203 Nmr Jobs - Page 3

About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and optimize Route of Synthesis (RoS) for novel medicinal drugs. Synthesize and purify medicinal compounds using advanced laboratory techniques. Conduct laboratory experiments to test the efficacy and safety of synthesized compounds. Analyse data from various analytical techniques to assess compound quality and properties. Improve the physicochemical properties of existing drugs to enhance performance and stability. Collaborate with other scientists and departments to advance drug development projects. Follow strict health and safety guidelines to ensure a safe working environment. Review and interpret the structure and purity of chemical compounds using modern analytical tools. Knowledge & Experience Bachelors in Medicinal Chemistry with Masters in Medicinal Chemistry, Organic Chemistry, or a related field. With M.Sc. (2 to 4 years of Experience) At least 2 years of hands-on experience in chemical synthesis within a pharmaceutical or biotech setting. Proficiency in modern synthetic techniques and analytical methods (e.g., NMR, HPLC, MS). strong problem-solving skills and the ability to design efficient synthetic routes. Excellent laboratory skills, including safe handling of chemicals and operation of laboratory equipment. Ability to work collaboratively in a team-oriented environment. Excellent written and verbal communication skills. Detail-oriented with strong organizational skills. Commitment to continuous learning and staying current with scientific advancements. Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans .

Conduct organic synthesis and chemical reactions as per R&D protocols. Perform purification, extraction, recrystallization, and characterization of organic compounds. Maintain lab records, chemical inventories, and ensure safety protocols. Assist senior scientists in process development and scale-up. Operate analytical instruments like HPLC, GC, IR, and NMR (basic knowledge acceptable). Support quality control and documentation work. Ensure compliance with standard operating procedures (SOPs). trong knowledge of organic chemistry and reaction mechanisms Basic handling of laboratory instruments Good documentation and reporting skills Ability to work in a team and follow instructions Attention to detail and safety-conscious approach Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹20,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Education: Master's (Preferred) Experience: Quality control: 1 year (Preferred) Research & development: 1 year (Preferred) Location: Hyderabad, Telangana (Preferred) Work Location: In person Application Deadline: 15/07/2025

Summary The job purpose is to lead and manage all assigned project/network activities and apply scientific/technical expertise to address complex R&D issues for the preparation and timely delivery of drug products (DP), processes and procedures; participate in teams and contribute to overall Technical Research and Development strategies and goals. To develop our growing pipeline of products we are looking for experienced professionals in the area of pharmaceutical development. In this challenging position, you will play a key role in the development of parenteral dosage form. The position is based in the Genome Valley, Hyderabad, within the Technical Research and Development Organization (TRD) of Global Drug Development (GDD). Role purpose Design, plan, perform, and interpret scientific experiments to perform chemical and pharmaceutical profiling of NCEs resulting in robust analytical method development, solid form characterization and formulation strategy development in collaboration within a multifunctional project team coordinated by a Project leader. Manage and contribute to maintenance of lab instruments/infrastructure. About The Role Major accountabilities: Ensure the selection of the appropriate NCE during discovery and early phase product development by performing appropriate risk assessments using physicochemical characterization, in vitro assessments, and in silico assessments. Design & formulate appropriate pre-clinical PK and tox formulations for parenteral and oral routes. Select, develop, and scaleup appropriate enabling technologies such as nanosuspension, amorphous solid dispersions, or microemulsion development per risk assessed. Design and perform analytical scientific experiments to characterize solubility, dissolution, pH, and permeability for DS and DP. Analysis by UV fiber optics, UPLC/HPLC, and other techniques as required (SEC, IC, Raman, FT-IR, XRPD, DSC, TGA, NMR, etc.). Design, plan and perform scientific experiments to support development of new technologies. Contribute to project related scientific/technical activities either independently or under minimal guidance from more experienced team member. Propose and provide input for the design of next experiments. Generate and evaluate data. Interpret results and document and report result using electronic notebooks(eLN) according to Novartis electronic documentation processes. Author development reports, laboratory protocols, etc. as per need. Communicate and address problems, perform literature searches. Adhere to all health and safety (HSE) practices appropriate to the site and country. Work according to appropriate SOP’s, and Novartis guidelines. Maintain a clean and safe working space. Utilize special tools/equipment and specialized facilities e.g., containment facilities, for potent compounds. Make sure that all deliverables are achieved against agreed project timelines and meeting quality expectations. Contribute to selection, installation, training, and maintenance of equipment and infrastructure. Manage inventory (chemicals, excipients, consumables, and solvents) within own area of responsibility. Evaluation and implementation of new methods and technologies, scientific contributions, supervision of research projects and initiation of new research activities. Enable Novel Delivery Technologies evaluation as per project needs Proactively support the overall culture of the organization through coaching, mentoring, providing feedback, driving innovation, external collaborations, and best practice sharing. Report and present scientific/technical results internally and contribute to peer reviewed publications, presentations, and patents. Fully adhere to all relevant Novartis Policies and Guidelines. Role model the Novartis Values and Behaviors. Minimum Requirements M. Pharm with 7 to 10 years of experience or PhD in Science with focus on pharmaceutical sciences and technology (e.g. Pharmacy, Chemistry) with 5+ years of experience Experience in the development, scale-up and technology transfer of Parenteral Drug Product manufacturing processes is required. Background in aseptic process development of parenteral product is required Thorough understanding of aseptic fill-finish unit operations (i.e. filling, filtration, mixing, lyophilization etc.) and equipment for scale-down model development and process characterization is required. Experience with regulatory filings (IND/IMPD etc.) is required. Demonstrated competency and experience in drug product development within the pharmaceutical industry is required. Successful work experience in a matrix organization is preferred. Good oral, written (good experience in writing of scientific reports and filing documentation) and presentation skills are essential. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Title: Senior Officer - ADL Custom Field 2: 2559 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. 2) Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. 3) Preparation and maintenance of volumetric solutions, buffers, etc 4) Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., as per calibration schedule 5) Knowledge of separation techniques in chemical separation in chromatography in Normal and reversed phase systems 6) Experience in chemical analysis like, titration, moisture, LOD, sulphated ash, TLC IR, SOR, Clarity of solutions and quantitative solubility tests 7) Exposure of GMP / GLP / GDP in laboratory. 8) Preparation of Standard operating procedures (SOP) for all the instruments, equipment and procedures. Job Segment: Chemical Research, Laboratory, Engineering, Science

