213 Nmr Jobs - Page 2

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive - API R&D Date: Jul 25, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Role: To execute activities related to R&D Peptide Process Development & Scale-ups, along with a group comprising of Research Officers/ Research Assistants in co-ordination with Team/Group Leader Details Of Previous Work Experience (Mandatory Requirement) Literature search and ROS (Route of Synthesis) finalization Basic knowledge of Orthogonal protected amino acid and Peptide Solid phase peptide Synthesis/Oligonucleodtide Synthesis Handling of hazardous chemical like Trifluoroacetic acid Knowledge of handling of analytical HPLC/Oligo Synthesis Purification using Preparative HPLC Preparative column packing and usage. Computer literacy etc. Knowledge of Phosphoramidalin /handling/storage Job Description: Literature search with respect to assigned project and finalizing the non-infringing synthetic route Experimentation (Process development, DoE study, optimization and validation). Purification of Peptide and knowledge of lyophilisation of pure solution. Handling of analytical HPLC and preparation of buffer. Characterisation of Peptide using HRMS,2D NMR, IR, Peptide mapping and sequencing. Preparation of Technology transfer documents. Scaling-up of process developed at R&D. Assisting to RA in filing DMF. General Laboratory Management etc. Apply Now » Apply Now Start applying with LinkedIn Please wait...

Role To execute activities related to R&D Peptide Process Development & Scale-ups, along with a group comprising of Research Officers/ Research Assistants in co-ordination with Team/Group Leader Details Of Previous Work Experience (Mandatory Requirement) Literature search and ROS (Route of Synthesis) finalization Basic knowledge of Orthogonal protected amino acid and Peptide Solid phase peptide Synthesis/Oligonucleodtide Synthesis Handling of hazardous chemical like Trifluoroacetic acid Knowledge of handling of analytical HPLC/Oligo Synthesis Purification using Preparative HPLC Preparative column packing and usage. Computer literacy etc. Knowledge of Phosphoramidalin /handling/storage Job Description Literature search with respect to assigned project and finalizing the non-infringing synthetic route Experimentation (Process development, DoE study, optimization and validation). Purification of Peptide and knowledge of lyophilisation of pure solution. Handling of analytical HPLC and preparation of buffer. Characterisation of Peptide using HRMS,2D NMR, IR, Peptide mapping and sequencing. Preparation of Technology transfer documents. Scaling-up of process developed at R&D. Assisting to RA in filing DMF. General Laboratory Management etc.

Aquaworks Private Limited As a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway—you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone’s empowered to be their best. Supervises a team of scientists who conduct theoretical or applied scientific research aimed at advancing technical knowledge and/or solving complex problems. Monitors progress of projects and reviews experiments to ensure that they adhere to established quality standards. Marmon Water Research Center – IIT-Madras ICCW, Chennai, India Position: Domain / Subject Matter Expert, Membrane Modification/ Adsorbent/Absorbent Innovation [Alternative: Sorption Innovation (Ion Exchange, Adsorption, Absorption] Marmon Water, Inc., a Marmon Holdings, Inc., Berkshire Hathaway Company, has established a research and innovation center at IIT-Madras ICCW Chennai, India. Marmon Water is an international leader in water treatment technologies, systems and chemistries with manufacturing and product development centers located in the United States, India, China and Singapore. The Marmon Water Research Center – India will be dedicated to working with all Marmon Water Business Units to develop innovative technologies that will be disruptive to our industry. Reports to: Director, Marmon Water India Research Center Responsibilities And Duties Independently research new sorption technologies: membranes/ adsorbent/ absorbents/ exchangers In collaboration with the Business Unit Technical Teams, maintain and update a pertinent literature and patent library, periodically report on status. Examine other global literature sources as available. In collaboration with the Business Unit Technical Teams, find, review and screen new technologies based on technical viability, potential IP position and ultimate cost to implement. Develop promising technologies to a proof of concept stage up to and including lab scale technology/process studies to prove/define process and viability. Document and report on all efforts. Interactively support ongoing development of technologies once past proof of concept stage. Directly design, conduct and analyze sorption experiments in coordination with the Business Units’ technical team. The Candidate Will Be Expected To Work with the business units to find, evaluate and develop new technologies from worldwide sources (universities, startups and other companies). Staff and develop a high-level team that can: Design patentable solutions through the proof-of-concept stage for handoff to the business units’ technical teams. Technology focus will be on water treatment solutions to improve water quality and consumer health. The candidate will need to have a working knowledge of Intellectual Property processes both in India and the United States. Understanding user needs through the eyes of our business and marketing teams; solving problems with unique technology(ies). Selection Criteria Qualifications: Ph.D. in Polymer/Organic Chemistry, Material Sciences, or closely related field. Preference to: Candidates who have shown a background in functional polymer synthesis and water treatment. 1-2 years minimum experience in a technology discovery/development role in water related field. Experience with experimental design Experience with polymer modification Experience in Analytical Instrumentation and analytical methods to support development and performance evaluation. Including: NMR, ICP-MS, GPC, GC-MS, FTIR, SEM, TGA, extractables, others Experience in contaminant reduction technologies a plus. Self-starting/motivated. Able to assess work, draw conclusions and move forward independently. Outstanding organizational skills. Lead by example – including conducting laboratory experiments, Strong team skills – will need to work sufficiently closely with Marmon Water Business Units. If chosen, candidate will be part of the Marmon Water Sorption Team, which meets monthly by conference call to discuss sorption related technologies and challenges in testing. Proficient computer skills (Microsoft Office, i.e., Word, Excel, PowerPoint, etc.). Physical Demands/Work Environment: Work in a laboratory environment safely with chemicals/materials/apparatuses as needed to develop/demonstrate sorption technologies. Due to the nature of this position, the applicant will be exposed to potentially hazardous substances. Leadership ability: Proven track record of accomplishment leading research efforts and teams. Technical achievement: Proven expertise in chosen discipline including patents and publications. Has presented at international academic or industrial conferences in English. Ideal Competencies Results oriented leader. Hands-on leader who leads by example. Collaborative. Strategic Thinker. Mastery of US English. Excellent presentation skills. Able to achieve results with limited resources. Desirable Personal And Professional Characteristics Candid, ethical, integrity Empathetic Able to make tough decisions. Travel International and regional travel required. Travel 10-20%. Salary Range Competitive salary and benefits. Marmon Water is seeking candidates for the position of Domain Expert, functional materials, to be a part of our innovative technology teams. The candidate must have knowledge of synthesis of the functional polymers and its characterization using NMR, FTIR, TGA, GPC etc. The candidate should have a personal and professional interest in clean-water technologies with a background in functional polymers/media / resin/membrane development and testing. The ideal candidate will hold a PhD in Polymer Chemistry, Materials Science, or similar with a research emphasis on the design or evaluation of advanced water treatment technologies. Candidates not having this specific research background will be considered if they have worked in a technology development role in the design or evaluation of media and fiber technologies to remove contaminants form water. The candidate will be responsible for coordinating research activities between the MW Business Units and the MWRC – India. The preferred candidate will have proven leadership experience, but will be expected to build equipment, carry out experiments and enjoy working in the laboratory. The preferred candidate will have a background in research and development, and experience in writing and evaluating patents. The ideal candidate will work with Marmon Water worldwide technical teams to find and evaluate new technologies to treat known and emerging contaminants. Travel up to and including 30% should be expected. This person will report to the Director of the Marmon Water Indian Research Center. The Domain Expert, Functional Polymer, will be working alongside other Domain Experts and is expected to generate innovative ideas and solutions for water treatment technologies (in the sorption field). Semiannual trips to international locations for collaboration both internal and external to Marmon Water will be expected. As the Marmon Water Research Center – India is being developed, Marmon Water seeks out candidates who are willing to work in a start-up like atmosphere. This is a great opportunity to build a research program and team to deliver innovative technologies to the water treatment market. Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.

Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (JRF) in a time bound research project for a temporary period, purely on contractual basis as per the following details. Position Junior Research Fellow (JRF) Number of Vacancy 01 Project Title High temperature corrosion and mechanical behavior of AM fabricated Haynes 282 alloy Department Mechanical Engineering Project Tenure 3 years Job Description The project aims to investigate the corrosion behavior and high temperature mechanical behavior of additively manufactured Haynes 282 alloy. Knowledge about Selective Laser Melting, corrosion, Fatigue, microstructural characterization is required. Strong communication and writing skills are desirable. Essential Qualification Minimum requirement: B.Tech in Mechanical Engineering/Materials Engineering/ Materials and Metallurgical Engineering with a valid GATE score. Desirable: M.Tech in Mechanical Engineering/ Materials Engineering/ Materials and Metallurgical Engineering with a valid GATE score. Age Limit JRF-28Yrs. Age relaxation The upper age limit is relax-able up-to 5 years in the case of candidates belonging to scheduled castes/tribes/OBC, women and physically handicapped candidates. Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m. Principal investigator Dr. Devasri Fuloria Assistant Professor Senior (Grade I) School of Mechanical Engineering Vellore Institute of Technology Vellore, Tamil Nadu - 632014 Send your resume along with relevant documents pertaining to the details of qualifications, GATE/NET score card, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (5/08/2025) through online http://careers.vit.ac.in Please note that the CV should include contact details (address, mobile phone no., email ID), date of birth, qualifications mentioned clearly. Complete information regarding publications of research papers in SCI Journals should be mentioned in the CV. Incomplete applications will be rejected. No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We are seeking a skilled and detail-oriented Analytical R&D Analyst with a strong foundation in organic chemistry and spectroscopy. The ideal candidate will bring hands-on experience in analytical method development and validation, along with expertise in operating a wide range of analytical instruments. This role supports API development and impurity profiling, while ensuring compliance with global regulatory standards. Key Responsibilities Analytical Method Development & Validation Develop and validate HPLC/GC test methods for diverse regulatory markets Perform troubleshooting and support OOS investigations during validations Conduct trace analysis, related substances testing, and carryover evaluations Prepare protocols and reports in line with data integrity and GMP guidelines Instrument Operation & Maintenance Handle routine operation and calibration of HPLC, IR, UV, Karl Fischer Titrator, Halogen Moisture Analyzer, Polarimeter, and wet lab techniques Operate advanced detection systems such as UV-PDA, ELSD, CAD, IR, and Mass detectors Manage routine troubleshooting and preventive maintenance of analytical instruments Spectroscopic Characterization & Data Interpretation Perform structure elucidation and characterization of APIs and impurities using spectroscopy Interpret analytical data using NMR, MS, DSC, TGA, and FTIR techniques Support identification of known/unknown impurities and intermediates Documentation & Compliance Maintain lab notebooks, calibration records, and validation documents Ensure compliance with GLP, GMP, and safety protocols during lab operations Work collaboratively with cross-functional teams including QA, QC, RA, and manufacturing Qualifications The ideal candidate will have: M.Sc. in Organic / Analytical Chemistry. 4 to 7 years of experience in a relevant field Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

LOCATION Hyderabad, India DEPARTMENT Chemistry Solutions Responsibilities– o Improvedelivery efficiency and quality through delivery management : o Collect samples forconducting analytical tests o Develop analytical methodsfor intermediates and final compounds o Prioritize and prepare samplesfor the required analysis o Conduct purification ofcompounds through prep HPLC/ MS - Prep HPLC/ SFC o Process HPLC/ LCMSchromatograms to analyze molecules and enrich purity of the intermediates/final compounds o Conduct calibration ofHPLC/ LCMS/ GCMS/ NMR instruments o Analyze the samples usingHPLC, Wet Analysis, NMR, GCMS and LCMS etc. o Prepare report with testresults and release as per agreed timelines o Prepare certificate ofanalysis for the final/ intermediate compounds o Ensure safety at work throughenforcement of best lab management practices : o Handle all chemicals and instrumentsin a safe manner, adhere to the lab safety practices and ensure compliance o Communicate to the in-houseengineer/senior team members immediately in case of any instrument break down o Record, maintain and updatethe analysis in an accurate manner on a continuous basis o Maintain data integrity andIP confidentiality : o Maintainstrict IP Confidentiality and adhere to all related policies o Ensure skill development of self and new teammembers: o Enhance knowledge relatedto NMR, HPLC, GCMS, LCMS, ATR generation and wet analysis etc. o Coach new joinees andjunior team members on various analytical instruments Additional Responsibilities: Reporting Team Reporting Designation: Reporting Department: Educational qualifications preferred Category: Field specialization: Degree: Academic score: Institution tier: Required Certification/s: Required Training/s: Required work experience Industry: Role: Years of experience: Key Performance Indicators: Required Competencies: Required Knowledge: Required Skills: Required abilities Physical: Other: Work Environment Details: Specific requirements Travel: Vehicle: Work Permit: Other details Pay Rate: Contract Types: Time Constraints: Compliance Related: Union Affiliation:

