119 Nmr Jobs - Page 2

Key Skills and Competencies Experience in Organic Synthesis/Multi-step Synthesis. Handling reactions from mg to gram scale. Sound Knowledge of isolation, separation & purifications techniques. Experience in characterization and identification of Organic molecules usingspectroscopy techniques like NMR, IR, LCMS, HPLC. Positive and confident individual with strong work ethics. Team player and good communications skills.

Job Title : Synthetic Chemist, NCE R&D Qualification : M.Sc. or Ph.D. in Organic/Medical Chemistry Experience : 3-8 years of relevant experience in CRO, Discovery R&D, API, Agrochemicals at R&D lab. Location: Dev Research Centre (SML Ltd), Nerul, Navi Mumbai-400706 Job Description: SML Limited is looking for a talented and motivated synthetic/medicinal chemist to support our internal agro-discovery program. The successful candidate will synthesize and purify compounds for the biological evaluation of insecticides, fungicides, nematicides, herbicides, and plant growth regulators using standard and advanced organic synthesis procedures. The applicant should be able to develop and troubleshoot synthetic routes directed to the target molecules as well as to carry out basic analytical and structural data analysis. In this position, the potential of the applicant to innovate both in the design of synthetic routes and in the generation of new target proposals will be valued. Good communication skills and the ability to work independently and within an international team environment are required. Candidate Specifications Education and Experience M.Sc. or Ph.D. in organic or medicinal chemistry having excellent experience in synthesis and characterization of organic compounds. Have a sound knowledge of mechanistic and organic chemistry principles. Experience with a broad range of organic synthesis techniques (e.g. handling sensitive chemicals and working under an inert atmosphere) Excellent laboratory skills in the purification of compounds using different chromatographic methods, recrystallization, and distillation. Sound experience in the analysis of compounds using TLC. Interpretation of results obtained by spectroscopic techniques (MS, NMR, IR, etc.) Sound knowledge and experience in all aspects of laboratory safety and industrial hygiene Demonstrated ability to work effectively across multi-disciplinary teams. Proven ability to root cause and resolve technically challenging problems. Experience in performing literature searches using chemistry databases (SciFinder, Reaxys) Preparation and maintaining lab record books and project reports.

Summary of Job: To support a team of 25-35 scientists and taking comprehensive responsibility of on time Analytical support for projects with minimal or no supervision. Role requires complete ownership of the project, cross-functional team coordination. Key Responsibilities: oTo lead the LC-MS, Prep HPLC, HPLC and NMR teams and responsible projects delivery. oResponsible to understand the scope of project and scope changes, accordingly, providing guidance to the team. oResponsible to scientific review and interpretation of the analytical data to ensure the correctness and quality. oProject execution support, as required: Providing scientific guidance and resolutions to the team as and when needed. oTo review the data presented by Team Leaders (Three TLs, associated each by 6-10 scientists) and team and technically guides them further/suggest course correction, wherever required. oMonitor all the responsible projects, sample load, planning and ensuring to meet the TAT. oRegularly review the progress of the analytical TAT and work on the corrective actions. oTo be responsible for prescribed data generation, timely completion and review of Analytical results and data. oCommunication: Responsible for attending the client telecons wherever required 1.Cross-functional coordination: Should ensure the regular interactions with the chemistry team and other functional group like Sourcing team ( SCM), Operation excellence team. oQuotes: Providing the costing for analytical activities as per the project scope. oLaboratory maintenance: Ensure safety practices are in place, constant review of the lab requirements and upgrading. oDepartment initiatives – Take at least one initiative in the department to improve the department and Active participation in all management initiatives, group discussions. oCompliance: Comply with rules, guidelines, and trainings. Participate in general lab maintenance efforts and comply with regulated environment. oSafety: To ensure that appropriate personal protective equipment’s (PPEs), responsible for the safe working of the team in the laboratory and follows the safety precautions. oTeam management and development: Guide, train, and support team members to ensure quality work is delivered as planned. Ensuring proper distribution of tasks and resource utilization. Identify skills and mentor associates; assign responsibilities and follow up; feedback at regular intervals and maintain a record. Provide leadership and direct contribution to functional and/or cross-functional improvements. ExperiencePh.D. with more than 6 years or MSc with more than 8- 15 year’s experience in a API / CDMO Industry, of which minimum 5 years should be in CDMO.