Key responsibilities of this job role include: Lead the development and optimization of chemical processes using flow reactors (microreactors, tubular reactors, packed-bed, etc.) Collaborate with synthetic chemists and process engineers to transition batch processes to continuous flow Develop and validate process parameters (residence time, flow rates, mixing, pressure, temperature, etc.) Integrate online/inline monitoring tools (PAT) such as FTIR, UV-Vis, NMR, or HPLC Ensure robust data analysis, modeling, and documentation of experiments and findings. Qualifications BE in chemical engineer with 4-5 years of experiences.

Overview Candidate need to be self motivated, technically sound, familiar with NMR- basic hardware and software uses, able to run 2D advance experiments. good knowledge about NMR-CryoProbe-SolidProbe and its peripherals. Good knowledge about windows and linux workstations Comfortable to use the system and report and communicate problems with Bruker Engineers on 1st level maintenance Provide On-site primary support to maintain all three systems 800MHz, 600MHz, 400MHz. Responsibilities On-Site support for all three systems 800MHz, 600MHz, 400MHz. Able to handle various probes and run advance NMR experiments. report all critical incidents and assist with on-line support provided. Provide help in Helium refilling in all three systems. Check and provide resolution for initial problems in the system, shimming, pulse check, experiments, rebooting and probe handling. Qualifications An Engineering background, worked with NMR or working presently on some projects. Application knowledge with technical expertise for basic NMR and its power and electronics issues, Strong oral and written communication, Flexible, willing to travel if required, Language proficiency English is required.

Title: Officer Custom Field 2: 2216 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. Preparation and maintenance of volumetric solutions, buffers, etc Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., as per calibration schedule Job Segment: Laboratory, Science

