242 Lcms Jobs

Role & responsibilities Collect samples for analysis from custodian. Processing of sample by using various sample extraction technique (to determine the concentration of analyte). Perform analysis via LCMS. Follow GXP. Sample extraction process using LLE, SPE, PPT. Stability issue handling, derivatization, etc. approach. Receive controlled forms for various activities. Document all linked activities and forms as per SOP. To check documents done by Jr. Analyst/ Fresher. Method development skills Trouble shooting of method Excel and MS Word.

Role & responsibilities Perform quality control testing of oncology products (raw materials, intermediates, and finished products) using validated analytical methods. Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, Dissolution Apparatus, FTIR, and other relevant equipment. Conduct stability testing as per ICH guidelines and prepare stability reports. Review and document analytical results in compliance with GDP and cGMP requirements. Identify and investigate deviations, OOS (Out of Specification) and OOT (Out of Trend) results, and implement corrective and preventive actions (CAPA). Support method validation, method transfer, and analytical troubleshooting. Ensure adherence to EHS (Environment, Health, and Safety) policies during laboratory operations. Maintain proper documentation, records, and ensure audit readiness for regulatory inspections (USFDA, MHRA, WHO, etc.). Collaborate with cross-functional teams to resolve quality issues and improve processes.

Role & responsibilities Perform quality control testing of oncology products (raw materials, intermediates, and finished products) using validated analytical methods. Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, Dissolution Apparatus, FTIR, and other relevant equipment. Conduct stability testing as per ICH guidelines and prepare stability reports. Review and document analytical results in compliance with GDP and cGMP requirements. Identify and investigate deviations, OOS (Out of Specification) and OOT (Out of Trend) results, and implement corrective and preventive actions (CAPA). Support method validation, method transfer, and analytical troubleshooting. Ensure adherence to EHS (Environment, Health, and Safety) policies during laboratory operations. Maintain proper documentation, records, and ensure audit readiness for regulatory inspections (USFDA, MHRA, WHO, etc.). Collaborate with cross-functional teams to resolve quality issues and improve processes.

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Planning/performing and reporting of acute toxicology studies Assist in preparation of SOP"™s, Protocols and Reports Participate in GLP / AAALAC related activities Literature search Maintenance of animal house and relevant documents as per GLP and AAALAC norms. To Assist and work along with SD and TC in Planning, initiation and conduct studies. Test item administration, dose formulation preparation and blood collection. Assistance in data collection, compilation and verification. Participate in GLP inspections and ensure relevant regulatory compliance guidelines. Support in interpretation and reporting of study data. Assist in report preparation and coordination of activities. Assist in archiving of all study related materials. Skills Required: Understanding of the agrochemical and pharmaceutical R&D process Behavioral Competencies: Good in oral / written communication skills. If you're interested in applying or learning more, send your updated resume to [email protected] with the subject line "Research Scientist/Senior Research Scientist - Acute "“ Toxicology - Bangalore". Qualifications Qualification M.Sc. in Zoology/Biosciences Additional Information Specialization Toxicology Department Acute "“ Toxicology Experience (years) 2 to 8 only

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Leadership role to manage team size of 10+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Managing multiple instruments (LC-MSMS, GC-MSMS, ICP-MS, IC etc.) Method development experience in LC-MSMS, GC-MSMS and ICPMS instrument Preparation and Implementation of SOP"™s related to E& L , general laboratory processes and best guidance. Good knowledge of 21 CFR part 11, Data Integrity principals, good documentation practices in cGMP lab Monitor and management of day-to-day laboratory activities Extensive knowledge of preparation, reviewing and approval capability for standard operating procedure (SOP) and COA Sound knowledge of structural elucidation and interpretation using analytical techniques such as NMR, IR, HPLC, GC, LC-MS etc. Resolving the team conflicts and provide training to the team for development and empowers team members Provide scientific and leadership direction to team members Good knowledge of laboratory safety and be a strong promoter of SHE activities in the lab. Skills Required: For M.Sc, 16-18 years of Discovery Analytical R&D experience and for PhD, 14-16 years of experience in CRO environment Excellent technical, problem-solving, writing, influencing and communication skills Strong leadership with excellent interpersonal skills, proven success of analytical projects and managing cross functional teams Demonstrative communication skills and confident in conveying information to internal/ external customers Skill for resolving the team conflicts and provide training to the team for development and empowers team members Behavioral Competencies: Excellent oral / written communication skills and flexibility to work in a dynamic environment Excellent in Knowledge sharing at all levels Qualifications Qualification M.Sc./PhD/Postdoc Additional Information Specialization Analytical Chemistry /Organic Chemistry, Department E&L Experience (years) 16 - 20