This position is no longer available. University: IRCELYON / CNRS (Université Claude Bernard Lyon 1) Country: France Deadline: Not specified Fields: Chemistry, Chemical Engineering, Materials Science, Environmental Science, Renewable Energy PhD Position – Solar Valorization of Biomass via Photoelectrochemistry IRCELYON / CNRS in Villeurbanne (Lyon), France, invites applications for a fully-funded, 3-year PhD position as part of the ANR SOLBIOPEC project, in collaboration with INL Lyon and CEA Saclay. Project Overview The project focuses on the development of photoelectrochemical (PEC) devices to convert biomass-derived compounds (such as furfural and HMF) into high-value chemicals, including furfuryl alcohol, 2-methylfuran (biofuel), and FDCA (bioplastic precursor). Research activities will involve the integration of advanced III-V photocathodes, oxide photoanodes (WO₃/BiVO₄), and operando spectroscopy techniques (Raman, XPS, FT-IR, XAS). The successful candidate will have access to synchrotron facilities (SOLEIL, ESRF, MAX IV). The ultimate objective is to develop a functional PEC demonstrator for rural biorefinery applications. Candidate Requirements Master’s degree in Chemistry or Chemical Engineering. Solid theoretical background in electrochemistry. Experience with analytical techniques (NMR, XRD, GC, HPLC) is desirable. Demonstrated interest in solar energy, green chemistry, and sustainable materials. Position Details Location: IRCELYON, CNRS – Lyon, France Start Date: October 2025 Salary: Approximately 1700 €/month Duration: 36 months Also See Postdoctoral Opportunity in Exsolution-Based Electrode Design for High-Temperature… Two Ph.D. Positions in Advanced Material Recovery and Printing Technologies at… PhD Opportunity in Digital Twin Development for Climate-Resilient Railway Infrastructure at… Fully Funded PhD Position in Advanced Water-In-Salt Electrolytes for Aqueous Batteries PhD Opportunity in Organic Chemistry – Exploring Prebiotic Peptide Synthesis via the Lossen… Application Procedure Interested candidates should send a CV and cover letter to mathieu.prevot@ircelyon.univ-lyon1.fr For further information, please visit: www.ircelyon.univ-lyon1.fr This position offers a unique opportunity to engage in interdisciplinary research at the intersection of renewable energy, electrochemistry, and biomass valorization, with access to world-class laboratories and research infrastructure in France. Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register

COMB Discovery Services is a Chemistry Services Provider with expertise in Organic Synthesis / Process Research and Development of Pharmaceuticals and Chemicals related to diverse segments viz. API intermediates, Dyes, Agrochemicals, Energy Materials etc. We are looking for highly motivated and dynamic young Research Chemist. Position : Trainee - Research Chemist Education Qualification : Master of Science – Chemistry Work Experience: Fresh Pass out from College / university. Job Responsibilities: · Independently responsible for the execution of Synthesis project in a timely manner under guidance of Senior Research Chemist. Carry out literature search and propose synthesis plan for discussion and approval. Resolve problems faced during synthesis and purification. · Adept at factual documentation of experiments as per GLP guidelines. · Eager to Learn, update and practice futuristic organic synthesis skills under the supervision of Senior Research Chemist. · As a member of synthesis team participate in all synthesis and scale up activities related to successful completion of project. · Follow good laboratory practices and safety protocols in a disciplined manner under guidance of Senior Colleague. Desired Skills: · Good knowledge of Organic Chemistry and Synthesis. · Interpretation of Characterisation data for structural elucidation viz. HNMR, 13C NMR, IR and Mass. · Knowledge of In-process control techniques viz. Chromatography (TLC, GC, HPLC etc.) · Self-Motivation to Work Hard and Desire to learn for the success of the Team. · Be a Positive and Supportive Team Member. Job Types: Full-time, Permanent, Fresher Pay: ₹10,000.00 - ₹20,000.00 per month Benefits: Health insurance Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Plan and conduct multi-step organic syntheses to develop novel molecules.Work closely with cross-functional teams, including medicinal chemists,biologists, and analytical scientists to advance drug discovery projects. Required Candidate profile - Experience in medicinal chemistry or CRO environment, preferably in drug discovery, or custom synthesis. - Proficiency in synthetic organic chemistry.

Job Description : Literature search, understanding of Quality by design, design of experiments, US-FDA product specific guidance, EMA guidelines, ICH guidelines, Statistical tools required in product development. Exposure of different software’s and tools required for QBD and DOE. Prototype formulation design to Lab scale development, process optimization using DOE and modern approach. Understating of complex APIs, Polymers, lipids and peptides APIs, Impurities. Characterization of complex formulations by advance techniques and interpretation of data. Understanding of DSC, AFM, DLS, SEM, TEM, Cryo-TEM, Raman-Spectroscopy, NMR, PXRD, SAXS, Zeta Sizer. Should be experience in Lab scale, scale up and technology transfer of complex process for exhibit/validation at GMP sites, optimization of critical process parameters at large scales. Should be experience in preparations and review of protocols, reports and Product development reports, Manufacturing Formulation Records, BMRs, Products Specifications. Should be experience in Product development as per the regulatory requirements of US-FDA, MHRA, and EMA. Different filling stages to approval process. Regulatory queries handling, preparation of justification. Should be experience in Product development by QbD approach (QTPP, CQA, CMA, CPP), Risk assessment by FMEA. Should be experience in Team handling and experiment design, planning, data interpretation, complex analytical methods. Should be experience in GLP/GMP compliance requirements, Different SOPS of Development Lab. Understanding of Pre-clinical studies, Bio equivalence studies, clinical studies (phases) Skills & Qualification : Microspheres Depot, Liposomes, Nanoparticles, Emulsion, Lyophilized injection - Minimum 07-12 years of experience required - M.Pharm (Pharmaceutics/Pharmaceutical Technology), Ph.D. (Preferred)

LOCATION Hyderabad, India DEPARTMENT Chemistry Solutions Responsibilities– Enhance client’ssatisfaction score: o Assessclient’s feedback to identify gaps o Closeidentified gaps to improve client satisfaction score Improve delivery efficiencyand quality through delivery management : o Collectsamples for conducting analytical tests o Developanalytical methods for intermediates and final compounds o PrepareStandard Operating Procedures (SOP) for instruments to be used for tests o Raiserequisition for procurement of chemicals/ consumables/ solvents/columns in atimely manner o Prioritizeand prepare samples for the required analysis o Conductpurification of compounds through prep HPLC/ MS - Prep HPLC/ SFC o ProcessHPLC/ LCMS chromatograms to analyze molecules and enrich purity of theintermediates/ final compounds o Conductcalibration of HPLC/ LCMS/ GCMS/ NMR instruments o Analyzethe samples using HPLC, Wet Analysis, NMR, GCMS and LCMS etc. o Preparereport with test results and release as per agreed timelines o Preparecertificate of analysis for the final/ intermediate compounds o Troubleshootthe analytical methods and instruments Ensure safety at workthrough enforcement of best lab management practices : o Handleall chemicals and instruments in a safe manner, adhere to the lab safetypractices and ensure compliance o Communicateto the in-house engineer/senior team members immediately in case of anyinstrument break down o Record,maintain and update the analysis in an accurate manner on a continuous basis Maintaindata integrity and IP confidentiality : o Maintainstrict IP Confidentiality and adhere to all related policies Ensure skill development ofself and new team members: o Enhanceknowledge related to NMR, HPLC, GCMS, LCMS, ATR generation and wet analysisetc. o Coach new joinees and junior team members on various analytical instruments Additional Responsibilities: Reporting Team Reporting Designation: Reporting Department: Educational qualifications preferred Category: Field specialization: Degree: Academic score: Institution tier: Required Certification/s: Required Training/s: Required work experience Industry: Role: Years of experience: Key Performance Indicators: Required Competencies: Required Knowledge: Required Skills: Required abilities Physical: Other: Work Environment Details: Specific requirements Travel: Vehicle: Work Permit: Other details Pay Rate: Contract Types: Time Constraints: Compliance Related: Union Affiliation:

💊 Job Title: Junior Medicinal Chemist 📍 Company: Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) 📌 Location: Gagillapur, Hyderabad. 📧 Apply at: jobs@morepenpdr.com 📞 +91 6302 451 459 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 Master’s 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 . Application Process To apply, submit your updated CV and a cover letter highlighting your relevant experience to: 📧 jobs@morepenpdr.com MPDRPL is an equal opportunity employer committed to a diverse and inclusive workplace.

Interested candidates, kindly mail to enpcareers.hr@ril.com Job Accountabilities: Design Scope of Work for Logging Services Evaluate EOI / Technical Bids Real time log monitoring, QA /QC Condition log data Handling Log Data Analysis Software Select side wall core, formation tester pertest and sample depths Process & Analyze Advanced Logs (Sonic Waveform, Image, NMR etc.) Petrophysical Evaluation, providing average reservoir parameters at the well for Geological model building and resource estimation Petrophysical facies identification by integrating log data, Image data, Core (RCA and SCAL) data for static geological model and Integrated subsurface description (ISD). Petrophysical evaluation of Unconventional Reservoirs Raise PRs & Verify Invoices Evaluate Casing & Cement Bond logs Adhere to Log Data compliance QC of Vendor Deliverables Support and deliver within budget Log data acquisition and processing Skills Required: Detailed Knowledge of Principles & Applications of Different Logs Qualification and Experience: Master’s degree in Geophysics or Geology from a recognized university Minimum 5 year’s experience in E&P Very Strong technical abilities in Integrated formation evaluation / petrophysical Interpretation. Interested candidates, kindly mail to enpcareers.hr@ril.com

Job Title: Jr. Scientific Officer, Department of Chemistry Reports to: Head, Department of Chemistry Location: Sonipat Experience (in years): Minimum 5 years in a similar role Nature of work: The Junior Scientific Officer (NMR) is responsible for the operation and supporting maintenance, the NMR instrument. The role involves sample analysis, data acquisition and processing, basic troubleshooting, and assisting in method development. The position requires sound knowledge of NMR principles, attention to detail, and a commitment to maintaining high-quality analytical results. The officer may also assist in training users, managing instrument schedules, and supporting collaborative research or industrial service projects. About Department of Chemistry: The Department of Chemistry at Ashoka University is a vibrant hub for interdisciplinary learning and advanced research in the chemical sciences. Located in Sonepat, Haryana, the department offers rigorous undergraduate and Ph.D. programs that bridge chemistry with physics, biology, and computational sciences, preparing students for diverse scientific challenges. The department emphasizes cutting-edge research in areas such as sustainable chemistry, nanoscience, materials, chemical biology, theoretical and computational chemistry. The department has state-of-the-art laboratory facilities with modern instrumentation. The department also fosters collaboration with industry and academic institutions, encouraging innovation, scientific curiosity, and real-world application of knowledge. Its mission is to produce high-quality research and cultivate a new generation of scientists equipped to contribute to global and national scientific advancement. Role and Responsibilities: 1. Operation, management, and maintenance of NMR instrument and facility lab 2. Analysis of samples using appropriate protocols 3. Documentation & Compliance Maintain detailed logs of experiments and sample data. Ensure compliance with laboratory safety and quality standards (e.g., GMP, GLP). 4. Method Development Develop or optimize NMR methods for new compounds or materials in consultation with research groups Validate new NMR protocols. 5. Instrument Maintenance Perform routine maintenance including tuning, calibration, and cryogen refills. Troubleshoot issues and liaise with technical support for repairs. 6. Training & Collaboration Train other staff or students in NMR operation and safety. Conduct training workshops Collaborate with research groups at Ashoka University and other institutes. 7. Inventory & Supplies Manage consumables like NMR tubes, deuterated solvents, and cryogens. Coordinate with vendors or purchasing departments. 8. Lab safety and waste management Follow and enforce lab safety protocols, including handling of solvents and cryogens. Manage chemical waste disposal in accordance with institutional and environmental regulations. Conduct regular checks to ensure safe working conditions in the NMR lab. 9. Advertisement of Facilities to Academia and Industry Promote the capabilities and availability of NMR services to external academic institutions and industry partners. Develop outreach materials, presentations, or participate in events to attract users and increase facility utilization. 10. Any other instructions received from Head, and HR.

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

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice. Process Development Scientist I POSITION PURPOSE: The Process Development Scientist-I with some supervision from the Chemical Development Lead focuses on the route scouting and Chemical Process Development of Bayers' existing and pipeline crop protective agents. Collaborates with all internal and external functional teams. The job holders ensure all the experimental work is done following the highest safety standards and document the generated data in the Electronic Lab Notebook. The applicant will have an excellent practical and theoretical understanding of synthetic organic chemistry or a relevant technology and can design and execute high-quality, thoughtful experimentation while making significant contributions both independently and as a member of a team. The candidate will work within an interdisciplinary and cross-divisional team in the Crop Protection Innovation organization. TASKS AND RESPONSIBILITIES: Conduct process chemistry research as an individual contributor, which includes, but is not limited to, research on inventing new synthetic routes and associated manufacturing processes that turn the molecules into agrochemical solutions Conduct experiments for route scouting, process optimization, safety evaluation, high throughput screening and chemo/biocatalytic reaction discovery and optimization. Invent synthetic routes and develop safe, robust, and cost-effective processes to manufacture Crop Protection Agents developing the synthetic routes Contribute to the Chemical Development Process by conducting laboratory experiments by own hand and providing experimental results, technical updates, documentation, data interpretation, recommendations for process optimization, etc. With the help of the Process Engineer optimize unit operations Investigate optimization, generate safety and process engineering data required for scale-up of chemical reactions This is a highly practical role where you will be working in the R&D laboratories to generate new synthetic routes and assist in the design, planning and execution of multi-step experimental studies guided by risk assessment to deliver safe, efficient, robust manufacturing processes. Collaborate within project teams by working closely with analytical chemists, process engineers, pilot plant team and project managers within the Crop Protection Innovation organization. Staying up to date with the latest advancements in chemistry and technologies. Find opportunities to use these technologies in solving process development challenges Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs. Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices. KEY WORKING RELATIONS: Internal Crop Protection Innovation Team Analytical Chemist from Pilot Plant Team AIM Production Team AIM Analytical team at Vapi External Coordinate with various vendors and engineers for instrument installation/maintenance activities WHO YOU ARE: M.Sc/M.Pharm in Organic Chemistry with more than 8 year’s experience or Fresh PhD or PostDoc in Organic Chemistry in designing and performing experiments in a laboratory setting to meet project timelines and objectives. Experience in independent planning and execution of experiments for multistep synthesis of complex organic molecules. Experience in independent interpretation of data from experiments and using it to make conclusions/decisions regarding the direction of future experimentation Comprehensive and state-of-the-art knowledge of modern synthetic methodologies as well as a basic understanding of organic reaction mechanisms and retrosynthesis. Strong understanding of small molecule analysis including chromatographic and spectroscopic techniques and structure elucidation by NMR and Mass Spectroscopy is required Embraces ambitious goals and drives progress with urgency. Consistently seeking opportunities to acquire knowledge, develop skills, and share insights. Possesses a strong willingness to learn and grow through challenging experiences, actively engaging in giving and receiving constructive feedback to foster continuous improvement. Effectively interacts with diverse teams across functions, cultivating strong working relationships with both internal and external collaborators to enhance overall performance Ability to work in the shifts Ever feel burnt out by bureaucracy? Us too. That’s why we’re changing the way we work— for higher productivity, faster innovation, and better results. We call it Dynamic Shared Ownership (DSO). Learn more about what DSO will mean for you in your new role here https://www.bayer.com/en/strategy/strategy Bayer does not charge any fees whatsoever for recruitment process. Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext. Please don’t rely upon any unsolicited email from email addresses not ending with domain name “bayer.com” or job advertisements referring you to an email address that does not end with “bayer.com”. YOUR APPLICATION Bayer is an equal opportunity employer that strongly values fairness and respect at work. We welcome applications from all individuals, regardless of race, religion, gender, age, physical characteristics, disability, sexual orientation etc. We are committed to treating all applicants fairly and avoiding discrimination. Location: India : Gujarat : Vapi Division: Crop Science Reference Code: 833702 Contact Us 022-25311234

. The Development Geologist cum Modeller will lead theintegration of geological, geophysical, petrophysical, and engineering data todevelop robust static models for field development and reservoir management.The incumbent will be a key player in multidisciplinary teams, contributing tostrategic decision-making through technical excellence and cross-functionalcollaboration. Key Responsibilities: 1. Geological Interpretation & Subsurface Understanding: Proficient in interpreting depositional environments acrossclastic, carbonate, mixed, deepwater, and shallow-marine systems. Conduct seismic facies analysis and generate detaileddepositional models. 2. Static Modelling Expertise: Develop complex structure models, apply both stochastic anddeterministic approaches to facies/property modelling. Perform volumetric analysis, uncertainty quantification, andmulti-scenario evaluations. 3. Reservoir Engineering Collaboration: Collaborate closely with REs on dynamic modelling,upscaling, and history matching. Provide static input for material balance (MBAL) andproduction forecasts using deterministic and probabilistic approaches. 4. Development & Appraisal Planning: Contribute to Field Development Plans (FDPs), full fieldreviews, and brownfield/greenfield development. Evaluate near-field exploration and behind casingopportunities. 5. Well Planning & Operations: Guide well planning, geo-steering, and real-time subsurfacedecision-making. Define and supervise data acquisition strategies inexploration, appraisal, and development wells. 6. Integration with Other Disciplines: Provide geological input into drilling, facilities, andeconomic models. Participate in risk and uncertainty analyses, decisiontrees, and support full-cycle E&P workflows from exploration torejuvenation. 7. Leadership & Mentoring: Lead and mentor junior geoscientists, foster technicaldevelopment within the team. Work effectively in integrated teams includinggeophysicists, petrophysicists, REs, PE, and drilling engineers. Education Requirement : Post graduate in Geology/Applied Geology from a recognizeduniversity Experience Requirement : 12-15 yrs Experience with very good modelling skill isrequired Skills & Competencies : Advanced level expertise insedimentology, sequence stratigraphy, structural geology, and basindevelopment. Expert user of industry tools -e.g., Petrel. Strong skills in structural andfacies mapping, petrophysical property mapping using geostatistical methods. Experience with seismicinversion, AVO analysis, and seismic attribute interpretation for facies andfluid characterization. Adequate understanding ofpetrophysical interpretation, RCA, SCAL, core sedimentology, image log, and NMRanalysis. Ability to integrate rock and logdata into geomodelling workflows. .

As a member of the New Chemical Entity(NCE) Research team located in Navi Mumbai, India, your primary responsibility will be the analysis of compounds for various projects from the medicinal chemistry team and lead NCEs. Your role will involve ensuring quality output within the set targets established by the Group leader, with approximately 60% of your time dedicated to this task. Another key aspect of your position will be the development of analytical methods for new NCEs using a range of instrumental techniques such as HPLC, LCMS, NMR, IR, SFC, and other wet analysis methods. This will require a high level of proficiency and attention to detail to deliver quality results within the specified targets, accounting for about 20% of your time. Additionally, a good understanding of analytical skills and basic knowledge of HPLC, LCMS, NMR, and SFC instruments will be essential for successful performance in this role. Achieving quality output within the designated targets set by the Group leader will be a core expectation, with approximately 20% of your time allocated to these tasks. Overall, your contributions to the NCE Research team will play a crucial role in advancing projects and lead NCEs, with a focus on maintaining high-quality standards and meeting set objectives under the guidance of the Group leader.,

As a Fortune 50 company with more than 400,000 team members worldwide, Target is an iconic brand and one of America's leading retailers. Joining Target means promoting a culture of mutual care and respect and striving to make the most meaningful and positive impact. Becoming a Target team member means joining a community that values different voices and lifts each other up . Here, we believe your unique perspective is important, and you'll build relationships by being authentic and respectful. Overview about TII At Target, we have a timeless purpose and a proven strategy. And that hasnt happened by accident. Some of the best minds from different backgrounds come together at Target to redefine retail in an inclusive learning environment that values people and delivers world-class outcomes. That winning formula is especially apparent in Bengaluru, where Target in India operates as a fully integrated part of Targets global team and has more than 4,000 team members supporting the companys global strategy and operations. Digital Strategy & Platform Right along with Targets distinctive retail brand, we are constantly improving and innovating our digital shopping experience. Are you ready to excel in the fast-changing retail environmentAre you a customer service enthusiast whos curious about the guest and can see the shopping journey through their eyesThen youll have success on the Digital Strategy & Platform team, whose goal is to offer guests a seamless online shopping experience across our platformsincluding Target.com and the store networks fulfillment capabilities. Here, youll collaborate to create and implement the digital strategies that enrich the online experience through the right mix of personalization, simplicity and intuitiveness. Your ideas will support Target in complementing the beloved in-store shopping interaction with a convenient, reliable and instantly gratifying digital experience. The Category Site Merchandising team focuses on increasing digital topline sales by optimizing conversion and the overall site experience. The team plays a crucial role in ensuring findability and discoverability of products, making it easy for guests to locate and discover items. By partnering with various teams within and outside of the Digital organization, the team drives the right experience for each category. Additionally, the team is responsible for delivering financial outcomes and plans for the digital business, ensuring that financial goals are met and sustained. As Senior Manager, Site Merchandising Category you will develop and lead teams to drive digital business growth through the development of effective site merchandising strategies for your categories. Your focus will be on leading your team to optimize the site experience to maximize guest engagement and sales. You will collaborate closely with cross-functional teams to ensure seamless execution of category strategies and alignment with business goals. Your leadership will be crucial in translating business objectives into actionable site merchandising tactics that enhance the digital shopping experience. Core Responsibilities: Category Digital Strategic Planning and Execution . Develop cohesive digital strategies for several categories and mobilize the team to execute those strategies, in close partnership with Merchandising, Marketing, Product/Technology, Operations, and Item partners. Key responsibilities included but are not limited to: Category Digital StrategyResponsible for partnering with merchant leaders to develop and prioritize initiatives to best drive category goals. Core Site MerchandisingImplement and optimize site merchandising strategies that focus on conversion, findability, maximizing guest engagement, and frictionless shopping. Senior Managers both set the vision for the category and work with the team to operationalize that vision within their team and by influencing across multiple partner teams. Analytics: Monitor, understand, and utilize data and key metrics from multiple and varied sources (devices and platforms, guest behavior, market trends, and competitive insights) to optimize short-term performance and to inform long-term strategies. Provide in-depth reporting and insights to partner teams and identify & highlight performance opportunities. Results & Financial Accountability: Maintain a strong sense of accountability for delivering financial results, ensuring strategies drive topline sales, profitability, and guest engagement. Team Leadership: Lead, mentor, and develop a team of site merchandisers, providing development, coaching, motivation, support, and feedback. Promote and model key Target behaviors. Champion diversity and inclusion. Create an atmosphere of teamwork, collaboration, agility, attention to detail, and drive. Cross-Functional Leadership: Establish strong cross-functional and cross-channel partnerships across Target. Influence and leverage other teams within the broader organization to advance digital objectives. Quarterly Planning and Activation Own & drive cross-functional category roadmap based on guest insights & business needs. Streamline processes, manage project timelines, and resolve operational challenges to improve task execution and efficiency. Core responsibilities of this job are described within this job description. Job duties may change at any time due to business needs. About You: 4 year college degree or equivalent experience 8+ years e-commerce experience Deep business acumen with an entrepreneurial, revenue-generating mindset Must have both strong technical acumen and a passion for customer experience Excellent understanding of mass merchandising, retail, e-commerce and multi-channel retailing Demonstrated experience in strategic and cross-functional influence, planning and execution High level of initiative and organization, with the ability to manage ambiguity, risk, uncertainty and changing directions Demonstrated experience in team leadership, with a personal interest in development Strong analytical and quantitative skills, including financial and business metrics Strong written and verbal communication skills with the ability to present to varying levels of leadership Demonstrate a deep understanding of e-commerce principles and the full customer journey funnel, to optimize site performance and enhance the digital shopping experience Experience in leading large-scale projects, track deliverables, allocate resources, and ensure alignment with strategic objectives Useful Links- Life at Target- https://india.target.com/ Benefits- https://india.target.com/life-at-target/workplace/benefits Culture- https://india.target.com/life-at-target/belonging