Job Description: We are seeking a highly motivated and skilled Medicinal Chemist with the industrial experience of 2 to 5 years to join our dynamic research and development team in Bengaluru. The candidate will be responsible for the design, synthesis, and characterization of novel chemical entities (NCEs) in accordance with client specifications and internal guidelines, contributing significantly to our drug discovery programs. Key Responsibilities: Synthesize and characterize novel NCEs efficiently and independently, adhering to client specifications. Apply broad knowledge of modern organic chemistry and synthetic methodologies to complex chemical problems. Execute various synthetic reactions, including but not limited to: heterocyclic chemistry, metal-catalyzed reactions, air/moisture-sensitive reactions, and hydrogenations, carrying out multi-step synthesis as required. Utilize a wide range of techniques for synthesis and purification, including chromatographic methods (e.g., MPLC, HPLC). Perform spectroscopic characterization of novel compounds using techniques such as NMR, LCMS, HPLC, and IR. Maintain accurate and up-to-date Lab Note Books in accordance with client specifications and internal guidelines. Generate final reports and other scientific documents as needed. Demonstrate a strong understanding of systems and processes pertaining to safety, health, and environmental regulations. Strictly adhere to EHS (Environmental, Health, and Safety) guidelines, maintaining a zero-tolerance policy for non-compliance. Required Candidate Profile: Education: M.Sc. in Organic Chemistry or Chemistry. Experience: 2 to 5 years of experience in Synthetic Chemistry (Small Scale). Interview Details (Walk-in Drive): Date: 5 th July'25 Time: 9:00 AM to 3:00 PM Interview Venues: Bengaluru: Aurigene Pharmaceutical Services Ltd. 39-40 Hosur Road KIADB Industrial Area, Phase 2, Electronic City, Bengaluru, Karnataka 560100 Hyderabad: Aurigene Pharmaceutical Services Ltd. Bollarum Road, Jaya Prakash Narayan Nagar, Miyapur, Telangana 500049, India Mandatory Documents to Carry for Interview: Your latest resume. Last three months' salary slips. Salary revision letter (if applicable). 3 Passport-size photographs. Note: The final job posting location will be Bengaluru, regardless of the interview location.

Description The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview This is a Non-supervisory position in Reference Standard Evaluation department, responsible for oversight and successful implementation and completion of all activities pertaining to a portfolio of Reference Standards (RS), Pharmaceutical Analytical Impurities (PAI) and Certified Reference Materials (CRMs) or any other physical materials USP intend to develop. The position is expected to contribute majorly in PAI activities. It is more of an operational and tactical role. This incumbent is responsible for, including but not limited to, timely preparation of procurement specification, collaborative testing protocols for RS, PAIs, CRMs , providing technical assistance for collaborating labs, analytical data review, preparation of scientific/technical reports, Certificates, Product Information Sheet (PIS), defining and preparation of packaging configuration, Quality Control testing instructions, resolving technical issues. How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist S-IV, RSE has the following responsibilities: Responsible for managing the development of PAIs by working in collaboration with internal and external stakeholders/partners as necessary Item creation, reviewing the data package from partners, preparation of packaging and labelling forms (PLF) Preparing the documentation including, but not limited to, the test protocol, PAI report, product information sheet. Communicate with internal stakeholders and external partner as and when required Addressing customer queries and complaints promptly after doing necessary investigation To have ability to do “Problem solving” at any step of development process Contribution to regular Reference Standard development process as and when required, that involves Responsible for timely preparation of procurement specifications and collaborative testing protocols for new/replacement RS lots, technical assistance for collaborating labs To review the analytical data received from the Collaborators and to prepare summary reports and Reference Standard Candidate Evaluation Package (RSCEP), preparation of packaging and QC testing instructions and assigning periodic re-test intervals. Independently maintains successful scheduling operations, necessary documents, complete and accurate information; and addresses quality issues to ensure availability of reference standards in a complex portfolio. To have discussion with Scientific Liaison (SL) and Expert Committee (EC) members during new monograph or monograph modernization processes. Participating in peer review of draft monograph before submission to Pubs. To Draft product planning documents (PPD), coordinates with labs, and reviews/interprets data from international collaborative studies. Submits collaborative study summary reports to review and subsequent approval for each RS lot. Addresses the concerns of balloters to achieve successful approval of RSCEPs. To have ability to do “Problem solving” at any step of RS development process. To produce quality documents (RSCEP, Addenda, TP) with minimum comments from RSTO and no “Major” observation from QA. To Coordinates for any additional necessary testing and assists other staff members in addressing the comments. To provide correct guidance on the interpretation of test data, Proposes and designs studies to obtain necessary data to resolve complaints. To demonstrate technical understanding to internal and external audiences regarding USP's Reference Standards program. Engages in conversation about reference standards issues. Addresses general customer technical inquiries and thoroughly investigates customer complaints with minimal guidance. Performs and participate in other related duties as assigned. Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: PhD in Chemistry/Pharmacy from a recognized University. Minimum of 4-7 years of Pharmaceutical industry experience MSc/MPharm from a recognized University. Minimum 8-10 years of Pharmaceutical industry experience Hands on experience on chromatographic techniques (HPLC, GC) Must have strong experience in analytical method development and analytical method validation Ability to handle multiple priorities in a fast-paced environment. Excellent written and verbal communications skills. Additional Desired Preferences Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration. Prior knowledge of working with and/or qualifying reference materials Adequate laboratory experience to handle sophisticated analytical equipment’s Ability to read and interpret spectroscopic analyses data (NMR, IR, MS) Ability to handle multiple priorities in a fast-paced environment. Excellent written and verbal communications skills. Ability to operate independently where appropriate, yet understand when to escalate issues and how to establish effective working relationships. Project Management skills. Must have ability to prioritize and manage multiple, concurrent projects in a fast-paced and high volume environment with changing deadlines and priorities Able to work flexible hours when needed to meet the project timelines Strong skills in troubleshooting, and solving technical problems. Experience with, and knowledge of the USP-NF is preferred. Basic knowledge / familiarity with statistical analysis Supervisory Responsibilities: NA Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview This is a Non-supervisory position in Reference Standard Evaluation department, responsible for oversight and successful implementation and completion of all activities pertaining to a portfolio of Reference Standards (RS), Pharmaceutical Analytical Impurities (PAI) and Certified Reference Materials (CRMs) or any other physical materials USP intend to develop. The position is expected to contribute majorly in PAI activities. It is more of an operational and tactical role. This incumbent is responsible for, including but not limited to, timely preparation of procurement specification, collaborative testing protocols for RS, PAIs, CRMs , providing technical assistance for collaborating labs, analytical data review, preparation of scientific/technical reports, Certificates, Product Information Sheet (PIS), defining and preparation of packaging configuration, Quality Control testing instructions, resolving technical issues. How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist S-IV, RSE Has The Following Responsibilities Responsible for managing the development of PAIs by working in collaboration with internal and external stakeholders/partners as necessary Item creation, reviewing the data package from partners, preparation of packaging and labelling forms (PLF) Preparing the documentation including, but not limited to, the test protocol, PAI report, product information sheet. Communicate with internal stakeholders and external partner as and when required Addressing customer queries and complaints promptly after doing necessary investigation To have ability to do “Problem solving” at any step of development process Contribution to regular Reference Standard development process as and when required, that involves Responsible for timely preparation of procurement specifications and collaborative testing protocols for new/replacement RS lots, technical assistance for collaborating labs To review the analytical data received from the Collaborators and to prepare summary reports and Reference Standard Candidate Evaluation Package (RSCEP), preparation of packaging and QC testing instructions and assigning periodic re-test intervals. Independently maintains successful scheduling operations, necessary documents, complete and accurate information; and addresses quality issues to ensure availability of reference standards in a complex portfolio. To have discussion with Scientific Liaison (SL) and Expert Committee (EC) members during new monograph or monograph modernization processes. Participating in peer review of draft monograph before submission to Pubs. To Draft product planning documents (PPD), coordinates with labs, and reviews/interprets data from international collaborative studies. Submits collaborative study summary reports to review and subsequent approval for each RS lot. Addresses the concerns of balloters to achieve successful approval of RSCEPs. To have ability to do “Problem solving” at any step of RS development process. To produce quality documents (RSCEP, Addenda, TP) with minimum comments from RSTO and no “Major” observation from QA. To Coordinates for any additional necessary testing and assists other staff members in addressing the comments. To provide correct guidance on the interpretation of test data, Proposes and designs studies to obtain necessary data to resolve complaints. To demonstrate technical understanding to internal and external audiences regarding USP's Reference Standards program. Engages in conversation about reference standards issues. Addresses general customer technical inquiries and thoroughly investigates customer complaints with minimal guidance. Performs and participate in other related duties as assigned. Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: PhD in Chemistry/Pharmacy from a recognized University. Minimum of 4-7 years of Pharmaceutical industry experience MSc/MPharm from a recognized University. Minimum 8-10 years of Pharmaceutical industry experience Hands on experience on chromatographic techniques (HPLC, GC) Must have strong experience in analytical method development and analytical method validation Ability to handle multiple priorities in a fast-paced environment. Excellent written and verbal communications skills. Additional Desired Preferences Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration. Prior knowledge of working with and/or qualifying reference materials Adequate laboratory experience to handle sophisticated analytical equipment’s Ability to read and interpret spectroscopic analyses data (NMR, IR, MS) Ability to handle multiple priorities in a fast-paced environment. Excellent written and verbal communications skills. Ability to operate independently where appropriate, yet understand when to escalate issues and how to establish effective working relationships. Project Management skills. Must have ability to prioritize and manage multiple, concurrent projects in a fast-paced and high volume environment with changing deadlines and priorities Able to work flexible hours when needed to meet the project timelines Strong skills in troubleshooting, and solving technical problems. Experience with, and knowledge of the USP-NF is preferred. Basic knowledge / familiarity with statistical analysis Supervisory Responsibilities: NA Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time