Key Responsibilities Lead the synthesis and process optimization for Anisole and downstream products. Design synthetic schemes with a focus on scalability, yield, cost, and environmental safety. Deep understanding of reaction mechanisms and transformation strategies. Hands-on experience with a wide range of reactions including oxidation, alkylation, halogenation, demethylation, and aromatic substitution. Strong command of analytical techniques: NMR, HPLC, GC, MS, IR, UV-Vis. Execute bench-scale experiments and develop SOPs and process documentation. Identify reaction bottlenecks and provide troubleshooting solutions. Supervise, train, and mentor junior chemists and research staff. Coordinate cross-functionally with scale-up, production, EHS, and quality teams. Continuously monitor recent literature and patents to drive innovation and ensure competitiveness. Ensure strict adherence to lab safety protocols and regulatory compliance. Skills Required Tech transfer experience to manufacturing teams. Exposure to continuous flow chemistry or green chemistry principles. Strong documentation, project planning, and communication abilities. Proficient in ELNs, MS Office, and scientific databases (SciFinder, Reaxys). Technical/Functional Proficiency Required Proven track record of successful scale-up from lab to pilot/plant. Strong problem-solving mindset and ability to work in a fast-paced, project-driven environment. Educational Qualifications - M.Sc. or Ph.D. in Organic Chemistry or related discipline. Show more Show less

Description 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. Brief Job Overview If you want to help pharmaceutical researchers improve the quality of drugs, and you have experience developing analytical methods with quantitative nuclear magnetic resonance (qNMR), then the United States Pharmacopeia (USP) wants to talk with you! We have an immediate opening for a Scientist III in our Digital and Innovation group. This position plays a critical role developing the next-generation analytical and digital technologies for pharmaceutical R&D. The successful applicant will drive product and application development by understanding the technical capabilities of qNMR and quantum mechanics (QM) for chemical analysis, developing validated methods, investigate the potential of non-targeted analysis using solvent solubility and the application of the Life Cycle approach through QbD principles. The successful candidate will also collaborate with on-going studies as appropriate. For over 200 years, USP has worked as an independent, scientific nonprofit organization to build trust where it matters most: in the world's medicines, dietary supplements and foods. Through our rigorous science and the public quality standards we set, USP builds trust in the supply of safe, quality medicines. With USP’s unique mix of rigorous scientific research, exceptional world-wide brand recognition, and a rapidly evolving suite of digital products and services, the successful applicant can make a tangible contribution to USP’s mission of protecting patient safety and improving the health of people around the world. How will YOU create impact here at USP? Duties The position's purpose should provide a high-level overview of why the position exists and briefly identify the most critical priorities of the position. This is an opportunity to highlight any features or duties of the role which includes: Perform studies to evaluate the key parameters of NMR and their impact on QM based analysis and qNMR non-target analysis. Develop, optimize, and publish high-quality analytical methods using high-field NMR and qNMR applications; publications may include white papers, application notes, or journal articles; Acquire high resolution qNMR spectra and implement structural elucidation for obtaining chemical structural information to develop QM spectral analysis models; Collaborate in on-going studies to expand the digital NMR spectral database; Provide sound technical guidance on related product development projects to advance qNMR applications and integrate them within USP Manage project tasks, create appropriate work schedules, and create experiment plans; Troubleshoot and resolve method and instrumentation issues and implement risk-mitigating process controls to ensure high data quality; Review, interpret, and evaluate available scientific literature to assist in the landscaping of both high-field and benchtop qNMR applications in the pharmaceutical, nutraceutical, and foods industries; Collaborate with appropriate internal stakeholders and experts from across academia and industry to drive USP’s mission of developing public standards. 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 MSc./ M. Pharm. having 6-8 years’ experience for S-III in a scientific discipline, with NMR, qNMR and Quantum mechanics along with method development experience. Ph.D. having 1-3 years’ experience for S-III in a scientific discipline, with NMR, qNMR, Quantum mechanics along with method development experience. Experience in performing research towards the development and validation of high-quality analytical methods; Hands-on experience in using NMR (qNMR, quantum mechanics for qNMR modeling and analysis, HPLC, and other appropriate technologies); We especially welcome applications from those who hold historically marginalized and/or underrepresented identities. This job description provides a portrait of an ideal candidate. Candidates who possess many, though perhaps not all, qualifications are encouraged to apply. 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. Capability to plan and conduct rigorous scientific research independently; Skilled in evaluation and interpretation of data; Strong ability to collaborate with various internal and external stakeholders to achieve intended outcomes; Ability to multi-task; Skilled in anticipating, troubleshooting, and solving technical problems; Familiarity and ability to execute good laboratory practices (GLP); Detailed oriented with excellent Organizational and Project Management skills; Excellent communication and presentation skills, both verbal and written; to communicate complex scientific ideas to non-scientists; Takes personal responsibility to ensure work is delivered on time and is of the highest quality; Knowledge in the design, plan and build guidelines for standardizing spectral library/database is a plus; Knowledge of potential applications of spectral libraries is a plus; Understanding of good manufacturing practices (GMP) is a plus. Benefits Supervisory Responsibilities NA 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 Show more Show less