Job Responsibilities : Design Scope of Work for Logging Services Evaluate EOI / Technical Bids Real time log monitoring, QA /QC Condition log data Handling Log Data Analysis Software Select side wall core, formation tester pretest and sample depths Process & Analyse Advanced Logs (Sonic Waveform, Image, NMR etc.) Petrophysical Evaluation, providing average reservoir parameters at the well for Geological model building and resource estimation Petrophysical facies identification by integrating log data, Image data, Core (RCA and SCAL) data for static geological model and Integrated subsurface description (ISD). Petrophysical evaluation of Unconventional Reservoirs Raise PRs & Verify Invoices Evaluate Casing & Cement Bond logs Adhere to Log Data compliance QC of Vendor Deliverables Support and deliver within budget Log data acquisition and processing. Education Requirement : Masters degree in Geophysics or Geology from a recognised university. Experience Requirement : Minimum 5 Years Experience In E&P Very Strong technical abilities in Integrated formation evaluation / petrophysical Interpretation. Skills & Competencies : Detailed Knowledge of Principles & Applications of Different Logs

As a Polymorph Screening Scientist at Morepen Proprietary Drug Research Pvt Ltd. (MPDRPL), your primary responsibility will be to lead the screening and selection of solid forms for drug candidates. You will play a crucial role in improving the physicochemical properties of active pharmaceutical ingredients (APIs) by overseeing polymorph screening activities. It is essential to identify the most stable and bioavailable forms of drug substances for regulatory submissions. Collaborating with cross-functional teams, you will mentor junior scientists and drive advancements in solid-state drug discovery. Your key responsibilities will include overseeing the screening of potential polymorphs, solvates, and hydrates for APIs, interpreting and analyzing solid-state data, scaling up identified novel polymorphs, collaborating with various teams to align polymorph selection with drug formulation strategies, preparing regulatory-compliant data for filings, troubleshooting any issues related to polymorph stability, and ensuring accurate documentation and reporting of experimental protocols and findings. The deliverables expected from you include the identification and characterization of stable polymorphs and crystal forms for drug candidates, detailed screening reports, regulatory-compliant data for solid-state forms, and methodologies for high-throughput screening, scaleup, and solid-state characterization. To qualify for this role, you should hold a Ph.D. in Pharmaceutical Sciences, Solid state Chemistry, Chemistry, or a related field, with a focus on solid-state chemistry or materials science. Alternatively, a Master's degree with equivalent experience will be considered. You should have a minimum of 6+ years of industry experience in solid-state chemistry, polymorph screening, or pharmaceutical development and proven expertise in solid-state characterization techniques and polymorph screening methods. Proficiency in solid-state characterization methods, high-throughput screening techniques, and knowledge of computational techniques for polymorph prediction are essential technical skills required for this role. In addition to technical skills, you should possess excellent problem-solving, troubleshooting, and decision-making skills. Effective communication skills, both written and verbal, are crucial for presenting complex data to diverse audiences. Being detail-oriented with strong organizational and documentation skills will contribute to your success in this role at MPDRPL.,

JOB DESCRIPTION Designation: Research Scientist (7-I) Job Location: Bangalore Department: DAS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines): Lead a team of scientists specializing in NMR spectroscopy. Key Responsibilities: (Maximum 5-8 Points) Structural elucidation of small molecules (organics) using state-of-the-art NMR methodologies Structure characterization of organic molecules. Collaborate closely with project teams. Solve complex technical problems with the equipment which could include software, hardware, or experimental set-ups. Maintains superconducting magnets, including scheduling cryogen deliveries; weekly liquid nitrogen fills and liquid helium fills. Proven hands-on experience in small-molecule NMR spectroscopy. Strong background in organic chemistry and structure elucidation Expertise in NMR methods with proficiency in NMR data systems and pulse sequence language. Strong written and communication skills. Ability to collaborate with project teams and work in a fast-paced team environment . Review of daily/monthly laboratory monitoring, verification, and calibration records of equipment and instruments. Understanding and demonstrating responsibility for the safety of self & colleagues by following all safety protocols provided by Syngene. Adherence to all environment, health, and safety (EHS) policies & standards are always in the workplace. Educational Qualification: MSc in analytical chemistry or allied disciplines. Technical/functional Skills: (Maximum 4-6 Points) NMR and LCMS. Experience: 10 to 15 years of hands-on experience on preparative HPLC Behavioral Skills: Must have very good communication skills Equal Opportunity Employer: .

Job Area: Engineering Group, Engineering Group > Hardware Engineering General Summary: As a leading technology innovator, Qualcomm pushes the boundaries of what's possible to enable next-generation experiences and drives digital transformation to help create a smarter, connected future for all. As a Qualcomm Hardware Engineer, you will plan, design, optimize, verify, and test electronic systems, bring-up yield, circuits, mechanical systems, Digital/Analog/RF/optical systems, equipment and packaging, test systems, FPGA, and/or DSP systems that launch cutting-edge, world class products. Qualcomm Hardware Engineers collaborate with cross-functional teams to develop solutions and meet performance requirements. Minimum Qualifications: Bachelor's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 3+ years of Hardware Engineering or related work experience. OR Master's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 2+ years of Hardware Engineering or related work experience. OR PhD in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 1+ year of Hardware Engineering or related work experience. Key Technical skills requirement: Candidate should have deep and sound understating of: Memory basic design understating for different architectures Memory measurement parameters Memory timing/power characterization and compiler engine building with all accuracy parameters involved Memory power views All the LVF/different forms of variation parameter Memory lib w.r.t. parameters/arcs/SDF conditions/variation parameters/QA steps/different formats Different Simulator tools Should have thorough understanding of release process to customers Knowledge of scripting languages such as Shell, Perl Good working knowledge of MS excel, PPT Mentoring skills to Juniors

Kenvue Is Currently Recruiting For A: Manager, R&D Analytical What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role Reports To: Director - Analytical Chemistry Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What You Will Do Kenvue is currently recruiting for: Manager, R&D Analytical This position currently would report to the Director, R&D Analytical and Microbiology Operations and is based at Mumbai. Who We Are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role reports to: Director, R&D Analytical and Microbiology Operations Location: Mumbai Travel %: 10 What You Will Do The Manager, R&D Analytical, would be responsible for leading the analytical activities for the Kenvue product portfolio such as defining the analytical strategy, execution planning, timing, resource requirements and interdependencies to complete the innovation and lifecycle management project deliverables. The role shall be responsible for delivering projects which deploy advanced analytical technologies and data interpretation tools and thus needs to be expert in these techniques. In addition, the role includes contributing to digital and data driven tools, lab automation and optimization of analytical processes to drive efficiencies through application of such advanced tools. The ideal candidate will be a subject matter expert in the Analytical domain and will have strong communication skills to partner with business partners independently lead projects. This is a people leader role, and hence specific skills related to people leader capabilities would be expected. Key Responsibilities Management of people, projects, lab systems and processes applied to Analytical R&D for the Innovation Pipeline in support of the portfolio. Deliver project milestones, excellence in execution of analytical studies (raw material and finished product) and documentation in compliance with requirements from internal policies and applicable regulations. Planning and executing the analytical strategy for new product development such as Test Method Development, Test Method Validation and Transfer to Quality Control Labs (internal and external) and CRO’s, Stability Studies, Impurity and degradation pathway assessments, etc. Advanced Analytical solutions (e.g. but not limited to Elemental impurities, Extractable and Leachable, Nitrosamines, etc.) and assessments using hi-tech instrumentation Technical documentation: protocols, reports, change controls, specifications, etc. Communicate the project progress to management, business partners, and team members. Attend and/or facilitate project and technical meetings. Assessment of internal processes identifying opportunities and implementing improvements such as organization of activities, redistribution of tasks, reduction of lead time and rework. Active participation in internal and external audits, from the preparation for the audit to responses to observation and closing out of action plans/commitments. Lead and manage team of scientific professionals: performance, development and coaching Representation on Global functional teams for specific assignments to lead future focused analytical strategies and solutions. Required Qualifications What we are looking for PhD preferred or Minimum Masters in Chemistry or with related field with minimum 12 to 15 years of experience. Work experience preferred in a consumer health or pharmaceutical industry, with at least 5 years in GMP working environment Strong knowledge and hand-on experience of advanced Analytical quantitative and qualitative techniques applied to finished products and raw materials e.g. MS, ICP-OES/MS, LC-MS/MS, NMR, etc. Deep knowledge and hands-on experience of lab operational and quality excellence tools to facilitate smart lab operations, workflows and data management. Experience of application of AI, data analytics, automation in Analytical domain highly preferred. Have strategic and operational skills to prioritize and complete projects based on business and compliance needs. Strong communication and presentation skills to effectively convey complex data insights Display of specific leadership attributes which indicate next level potential to take up higher roles Experience with change control processes and providing technical assessments and documentation to support changes for Finished Products Specifications, Raw Material, and/or Test Methods used at Internal and External Manufacturing sites. Strong and effective communication skills across different layers of the organization, as this role requires consistent, frequent collaborations with global sites, through virtual meetings and email correspondences. Strong knowledge in current compendia, industry standards, product registrations Experience in leading without follow-ups and frequent guidance assigned projects to meet business objectives Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

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 The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities (small molecules and peptides) through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices 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 Senior Scientist I has the following responsibilities: Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules & peptides. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Execute small molecule synthesis and, solid-phase and solution-phase peptide synthesis with a focus on quality. Perform peptide modification techniques, including cyclization, disulfide bridge formation, stapling, and derivatization. Support in characterization of peptides by utilizing advanced characterization techniques such as LCMS, HPLC, and NMR to ensure peptide quality and accuracy. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab. Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. 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: M Sc (Organic Chemistry) from a reputed university with minimum 11-13 years of industrial experience in API Process R&D/CDMO/CRO (OR) Ph.D (Full Time) in Synthetic Organic Chemistry from a reputed group with 7-10 years of post doctoral and/or industrial research experience in API Process R&D/CDMO/CRO. Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of Small Molecule APIs/ NCEs on lab scale and production. Experience in handling automated peptide synthesizers and purification processes is highly desirable. Proven ability for adoption of QMS and documentation procedure Adherence to lab safety guidelines Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions, solid phase and complex peptide synthesis and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Good practical, documentation & presentation skills. Attention to detail, stratregic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. 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.