1. Understand the project requirements & deliverables from supervisor/manager 2. Carry out literature search by using SciFinder, Reaxys and other search engines 3. Comprehend and discuss the MSDS with supervisor/ team members. 4. Identify and mitigate any potential safety risk with the help of Manager 5. Plan, setup, monitor, and workup chemical reactions independently 6. Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) 7. Isolate product and Optimize reaction conditions for improved yields and output 8. Purify compounds by different methods using chromatography, distillation and crystallization etc. 9. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc 10. Ensure parallel execution of multiple reactions conducted both by self and the team 11. Scale up of R&D developed products to kg scale and then technology transfer to pilot plant 12. Troubleshoot as appropriate for successful execution with intimation to supervisor 13. Discuss research findings and work plan on daily basis with supervisor/ manager and Mentor junior lab personnel 14. Document reactions, research findings/ observations accurately in lab note books to ensure data integrity 15. Participate in project meetings and prepare daily, weekly and monthly reports and submit to Manager 16. Writing regular updates, final reports, PDR preparations and inter departmental communications 17. Regular lab duties including equipment maintenance, chemical inventory and lab clean-up Job Types: Full-time, Permanent Pay: ₹232,834.74 - ₹309,279.35 per year Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Education: Diploma (Required) Work Location: In person

Walk-In Drive For API Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Saturday 05-07-2024. Requirement for Executive / Senior Executive - API AR&D - API Analytical Research & Development(AR&D) HPLC,GC,GCMS,LCMS,PXRD High performance liquid chromatography (HPLC) & GC HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of drug development. Method Validation of analytical methods as per internal and country specific regulatory guidelines and execution through proper protocols. Compliance of Good Laboratory Practice in the lab Responsible for providing support to technical issues related to R&D to file the Drug Master files. Effective method development ensures that laboratory resources are optimized, while methods meet the objectives required at each stage of drug development. Responsible for ensuring delivery time-lines and adherence to quality and standards and customer Relationship management. Facilitating scientific and technical discussions with team members and external collaborators to resolve issues and communicating conclusions from stability studies. Interview Date : Saturday 05-07-2024 Department : Analytical Research & Development(API AR&D) HPLC,GC,GCMS,LCMS,PXRD Experience : 1 to 6 Years Qualification : M.Sc Position: Executive / Senior Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details :Venue Details : MSN Laboratories Pvt. Ltd, R&D Centre, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana

Job Title -AM Research and Development Qualification: MSc (Organic Chemistry with first class), Experience: 4+ years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 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 and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor

Job Title - R&D Chemist Qualification: MSc (Organic Chemistry with first class), Experience: 4+ years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 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 and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor

1.Understand the project requirements & deliverables from supervisor/manager 2.Carry out literature search by using SciFinder, Reaxys and other search engines 3.Comprehend and discuss the MSDS with supervisor/ team members. 4.Identify and mitigate any potential safety risk with the help of Manager 5.Plan, setup, monitor, and workup chemical reactions independently 6.Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) 7.Isolate product and Optimize reaction conditions for improved yields and output 8.Purify compounds by different methods using chromatography, distillation and crystallization etc. 9. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc 10.Ensure parallel execution of multiple reactions conducted both by self and the team 11.Scale up of R&D developed products to kg scale and then technology transfer to pilot plant 12.Troubleshoot as appropriate for successful execution with intimation to supervisor 13.Discuss research findings and work plan on daily basis with supervisor/ manager and Mentor junior lab personnel 14.Document reactions, research findings/ observations accurately in lab note books to ensure data integrity 15.Participate in project meetings and prepare daily, weekly and monthly reports and submit to Manager 16.Writing regular updates, final reports, PDR preparations and inter departmental communications 17.Regular lab duties including equipment maintenance, chemical inventory and lab clean-up 18.Maintain strict IP Confidentiality and adhere to all related data privacy policies

Job Title -Manager Research & Development(R&D) - Agrochemical Qualification: MSc (Organic Chemistry with first class), Experience: 4+ years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 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 and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor Experience 8 - 14 Years Industry Engineering Engineering Design R&D Quality Qualification M.Sc, Ph.D/Doctorate Key Skills Research & Development R&D Chemist Research & Development Executive HPLC UPLC GC R&D Manager

JOB DUTIES AND RESPONSIBILITIES (Please Mention In Below Table) 1. Understand the project requirements & deliverables from supervisor/manager 2. Carry out literature search by using SciFinder, Reaxys and other search engines 3. Comprehend and discuss the MSDS with supervisor/ team members. 4. Identify and mitigate any potential safety risk with the help of Manager 5. Plan, setup, monitor, and workup chemical reactions independently 6. Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) 7. Isolate product and Optimize reaction conditions for improved yields and output 8. Purify compounds by different methods using chromatography, distillation and crystallization etc. 9. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc 10. Ensure parallel execution of multiple reactions conducted both by self and the team 11. Scale up of R&D developed products to kg scale and then technology transfer to pilot plant 12. Troubleshoot as appropriate for successful execution with intimation to supervisor 13. Discuss research findings and work plan on daily basis with supervisor/ manager and Mentor junior lab personnel 14. Document reactions, research findings/ observations accurately in lab note books to ensure data integrity 15. Participate in project meetings and prepare daily, weekly and monthly reports and submit to Manager 16. Writing regular updates, final reports, PDR preparations and inter departmental communications 17. Regular lab duties including equipment maintenance, chemical inventory and lab clean-up If any candidates is suitable for this opening please sent me your updated profile on this mail id. Experience 4 - 10 Years Industry Engineering Engineering Design R&D Quality Qualification Other Bachelor Degree Key Skills R&D Executive Agro Chemical Synthesis HPLC LCMS Methods & Analytical UV Troubleshoot Chemical Reactions Chemical Research

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 Preparation and review of Specifications, Method of analysis procedures and Analytical development reports Experience in making lab SOPs & study reports Experience 9 - 15 Years Industry Pharma R&D Biotech Qualification Ph.D/Doctorate Key Skills Analytical Development R&D Manger AM R&D R&D Method Feasibility Green Field Projects Research and Development UPLC HPLC GC Chemical Research

AM R & D For Agrochemical Industry Job Title : AM R and D Department : ADL Experience Required : 7+ Yrs Qualification : MSc (Organic chemistry) 1 Plan, setup, monitor, and workup chemical reactions 2 Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) 3 Isolate product and Optimize reaction conditions for improved yields and output 4 Purify compounds by different methods using chromatography, distillation and crystallization etc. 5 Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc 6 Ensure parallel execution of multiple reactions conducted both by self and the team 7 Scale up of R&D developed products to kg scale 8 Coordinate with senior team members to manage & deliver projects on time with high-quality standards of the deliverables 9 Regular lab duties including equipment maintenance, chemical inventory and lab clean-up 10 Document reactions, research findings/ observations accurately in lab note books to ensure data integrity 11 Participate in project meetings and prepare daily, weekly and monthly reports and submit to Manager 12 Maintain strict IP Confidentiality and adhere to all related data privacy policies Experience 5 - 11 Years Industry Engineering Engineering Design R&D Quality Qualification Other Bachelor Degree Key Skills Research & Development R&D Executive Agro Chemical Synthesis UPLC HPLC AM R & D ADL Chemical Analyst