Description 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 III 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 1-3 years of Pharmaceutical industry experience MSc/MPharm from a recognized University. Minimum 6-8years 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 Show more Show less

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 Companies- Jubilant 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 services–from 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-vitro models 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 world’s 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: - Trainee research Associate/ A0 Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification and characterization of chemical intermediates. Deliver small to large quantities of novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Excellent knowledge of basic organic chemistry with mechanism. Good knowledge of Name Reactions & functional group transformation. Good knowledge of molarity, normality, equivalency. Practical experience in thin-layer chromatography, column purification and extraction. Good understanding of NMR, IR and mass spectrometry. Interest to adapt and knowledge of laboratory safety practices. Enthusiasm to work in a dynamic research environment. Good Soft & Scientific Communication skills. Person Profile Qualification: - M.Sc. in Chemistry/Organic Chemistry/Pharmaceutical Chemistry or related field or M. Pharma (Specialized in Organic Synthesis) with 0-1 years’ project experience. Experience: - 0-1 year of exp. 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. Show more Show less

We are actively looking for credible team members who would be primarily responsible for: Encompassing literature survey. Identifying techno commercially attractive and non infringing route for fluoro-specialty molecules identified for commercialization in time bound manner. Develop & standardize industrially feasible processes and also meet long term cost targets. Identify & develop new products. Prepare feasibility report, cost analysis report, monthly progress report and TDR Demonstrate/validate the lab scale process up to commercial scale Essential Lead a team of scientist and chemists for new products / process development and improvement of the existing products. Knowledge and understanding of synthetic methods, analytical methods and relevant products. Excellent skills in interpretation of analytical data from UV, IR, NMR, GC, GCMS & HPLC, LCMS, MS and so on. Well versed with GLP, GMP and IMS guidelines. Understanding of literature/ patents. Understanding and accomplishment of Customer requirements. Knowledge of SAP & IMS Educational Requirements : M.Sc. / Ph. D. with Organic Chemistry Experience required : 12-13 years of relevant experience in R&D, candidates with background of Fluoropolymers will be preffered Relevant and total experience Total Number of experience required - 12-15 Relevant experience required in - Fluorospecialities

Description 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 hands-on non-supervisory position responsible for the oversight and successful implementation and completion of all activities pertaining to a portfolio of Reference Standards (RS)/Analytical Reference Materials (ARMs) including but not limited to pharmaceutical analytical impurities, extractables & leachables, polymers and certified reference materials (CRMs). This incumbent is responsible for the timely preparation of procurement specification and collaborative testing protocols for all candidate lots, technical assistance for collaborating labs, analytical data review and preparation of summary reports, preparation of packaging and Quality Control testing instructions 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 SIII/SIV Position Has The Following Responsibilities Responsible for timely preparation of testing protocols for new/replacement reference materials, technical assistance for collaborating labs To review the analytical data received from the Collaborators and to prepare summary reports, 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. Coordinate with labs, and reviews/interprets data from international collaborative studies. To Coordinates for any additional necessary testing and assists other staff members in addressing the comments. To provide guidance on the interpretation of test data, Proposes and designs studies to obtain necessary data to resolve complaints. To support Documentary Standard team by peer review of draft monograph 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. Presents information to USP staff and external audiences. Facilitates additional cross-functional activities with other departmental staff and other USP staff. Performs 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 Scientist IV MSc in chemistry or related field with 8-10 yrs of experience (or) Ph.D. in chemistry or related field with 3-5 yrs of experience Scientist III MSc in chemistry or related field with 6-8 yrs of experience (or) Ph.D. in chemistry or related field with 1-3 yrs of experience with the following skills Hands on experience in interpretation of results, characterization of the compound by spectral techniques (NMR, MASS, and IR). Knowledge on chromatographic techniques (HPLC, GC) Ability to handle multiple priorities in a fast-paced environment. Excellent written and verbal communications skills. Additional Desired Preferences Ability to read and interpret spectroscopic analyses data (NMR, IR, MS etc.) Hands on experience on chromatographic techniques such as (HPLC, GC). Prior experience with materials characterization using a variety of analytical techniques. Prior experience with lab investigations. Stability studies exposure. 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 Show more Show less