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. : Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.

Urgent opening for QC Officer-Sr. Officer in Dahej, Bharuch. Note: Walk In Interview at Bharuch Date & Time: 24th August, 2025 at 09:00 AM Onwards Job Location: Dahej, Bharuch Experience: 2 to 7 years in API Qualification: M.Sc./B.Pharm/M. Pharm Required Candidate profile Roles and Responsibilities: -Experience in Section LCMS / PSD / HPLC / GC /Method Validation -Candidate preferred from Pharma API (Active Pharmaceutical Ingredient).

Role & responsibilities Should perform sample processing smoothly as well as project execution with in assign time. Should handle instrument as well as QA observation. Should coordinate with Group members/ Group leader/ Lab manager Should be able to inspect raw data as per defined procedure. Should report inspection result properly. Should verify calibration record. Should maintain GLP in Lab. Preferred candidate profile 5-6 Years of Experience in Clinical Research Organizations only (Bio-Analytical Department) Qualification: MSC Immediate to 20 days joiners are preferred. You can also share your resumes on: pradnya.raut@accutestglobal.com for quicker callback

Job Requirements table {mso-displayed-decimal-separator:"\."; mso-displayed-thousand-separator:"\,";} tr {mso-height-source:auto;} col {mso-width-source:auto;} td {padding-top:1px; padding-right:1px; padding-left:1px; mso-ignore:padding; color:black; font-size:11.0pt; font-weight:400; font-style:normal; text-decoration:none; font-family:Calibri, sans-serif; mso-font-charset:0; text-align:general; vertical-align:bottom; border:none; white-space:nowrap; mso-rotate:0;} .xl16 {color:windowtext; font-size:14.0pt; font-weight:700; font-family:EMprint, sans-serif; mso-font-charset:0; text-align:center; vertical-align:middle; border-top:1.0pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:.5pt solid windowtext; border-left:1.0pt solid windowtext; white-space:normal;} .xl17 {font-family:Aptos, sans-serif; mso-font-charset:0; text-align:left; vertical-align:middle; border-top:.5pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:.5pt solid windowtext; border-left:1.0pt solid windowtext;} .xl18 {font-family:Aptos, sans-serif; mso-font-charset:0; text-align:left; vertical-align:middle; border-top:.5pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:.5pt solid windowtext; border-left:1.0pt solid windowtext; white-space:normal;} .xl19 {font-family:Aptos, sans-serif; mso-font-charset:0; text-align:left; vertical-align:middle; border-top:.5pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:1.0pt solid windowtext; border-left:1.0pt solid windowtext; white-space:normal;} Job Description - ICSR EngineerInvolve & support all phases in the ICS Cybersecurity (Work Practices) including implementation, deployment and stewardship.Operations & Maintenance - Support regular operations & maintenance stewardship and reporting activities for ICSR systems (i.e., review local operating procedures of BU against the ICSR WPs to ensure alignment, perform access reviews and periodic verification for ICSE, listing and reporting of cyber KPIs etc.)Support and involve in application of discipline design standards, specifications, codes, and appropriate safety/ security criteria.Support and involve in meeting industry standards (IEC 62443, NIST Cybersecurity Framework etc.) and regulatory requirements pertaining to ICS Cybersecurity.Support and involve in implementing cyber secure architecture of controls and safety systems.Support in management and assessment of cybersecurity controls and provide relevant improvement recommendations.Perform data collection and analysis related to ICSR with common database and software data analysis tools. Provide support for appropriate documentation.Support and involve in implementing technologies for ICSR.Support in inventory listing - Support to update BU ICSR inventory list in the WP recommended format, review of available documentation and gathering of informationSupport in assessment of threats to Control Systems (i.e. take inventory of required templates/documents to determine the key components/ equipment for risk assessments, stewarding/ participating in risk assessments, appropriate assignment of risk ratings, identification of Controls for the risk scenario or threat vector, obtain endorsement / approvals from Custodian and/or Business Owner, Perform periodic verifications to ensure that approved risk-reduction controls are in place and functioning for each ICSE zone) and management of security controls and processes.Information and Documentation - Identify and support required updates to documentation related to ICSR (i.e. organize required documents in designated folders (hard and soft), monitor and approve access to ICSR folders/ documentation via IT Help, ensure alignment with end-users on updates, document deviations for ICSR non-compliant systems, document all local operating procedures applicable to ICS environment, obtain endorsement and ensure availability for appropriate BU personnel)Third Party Services - Support the stewardship of controls for third party services (i.e., Document processes or procedures for Third Party Access, maintain/verify controls pertaining to Third Party access and External Connections, collaborate with ENC task force team, perform risk assessments for systems with ICSE External Connections, complete controls catalogs to meet ICSR requirements for external connections and ensure certification, Perform periodic verifications to ensure that approved risk-reduction controls are in place and functioning for each ENC)Personnel and Training - Support training activities for alignment on ICSR (i.e. Provide staff, visitors and guests who may have access to in-scope equipment with a brief training document, Follow Industrial Control Systems Visitor/ Guest ICSR Communication checklist, train BU personnel in performing Risk Assessments/Threat Vector Assessments using ASSET/ Other Tools, if any)Community Awareness and Emergency Preparedness - Support documentation of Cybersecurity Emergency Response Plan (CSERP) and Disaster Recover Plan (DRP), facilitate/ participate in CSERP/ DRP drills/ table-top exercise, document reports, implementation of drill recommendations and update the CSERP/DRP if necessary.Vulnerability Management - Review advisories/ vulnerability notifications pertaining to ICSE in scope equipments, document forward path/ mitigations/ workaround, execute/ plan for implementation.Assessment and Improvement - Support Continuous Improvement activities for ICSR (i.e., Work with ICSR CoE and BU controllers in assisting ICSR UIA and external audits, Review and endorsement of BU's deviations from ICSR v4 requirements, Help BU to close audit gaps and in sustaining closure actions.) Work Experience table {mso-displayed-decimal-separator:"\."; mso-displayed-thousand-separator:"\,";} tr {mso-height-source:auto;} col {mso-width-source:auto;} td {padding-top:1px; padding-right:1px; padding-left:1px; mso-ignore:padding; color:black; font-size:11.0pt; font-weight:400; font-style:normal; text-decoration:none; font-family:Calibri, sans-serif; mso-font-charset:0; text-align:general; vertical-align:bottom; border:none; white-space:nowrap; mso-rotate:0;} .xl16 {color:windowtext; font-size:14.0pt; font-weight:700; font-family:EMprint, sans-serif; mso-font-charset:0; text-align:center; vertical-align:middle; border-top:1.0pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:.5pt solid windowtext; border-left:1.0pt solid windowtext; white-space:normal;} .xl17 {font-family:Aptos, sans-serif; mso-font-charset:0; text-align:left; vertical-align:middle; border-top:.5pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:.5pt solid windowtext; border-left:1.0pt solid windowtext;} .xl18 {font-family:Aptos, sans-serif; mso-font-charset:0; text-align:left; vertical-align:middle; border-top:.5pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:.5pt solid windowtext; border-left:1.0pt solid windowtext; white-space:normal;} .xl19 {font-family:Aptos, sans-serif; mso-font-charset:0; text-align:left; vertical-align:middle; border-top:.5pt solid windowtext; border-right:1.0pt solid windowtext; border-bottom:1.0pt solid windowtext; border-left:1.0pt solid windowtext; white-space:normal;} Job Description - ICSR EngineerInvolve & support all phases in the ICS Cybersecurity (Work Practices) including implementation, deployment and stewardship.Operations & Maintenance - Support regular operations & maintenance stewardship and reporting activities for ICSR systems (i.e., review local operating procedures of BU against the ICSR WPs to ensure alignment, perform access reviews and periodic verification for ICSE, listing and reporting of cyber KPIs etc.)Support and involve in application of discipline design standards, specifications, codes, and appropriate safety/ security criteria.Support and involve in meeting industry standards (IEC 62443, NIST Cybersecurity Framework etc.) and regulatory requirements pertaining to ICS Cybersecurity.Support and involve in implementing cyber secure architecture of controls and safety systems.Support in management and assessment of cybersecurity controls and provide relevant improvement recommendations.Perform data collection and analysis related to ICSR with common database and software data analysis tools. Provide support for appropriate documentation.Support and involve in implementing technologies for ICSR.Support in inventory listing - Support to update BU ICSR inventory list in the WP recommended format, review of available documentation and gathering of informationSupport in assessment of threats to Control Systems (i.e. take inventory of required templates/documents to determine the key components/ equipment for risk assessments, stewarding/ participating in risk assessments, appropriate assignment of risk ratings, identification of Controls for the risk scenario or threat vector, obtain endorsement / approvals from Custodian and/or Business Owner, Perform periodic verifications to ensure that approved risk-reduction controls are in place and functioning for each ICSE zone) and management of security controls and processes.Information and Documentation - Identify and support required updates to documentation related to ICSR (i.e. organize required documents in designated folders (hard and soft), monitor and approve access to ICSR folders/ documentation via IT Help, ensure alignment with end-users on updates, document deviations for ICSR non-compliant systems, document all local operating procedures applicable to ICS environment, obtain endorsement and ensure availability for appropriate BU personnel)Third Party Services - Support the stewardship of controls for third party services (i.e., Document processes or procedures for Third Party Access, maintain/verify controls pertaining to Third Party access and External Connections, collaborate with ENC task force team, perform risk assessments for systems with ICSE External Connections, complete controls catalogs to meet ICSR requirements for external connections and ensure certification, Perform periodic verifications to ensure that approved risk-reduction controls are in place and functioning for each ENC)Personnel and Training - Support training activities for alignment on ICSR (i.e. Provide staff, visitors and guests who may have access to in-scope equipment with a brief training document, Follow Industrial Control Systems Visitor/ Guest ICSR Communication checklist, train BU personnel in performing Risk Assessments/Threat Vector Assessments using ASSET/ Other Tools, if any)Community Awareness and Emergency Preparedness - Support documentation of Cybersecurity Emergency Response Plan (CSERP) and Disaster Recover Plan (DRP), facilitate/ participate in CSERP/ DRP drills/ table-top exercise, document reports, implementation of drill recommendations and update the CSERP/DRP if necessary.Vulnerability Management - Review advisories/ vulnerability notifications pertaining to ICSE in scope equipments, document forward path/ mitigations/ workaround, execute/ plan for implementation.Assessment and Improvement - Support Continuous Improvement activities for ICSR (i.e., Work with ICSR CoE and BU controllers in assisting ICSR UIA and external audits, Review and endorsement of BU's deviations from ICSR v4 requirements, Help BU to close audit gaps and in sustaining closure actions.)