Job Description Jubilant Bhartia Group 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, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services Jubilant Bhartia Group has four flagships CompaniesJubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited Currently the group has a global workforce of around 43,000 employees About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research servicesfrom target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)in partnership with leading worldwide healthcare companies With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology,in-vivo,in-vitromodels and translational sciences Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the worlds leading pharmaceutical, biotech companies, academic institutions and research foundations Find out more about us at www jubilantbiosys com The Position Organization : Jubilant Biosys Designation & Level: RA / SRA (S1/S2/S3/S4) Location: Greater Noida Department: Analytical Key Responsibilities Having exposure of 1-8y in analytical chemistry (HPLC/LCMS/NMR or purification) Interaction with synthetic team and problem solving skills Should be able to handle the respective instrument Knowledge of instrumental technique with its application Should be able to handle routine analysis independently on respective instrument Experience in method development on HPLC/LCMS will be desirable but not necessary Maintenance, cleaning, documentation and calibration of analytical instruments Maintain laboratory as safe working place Person Profile Qualification: - Sc (Analytical Chemistry) Experience: - 2 years of relevant experience Jubilant is an equal opportunity employer All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances

Job Description Jubilant Bhartia Group 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, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services Jubilant Bhartia Group has four flagships CompaniesJubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited Currently the group has a global workforce of around 43,000 employees About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research servicesfrom target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)in partnership with leading worldwide healthcare companies With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology,in-vivo,in-vitromodels and translational sciences Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the worlds leading pharmaceutical, biotech companies, academic institutions and research foundations Find out more about us at www jubilantbiosys com The Position Organization : Jubilant Biosys Designation & Level: Senior Research Associate (SRA-1/ SRA-2) (S3/S4) Location: Greater Noida Department: Synthesis Key Responsibilities Synthesis, purification, and characterization of novel intermediates Deliver small to large quantities of by novel chemical entities for drug discovery Work collaboratively in a team to drive chemistry projects forward Responsible for safe conduct of reactions Excellent knowledge in basic and advance organic chemistry Good knowledge in functional group conversion and multiple step synthesis Basic knowledge retrosynthetic analysis (desirable) Good expertise in handling pyrophoric reactions Good knowledge of TLC, column purification, extraction Excellence in analysing NMR, IR and Mass Spectrometry data Always adhere to safe laboratory practices Enthusiasm to work in a dynamic research environment Always stretch when project challenge increases Good knowledge in computer (MS-word/Excel/Power point) and structure drawing (Chem Draw/ISIS) and recording in electronic lab notebook Good communication and presentation skill Good in literature search using Sci Finder Person Profile Qualification: - Sc in Organic Chemistry or related field/ M Experience: (below are Sample points) 5-10 years of industry experiences with any leading CRO organization Jubilant is an equal opportunity employer All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances

Job Title - R&D Chemist Qualification: MSc (Organic Chemistry with first class), Experience: 4+ years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 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 and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor Experience 5 - 11 Years Industry Pharma R&D Biotech Qualification M.Sc Key Skills R & D Executive Synthesis LAB Agrochemical ADL R&D R&D Chemist GC UPLC HPLC

Job Title - R&D Chemist Qualification: MSc (Organic Chemistry with first class), Experience: 4+ years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 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 and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor Experience 5 - 10 Years Industry Pharma R&D Biotech Qualification M.Sc Key Skills Green Field Projects R&D Chemist UPLC GC R&D Developed R&D Executive Synthesis HPLC R&D Manager

Job Title - Sr.Officer/Officer- R&D Chemist Qualification: MSc (Organic Chemistry with first class) Experience: 1-7 years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 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 and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor Experience 3 - 9 Years Industry IT Software - Others Qualification M.Sc Key Skills Green Field Projects Agro Chemical Research and Development R&D Chemist CRO Scifinder Bharuch R & D Executive Research Analysis PDR Preparations Research Research Projects Chemical Agrochemical GC HPLC LCMS

Job Description Understand the project requirements & deliverables from supervisor/managerCarry out literature search by using SciFinder, Reaxys and other search engines.Comprehend and discuss the MSDS with supervisor/ team members.Identify and mitigate any potential safety risk with the help of Manager 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 and output Purify compounds by different methods using chromatography, distillation and crystallization etc.Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team cale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor Discuss research findings and work plan on daily basis with supervisor/ manager and Mentor junior lab personnel.Document reactions, research findings/ observations accurately in lab note books to ensure data integrity.Participate in project meetings and prepare daily, weekly and monthly reports and submit to ManagerWriting regular updates, final reports, PDR preparations and inter departmental communications