565 Chromatography Jobs - Page 8

Job Overview JOB DESCRIPTION As a Peptides Production Trainee, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes Key Responsibilities Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Preferred Candidate Profile Masters/Bachelors degree in Chemistry or a related field. Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Qualifications Masters/Bachelors degree in Chemistry or a related field. About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer 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. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

Title: Senior Officer Custom Field 2: 2727 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. Preparation and maintenance of volumetric solutions, buffers, etc Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., as per calibration schedule Experience in chemical analysis like, titration, moisture, LOD, sulphated ash, TLC IR, SOR, Clarity of solutions and quantitative solubility tests Exposure of GMP / GLP / GDP in laboratory. Knowledge of separation techniques in chemical separation in chromatography in Normal and reversed phase systems Preparation of Standard operating procedures (SOP) for all the instruments, equipment and procedures. Qualification of instruments Job Segment: Chemical Research, Laboratory, Engineering, Science

Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP for Oil & Gas Downstream Good to have skills : NAMinimum 12 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your day will involve overseeing the application development process and ensuring seamless communication within the team and stakeholders. Roles & Responsibilities:- Expected to be an SME- Collaborate and manage the team to perform- Responsible for team decisions- Engage with multiple teams and contribute on key decisions- Expected to provide solutions to problems that apply across multiple teams- Lead the application development process effectively- Ensure timely delivery of high-quality applications- Provide guidance and mentorship to team members Professional & Technical Skills: - Must To Have Skills: Proficiency in SAP for Oil & Gas Downstream- Strong understanding of application development processes- Experience in leading application design and configuration- Knowledge of industry-specific best practices in Oil & Gas Downstream sector- Hands-on experience in implementing SAP solutions for Oil & Gas industry Additional Information:- The candidate should have a minimum of 12 years of experience in SAP for Oil & Gas Downstream- This position is based at our Hyderabad office- A 15 years full-time education is required Qualification 15 years full time education

𝐖𝐞 𝐚𝐫𝐞 𝐡𝐢𝐫𝐢𝐧𝐠 𝐚 𝐏𝐫𝐨𝐝𝐮𝐜𝐭 𝐌𝐚𝐧𝐚𝐠𝐞𝐫 𝐭𝐨 𝐥𝐞𝐚𝐝 𝐨𝐮𝐫 𝐂𝐏𝐂 𝐒𝐲𝐬𝐭𝐞𝐦𝐬 𝐩𝐨𝐫𝐭𝐟𝐨𝐥𝐢𝐨 𝐚𝐜𝐫𝐨𝐬𝐬 𝐈𝐧𝐝𝐢𝐚 . Here is the thing. This is not your regular sales job. You will 𝐨𝐰𝐧 𝐚 𝐧𝐢𝐜𝐡𝐞 𝐩𝐫𝐨𝐝𝐮𝐜𝐭, work with people who take science seriously, and build something meaningful over time. The product is 𝐬𝐭𝐫𝐨𝐧𝐠, but not well-known. That means your approach has to be 𝐟𝐨𝐜𝐮𝐬𝐞𝐝, 𝐜𝐥𝐞𝐚𝐫, and 𝐜𝐨𝐧𝐬𝐢𝐬𝐭𝐞𝐧𝐭. You will work with 𝐩𝐞𝐩𝐭𝐢𝐝𝐞 𝐦𝐚𝐧𝐮𝐟𝐚𝐜𝐭𝐮𝐫𝐞𝐫𝐬, 𝐩𝐫𝐨𝐜𝐞𝐬𝐬 𝐜𝐡𝐞𝐦𝐢𝐬𝐭𝐬, and 𝐞𝐱𝐭𝐫𝐚𝐜𝐭𝐢𝐨𝐧 𝐬𝐜𝐢𝐞𝐧𝐭𝐢𝐬𝐭𝐬. They know what they want, and it is not marketing talk. It is real science. 𝐁𝐚𝐬𝐞𝐝 𝐢𝐧 𝐇𝐲𝐝𝐞𝐫𝐚𝐛𝐚𝐝 (𝐇𝐞𝐚𝐝 𝐎𝐟𝐟𝐢𝐜𝐞) 𝐖𝐡𝐨 𝐬𝐡𝐨𝐮𝐥𝐝 𝐚𝐩𝐩𝐥𝐲 ? 𝐁𝐚𝐜𝐡𝐞𝐥𝐨𝐫𝐬/𝐌𝐚𝐬𝐭𝐞𝐫𝐬 𝐢𝐧 𝐂𝐡𝐞𝐦𝐢𝐬𝐭𝐫𝐲, 𝐁𝐢𝐨𝐭𝐞𝐜𝐡, 𝐨𝐫 𝐏𝐡𝐚𝐫𝐦𝐚 𝟒–𝟔 𝐲𝐞𝐚𝐫𝐬 𝐞𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞 𝐢𝐧 𝐜𝐡𝐫𝐨𝐦𝐚𝐭𝐨𝐠𝐫𝐚𝐩𝐡𝐲 𝐨𝐫 𝐩𝐫𝐞𝐩𝐚𝐫𝐚𝐭𝐢𝐯𝐞 𝐩𝐮𝐫𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧 𝐇𝐚𝐧𝐝𝐬-𝐨𝐧 𝐰𝐢𝐭𝐡 𝐩𝐞𝐩𝐭𝐢𝐝𝐞 𝐬𝐲𝐧𝐭𝐡𝐞𝐬𝐢𝐳𝐞𝐫𝐬 = 𝐛𝐢𝐠 𝐩𝐥𝐮𝐬 𝐂𝐚𝐧 𝐛𝐫𝐞𝐚𝐤 𝐝𝐨𝐰𝐧 𝐜𝐨𝐦𝐩𝐥𝐞𝐱 𝐬𝐭𝐮𝐟𝐟 𝐢𝐧𝐭𝐨 𝐜𝐥𝐞𝐚𝐫 𝐥𝐚𝐧𝐠𝐮𝐚𝐠𝐞 𝐎𝐰𝐧𝐬 𝐭𝐡𝐞 𝐣𝐨𝐛. 𝐃𝐨𝐞𝐬 𝐧𝐨𝐭 𝐰𝐚𝐢𝐭 𝐭𝐨 𝐛𝐞 𝐭𝐨𝐥𝐝. If you want to 𝐛𝐮𝐢𝐥𝐝 𝐚 𝐭𝐞𝐜𝐡𝐧𝐢𝐜𝐚𝐥 𝐜𝐚𝐫𝐞𝐞𝐫, not just chase monthly numbers, this could be your thing. You will work closely with 𝐠𝐥𝐨𝐛𝐚𝐥 𝐭𝐞𝐚𝐦𝐬, get visibility across a growing niche, and shape how this product evolves in India. 𝐃𝐌 𝐝𝐢𝐫𝐞𝐜𝐭𝐥𝐲 𝐢𝐟 𝐲𝐨𝐮 𝐚𝐫𝐞 𝐢𝐧𝐭𝐞𝐫𝐞𝐬𝐭𝐞𝐝. www.inkarp.co.in #lifesciences #productmanagement #chromatography #hiringnow #peptides #scientificsales #jobsearchindia #hyderabadjobs #sciencecareers #biotechindia #pharmaroles #CPCsystems #inkarp

Trending Job Description Key responsibilities of this job role include: Design and execute multistep organic syntheses under the supervision of senior scientists. Having knowledge of enzymatic reactions. Perform compound purification using techniques such as column chromatography, recrystallization, HPLC, etc. Characterize synthesized compounds using analytical techniques (NMR, LC-MS, IR, UV-Vis, etc.). Maintain accurate and detailed records of all experiments Participate in group meetings and contribute to scientific discussions. Ensure compliance with laboratory safety protocols and chemical handling guidelines. Assist in the preparation of reports, presentations, and research publications. Qualifications M.Sc. in Organic Chemistry, Medicinal Chemistry with 3-4 years of experiences or fresh Ph.D in organic chemistry. About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer 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. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 8460 Job Category R & D Posting Date 07/07/2025, 05:40 AM Job Schedule Full time Locations Piramal Enterprises Limited, Navi Mumbai, Maharashtra, 400701, IN

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities (small molecules and peptides) through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Senior Scientist I Has The Following Responsibilities Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules & peptides. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Execute small molecule synthesis and, solid-phase and solution-phase peptide synthesis with a focus on quality. Perform peptide modification techniques, including cyclization, disulfide bridge formation, stapling, and derivatization. Support in characterization of peptides by utilizing advanced characterization techniques such as LCMS, HPLC, and NMR to ensure peptide quality and accuracy. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab. Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience M Sc (Organic Chemistry) from a reputed university with minimum 11-13 years of industrial experience in API Process R&D/CDMO/CRO (OR) Ph.D (Full Time) in Synthetic Organic Chemistry from a reputed group with 7-10 years of post doctoral and/or industrial research experience in API Process R&D/CDMO/CRO. Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of Small Molecule APIs/ NCEs on lab scale and production. Experience in handling automated peptide synthesizers and purification processes is highly desirable. Proven ability for adoption of QMS and documentation procedure Adherence to lab safety guidelines Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions, solid phase and complex peptide synthesis and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Good practical, documentation & presentation skills. Attention to detail, stratregic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist I/II Has The Following Responsibilities Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience M Sc (Organic Chemistry) from a reputed university with minimum 1-6 years of industrial experience in API Process R&D/CDMO/CRO Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale and production. Proven ability for adoption of QMS and documentation procedure Adherence to lab safety guidelines Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Good practical, documentation & presentation skills. Attention to detail, strategic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons. 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 DESCRIPTION Designation: Associate Scientist Job Location: Bangalore Department: DDS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Key Responsibilities: Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipmentEnsure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipmentRecord the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. Ensure that the instrument / equipment s are calibrated, undergone preventive maintenance, and are kept clean before use and in case of any breakdown, report to maintenance immediatelyEnsure that they know the MSDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS normsAttend all mandatory trainings and update training records as and when trainings are completedAlways ensure confidentialityPrepare SOPs/IOPs/EOPs/OCPs when any new lab activity is identified or existing one requires updatingAny other lab responsibilities as indicated by the EHSQ team member/ supervisor / group leader. Understanding and demonstrating responsibility for safety of self & colleagues by following all safety protocols provided by SyngeneAdherence to all environment, health, and safety (EHS) policies & standards always in the workplaceWearing all PPE as required. Adherence to all procedures related to Syngene s data integrity policiesCompliance to Syngene s quality standards at all times. For running independent project(s) in the areas of immuno-oncologyFor driving the assigned project with full commitment, To champion the biology of project, establish all assays, models required to drive the project and work in collaboration with team members within the domain, across different domains and across departmentTo take active participation in running experiments, compiling the data in required format and prepare study reportsTo train and mentor other scientists in a timely mannerTo work in a collaborative fashion with research scientists from various disciplines Educational Qualification: MSc (Chemical Sciences). Experience: 5 - 8 Years Required Skills: Should be familiar with concepts of chemical synthesisFamiliar with operations of relevant apparatus - instrument / equipment. Good Knowledge of analytical techniques and analytical data interpretation. Good communication skills Behavioral Skills: Good communication skills, good presentation skills, hardworking, sincere and a team player. Must demonstrate integrity and take accountability of their work Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Description The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist III/IV has the following responsibilities: Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: Scientist III/IV – M Sc (Organic Chemistry) from a reputed university with minimum 6-10 years of industrial experience in Pharmaceutical Process R&D or CRAMS or CRO set up (Or) Ph.D (Full Time) in Synthetic Organic Chemistry from a reputed group with minimum 1-7 years post-doctoral/industrial research experience in organic synthesis Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale. Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions, and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Have good practical, documentation & presentation skills. Attention to detail, strategic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

Company Description SMART Labtech is a leading developer and supplier of high-value Laboratory Analytical, Biotechnological, Environmental, Microscopic, and Weighing equipment. Headquartered in Hyderabad, India, SMART Labtech focuses on innovation and state-of-the-art scientific tools for various applications. The company prioritizes customer satisfaction by providing quality products and effective after-sales service. Our products comply with CE certifications and advance discoveries in genomics and proteomics, drug discovery processes, and life science research. SMART Labtech maintains a strong sales and distribution network with extensive training for our sales representatives. Role Description This is a full-time on-site role for a Sales Executive (Chromatography) at our Hyderabad Location .The Sales Executive is responsible for identifying and meeting potential customers, understanding their requirements, and offering suitable chromatography solutions. The role includes managing sales cycles, establishing and maintaining customer relationships, presenting product demonstrations, and providing effective after-sales support. The Sales Executive will ensure that customer needs are met with top-quality laboratory products and services. Qualifications One or two years Experience in chromatography sales is an advantage Knowledge of chromatography and laboratory equipment Excellent communication, presentation, and negotiation skills Strong organizational and time management abilities Ability to work independently and as part of a team Bachelor's degree in Chemistry, Biotechnology, or related field

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist III/IV Has The Following Responsibilities Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience Scientist III/IV – M Sc (Organic Chemistry) from a reputed university with minimum 6-10 years of industrial experience in Pharmaceutical Process R&D or CRAMS or CRO set up (Or) Ph.D (Full Time) in Synthetic Organic Chemistry from a reputed group with minimum 1-7 years post-doctoral/industrial research experience in organic synthesis Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale. Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions, and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Have good practical, documentation & presentation skills. Attention to detail, strategic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time

Job Title: General Manager (Sales & Marketing) Location: Thane, Maharashtra Experience Required: 7 to 10 Years Qualification: MBA in Sales and Marketing Salary: ₹12 to ₹15 LPA About the Company: BSB Pharma Analytic Pvt. Ltd. (A Client Company of FireSpark Services) is a fast-growing company based in Mumbai, specializing in high-quality chromatography consumables for HPLC and GC applications. We are committed to precision, innovation, and delivering world-class products such as vials, caps, syringe filters, and lab accessories. With a strong focus on quality, research, and customer satisfaction, we are scaling rapidly and looking for passionate professionals to grow with us. About the Role: We are seeking a dynamic and experienced General Manager to lead our operations and drive strategic growth. The ideal candidate will possess strong leadership capabilities, a proven track record in sales and marketing, and the ability to oversee cross-functional teams to ensure the compan meets its business goals. Key Responsibilities: • Lead and manage all business operations across departments including sales, marketing, finance, HR and administration. • Develop and execute growth strategies in line with company objectives. • Drive business development and client acquisition to expand market presence. • Analyze sales and marketing performance metrics and identify areas for improvement. • Set quarterly and annual performance goals for teams and monitor KPIs. • Foster a high-performance work culture through leadership, mentoring, and team engagement. • Ensure efficient allocation of resources and manage budgets effectively. • Oversee compliance with company policies, legal standards, and industry regulations. • Report directly to senior leadership and provide regular updates on progress and challenges. Requirements: • MBA in Sales and Marketing from a reputed institution. • 7–10 years of proven experience in a managerial or leadership role, preferably in a similar industry. • Strong understanding of sales, marketing, and business operations. • Exceptional leadership, communication, and decision-making skills. • Proficiency in data-driven strategy planning and execution. • Ability to thrive in a dynamic and fast-paced environment. What We Offer: • Competitive annual package of ₹12 to ₹15 LPA based on experience and skill set. • Opportunity to work with a growing and innovative team. • Performance-based incentives and growth opportunities. • Professional development and leadership training.

Akshara Consultancy - Laboratory Items Distribution Company Qualifications: Bachelors degree,or masters preferably Pharmaceutics, or Pharmacology 2-3 years of sales experience, preferably in pharmaceutical laboratory items. Key Responsibilities: Sell laboratory items, including microbiology and chromatography products (HPLC/GC vials and columns). Develop and expand client relationships. Conduct regular field visits to follow up with clients and secure orders. Maintain and enhance sales performance for both existing and new business. Travel across Telangana to meet clients and ensure customer satisfaction. Desired Skills and Attributes: Strong interpersonal and communication skills. Ability to work independently and manage time effectively. Self-motivated with a proactive sales approach. Willingness to travel extensively within the region.

Date: 3 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Dedicated Centre JOB DESCRIPTION Designation: Associate Scientist Job Location: Bangalore Department: DDS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Key Responsibilities: Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipmentEnsure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipmentRecord the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially.Ensure that the instrument / equipment’s are calibrated, undergone preventive maintenance, and are kept clean before use and in case of any breakdown, report to maintenance immediatelyEnsure that they know the MSDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS normsAttend all mandatory trainings and update training records as and when trainings are completedAlways ensure confidentialityPrepare SOPs/IOPs/EOPs/OCPs when any new lab activity is identified or existing one requires updatingAny other lab responsibilities as indicated by the EHSQ team member/ supervisor / group leader.Understanding and demonstrating responsibility for safety of self & colleagues by following all safety protocols provided by SyngeneAdherence to all environment, health, and safety (EHS) policies & standards always in the workplaceWearing all PPE as required.Adherence to all procedures related to Syngene’ s data integrity policiesCompliance to Syngene’ s quality standards at all times.For running independent project(s) in the areas of immuno-oncologyFor driving the assigned project with full commitment,To champion the biology of project, establish all assays, models required to drive the project and work in collaboration with team members within the domain, across different domains and across departmentTo take active participation in running experiments, compiling the data in required format and prepare study reportsTo train and mentor other scientists in a timely mannerTo work in a collaborative fashion with research scientists from various disciplines Educational Qualification: MSc (Chemical Sciences). Experience: 5 - 8 Years Required Skills: Should be familiar with concepts of chemical synthesisFamiliar with operations of relevant apparatus - instrument / equipment.Good Knowledge of analytical techniques and analytical data interpretation.Good communication skills Behavioral Skills: Good communication skills, good presentation skills, hardworking, sincere and a team player. Must demonstrate integrity and take accountability of their work Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

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

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard Office Hours (40/wk) Environmental Conditions Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description About Chromatography & Mass Spectrometry Division! The Chromatography and Mass Spectrometry business creates innovative instruments, consumables, and software solutions for analytical sciences. Roles And Responsibilities Support Thermo Fisher customers through technical service, installation, operation, training, and repair of specialized analytical equipment like HPLC and CAD (Aerosol detector). Undertake product installation on client premises and demonstrate features related to 21 CFR compliance. Provide training and technical advice on instrument use, both in person and by phone, sharing Dos and Don’ts for optimum performance of the system. Investigate difficulties and solve faults arising from operation or utilization. Rectify problems, suggest solutions, or arrange for repairs to be made. Provide a vital link between customers and Sales and Marketing. Ensure effective service is provided to the customer by maintaining communication between the customer and the company. Monitor repairs in terms of the organization’s service/warranty cover and make suggestions for product improvements. Carry out planned maintenance calls and perform regular customer visits. Make recommendations about spare parts requirements and assist with monitoring equipment. Achieve assigned spares and service revenue targets by promoting PM kits, instrument upgrades, and software upgrades. Extensive traveling within the territory is required, with potential travel outside the territory if needed. Knowledge, Skills, And Abilities Bachelor of Technology (Biotechnology/Electronics). 4 to 5 experience in analytical equipment like HPLC and CAD (Aerosol detector). Proficient in written and verbal communication. Interpersonal skills needed for a role that involves interacting with various individuals within and outside the company. Ability to prioritize service requests and produce clear and concise documentation. Self-motivated and proactive in technical and support approaches. Work closely with customers to understand their pain areas and act as a consultant between the organization and the customer, helping both achieve regional commercial goals. Build good rapport with customers and educate them about the procurement of PM kits annually, reducing system downtime.

Sales of Filtration Products from leading Filtration brands in Pharmaceuticals (API & Formulation), Biopharma (Mabs, Vaccines, Other Biosimilars), Oil & Gas industries, Ultrapure Water, Digital Inks & Printers Visiting Industrial across the assigned region for pitching High Performance Industrial products for various applications. The candidate will undergo training and will be meeting key decision makers in the industry and do value selling. Candidate will hold Technical/Commercial discussions with R&D, Manufacturing, Production providing them product benefits, commercial offers, negotiations, order execution followed by payment collection. The candidate will adhere to the visit plans & provide regular visit report to Manager. Candidate will be empowered with data for Sales forecasting Monthly, Quarterly and Annually based on sales history and new developments. All new developments will be uploaded in Sales Funnel for Customer mapping and keeping Track of competitors activities in the region. Candidate will partner with the Sales Manager to meet and exceed sales targets and developing new accounts to grow the business. Role & responsibilities Preferred candidate profile

BD & provide technical support. Handle Multistep Synthesis. Peptides Synthesis using Solid Phase Peptide Synthesis. Design & synthesis of small molecules in API. Handling synthesis of organic chemical reactions.Knowledge on Instrumentation is a must. Annual bonus Provident fund Health insurance

Job description Job title: Senior Research Associate Job location: Hyderabad Job grade: 9-II About Syngene: Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: Personnel handling this profile will be working in Syngene reaction screening facility and responsible for setting library of reaction in small scale to optimize one reaction condition. The candidate should be good in data analysis and report making and metal catalyzed coupling reactions. Experience of handling glove box will be preferred. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene. Role Accountabilities: Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipments . Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. The candidate should be capable of meeting Syngene s productivity expectations (# of compounds/month and # of steps/month) without compromising on safety and quality. The candidate should have excellent analytical interpretation and making report. Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 4-6 years Skills and Capabilities: Should have deeper knowledge with concepts of organic synthesis and reaction mechanism and metal catalyzed coupling reactions. Candidate should be capable of solving synthetic problems independently Should be excellent in purification and analytical interpretation, especially LCMS, UPLCMS skills. Familiar with operations of relevant apparatus - instrument / equipment. Glove-box uses experience will be preferred Handling small scale reaction Education M. Sc in general or organic chemistry

We are seeking a dedicated and detail-oriented Junior R&D Lab Chemist to support research and product development activities in our laboratory. The role involves assisting in experiments, analyzing chemical compounds, and maintaining lab equipment and documentation under the guidance of senior scientists or chemists. Key Responsibilities: Assist in the formulation and testing of new products or materials. Conduct laboratory experiments according to established protocols and safety standards. Analyze samples using techniques such as titration, spectroscopy, chromatography, or other analytical methods. Maintain accurate and detailed records of experiments, results, and observations. Prepare chemical solutions and reagents as required for experiments. Calibrate, clean, and maintain laboratory equipment s. Support scale-up trials and process optimization efforts. Ensure compliance with internal safety, health, and environmental policies. Collaborate with cross-functional teams including production, quality control, and regulatory. Qualifications: Bachelor s degree in Chemistry, Chemical Engineering, or a related field. 1 to 3 years of experience in a laboratory or R&D environment (freshers, internship or training experience is also preferred). Knowledge of laboratory practices, chemical handling, and safety procedures. Familiarity with analytical instruments and lab software is a plus. Strong attention to detail, analytical thinking, and documentation skills. Willingness to learn and take direction in a fast-paced research environment. Working Conditions: Laboratory environment; exposure to chemicals and lab equipment. Use of personal protective equipment (PPE) is mandatory. May involve standing for extended periods and handling hazardous materials. Key Skills : Titration Spectroscopy Calibrate

Job Overview As a Peptides Production Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Roles & Responsibilities: Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunitie Experience 4 to 6 Yrs experience in Peptides Manufacturing Preferred candidate profile: Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes.

Job Overview As a Peptides Production Sr Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities: Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Experience 4 to 6 Yrs experience Peptides Production Preferred candidate profiles Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Qualifications Masters/Bachelors degree in Chemistry or a related field.

Job description Job Description: HPLC Analyst - Pharma Background only. Company: Sain Medicaments Pvt Ltd, UPPAL, HYDERABAD. Location: Uppal, Hyderabad Industry: Pharmaceutical (Pharma Experience Required) We are seeking a skilled and experienced HPLC Analyst to join our Quality Control (QC) team. The ideal candidate should have a strong background in the pharmaceutical industry and hands-on experience in laboratory analysis. Job Responsibilities: Perform analysis of raw materials and finished products. Operate and maintain HPLC (High-Performance Liquid Chromatography) equipment. Conduct UV, pH, and Karl Fischer (KF) titration analyses. Ensure accurate and reliable testing results in line with industry standards. Follow Good Laboratory Practices (GLP) and ensure compliance with quality protocols. Experience: Minimum of 2 to 3 years of experience in a clinical, industrial, or pharmaceutical laboratory. Qualifications: M.Sc. / B.Sc. / M.Pharm / B.Pharm in a scientific or related field. If you have the required experience and are passionate about working in a dynamic pharmaceutical environment, we invite you to apply! Industry Pharmaceutical Manufacturing

Job Description Primary role : Provides technical & application field services & support to external customers and Agilent customer engineers. This includes reactive and pro-active actions that result in a timely and cost-effective problem resolution. Responsibilities of this position include but are not limited to; Responsible for providing technical & application support for Agilent analytical instruments to existing & new customers & field engineers at identified locations at PAN India level To perform Installations, Preventive Maintenance, Repair, software & hardware IQ OQ on Agilent products Leads projects requiring coordination with other functions & customers Deliver customer education courses on-site as well at COE labs Cost & time effective application method deployment on Agilent instruments Promptly troubleshoot method/technology transfers issues from one instrument to another. Respond promptly to related customer queries & help in prompt resolution of customer escalations Training of internal & external team and provide technical support. To participate in programs to stimulate demand for all Agilent range of products/services and ensure timely and proper execution of those programs Holds product seminars for customers, prospects and employees To co-ordinate internally with all the field, sales team and Managers to ensure that the key customers are delighted Must be willing to travel extensively. Qualifications Master’s/Bachelor’s Degree in Biotechnology/Chemistry/Analytical Chemistry/Instrumentation/Pharmacy or equivalent Relevant 4-5 years of professional experience on analytical instruments in Gas Phase chromatography domain like GC, GCHS, GCHSMS, GCMSMS etc. in Food, Pharma, Chemical & Energy, Petroleum markets etc. Experience working on Gas Analyzers & special products like GCQTOF would be preferable Excellent numerical, verbal and written communication skills along with good organizational & negotiation skills. Microsoft Outlook, Excel, PowerPoint, SQL etc. Additional Details This job has a full time weekly schedule. It includes the option to work remotely. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws. Travel Required: 75% of the Time Shift: Day Duration: No End Date Job Function: Services & Support

Kenvue Is Currently Recruiting For a Scientist, R&D Analytical What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role Reports To Director - Analytical Chemistry Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Hybrid What You Will Do Kenvue is currently recruiting for: Scientist, R&D Analytical This position reports into Principal Scientist, R&D Analytical and is based at Mumbai, India Who We Are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role reports to: Principal Scientist, R&D Analytical Location: Mumbai Responsibilities The Scientist, R&D Analytical is responsible for performing analytical and stability testing, conducting advanced research activities and utilizing technology and programs to enable Innovation projects: Key Responsibilities Lead and manage analytical research projects in R&D department Develop, optimize, validate and transfer analytical methods to support product development and life cycle management projects Execute developmental stability testing for Drug and Cosmetic products Collaborate with cross-functional teams to drive scientific advancements Provide technical expertise in analytical instrumentation and data analysis Ensure expertise in a wide range of analytical technologies and instrumentation for testing capabilities. Execute the assigned stability testing for shelf-life assessment of stability studies. Participate in method transfer process regarding testing activities. Work on specific research projects, if required. Stay current with industry trends and technologies to drive innovation Support process owners or subject matter experts for assigned responsibilities, critical laboratory processes and quality systems. Required Qualifications What we are looking for Minimum Masters in Chemistry or equivalent science (e.g. Biochemistry, Pharmaceutical Sciences) or Ph.D with 4-8 years of proven working experience in Analytical Chemistry and/or Medicinal chemistry, Quality Control or related functions in healthcare/pharma/FMCG sector with exposure to GMP and Quality environment preferred Proven track record of leading successful scientific projects Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health or Pharmaceutical environment Strong knowledge in UPLC, HPLC, and GC to execute Analytical test method development, validation and optimization in a cGMP environment Solid understanding of analytical and physical testing capabilities, technical skills related to instrumentation principles and working, basic troubleshooting, good documentation practices, data integrity aspects, etc. Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment Excellent communication and collaboration skills Strong experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems. Ability to grasp technical/compliance requirements and execute assigned work to meet the key performance indicators Excellent oral and written communication and articulation skills Challenges the status quo and brings innovative ideas and suggestions Displays technical curiosity and self-initiative to deliver beyond usual activities Good interpersonal skills to partner across functions, sites, and regions If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.