: As a Chemist in the Instrumentation Laboratory (Residue Lab), you will be responsible for the preparation and analysis of samples using various Instrument techniques while ensuring strict adherence to safety and documentation protocols. Your role will involve receiving, handling, and storing samples and standards, conducting analysis on instruments in compliance with regulations, and contributing to method development and validation. Strong analytical skills and knowledge of NABL and ISO/IEC 17025:2017 standards are essential for this role. Key Responsibilities: - Sample Preparation & Analysis: - Receive, handle, and store samples - Prepare samples, conduct analysis, and generate reports - Prepare chemicals, reagents, diluents, and standardization solutions - Instrument Operation & Maintenance: - Operate instruments such as HPLC, GC, LC-MS/MS, GC-MS/MS, or ICP-MS for residue analysis - Interpret analytical data and troubleshoot technical issues - Perform testing according to specified methods and standards - Calibration & Intermediate check of Instruments: - Maintain records for verifications, intermediate checks, and preventive maintenance - Monitor cylinder maintenance - Method Development & Validation: - Develop, validate, and verify methods - Prepare SOPs and STPs - Handle certified reference materials - Data Management & Indent: - Process raw data, perform calculations, and generate analytical reports - Maintain records in compliance with GLP and ISO 17025 requirements - Collaborate with other departments and chemists - Compliance & Quality Control: - Participate in ILC, IQC, and Professional testing - Follow GLP, 5S, and safety guidelines - Ensure analysis compliance with regulatory standards - Safety & Housekeeping: - Adhere to lab safety protocols and waste disposal procedures - Maintain cleanliness and orderliness in the laboratory - Team Collaboration & Learning: - Work under supervision and participate in training sessions - Stay updated with new analytical methods and technologies - Coordinate with team members and report any deviations promptly Qualification Required: - Post Graduation/B.Tech in Food Technology/Chemistry/Bio Technology or Equivalent - 2-5 years of experience in an NABL Food testing laboratory - Knowledge of NABL, ISO/IEC 17025:2017 standards/rules regulations - Analytical mindset with attention to detail Working Conditions or Location: On-Site at Sangariya Fanta, Jodhpur, Rajasthan (Note: Any additional details of the company were not included in the provided job description.),

About the Team At Nutanix Cloud Manager, we are trying to build the next generation platform to help enterprises model, develop and manage applications. We want to give them the ability to encapsulate not only infrastructure but even the application its architecture and deployment as code. You will be reporting to the Senior Manager Engineering, QA - NCM Team. Your Role As the gatekeeper of our product quality, you would be required to ensure that product releases adhere to the highest quality norms. You will design and develop a testing framework for our products and be part of a ruthless quality team. You will develop test tools, test cases, maintain test beds, and provide metrics and test/quality status. What You Will Bring: Be a self-starter who can flourish in a fast-paced technology company Be the owner of our automation and delivery systems Be actively participating in Coding & Code reviews Have expertise in languages like Python, JAVA Have expertise with automation and building tools such as Selenium, JMeter and Jenkins Strong systems background (Linux systems with exposure to Process, Memory and IO Management tools You will enable our engineers to generate known-quality releases with every commit, discover defects early and iterate fast. Thrive on working on open-source technologies. Excellent programming and scripting capabilities to develop code for automated tests. Should have an extremely good problem-solving approach with good hands-on knowledge of Algorithms & Data Structures.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 20-09-2025. 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 interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 20-09-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

Conduct chemical synthesis of new and existing agrochemical compounds in the lab. Develop and optimize synthetic routes and reaction conditions to improve yield, purity, and cost-effectiveness.

Plan, setup, monitor, and workup chemical reactions Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) Isolate product and Optimize reaction conditions for improved yields and output.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

As a candidate for this role, you will be responsible for the following key responsibilities: - Thorough knowledge of HPLC based analysis of recombinant proteins including RP-HPLC, SE-HPLC, and glycan analysis. - Independently design method development of proteins, qualification, transfer following ICH/USP/EP/IP guidelines. This includes writing and reviewing protocols, transfer plans, and reports. - Carry out day-to-day analytical work and collaborate with the Cell culture and downstream teams in Biotech R&D. - Set up product-related test/release specifications and analytical protocols for Biotech products. - Design in-house/outsource methods for Physico-chemical characterization of biological products. - Coordinate with QC for the smooth implementation of new methods. - Maintain equipment logs and documentation in the lab. - Monitor and maintain stability of various products in Biotech. - Prepare lab-related documents, regulatory submission documents, and provide QC support (SOP, STP, COA, MOA, Specification). - Interpret data and write reports in support of regulatory submissions. - Review analytical data for in-process & stability related activities. Qualifications required for this role: - Strong knowledge of HPLC based analysis of recombinant proteins. - Experience in method development, qualification, and transfer following ICH/USP/EP/IP guidelines. - Good understanding of analytical work in a Biotech R&D setting. - Ability to design analytical protocols for Biotech products. - Knowledge of Physico-chemical characterization of biological products. - Proficiency in interpreting data and writing reports for regulatory submissions.,

Plan, setup, monitor, and workup chemical reactions independently Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) Isolate product and Optimize reaction conditions for improved yields

Develop, optimize, and validate analytical methods for raw materials, in-process samples, and finished products.Perform analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, dissolution, and others.

Develop, validate, and optimize analytical methods for qualitative and quantitative analysis of raw materials, intermediates,and finished products. Perform instrumental analysis using techniques such as HPLC,GC.

Research Assistants will be expected to conduct research to identify contacts and set up interviews with select industry sources, prepare detailed notes or call reports, and support other members of the team in their projects.

SUMMARY Job Description: Job Description : As a Low Code No Code (LCNC ) Developer, you will be responsible for developing and supporting Power Apps and must have strong solutioning and troubleshooting skills. Creating reusable components for an application and working in Agile environment and ensuring consistency in delivering application. You will play a key role in development and support of LCNC applications. As a member of global team excellent communication and analytical skills are essential to this role. JOB REQUIREMENTS: 1. Experience Range Min 2- Max 7 Years 2. 100% Alignment required with Rotational Shifts and Project Timelines 3. Excellent Communication skills. 4. Strong Hands on Power App development Canvas and Model-driven. 5. Strong experience in developing Power Automate or MS Flows. 6. Excellent UI/UX designing skills in Power Apps. 7. Proficient in developing Power BI reports and dashboards 8. Hands on experience in integrating SharePoint online with third party applications - using CSOM, JSOM, API, Connectors etc. 9. Hands on experience in applying Power Apps including an in-depth understanding of customization, configuration, integration, and extensibility, as well as boundaries and constraints 10. Strong understanding of PowerApps formulas and development methods including Powe FX programing language. 11. Excellent knowledge on Microsoft Dataverse aka Common Data Services. 12. Hands on experience on creating custom connectors 13. Able to develop cost effective solutions by choosing correct licensing model. 14. Ability to develop Components and leverage reusability in deliverables. 15. Ability to integrate solutions with SharePoint and Microsoft Teams, 16. Strong hands on experience in SQL Server, PostgreSQL, SSIS, SSRS, Power BI 17. Good to have experience in AWS and Azure Cloud. 18. Good to have experience in Front end frameworks like Angular or React. 19. Ability to Cross skill and function on Multi Skill / Tech Stack assignments 20. Should be able to support, develop and enhance application on clouds platform as per best practices. 21. Ability to Work Independently on application issues and enhancements. 22. Should have good troubleshooting and analytical skills. 23. Ability to learn and work on different technology stacks. 24. Working knowledge of ITIL module. Must have understanding on Critical Incident Management Process, Change Management and Problem Management Process. 25. Hands on knowledge on any ITSM tool preferably ServiceNow. 26. Excellent Troubleshooting and Analytical Skills.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department. Required Candidate profile with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc