341 Nmr Jobs - Page 6

Description 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 The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients and dietary supplements manufactured, distributed, and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries. This is a hands-on, non-supervisory individual contributor position in which the incumbent applies their knowledge and practical experience in execution of bioanalytical projects on collaborative testing of Reference Standards, Analytical Reference Materials, documentary standards and characterization of different biological products. Additionally, the incumbent will also actively engage and contribute in verification, international and national reference standard development programs as assigned. 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. Roles And Responsibilities Aligns with USP’s mission, goals and objectives and complies with USP’s guidelines and other requirements. Demonstrates laboratory skills and hands on expertise in analytical Chromatography _,_ SEC-MALS, LC-MS, HPLC/UPLC, Ion-chromatography, Capillary Electrophoresis, Biochemical assays, SDS-PAGE, Western blot, IEF, Enzymatic/Protein assays (Spectrophotometer and Plate readers). Technical knowledge in Circular dichroism, FTIR, Gas chromatography, NMR is an added advantage. Plans and executes Compendial and R&D projects besides contributing in the new initiatives viz., proof of concept studies in Biologics for product classes such as proteins, enzymes, vaccines, monoclonal antibodies, cell and gene therapy, peptides, antibiotics, raw material and any other biological products as assigned. Ability to plan, design, execute, and resolve technical issues within the scope. Evaluates and analyzes scientific reports, applies personal experience, academic training, and technical insights to troubleshoot and solve problems in the laboratory within the scope. Performs administrative responsibilities, mentors and trains team member/members as assigned. Actively engages in project coordination with cross-functional/global teams and aligns with Global Biologics objectives. Prepares and reviews project reports, SOPs, and other documents to ensure compliance to USP’s Quality Management System and contribute in Internal audits, ISO 9001, and ISO 17025 audits Assists and recommends improvements in laboratory/project management methods and processes. Performs other 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 Senior Scientist I - MSc./M.Tech./M.Pharm. in relevant stream of Biological Sciences with 11-13 (Or) Ph.D with 7-10 years of industry experience working in Analytical R&D and/or QC department of Biopharmaceutical industry and has hands on experience in work recombinant therapeutic proteins, peptides, mAbs and /or CGT and Vaccines. The candidate should be well-versed with operation and troubleshooting of all instruments used in performing the analytical characterization of the molecules and should have sound knowledge of QMS systems. The candidate should have strong competencies in technical writing, communication, and presentation skills. Scientist IV – MSc./M.Tech./M.Pharm. in relevant stream of Biological Sciences with 8-10 (Or) Ph.D with 4-7 years of industry experience working in Analytical R&D and/or QC department of Biopharmaceutical industry and has hands on experience in work recombinant therapeutic proteins, peptides, mAbs and /or CGT and Vaccines. The candidate should be well-versed with operation and troubleshooting of all instruments used in performing the analytical characterization of the molecules and should have sound knowledge of QMS systems. Experience in method development, validation and technology transfer and analytical characterization for biomolecules is an added advantage, Work experience in cGLP/cGMP environment is preferred. The candidate should have strong competencies in technical writing, communication, and presentation skills. Additional Desired Preferences The candidate should be well-versed with operation and troubleshooting of all instruments used in performing the above-mentioned analytical techniques and should have sound knowledge of QMS systems. Previous experience working in biopharma cGLP/cGMP/QMS environment with practical experience in good documentation practices would be an advantage. The candidate should have strong competencies in technical writing, communication, and presentation skills. Good written and verbal communications skills Supervisory Responsibilities None 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

Job Title CMC-IRA Job Grade G11B/G11A Function India Regulatory Affairs Location: Baroda Job Summary Review of CMC documents. Documents include but not limited to following: Drug Substance Structural formula, molecular formula and relative molecular weight General description of raw materials Identification of critical steps in process and control Flow diagram of manufacturing process Description and characterization of drug substance Physiochemical data: (Chemical name and structure, Empirical formula, Molecular weight) Physical properties:- Description, Solubility, Rotation, Partition coefficient, Dissociation constant. Analytical Data: Elemental analysis, Mass spectrum, NMR spectra, IR spectra, UV spectra, Polymorphic identification Complete monograph specification and STP Impurities (name, manufacturer) Residual solvent/ other volatile impurities (OVI) estimation Manufacturing process for drug substance Validation of manufacturing process [assay method, impurity estimation method, residual solvent/other volatile impurities(OVI) estimation method] Manufacturer(s) Stability of drug substance Tests and evaluation of packaging materials Specifications of primary and secondary packing Container closure system Reference standards Justification of specifications Storage and shipping conditions of drug substance Protocol of stability study, results and conclusions Manufacturing process development Selection and justification of critical steps Filling procedure for the active ingredient, in-process controls Stabilization of active ingredient Drug Product Justification of final qualitative/quantitative formula Manufacture of drug product Description and composition of drug product Description of manufacturing process Protocol of stability study, results and conclusions Stability of drug product Tests and evaluation of packaging materials Specifications of primary and secondary packing Container closure system Finished product specification and STP Justification of specifications Excipient compatibility study Dissolution Study In process quality control check and report Certificate of analysis Validation of analytical procedures Forced degradation study Process validation protocol and Report Labeling Details of equipment and facilities for production of drug product: master formula, batch record and set release documentation in respect of consistency batches Description of batch identification system Control of excipients (adjuvant, preservative, stabilizers and others) Use of new adjuvants, preservatives, stabilizers and excipients Areas Of Responsibility Checking of CMC documents. Discussion with CFT for corrections Co-ordination for finalized CMC documents from stakeholders Review and approval of CCR Compilation of CMC dossier for regulatory submission including query responses Travel Estimate Only if required Job Scope Internal Interactions (within the organization) Yes External Interactions (outside the organization) Yes, in case of CMO projects Geographical Scope Financial Accountability (cost/revenue with exclusive authority) Job Requirements Educational Qualification M. Pharma Specific Certification Experience 5-10 years Skill (Functional & Behavioural): Knowledge of CMC requirements/understanding of ICH quality guidelines

We are looking for an experienced medicinal chemist with hands-on expertise in small-molecule drug discovery. This role involves driving the design, synthesis, and optimization of chemical compounds from early hit identification through to lead optimization. The ideal candidate will bring strong experimental chemistry capabilities, SAR insight, and cross-functional collaboration skills to advance high-quality drug candidates. Key Responsibilities Design, plan, and execute synthetic routes to support iterative compound design and structure-activity relationship (SAR) studies. Analyze and prioritize screening hits based on potency, selectivity, and chemical tractability. Apply biophysical and biochemical assay data (e.g., SPR, NMR, IC₅₀) to assess compound binding and refine structures. Collaborate with computational chemists for structure-guided drug design, virtual screening, and docking studies. Optimize compounds for multiple parameters including potency, solubility, selectivity, metabolic stability, and pharmacokinetic properties. Incorporate early ADME and safety profiling data (e.g., microsomal stability, permeability, CYP inhibition) into lead selection decisions. Troubleshoot synthetic challenges and improve efficiency in compound production and purification. Work cross-functionally with biology, DMPK, and pharmacology teams to support candidate advancement. Maintain accurate records, contribute to project meetings , and present experimental findings and SAR rationale. Required Qualifications Ph.D. or M.Sc. in Organic or Medicinal Chemistry with 5+ years of relevant experience in small-molecule drug discovery. Demonstrated expertise in synthetic organic chemistry and medicinal chemistry principles. Strong understanding of DMTA cycles and hands-on experience in SAR-driven lead development. Proficiency with analytical tools (NMR, LC-MS, HPLC) and compound characterization techniques. Effective collaboration in multidisciplinary project teams and clear scientific communication.