At USP, inclusive scientific collaboration is highly valued, recognizing the importance of diverse expertise in strengthening the development of trusted public health standards. The organizational culture at USP supports equitable access to mentorship, professional development, and leadership opportunities, reflecting the belief that broad participation in scientific leadership leads to more impactful global health outcomes. As an equal employment opportunity employer, USP is committed to fair, merit-based selection processes that enable the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Reasonable accommodations are provided to individuals with disabilities, and policies are in place to create an inclusive and collaborative work environment. This non-supervisory position at USP involves supporting the process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. The successful applicant will work on projects, including Analytical Method Development and evaluation for in-process samples in synthetic chemistry. Responsibilities also include performing a variety of routine and non-routine analytical tests, maintaining safety and GLP environment in the lab, development/validation of methods, stability studies, and research projects in analytical chemistry. The role requires directing, troubleshooting, and sharing insights on complex projects, collaborating closely with other scientists and/or USP personnel. As part of the mission to advance scientific rigor and public health standards, the individual in this position will contribute significantly to increasing global access to high-quality medicines through public standards and related programs. USP emphasizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure that health systems worldwide can rely on strong, tested, and globally relevant quality standards. The People and Culture division at USP, in collaboration with the Equity Office, invests in leadership and workforce development to equip all employees with the skills necessary to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist IV at USP will have responsibilities including supporting reaction monitoring, scale-up, and final analysis of samples, preparing development reports, executing projects as per specifications, timelines, and budget, reviewing SOPs, protocols, reports, and more. Collaboration with the synthetics team, evaluation and implementation of Process Analytical Technologies (PAT) capabilities, planning and completion of projects, participation in ISO-9001 certification, maintenance of GLP, and safety procedures in the lab are key aspects of the role. The successful candidate will have a Master's degree in Analytical Chemistry/Organic Chemistry/M. Pharm with 8-10 years of experience or a Ph.D. with 4-7 years of experience in Analytical Research and Development. Hands-on experience with chemical methods and various instruments, understanding of process analytical technology, analytical testing and development, technical writing, communication skills, and the ability to function in a team-oriented environment are essential qualifications. USP welcomes applications from individuals holding historically marginalized and/or underrepresented identities. Desired preferences include hands-on experience with PAT instruments and techniques, knowledge of API manufacturing and product testing, expertise with USP compendial methods and requirements, pharmaceutical laboratory experience, strong project management skills, and proficiency in data evaluation and problem-solving. USP provides benefits to protect the personal and financial well-being of employees and their families. USP, the U.S. Pharmacopeial Convention, is an independent scientific organization collaborating with top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. With a core value of Passion for Quality, USP aims to strengthen the supply of safe, quality medicines and supplements worldwide. In building an inclusive organizational culture, USP affirms the value of Diversity, Equity, Inclusion, and Belonging to ensure confidence in health and healthcare quality for all.,