Description 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. Brief Job Overview This is a hands-on non-supervisory position responsible for the oversight and successful implementation and completion of all activities pertaining to a portfolio of Reference Standards (RS)/Analytical Reference Materials (ARMs) including but not limited to pharmaceutical analytical impurities, extractables & leachables, polymers and certified reference materials (CRMs). This incumbent is responsible for the timely preparation of procurement specification and collaborative testing protocols for all candidate lots, technical assistance for collaborating labs, analytical data review and preparation of summary reports, preparation of packaging and Quality Control testing instructions. How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The SIII/SIV Position Has The Following Responsibilities Responsible for timely preparation of testing protocols for new/replacement reference materials, technical assistance for collaborating labs To review the analytical data received from the Collaborators and to prepare summary reports, 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. Coordinate with labs, and reviews/interprets data from international collaborative studies. To Coordinates for any additional necessary testing and assists other staff members in addressing the comments. To provide guidance on the interpretation of test data, Proposes and designs studies to obtain necessary data to resolve complaints. To support Documentary Standard team by peer review of draft monograph 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. Presents information to USP staff and external audiences. Facilitates additional cross-functional activities with other departmental staff and other USP staff. Performs 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 Scientist IV MSc in chemistry or related field with 8-10 yrs of experience (or) Ph.D. in chemistry or related field with 3-5 yrs of experience Scientist III MSc in chemistry or related field with 6-8 yrs of experience (or) Ph.D. in chemistry or related field with 1-3 yrs of experience with the following skills Hands on experience in interpretation of results, characterization of the compound by spectral techniques (NMR, MASS, and IR). Knowledge on chromatographic techniques (HPLC, GC) Ability to handle multiple priorities in a fast-paced environment. Excellent written and verbal communications skills. Additional Desired Preferences Ability to read and interpret spectroscopic analyses data (NMR, IR, MS etc.) Hands on experience on chromatographic techniques such as (HPLC, GC). Prior experience with materials characterization using a variety of analytical techniques. Prior experience with lab investigations. Stability studies exposure. 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 Show more Show less

Description 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. Brief Job Overview If you want to help pharmaceutical researchers improve the quality of drugs, and you have experience developing analytical methods with quantitative nuclear magnetic resonance (qNMR), then the United States Pharmacopeia (USP) wants to talk with you! We have an immediate opening for a Scientist III in our Digital and Innovation group. This position plays a critical role developing the next-generation analytical and digital technologies for pharmaceutical R&D. The successful applicant will drive product and application development by understanding the technical capabilities of qNMR and quantum mechanics (QM) for chemical analysis, developing validated methods, investigate the potential of non-targeted analysis using solvent solubility and the application of the Life Cycle approach through QbD principles. The successful candidate will also collaborate with on-going studies as appropriate. For over 200 years, USP has worked as an independent, scientific nonprofit organization to build trust where it matters most: in the world's medicines, dietary supplements and foods. Through our rigorous science and the public quality standards we set, USP builds trust in the supply of safe, quality medicines. With USP’s unique mix of rigorous scientific research, exceptional world-wide brand recognition, and a rapidly evolving suite of digital products and services, the successful applicant can make a tangible contribution to USP’s mission of protecting patient safety and improving the health of people around the world. How will YOU create impact here at USP? Duties The position's purpose should provide a high-level overview of why the position exists and briefly identify the most critical priorities of the position. This is an opportunity to highlight any features or duties of the role which includes: Perform studies to evaluate the key parameters of NMR and their impact on QM based analysis and qNMR non-target analysis. Develop, optimize, and publish high-quality analytical methods using high-field NMR and qNMR applications; publications may include white papers, application notes, or journal articles; Acquire high resolution qNMR spectra and implement structural elucidation for obtaining chemical structural information to develop QM spectral analysis models; Collaborate in on-going studies to expand the digital NMR spectral database; Provide sound technical guidance on related product development projects to advance qNMR applications and integrate them within USP Manage project tasks, create appropriate work schedules, and create experiment plans; Troubleshoot and resolve method and instrumentation issues and implement risk-mitigating process controls to ensure high data quality; Review, interpret, and evaluate available scientific literature to assist in the landscaping of both high-field and benchtop qNMR applications in the pharmaceutical, nutraceutical, and foods industries; Collaborate with appropriate internal stakeholders and experts from across academia and industry to drive USP’s mission of developing public standards. 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 MSc./ M. Pharm. having 6-8 years’ experience for S-III in a scientific discipline, with NMR, qNMR and Quantum mechanics along with method development experience. Ph.D. having 1-3 years’ experience for S-III in a scientific discipline, with NMR, qNMR, Quantum mechanics along with method development experience. Experience in performing research towards the development and validation of high-quality analytical methods; Hands-on experience in using NMR (qNMR, quantum mechanics for qNMR modeling and analysis, HPLC, and other appropriate technologies); We especially welcome applications from those who hold historically marginalized and/or underrepresented identities. This job description provides a portrait of an ideal candidate. Candidates who possess many, though perhaps not all, qualifications are encouraged to apply. 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. Capability to plan and conduct rigorous scientific research independently; Skilled in evaluation and interpretation of data; Strong ability to collaborate with various internal and external stakeholders to achieve intended outcomes; Ability to multi-task; Skilled in anticipating, troubleshooting, and solving technical problems; Familiarity and ability to execute good laboratory practices (GLP); Detailed oriented with excellent Organizational and Project Management skills; Excellent communication and presentation skills, both verbal and written; to communicate complex scientific ideas to non-scientists; Takes personal responsibility to ensure work is delivered on time and is of the highest quality; Knowledge in the design, plan and build guidelines for standardizing spectral library/database is a plus; Knowledge of potential applications of spectral libraries is a plus; Understanding of good manufacturing practices (GMP) is a plus. Benefits Supervisory Responsibilities NA 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 Show more Show less

Hi, Greetings from Biophore India Pharmaceuticals!! We are hiring for Synthesis R&D /Process R&D/CRO Experience: 3 to 6 Years Qualification: M. Sc ( Organic Chemistry) Walk In date : 19th November 2024, Tuesday . Timings : From 10:00 AM to 02:00 PM . Preferable Male Candidates only If any one not able to attend the interviews , share your CV to " recruitments@biophore.com "

SUMMARY Looking Both Fresher/Exp candidates ready to work in blended Process in Leading KOLKATA MNC , Salary upto 4 lpa Requirements Requirements * Any Undergraduate / Graduate fresher and exp with excellent english communication can apply * Should have excellent communication (read/write/speak) * Should be smart and have convincing skills * Doing outbound calls and providing information * Selling products and promos * Helping customer * Comfortable to work in rotational shift Benefits Benefits Direct Company payroll , PF+ESI+Incentives , Telephonic interview

Department ANKLESHWAR MFG.- U1 Job posted on Jun 02, 2025 Employment type P-P7-Probationer-HO Staff Investigation related support for quality/yield failures OOS/OOT/Deviations/Market complaints investigations Chemistry literature search, Interpretation of LCMS, GCMS, NMR etc., Structure Elucidation and Characterization report preparation Ecofriendly cost-effective process development related work (Cost reduction, Yield improvement etc) New Vendor Qualification related support (NVQ) Plant trouble shooting support (Plant monitoring, CFT discussions etc) Responsible for maintaining Lab Safety compliance (SMS ratings etc) Responsible for maintaining laboratory GMP/RA compliance To support HAZOPs, SHE Risk assessments etc Responsible for Capacity enhancement, effluent reduction etc support Capable to lead a synthesis lab Qualification : M.Sc (Chemistry) Background with ADL/QC IS Preferred. Experience : Min. 2 years + Experience in Zydus : Min. 12 months Apply on : Karishma.r.kadu@zyduslife.com with subject of ZTMP – PD lab

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Research Associate II – Nitrosamines (Characterization Team) Baxter Pharmaceuticals R&D is seeking a highly motivated scientist with proven expertise in liquid chromatography and mass spectrometry to join its Characterization team. As a key contributor within the Pharmaceuticals Global Business Unit, the successful candidate will oversee and apply state-of-the-art technologies in LC-MS and GC-MS in support of new and existing pharmaceutical products. The scientist in this role will support Nitrosamine studies, extractables and leachable studies, using mass spectrometry-based approaches to identify nitrosamines, potential leachables from container extracts and develop and validate LC/MS methods to quantify leachable compounds in finished drug product solutions. The candidate is expected to work independently in the laboratory, to direct studies, conduct independent experiments, and generate and interpret data to solve challenging analytical problems. What you'll be doing Perform chemical extractions of container closure systems and drug product solutions in the laboratory. Apply state-of-the-art mass spectrometry-based approaches to solve challenging problems. Develop and validate novel mass spectrometry-based analytical methods. Independently plan, execute, and manage projects/programs that both span multiple disciplines and utilize established methods, techniques, or approaches. Approve technical feasibility of complex design concepts within area of expertise; advise management regarding appropriate action. Interpret data, evaluate analytical results, identify trends/exceptions relative to product requirements, definitions, and/or project goals. Reach conclusions based on research analysis and incorporate recommendations into larger projects. Share research outcomes and methodology with team members and other divisional personnel. Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development to ensure compliance in all research, data collection, and reporting activities. Maintain an in-depth knowledge and understanding of GxP and related regulations and guidance. Be able to provide expert insights into such regulations so as to facilitate efficient product registration. Be an active participant in the generation, review, adoption, and interpretation of such regulations. What you'll bring Masters degree with at least 8-12 years, or PhD with 6-7 years in relevant discipline required. Must have formal training in mass spectrometry. Must be skilled in carrying out sophisticated mass spectrometric experiments, such as accurate mass and MS/MS, and in the interpretation of mass spectrometric data. Must have good knowledge of organic chemistry and other analytical disciplines, such as chromatography, NMR, IR, etc. Possess skills, or demonstrated scientific background for the development of the necessary skills, for the elucidation of unknown compound structure using a multidisciplinary approach. Experience in Nitrosamine, E&L testing/study design, environmental chemistry testing, and/or trace organic analysis preferred. Experience with complex method development and validation, particularly for quantitative LC/MS methods, preferred. Must be able to able to carry out strategy and vision set by upper management and be able to communicate the vision to more junior associates. Ability to make routine, and some less routine, decisions independently. Can effectively communicate with internal and external partners. Experience working in a regulated pharmaceutical environment (e.g., cGXP) preferred. Ability to learn quickly and to tackle problems in a timely manner using analytical chemistry skills. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

Key responsibilities of this job role include: Design and execute multistep organic syntheses under the supervision of senior scientists. Having knowledge of enzymatic reactions. Perform compound purification using techniques such as column chromatography, recrystallization, HPLC, etc. Characterize synthesized compounds using analytical techniques (NMR, LC-MS, IR, UV-Vis, etc.). Maintain accurate and detailed records of all experiments Participate in group meetings and contribute to scientific discussions. Ensure compliance with laboratory safety protocols and chemical handling guidelines. Assist in the preparation of reports, presentations, and research publications. Responsibilities Qualifications M.Sc. in Organic Chemistry, Medicinal Chemistry with 3-4 years of experiences or fresh Ph.D in organic chemistry.

Key Responsibilities Polymer Synthesis: Design, develop, and optimize emulsion polymerization, Polyurithane Dispersion (PUD) processes for the synthesis of water-based polymers for various applications Characterization: Conduct detailed chemical, physical, and mechanical testing of polymer products, including particle size analysis, viscosity measurements, and glass transition temperature (Tg) analysis. Scale-Up: Lead the scale-up of laboratory-scale processes to pilot and production-scale manufacturing while ensuring consistent quality and performance. Process Optimization: Improve process efficiencies, yields, and reproducibility through continuous process improvement strategies. Cross-Functional Collaboration: Collaborate with product development, marketing, and manufacturing teams to ensure that polymer products meet customer and regulatory requirements. Troubleshooting: Provide technical support for solving production issues related to emulsion polymerization processes and product quality. Documentation: Maintain comprehensive lab notebooks, write technical reports, and prepare presentations to communicate results and findings to internal and external stakeholders. Market Research: Stay updated with the latest trends and advancements in polymer science, particularly in emulsion polymerization, and provide input into the development of new product lines. Skills Required In-depth knowledge of emulsion polymerization techniques such as batch, semi-batch, and continuous processes. Strong understanding of polymer structure-property relationships. Experience with analytical techniques such as GPC, DSC, TGA, FTIR, NMR, GCMS, GPC etc. Familiarity with the development of polymer products for coatings, adhesives, paints, or similar industries. Knowledge of regulatory standards and environmental considerations for water-based polymers. Strong problem-solving, analytical, and communication skills. Technical/Functional Proficiency Required Emulsion Polymerization and PUD Techniques: Expertise in batch, semi-batch, and continuous emulsion polymerization processes. In-depth knowledge of free radical polymerization, dispersion polymerization, and miniemulsion polymerization. Knowledge of comonomers to tailor polymer properties, including hydrophobic/hydrophilic balance, Tg, and mechanical properties. Surfactants and Emulsifiers: Proficiency in selecting and using surfactants, emulsifiers, and stabilizers for emulsion polymer systems. Understanding of the impact of surfactants on particle size, stability, and final polymer properties. Polymer Characterization: Ability to use analytical tools for the characterization of polymer products: Particle size and distribution analysis using DLS or laser diffraction. Molecular weight distribution using Gel Permeation Chromatography (GPC). Glass transition temperature (Tg) and thermal stability using Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA). Mechanical properties such as tensile strength and elongation. Surface and interfacial properties using techniques like contact angle measurement. Formulation Chemistry: Experience with the formulation of emulsion polymers, PUD for specific applications such as adhesives, coatings, paints, textiles, or paper. Knowledge of additives (e.g., thickeners, coalescing agents, plasticizers) and their role in improving product performance. Educational Qualifications - Bachelor's/Master’s Degree in Chemistry, Polymer Science, Materials Engineering, or Chemical Engineering. Experience Level (If applicable) - Minimum 5-10 years of experience in emulsion polymer, PUD synthesis preferably in an industrial setting. Show more Show less

Job Description Sr. Responsibility Result Expected % of Time Spent 1 Analysis of compounds for various projects from medicinal chemistry team and lead NCEs. Quality output within set target by Group leader 60% 2 Analytical method development for new NCEs using different instrumental techniques like HPLC, LCMS, NMR, IR and SFC and other wet analysis Quality output within set target by Group leader 20% 3 Good analytical skills and basic knowledge of HPLC, LCMS, NMR and SFC instruments Quality output within set target by Group leader 20% Show more Show less

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. BE in chemical engineer with 4-5 years of experiences.

Key responsibilities of this job role include: Design and execute multistep organic syntheses under the supervision of senior scientists. Having knowledge of enzymatic reactions. Perform compound purification using techniques such as column chromatography, recrystallization, HPLC, etc. Characterize synthesized compounds using analytical techniques (NMR, LC-MS, IR, UV-Vis, etc.). Maintain accurate and detailed records of all experiments Participate in group meetings and contribute to scientific discussions. Ensure compliance with laboratory safety protocols and chemical handling guidelines. Assist in the preparation of reports, presentations, and research publications. M.Sc. in Organic Chemistry, Medicinal Chemistry with 3-4 years of experiences or fresh Ph.D in organic chemistry.

Summary of Job To be responsible for pre-formulation and preclinical formulation activities. To be responsible for designing the experiment under supervision and handling associated equipment's and operations along with interpretations. Key Responsibilities 1.Ability to design and execute pre-formulation experiments like solubility, pKa, log P, dissolution, intrinsic dissolution, bulk density, flow indices, solid-state assessment, excipient compatibility etc. 2.Completely conversant with hands on experience and/or interpreting data from pre-formulation studies of a compound including physicochemical, bulk, surface and particle properties. 3.Ability to design and execute preclinical formulations to support lead ID, lead optimization and clinical candidate selection, including but not limited to solution, suspension, powder for constitution, compound filled in capsules and basic tablet ability. 4.Reasonably conversant with hands on experience and/or interpreting data from solid-state equipment's like PXRD, MDSC, TG, DVS and other techniques like Polarizing and Hot-stage Microscopy and other dynamic image analysis techniques, specially during supporting solid form and salt screening. 5.An additional benefit would be to have operational experience of handling Particle size analyzer, HPLC, GC, Dissolution apparatus and Disintegration apparatus. 6.Ability to collate and scientifically present data & observations and provide scientific inputs in discussion with internal or external customers. 7.Proactively maintain the equipment's, facility and supporting systems as per established good lab handling processes, maintain requisite equipment and process SOPs and lean tools 8.Follow good documentation practices and have adequate exposure to record observations in Electronic Lab Notebook (ELN). 9.Proactive in aligning with new technologies and approaches to participate in continuous improvement needs of the business. 10.He/she should have sufficient knowledge chemical safety, comprehensive risk assessment of drug substance and safe handling. Qualification M. Pharma, M.Sc. or M Tech with relevant specialization in Pharmaceutical Sciences Experience 1-5 years Key Competencies (Technical, Functional & Behavioral) Technical & Functional Sound experience of fundamentals of pre-formulation and approaches used for preclinical formulation development of compounds. Basic knowledge on developing clinical formulation would be an added plus. Demonstrated capability in having understanding to design and interpret data from PXRD, modulated DSC, TGA, DVS, Microscopy and working operations of HPLC, GC, FT-IR, NMR, Dissolution, BET and other physical and physicochemical characterization techniques. Hands-on operating would be an added plus. Behavioral Aptitude to learn and excel. Proactive in technical & operational space. Ability to work in cross-functional team environment. Ability to contextualize the observations and attention to detailing. Effective communication skills and absorbing attitude.

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 Companies- Jubilant 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 services–from 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-vitro models 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 world’s 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: - Trainee research Associate/ A0 Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification and characterization of chemical intermediates. Deliver small to large quantities of novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Excellent knowledge of basic organic chemistry with mechanism. Good knowledge of Name Reactions & functional group transformation. Good knowledge of molarity, normality, equivalency. Practical experience in thin-layer chromatography, column purification and extraction. Good understanding of NMR, IR and mass spectrometry. Interest to adapt and knowledge of laboratory safety practices. Enthusiasm to work in a dynamic research environment. Good Soft & Scientific Communication skills. Person Profile Qualification: - M.Sc. in Chemistry/Organic Chemistry/Pharmaceutical Chemistry or related field or M. Pharma (Specialized in Organic Synthesis) with 0-1 years’ project experience. Experience: - 0-1 year of exp. 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. Show more Show less

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 Companies- Jubilant 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 services–from 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-vitro models 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 world’s 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: - Trainee research Associate/ A0 Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification and characterization of chemical intermediates. Deliver small to large quantities of novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Excellent knowledge of basic organic chemistry with mechanism. Good knowledge of Name Reactions & functional group transformation. Good knowledge of molarity, normality, equivalency. Practical experience in thin-layer chromatography, column purification and extraction. Good understanding of NMR, IR and mass spectrometry. Interest to adapt and knowledge of laboratory safety practices. Enthusiasm to work in a dynamic research environment. Good Soft & Scientific Communication skills. Person Profile Qualification: - M.Sc. in Chemistry/Organic Chemistry/Pharmaceutical Chemistry or related field or M. Pharma (Specialized in Organic Synthesis) with 0-1 years’ project experience. Experience: - 0-1 year of exp. 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. Show more Show less

For day to day sample extractions & instrument (LCMS/MS - GCMS/MS) sequencing Roles and Responsibilities Testing of various agriculture and food products for chemical and nutritional testing by standard and in-house methods Hands on expireance in Proximate Analysis Operating the lab instruments like pH meter, weighing balance, incubator, GCMS/MS & LCMS/MS, UPLC Preparation of standard solutions Daily maintenance of lab equipment. Following good laboratory practices Following disposal process for samples & solutions as per SOP. Accurate analysis and interpretation of test results Maintenance of laboratory documents and records Validation of methods and calibration/verification of instruments Ensuring purity and validity of CRMs Conduct sensory evaluations of food samples

Job description: Leadership role to manage team size of 20+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Planning and excution of projets in Analytical services Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Ensuring the compliance related to all the activities Method development/Validation experience in LC-MSMS, GC-MSMS and ICPMS instrument Preparation and Implementation of SOPs related to E& L,Stability studies, general laboratory processes and best guidance. Good knowledge of 21 CFR part 11, Data Integrity principals, good documentation practices in cGMP lab Monitor and management of day-to-day laboratory activities Subject Matter Expert for guiding extractables and leachable studies, Stability studies, Nitrosamine studies, PSD, PXRD, HPLC, GC-MS/MS, LC-MS/MS, ICP-MS, IC, Dissolution, UV-Vis, etc., including designing the preparation of protocols and report Extensive knowledge of preparation, reviewing and approval capability for standard operating procedure (SOP) and COA Sound knowledge of structural elucidation and interpretation using analytical techniques such as NMR, IR, HPLC, GC, LC-MS etc. Resolving the team conflicts and provide training to the team for development and empowers team members Provide scientific and leadership direction to team members Knowledge on LIMS Supporting in setting up lab facility and instrument distribution Good knowledge of laboratory safety and be a strong promoter of SHE activities in the lab. Skills Required: For M.Sc, 20-25 years of Analytical R&D/QC experience in CRO environment Excellent technical, problem-solving, writing, influencing and communication skills Strong leadership with excellent interpersonal skills, proven success of analytical projects and managing cross functional teams Demonstrative communication skills and confident in conveying information to internal/ external customers Skill for resolving the team conflicts and provide training to the team for development and empowers team members Behavioral Competencies: Excellent oral / written communication skills and flexibility to work in a dynamic environment Excellent in Knowledge sharing at all levels. If you're a fit, send your resume to . Please share only relevant profiles. Qualifications M.Sc -Analytical Chemistry/Organic Chemistry/General Chemistry/Industrial Chemistry