Scientist med chem: 2 5 years To Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. To have broad knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. To work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports, powerpoint presentations and other scientific documents by using the chemdraw as needed. Should be able to scout new / alternate schemes & know the use of scifinder, reaxys etc. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Show more Show less

Job Description Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. Broad knowledge of modern organic chemistry and synthetic methods Heterocyclic chemistry, metal catalyzed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. Work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports and other scientific documents, as needed. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Required Candidate Profile M.Sc. Organic Chemistry/Chemistry Experience:- 2 to 8 years in Synthetic Chemistry(Small Scale) Job Location: Bengaluru. Show more Show less

Aurigene Pharmaceutical Services Limited is seeking a talented and motivated Scientist - Medicinal Chemistry - to join our growing team. In this role, you will play a key role in the discovery and development of novel drug candidates by designing, synthesizing, and characterizing target molecules. Responsibilities Synthesize novel target molecules according to client specifications, working independently and efficiently. Utilize your broad knowledge of modern organic chemistry and synthetic methods, including: Heterocyclic chemistry Metal-catalyzed reactions Handling air/moisture sensitive reagents Hydrogenations Multi-step synthesis Apply a wide range of techniques in synthesis and purification: Chromatographic methods (including expertise in MPLCs) Spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR) Demonstrate problem-solving skills and the ability to think creatively to overcome synthetic challenges. Maintain laboratory notebooks and meticulously, adhering to client guidelines. Generate final reports and other scientific documents as required. Demonstrate a strong understanding of safety protocols and adhere to EHS guidelines as per our zero-tolerance policy. Key Skills And Competencies M.Sc. in Organic Chemistry with 2to 8 years of relevant experience. Strong knowledge of modern organic chemistry principles and synthetic methods. Expertise in various techniques for organic synthesis, purification, and characterization. Excellent problem-solving and critical thinking skills. Ability to work independently and as part of a team. Strong communication and interpersonal skills. Proficiency in scientific writing and record keeping. Show more Show less

Position Scientist Medicinal Chemistry (CRO) Location Hyderabad/Bangalore Desired Profile M.Sc. (Organic Chemistry/Chemistry) with 3-8 years Job Description, Key Skills And Competencies To synthesize, and characterize novel target molecules as per client specifications, in an efficient and independent manner. To have broad knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc.. Hands-on experience with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Ability to think outside the box and independently solve synthetic problems. Troubleshooting for the whole team and being able to take quick and decisive actions (for PhD candidates and/or lab leaders). Maximize the productivity of the group and provide intellectual input to the department. Ability to manage a small team of 3-4 chemists, in addition to his/her individual work (for lab leaders/PhDs). Interaction with the clients and smooth communication of project goals/results during the weekly TCs/VCs (for lab leaders/PhDs). Up to date maintenance of Lab Note Books, as per client guidelines. Generation of final reports and other scientific documents, as needed. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Competencies Good Communication Skills Interpersonal Skills Team Player Show more Show less

Department Chemistry Salary £37,174 - £45,413 per year Grade Grade 6 Contract status Fixed term Hours of work Full-time Based at University of York campus Interview date To be confirmed Posted Date 30/07/2025 Apply by 27/08/2025 Job Reference 14271 Documents Job description 14271.pdf (PDF, 329.73kb) Role Description Applications are invited for a Postdoctoral Research Associate position for up to 36 months to work with Professor Gideon Grogan and Dr William Unsworth in the Department of Chemistry. The project is funded by the EPSRC. Department The Department of Chemistry is one of the largest and most successful departments at York and we are renowned internationally for our research. As a department, we strive to provide a working environment that allows all staff and students to contribute fully, to flourish, and to excel. We are proud of our Athena Swan Gold Award Role The project will focus on exploring the application of Amine Dehydrogenase enzymes to the generation of pharmaceutically relevant intermediates. There will be a special focus on the evolution of these enzymes and their applications in synthetic organic and process chemistry. This appointment will suit a candidate with strong training in chemical synthesis and analysis, ideally also with experience in enzyme production and biocatalytic approaches. The position is tenable for a period of 36 months available from September 2025. Main Duties And Responsibilities To conduct research under the supervision of Professor Gideon Grogan and Dr William Unsworth and to contribute to the production of research into the application of Amine Dehydrogenase enzymes to the generation of pharmaceutically relevant intermediates. To assist in the identification and development of potential areas of research and the development of proposals for independent or collaborative research projects. To provide guidance to other staff and students, as required, as well as coordinating the work of small research teams and assist with undergraduate project supervision. Skills, Experience & Qualification Needed An undergraduate degree and PhD in Chemistry or equivalent Knowledge in organic synthesis and analysis to engage in high quality research using a range of research techniques and methodologies Extensive skills in synthetic organic chemistry and analysis including analysis of small organic molecules using NMR spectroscopy Experience of enzyme production and biocatalytic reactions advantageous Highly developed communication skills, attention to detail and commitment to high quality Evidenced ability to develop research objectives, plan and prioritise work, and conduct individual and collaborative research Ability to write up research work for publication and competency at presenting at conferences Positive attitude to colleagues and students and a willingness to work proactively Commitment to personal development and an understanding of equality and diversity issues Interview date: To be confirmed For informal enquiries: please contact Prof Gideon Grogan, email gideon.grogan@york.ac.uk, or Dr William Unsworth, email william.unsworth@york.ac.uk The University strives to be diverse and inclusive – a place where we can ALL be ourselves. We particularly encourage applications from people who identify as Black, Asian or from a Minority Ethnic background, who are underrepresented at the University. We offer family friendly, flexible working arrangements, with forums and inclusive facilities to support our staff. #EqualityatYork

LOCATION Hyderabad, India DEPARTMENT Chemistry Solutions Responsibilities– Conduct analysis, testingand purification of product samples: o Developanalytical methods for intermediates and final compounds o Collectall the samples and record the content into the register o Collectsolvents from the store and check for its quality o Prioritizeand prepare samples for the required analysis o Preparemobile phase for HPLC, LCMS and preparative HPLC o ProcessHPLC/ LCMS chromatograms to analyze molecules and enrich purity of theintermediates/ final compounds o Developmethods and purify compounds using prep HPLC/ MS - Prep HPLC/ SFC o Analyzethe samples using HPLC, NMR, GCMS and LCMS etc. o Supportsenior team members in preparing reports with test results Ensure safety at workthrough adherence 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 any instrumentbreak down o Record,maintain and update the analysis in an accurate manner on a continuous basis Maintain dataintegrity and IP confidentiality : o Maintainstrict IP Confidentiality and adhere to all related policies Ensure skill development ofself: o Enhanceknowledge related to NMR, HPLC, LCMS, GCMS, POLARIMETER, ATR generation and wetanalysis etc. 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:

As a Process Development Chemist, you will be responsible for designing and conducting experiments to create new chemical processes and enhance existing ones. You will scale up laboratory procedures to pilot and production levels, ensuring scalability and reproducibility. Analyzing current processes, identifying areas for enhancement, and implementing modifications to boost efficiency, yield, and safety will be a key aspect of your role. Utilizing statistical methods and tools to assess process performance will be crucial. You will collaborate closely with cross-functional teams, such as R&D, quality assurance, production, and regulatory affairs, to seamlessly integrate processes. Providing technical support and expertise to production teams will be essential. Additionally, you will prepare detailed documentation for processes, including protocols, reports, and standard operating procedures (SOPs), while ensuring compliance with safety, environmental, and quality standards. In the event of issues during production, you will investigate and resolve them promptly to minimize downtime. Conducting root cause analysis and implementing corrective actions will be part of your troubleshooting responsibilities. Staying updated on the latest advancements in chemical processes and technologies, and evaluating and recommending the use of new tools and technologies to enhance process performance will be vital for research and development. To qualify for this role, you should hold a Bachelors or Masters degree in Chemistry, Chemical Engineering, or a related field, along with years of experience in chemical process development or a related area. A strong understanding of chemical reactions, kinetics, thermodynamics, and safety regulations is required. Proficiency in analytical techniques such as HPLC, GC, NMR, and others relevant to process chemistry is essential. Excellent problem-solving skills, attention to detail, and strong communication and teamwork abilities are desired qualities. This is a full-time, permanent position with benefits such as provided food, paid sick time, and Provident Fund. The work schedule may involve day shifts or rotational shifts, with the work location being in person.,

Job Responsibilities : The Development Geologist cum Modeller will lead the integration of geological, geophysical, petrophysical, and engineering data to develop robust static models for field development and reservoir management The incumbent will be a key player in multidisciplinary teams, contributing to strategic decision-making through technical excellence and cross-functional collaboration, Key Responsibilities: Geological Interpretation & Subsurface Understanding: Proficient in interpreting depositional environments across clastic, carbonate, mixed, deepwater, and shallow-marine systems, Conduct seismic facies analysis and generate detailed depositional models, Static Modelling Expertise: Develop complex structure models, apply both stochastic and deterministic approaches to facies/property modelling, Perform volumetric analysis, uncertainty quantification, and multi-scenario evaluations, Reservoir Engineering Collaboration: Collaborate closely with REs on dynamic modelling, upscaling, and history matching, Provide static input for material balance (MBAL) and production forecasts using deterministic and probabilistic approaches, Development & Appraisal Planning: Contribute to Field Development Plans (FDPs), full field reviews, and brownfield/greenfield development, Evaluate near-field exploration and behind casing opportunities, Well Planning & Operations: Guide well planning, geo-steering, and real-time subsurface decision-making, Define and supervise data acquisition strategies in exploration, appraisal, and development wells, Integration with Other Disciplines: Provide geological input into drilling, facilities, and economic models, Participate in risk and uncertainty analyses, decision trees, and support full-cycle E&P workflows from exploration to rejuvenation, Leadership & Mentoring: Lead and mentor junior geoscientists, foster technical development within the team, Work effectively in integrated teams including geophysicists, petrophysicists, REs, PE, and drilling engineers, Education Requirement : Post graduate in Geology/Applied Geology from a recognized university Experience Requirement : 12-15 yrs Experience with very good modelling skill is required Skills & Competencies : Advanced level expertise in sedimentology, sequence stratigraphy, structural geology, and basin development, Expert user of industry tools e-g , Petrel, Strong skills in structural and facies mapping, petrophysical property mapping using geostatistical methods, Experience with seismic inversion, AVO analysis, and seismic attribute interpretation for facies and fluid characterization, Adequate understanding of petrophysical interpretation, RCA, SCAL, core sedimentology, image log, and NMR analysis, Ability to integrate rock and log data into geomodelling workflows, Show

Scientist med chem: 2 – 5 years To Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. To have broad knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. To work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports, powerpoint presentations and other scientific documents by using the chemdraw as needed. Should be able to scout new / alternate schemes & know the use of scifinder, reaxys etc. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy.

Position Scientist – Medicinal Chemistry (CRO) Location Hyderabad/Bangalore Desired Profile M.Sc. (Organic Chemistry/Chemistry) with 3-8 years Job Description, Key Skills And Competencies To synthesize, and characterize novel target molecules as per client specifications, in an efficient and independent manner. To have broad knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc.. Hands-on experience with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Ability to think outside the box and independently solve synthetic problems. Troubleshooting for the whole team and being able to take quick and decisive actions (for PhD candidates and/or lab leaders). Maximize the productivity of the group and provide intellectual input to the department. Ability to manage a small team of 3-4 chemists, in addition to his/her individual work (for lab leaders/PhDs). Interaction with the clients and smooth communication of project goals/results during the weekly TCs/VCs (for lab leaders/PhDs). Up to date maintenance of Lab Note Books, as per client guidelines. Generation of final reports and other scientific documents, as needed. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Competencies Good Communication Skills Interpersonal Skills Team Player

Job Description Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. Broad knowledge of modern organic chemistry and synthetic methods Heterocyclic chemistry, metal catalyzed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. Work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports and other scientific documents, as needed. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Required Candidate Profile M.Sc. Organic Chemistry/Chemistry Experience:- 2 to 8 years in Synthetic Chemistry(Small Scale) Job Location: Bengaluru.

Aurigene Pharmaceutical Services Limited is seeking a talented and motivated Scientist - Medicinal Chemistry - to join our growing team. In this role, you will play a key role in the discovery and development of novel drug candidates by designing, synthesizing, and characterizing target molecules. Responsibilities Synthesize novel target molecules according to client specifications, working independently and efficiently. Utilize your broad knowledge of modern organic chemistry and synthetic methods, including: Heterocyclic chemistry Metal-catalyzed reactions Handling air/moisture sensitive reagents Hydrogenations Multi-step synthesis Apply a wide range of techniques in synthesis and purification: Chromatographic methods (including expertise in MPLCs) Spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR) Demonstrate problem-solving skills and the ability to think creatively to overcome synthetic challenges. Maintain laboratory notebooks and meticulously, adhering to client guidelines. Generate final reports and other scientific documents as required. Demonstrate a strong understanding of safety protocols and adhere to EHS guidelines as per our zero-tolerance policy. Key Skills And Competencies M.Sc. in Organic Chemistry with 2to 8 years of relevant experience. Strong knowledge of modern organic chemistry principles and synthetic methods. Expertise in various techniques for organic synthesis, purification, and characterization. Excellent problem-solving and critical thinking skills. Ability to work independently and as part of a team. Strong communication and interpersonal skills. Proficiency in scientific writing and record keeping.

Job Purpose and Impact The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up. Perform method validation and verification to roll out new testing method in the lab. Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system. Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports. Maintain systems and techniques for reporting data across functional areas. Organize and participate ring tests with the goal to check and control methods and equipment. Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff. Other duties as assigned Qualifications Minimum Qualifications Bachelor's degree in a related field or equivalent experience Preferred Qualifications "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively" Necessary English reading capacity Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc. Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing Minimum of Three years of working experience in the Food industry Lab.

Website: www.chemcointernationalgroup.com Research & Development Head – Specialty & Fine Chemicals / Pharmaceuticals Research & Development Operations Oversee R&D laboratory operations involving synthesis, process development, scale-up, and analytical activities for pharma and specialty/fine chemicals. Ensure strict compliance with regulatory guidelines such as APIC, GMP, GLP, ISO, and industry-specific requirements. Supervise, mentor, and train R&D staff to strengthen capabilities across organic synthesis, process development, and analytical research. Manage advanced R&D instrumentation, including: Reaction optimization equipment (lab and kilo scale reactors) Analytical tools (HPLC, GC, NMR, Mass Spectrometry) Other specialized instruments relevant to NPD and scale-up New Product Development & Innovation Lead ideation, design, and execution of new product development (NPD) projects from concept through pilot scale. Conduct and oversee patent landscaping, FTO (Freedom to Operate) analysis, and literature/patent searches to ensure IP compliance. Guide manufacturing development, technology scouting, and process optimization for new and existing APIs, intermediates, and specialty chemicals. Collaborate with cross-functional teams (QC, Regulatory, Operations, Marketing) to support commercialization of new products. Process Development and Scale-up Design, optimize, and validate robust, scalable processes for targeted molecules. Ensure efficient and safe transfer of processes from R&D to pilot and production scale. Troubleshoot and resolve technical challenges during process scale-up and technology transfer. Analytical Method Development Collaborate with QC and analytical teams on method development, validation, and transfer for new products and intermediates. Support analytical troubleshooting and data interpretation for R&D projects. Documentation and Compliance Maintain comprehensive documentation for all R&D activities: method development, process reports, patent search summaries, scale-up protocols. Ensure all work meets applicable regulatory, safety, and environmental guidelines (GMP, ISO, ICH, etc.). Interface with QA/QC and Regulatory teams to ensure approval-readiness and compliance. Continuous Improvement and Cost Reduction Identify and implement improvements in R&D processes, technology, and workflow for enhanced productivity and reduced costs. Foster a culture of innovation, continuous learning, and scientific excellence. Requirements: PhD or Master’s degree in Chemistry, Organic Chemistry, Pharmaceutical Sciences, or Chemical Engineering. Minimum 5 years' R&D experience in the pharmaceutical or specialty chemical industry, including substantial leadership/people management. Proven track record in patent research, new product/process development, and successful pilot scale-up and tech transfer. Strong working knowledge of regulatory and quality standards (GMP, ISO, ICH, etc.). In-depth experience with analytical instrumentation (HPLC, GC, NMR, MS) and process equipment. Demonstrated problem-solving, project management, and leadership abilities. Excellent written and verbal communication, with a collaborative, hands-on working style. Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹80,000.00 per month Benefits: Health insurance Leave encashment Paid sick time Paid time off Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Palghar, Maharashtra: Reliably commute or planning to relocate before starting work (Preferred) Education: Master's (Required) Experience: QC: 5 years (Preferred) Language: English (Required) Location: Palghar, Maharashtra (Required) Work Location: In person

Are you looking for exciting career opportunity. We are hiring talented professionals with 3-5 years of relevant experience. Responsibilities Experience in organic synthesis/multi-step synthesis Handling reactions in mg to gram scale Sound knowledge of isolation, separation, purification techniques Experience in characterization and identification of organic molecules using spectroscopic techniques like NMR, HPLC, LCMS, GC, GCMS Positive and confident individual with a strong work ethics Team player and good communication skills. Qualifications MSc in organic chemistry/Medicinal chemistry with 3-5 years of experience. Medium of study in English Post graduation from premium institutes is preferred Interested candidates may please write to nageswararao.i@bioplus.in

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!

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 This position calls for a seasoned analytical scientist with deep expertise in the characterization of pharmaceutical compounds and impurities. The incumbent will lead complex analytical investigations, support cross-functional development teams, and uphold compliance with GLP and GMP requirements in a regulated environment. Key Responsibilities Perform structure elucidation and characterization of APIs, intermediates, and impurities using advanced spectroscopic techniques Conduct impurity profiling using LC-MS/MS and qualify standards and markers Provide analytical support to chemical research, pharmaceutical research, and manufacturing units Troubleshoot issues arising in process development (PD Lab) and quality control (QC) settings Prepare comprehensive characterization reports for DMFs, investigations, and standard qualifications Maintain laboratory operations as per GLP/GMP and safety guidelines Support regulatory and documentation activities Core Competencies Independently manage research tasks with minimal supervision Train and supervise junior analysts, ensuring high-quality output Lead and execute analytical deliverables within project timelines Review lab notebooks (LNBs), analytical reports, data files, and excel logs for accuracy and completeness Serve as a subject matter expert for function-specific queries and problem-solving Apply scientific principles to interpret complex analytical outcomes Draft and revise SOPs, STPs, technical forms, and project documentation Collaborate effectively with multi-disciplinary and cross-functional teams Comply with all EHS and regulatory standards during laboratory operations Qualifications The ideal candidate will have: M.Sc. in Chemistry or M.Pharm with minimum 10 years of industrial experience Ph.D. in a relevant field with at least 5 years of experience 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!

We are looking for a Chemistry Research Intern who is eager to learn best laboratory practices, assist in ongoing research activities, and contribute to experimental workflows to drive innovation at altM. The candidate will get hands-on exposure to organic synthesis, characterization techniques, and cross-functional research environments, working closely with senior scientists and engineers. Responsibilities include supporting lab-scale synthesis and formulation activities, assisting in purification and characterization of compounds using instruments such as NMR, GC-MS, HPLC, and IR, helping prepare reagents, setting up reactions, and monitoring experimental progress. The role also involves maintaining accurate lab records, inventory, and data logs, staying curious and engaged, with support provided for literature review, method development, and data interpretation over time, as well as adhering to safety protocols and best practices in lab settings. Requirements for the role include being a student or recent graduate with a Bachelors or Masters in Chemistry (preferably Organic or Applied Chemistry), with prior lab and project experience and internships being a nice-to-have. Strong theoretical and practical knowledge of organic chemistry principles and techniques, proficiency in using lab equipment and analytical instruments, excellent problem-solving skills, attention to detail, strong communication and interpersonal skills, with the ability to collaborate effectively in a team, commitment to safety, compliance, and ethical conduct in scientific research, and the ability to work from our lab in Bangalore with a willingness to travel for fieldwork or partner projects. The compensation and benefits offered include competitive cash compensation, negotiable for the right talent and qualifications.,

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.

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.

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.