At USP, we highly value inclusive scientific collaboration and acknowledge that attracting diverse expertise strengthens our ability to develop trusted public health standards. We cultivate an organizational culture that supports fair access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research embody our belief that ensuring broad participation in scientific leadership leads to stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is dedicated 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 offer reasonable accommodations to individuals with disabilities and uphold policies that foster an inclusive and collaborative work environment. This non-supervisory position is designed to support the process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. As a successful applicant in this role, you will work on projects involving Analytical Method Development and evaluation for in-process samples in synthetic chemistry. You will be responsible for performing a variety of non-routine and routine analytical tests, maintaining a safe & GLP environment in the lab, including the development/validation of methods, stability studies, and research projects in analytical chemistry. Additionally, you will direct, troubleshoot, and share insights on complex projects, draw independent conclusions about the results, and determine the project's next steps. Collaboration with other scientists and/or USP personnel will be a key aspect of this role. As part of USP's 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. Our organization prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure that health systems worldwide can rely on robust, tested, and globally relevant quality standards. The Scientist IV will have the following responsibilities: - Support reaction monitoring, scale-up, and final analysis of samples as per monograph / in-house procedures. - Prepare development reports for Synthetic Support projects. - Execute projects per approved test protocols. - Evaluate, implement, and enhance Process Analytical Technologies (PAT) capabilities in collaboration with the synthetics team. - Plan, execute, and complete projects as per specifications, timelines, and budget. - Prepare and review SOPs, protocols, reports, etc. - Coordinate with external vendors and relevant internal departments to ensure project requirements are met. - Ensure maintenance and calibration of equipment, IQ/OQ/PQ of new instruments, and preparation for ISO-9001 certification/recertification. - Maintain GLP and implement safety procedures in the lab. - Work on any other assigned tasks/lab management activities. - Collaborate within the team and cross-functional teams. - Learn and practice Diversity, Equity, Inclusion & Belonging culture. The successful candidate should have a demonstrated understanding of the organization's mission, a commitment to excellence through inclusive and equitable behaviors, and the ability to quickly build credibility with stakeholders. Additionally, the following competencies and experience are required: - MSc. in Analytical Chemistry / Organic Chemistry/M. Pharm with 8-10 years of experience or Ph.D. with 4-7 years of experience in Analytical Research and Development. - Hands-on experience with chemical methods and instruments like HPLC, GC, LC-MS, GC-MS, FTIR, UV-Visible, wet chemistry, etc. - Understanding of process analytical technology, chemometrics, and knowledge of in-line, online, at-line process analytical tools. - Experience in analytical testing and development with a focus on process analytical chemistry. - Comprehensive understanding of synthetic organic molecules development and analytical chemistry. - Ability to perform analytical method developments and validations. - Excellent technical writing and verbal communication skills. - Good interpersonal skills and ability to function in a team-oriented environment. USP welcomes applications from individuals with historically marginalized and/or underrepresented identities. Candidates possessing many, though perhaps not all, qualifications are encouraged to apply. Additional desired preferences include hands-on experience with PAT instruments, familiarity with a variety of software and laboratory information systems, knowledge of API manufacturing and product testing, expertise with USP compendial methods and requirements, and strong project management skills. USP provides benefits to protect the well-being of employees and their families, including company-paid time off, comprehensive healthcare options, and retirement savings. Please note that USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under a specific written agreement with USP.,

We are seeking a proactive Sr. Research Associate I- Analytical to independently handle analytical chemistry tasks. You will be responsible for method development and purification of samples using various chromatographic instruments. This role requires the ability to troubleshoot instruments and apply a strong knowledge of instrumental techniques to support drug discovery and development services. Roles & Responsibilities: Independently handle routine analysis on respective instruments. Conduct method development and purification of samples on chromatographic instruments such as HPLC, Prep-HPLC, SFC, and Prep-SFC . Troubleshoot analytical instruments to ensure their reliable operation. Apply knowledge of instrumental techniques and software in practical applications. Skills Required: Strong knowledge of instrumental techniques and their software applications. Ability to troubleshoot analytical instruments. Experience in method development on LCMS is desirable. QUALIFICATION: Master's or Bachelor's degree in Chemistry, Analytical Chemistry, or a related field.

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

As a member of our team, you will be responsible for handling various analytical instruments such as HPLC, LCMS, GC, Prep HPLC, SFC, Prep SFC, KF, and SOR including the associated software. Your main duties will involve method development using HPLC/GC for raw materials, intermediates, and final products, in accordance with ICH guidelines. You will also provide in-process analysis support, calibrate HPLC and GC instruments, prepare SOPs and GDLs as necessary, and handle documentation including STP and report preparation. Troubleshooting of analytical instruments like HPLC and GC, as well as analytical data for purity confirmation, will be part of your routine tasks. Additionally, you will be involved in isolation and purification by Prep HPLC for various products, known and unknown impurities. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that offers comprehensive services across the drug life cycle. With a global network of facilities in North America, Europe, and Asia, we provide drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products are also within our scope. PPS extends its services to biologics including vaccines, gene therapies, and monoclonal antibodies, facilitated by Piramal Pharma Limited's investment in Yapan Bio Private Limited. With a proven track record as a trusted service provider across diverse technologies, we are the preferred partner for innovators and generic companies globally. At Piramal Group, we uphold equal employment opportunities, making our decisions based on merit, qualifications, skills, performance, and achievements. We are committed to ensuring that all applicants and employees are treated fairly in personnel matters, including recruitment, selection, training, promotion, compensation, and working conditions. We provide equal opportunities for individuals with disabilities and accommodate needs related to religious observance or practice. Our core values drive us towards inclusive growth while maintaining ethical and values-driven practices.,

As an Analytical Chemist at our company, you will be responsible for developing analytical methods using techniques such as HPLC, GC, LCMS, KF, and FTIR for routine analysis. You will also be in charge of maintaining analytical documentation including protocols, specifications, etc. Calibration of HPLC and GC instruments will be part of your regular tasks. It is essential that you are knowledgeable about data integrity and ALCOA guidelines. Additionally, you will be involved in chiral method development to support our analytical processes.,

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

Analytical method development Routine Analysis by HPLC, GC, LCMS, KF and FTIR Analytical documentation as like Protocols, specifications etc. Calibration of HPLC, GC instruments Aware about data integrity and ALCOA Chiral method development 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

Overview Waters, the world&aposs leading specialty measurement company that cares about inclusion and diversity is seeking for an Account Manager Systems / Instruments to support the very successful growth of our businesses across Ahmedabad, Gujarat. . Waters deliver benefits through innovation and people that enable customer success in the life, materials and food sciences. People create the Waters difference. By engaging with our talented and diverse workforce we continuously evolve, develop and improve our products. We believe in delivering innovative technology and system solutions to our valued customers to enable their success. Our talented field sales/service and specialist teams have over the years delivered great and sustainable business results. With a constant focus on growth and by developing new markets we are able to increase the business even within very challenging economic circumstances. As Account Manager , you are an ambassador of Waters and will bring to the market Waters products and services. You will demonstrate a clear grasp of understanding the customers business and its growth plans, as well as be able to take the knowledge and convert that into a solution and offering from Waters, with a primary aim of bringing customer success. This position brings you a great degree of flexibility working in the field. Your role will be designated to either a territory and/or markets. Responsibilities Addressing new and existing customers in diverse markets (Pharma, Biopharma, Chemical materials, Food, Environmental, Clinical, Academia); Maintaining and developing existing customer and identifying and developing new accounts; Visiting regularly customers within the assigned territory; Organising, delivering and following up seminars and workshops at customer sites; Providing customers with high quality technical advice whilst maintaining a focus on maximising the sales potential; Collaborating, liaising and providing guidance and support across departments to ensure customer success. You will be working closely with all other groups at Waters (e.g. Instrument Sales, Chemistry Operation and Informatics etc.); Formulating and successfully implementing business plans; Planning and prioritising personal time and sales activities; Adhering to Waters and customers relevant Health, Safety and Environment requirements when on site and as an individual employee; Using related systems, e.g. CRM, Service Plan, Quotation system, with a keen mind on improvements and upgrades. Qualifications Education: Bachelors Degree, Masters, or PhD in scientific area such as chemistry, biology, or biochemistry Experience: Knowledge of Liquid Chromatography and Sample Preparation; Nice to have technical and practical solution Selling Experience, particularly in LC, LCMS & Informatics Products. Exposure w ithin a HPLC laboratory. Method development preferred; Skills: Action oriented and eager to achieve results Strong technical background in analytical technologies, especially LC and MAction oriented and eager to achieve results Sound communication and presentation skills Highly organized / well-prepared / time management skills Strong interpersonal skills and a good listener Matured disposition, positive attitude and strong sense of commitment Strong technical background in analytical technologies, especially LC and MS Travel: This is a territory-based position with travelling within your designated territory, and occasional travels to other countries for activities such as governance of department, local business support, meetings and training. Company Description Waters Corporation (NYSE:WAT) is a global leader in analytical instruments, separations technologies, and software, serving the life, materials, food, and environmental sciences for over 65 years. Our Company helps ensure the efficacy of medicines, the safety of food and the purity of water, and the quality and sustainability of products used every day. In over 100 countries, our 7,600+ passionate employees collaborate with customers in laboratories, manufacturing sites, and hospitals to accelerate the benefits of pioneering science . Diversity and inclusion are fundamental to our core values at Waters Corporation. It benefits our employees, our products, our customers and our community. Waters complies with all applicable federal, state, and local laws. Qualified applicants are considered without regard to sex, race, color, ancestry, national origin, citizenship status, religion, age, marital status (including civil unions), military service, veteran status, pregnancy (including childbirth and related medical conditions), genetic information, sexual orientation, gender identity, legally recognized disability, domestic violence victim status, or any other characteristic protected by law. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. All hiring decisions are based solely on qualifications, merit, and business needs at the time. Show more Show less

Responsibilities: * Perform preventative maintenance on analytical instruments * Conduct field instrumentation checks * Maintain electrical instrumentation * Calibrate equipment according to schedule Health insurance Accidental insurance Gratuity Provident fund

You get to collaborate on: Work closely with discovery specialists, disease area scientists and in vivo team members. Handling of laboratory animals like rat, mice, Guniea Pig and Rabbits. Dose administration to experimental animals by different routes and small animals surgery (like cannulations, CSF fluid collection) and handling, followed by compound dose preparation, administration to experimental animals. Contributing to the ongoing drug discovery programs by conducting in vivo DMPK studies for NCEs with a good knowledge of in vivo animal models. Data generation, analysis, compilation, report preparation. Regular uploading of the data. Conduct statistically supported data (analysis using win online) and deliver results in a timely manner to enable informed decision-making Understanding systems, processes, and compliance. Prepare, review, and deliver scientific presentations for internal/external use. Participate in cross-functional team activities, add value to research projects through creative ideas. Learn from top-notch drug discovery scientists across the world and opportunity to get trained in people skills. PK-PD studies in rat and mice of NCE.

HIRING FOR OSD - PRODUCTION & QC PRODUCTION(OSD) Experience: (01-07Years) Compression, Granulation, Coating, Capsule filling, Inspection QC Experience: (02-09Years) HPLC, GC, RM,PM, Stability, IP/FP, Method Development, Method Transfer QUALIFICATION : ITI/DIPLOMA/BSC/MSC/B PHARM/M PHARM With relevant Experience ITI/DIPLOMA/BSC/MSC/B PHARM Freshers can Apply DESIGNATIONS: Operator/Sr Operator/Jr Officer/Officer/Jr Executive/Executive INTERVIEW VENUE: SK Consultancy Services, H.No-1-77, 3rd Floor, Bachupally X Road, Opposite Sri Swastik Multi Specialty Hospital, Towards Nizampet Road DATE &TIME: 26th July 2025 ( Saturday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume 3 Month Pay slips Increment letter Previous company relieving letters Education Documents and ID Proofs Help Us Spread the Word (Refer): Circulate it in your Social Networking sites and groups for better reach and Refer your friends and colleagues, it could be a great opportunity for someone in need! WORK LOCATION: Hetero Labs Limited, UNIT V Polleypally, Jadcherla, Mahabubnagar CONTACT INFO: E-mail: Ashok.ch@hetero.com & Contact:8555912639 for further info.

Role & responsibilities Experience Minimum 3-5 years of experience in handling ADME assays and HPLC and LCMS/MS Skills and Capabilities Expertise in column selection, mobile phase selection, solvent preparations and sample processing techniques such as protein precipitation, liquid-liquid extraction and solid phase extraction is mandatory Sample processing of New chemical entities from various in-vitro and in-vivo studies executed in Preclinical discovery by using appropriate extraction methods Should be able to develop and validate LC-MS based qualitative/quantitative methods and apply them in routine analysis Should be well versed with internet-based literature search and capable of implementing the Learnings as and when required Candidate is expected to have basic understanding in interpretation of Mass/UV Spectra Should ensure preventative maintenance and calibration schedules of HPLC & mass spec by coordinating with vendor and support staff General understanding of Drug metabolism and Pharmacokinetics Should be able to deliver scientific presentation in departmental journal club and write official Project reports Preferred candidate profile M. Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis.