2105 Hplc Jobs - Page 24

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.,

As an in-vitro Bioanalytical Scientist at Syngene, your core purpose will be to provide expert DMPK support to multidisciplinary integrated Drug Discovery projects. Your responsibilities will include defining and implementing the DMPK strategy to expedite project progression, participating in capability building projects as per business requirements, and providing input into the design of experimental protocols and Bioanalytical procedures for the analysis of drug candidates in biological samples. Additionally, you will be expected to deliver scientific presentations in departmental journal clubs and write official project reports. Your role accountabilities will involve planning and supervising routine Bioanalytical workflow to ensure deliverables and productivity, verifying analytical study data for accuracy and integrity, mentoring and supervising fellow scientists for method development and troubleshooting, and playing a key role in evaluating and interpreting bioanalytical results. Troubleshooting LC-MS/MS based bioanalytical methods, having a basic understanding of interpreting Mass/UV Spectra, and ensuring preventative maintenance and calibration schedules of HPLC & mass spec will also be part of your responsibilities. In terms of leadership capabilities, you are expected to demonstrate skills in people management, strong communication, team building, problem-solving attitude, and interpersonal skills. You should consistently align with Syngene's core values of Excellence, Integrity, and Professionalism. As a Syngene leader, you will champion effective Environment, Occupational Health, Safety, and Sustainability (EHSS) practices for the company, oversee compliance within the Biologics business, and foster a corporate culture that promotes an EHSS mindset, quality, integrity, and compliance. People management, career planning, and talent retention will be key areas where you will provide clear, active leadership. Specific requirements for this role include a minimum of 10-15 years of experience in the relevant industry, with demonstrated capabilities in collaboration, leading teams, and Bioanalytical Excellence. The educational background required is an M. Pharm in Pharmaceutical sciences or Pharmaceutical Analysis with a minimum of 10 years of experience in handling ADME assays and HPLC and LCMS/MS, or a fresh Ph.D. in similar disciplines. Syngene is an Equal Opportunity Employer, and all employees are expected to uphold the company's values of Excellence, Integrity, and Professionalism in their daily work.,

As a Chemist at HEPL, a Group company of a 35-year-old FMCG Brand, you will be responsible for conducting various analytical tests and quality control activities in industries such as FMCG, Cosmetics, Foods, and Pharmaceuticals. You should hold an M.Sc. degree in Chemistry, Food Science, or Life Sciences with 0 to 5 years of relevant experience. Your primary responsibilities will include operating, calibrating, and maintaining various laboratory equipment such as UV-Vis spectrophotometer, K.F. Titrator, Conductivity meter, Viscometer, FT-IR, Tinto meter, Analytical balance, pH meter, GC, and HPLC. You should also have hands-on experience in handling Kjeldahl digestion and Distillation Unit, as well as in the preparation and maintenance of reference standards and volumetric standard solutions. In addition, you will be involved in quality control and quality assurance activities, including testing retained samples, spiked samples, and participating in inter-laboratory comparisons and proficiency testing programs related to skincare, hair care, hair color, specialty products, foods, snacks, dairy products, beverages, and bakery products. Furthermore, you will be responsible for preparing Standard Testing Procedures (STPs), validation documents, raw material, and product specifications. Good documentation and adherence to Good Laboratory Practices are essential aspects of this role. You should possess strong communication skills to effectively convey analytical results to both scientific and non-scientific stakeholders. The ideal candidate should have excellent written and oral communication skills in English and be able to join immediately. Prior experience in Research, NABL, and Laboratory settings will be preferred. The role is based in Ekkatuthangal, Chennai, and involves working full-time on day shifts from Monday to Friday. HEPL offers benefits such as health insurance and Provident Fund, along with yearly bonuses. If you meet the qualifications and requirements mentioned above and are keen on contributing to a renowned FMCG brand, we encourage you to apply for this position.,

As the leading supplier of active pharmaceutical ingredients (APIs), TAPI is dedicated to advancing global health. With a legacy of over 80 years and a diverse portfolio of more than 350 products, along with custom CDMO services, we are shaping the future of the healthcare industry worldwide. Our team of over 4,200 professionals across 13 state-of-the-art facilities in various countries collaborates to innovate, problem-solve, and deliver excellence. By joining us, you will become part of a mission that transforms lives. Key Responsibilities: - Perform analysis of stability samples and working standard qualification following defined procedures and pharmacopeial monographs. - Operate and maintain analytical instruments, ensuring smooth function and troubleshooting in accordance with GLP standards. - Maintain accurate documentation of methods, specifications, logbooks, certificates, and stability reports, including data archiving. - Monitor stability studies based on ICH Q1 guidelines. - Conduct analytical method validation activities as per ICH Q2 standards. - Initiate LIR/OOS investigations for any deviations or gaps related to SOPs or monographs during routine operations. - Ensure qualifications and calibrations of all analytical instruments within the stability section. - Strictly comply with laboratory safety procedures during daily activities. Minimum Required Skills: - Solid understanding of Quality Control procedures. - Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices). - Hands-on expertise with HPLC, GC, KF, Auto titrator, and Vacuum oven operations. - Ability to handle instrument troubleshooting and follow documentation protocols. Qualifications: - Experience Level: 4+ Years - Industry Experience: API Experience is required - Qualification: B.Sc. / M.Sc. in Chemistry or B. Pharmacy Join TAPI and embark on a journey to leave a lasting impact on global health. If you are prepared to lead, innovate, and inspire, we are thrilled to have you on our team. Lets together shape the future of pharmaceuticals. Apply on top of this page, and our talent acquisition team will reach out to you soon!,

As a candidate for this role, you will be responsible for working in accordance with organizational compliance requirements. Your main tasks will include developing methods for various quality attributes for complex injectable drug products such as Liposomes and Ophthalmic Drug products. You will also be in charge of performing method validation and verification, as well as analyzing drug products using a variety of analytical techniques including HPLC, GC, UV, and other relevant methods. In addition, you will be tasked with identifying, investigating, and troubleshooting issues as they arise. Your responsibilities will also involve conducting chemical analyses such as Extraction, Refluxing, Residue on ignition, Centrifuging, and Evaporation. Furthermore, you will be expected to prepare study templates, analytical method validation and verification reports, as well as protocols to support your findings. Overall, this role will require a high level of attention to detail, strong analytical skills, and the ability to work effectively within a regulated pharmaceutical environment.,

As an Analyst or Senior Analyst in Bioanalytical Research at Veeda Lifesciences, you will play a crucial role in conducting bioanalytical research activities. This includes method development, validation, and sample analysis utilizing a variety of techniques such as HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Your responsibilities will also involve developing and validating methods for bioanalysis of biologics and biosimilars in compliance with regulatory requirements, such as those set by the USFDA. Collaboration with cross-functional teams will be essential to ensure the timely delivery of high-quality results. Additionally, you will be tasked with performing stability testing of biological products under different conditions. Troubleshooting issues related to instrument calibration, maintenance, and operation will also fall within your scope of duties. The ideal candidate for this role should hold a Bachelor's degree in Pharmacy (B.Pharm) or a Master's degree in Pharmacy (M.Pharm) from an accredited institution, or alternatively an M.Sc. degree. Previous experience ranging from 0 to 4 years is preferred. A strong understanding of analytical instruments like HPLC, UPLC, GC, MS, ICP-MS, and wet analysis is highly desirable for this position.,

Rubicon Research Limited is a rapidly growing pharmaceutical formulation company focused on developing, manufacturing, and marketing branded specialty and generic prescription pharmaceutical products in regulated markets. With a diverse product portfolio of over 250 SKUs spanning more than 70 product families, we have established marketing, sales, and distribution platforms in the US through our subsidiaries AdvaGen Pharma and Validus Pharmaceuticals. Our US FDA-inspected R&D facilities in India and Canada, along with manufacturing facilities in Maharashtra, India, equipped with various drug development and manufacturing capabilities, demonstrate our commitment to quality and innovation. As a Manager in Analytical Method Validation at Rubicon Research Limited, you will play a crucial role in overseeing end-to-end activities related to validation and documentation for various regulatory markets. Your responsibilities will include ensuring accurate documentation for analytical method validation, planning daily validation activities, coordinating with the Analytical Development team, reviewing protocols and reports, managing incidences, investigations, and change control processes, and ensuring compliance with quality management systems. Additionally, you will be responsible for training and supporting the Analytical Method Validation team, providing technical input for analytical data generation, addressing analytical issues, and preparing material budgets. Key Qualifications & Experience: - M. Pharm/M. Sc in Organic or Analytical Chemistry - Proficiency in handling instruments such as HPLC, GC, KF, IC, PSD, etc. - Familiarity with US, UK, EU, and ROW regulatory bodies - Experience with GDP and regulatory query handling In this role, you will need to demonstrate a strong understanding of regulatory guidelines, ensure compliance in the laboratory, provide technical training to team members, and review documents through the Document Management System (DMS) following the Quality Management System (QMS). Your expertise will be crucial in maintaining GLP standards, meeting regulatory and quality expectations, and ensuring that all analytical work is audit-ready to meet FDA standards. Please note that the candidate is expected to work in various shifts as required and may need to visit external sites based on project requirements. If you are passionate about pharmaceutical development, regulatory compliance, and analytical method validation, we encourage you to join our dynamic team at Rubicon Research Limited.,

You should possess a DMPK background with hands-on experience in DMPK-ADME assays and bioanalysis using LCMS/MS & HPLC techniques. Your strong scientific knowledge and excellent communication skills will be key in this role. As part of the team, you will work in the lab under supervision, ensuring the generation of quality data consistently and maintaining high individual productivity levels. Your responsibilities will include running ADME assays and taking charge of the archival of documents and data. Additionally, your ability to learn new techniques, experiments, and instruments will be crucial for success in this position.,

The pharmaceutical Quality Control (QC) professional ensures that drugs and related products meet quality standards throughout their lifecycle, from raw materials to finished goods. This involves a range of activities including testing, analysis, and documentation, all while adhering to regulatory guidelines and company procedures. Key Responsibilities: Testing and Analysis: Conducting various tests on raw materials, in-process samples, and finished products using analytical techniques like HPLC, GC, UV, and spectroscopy. Quality Standards Compliance: Ensuring products meet established quality standards, specifications, and regulatory requirements (e.g., GMP, ICH, USFDA, WHO). Documentation and Reporting: Maintaining detailed records of all testing, analysis, and investigations, including preparing certificates of analysis and other relevant reports. Equipment Management: Calibrating, maintaining, and troubleshooting analytical instruments and equipment. Deviation Investigations: Investigating and documenting any deviations from established quality standards or procedures (e.g., Out of Specification (OOS) results) and implementing corrective and preventive actions (CAPA). Stability Studies: Conducting and documenting stability studies to assess product shelf life and storage conditions. Method Validation: Validating analytical methods to ensure they are suitable for their intended use. Training and Supervision: Training and supervising QC technicians, ensuring they adhere to quality standards and procedures. Audits and Inspections: Participating in internal and external audits and inspections, addressing any findings, and ensuring compliance. Inventory Management: Managing the inventory of reagents, standards, and other materials needed for QC analysis. Process Improvement: Identifying opportunities to improve the efficiency and effectiveness of QC processes. Skills and Qualifications: Education: Typically requires a Bachelor's or Master's degree in Chemistry, Biochemistry, Microbiology, or a related field. Analytical Skills: Strong analytical and problem-solving skills, including the ability to interpret data, troubleshoot issues, and make informed decisions. Technical Skills: Hands-on experience with relevant analytical techniques and instrumentation. Regulatory Knowledge: Understanding of cGMP, ICH guidelines, and other relevant regulatory requirements. Attention to Detail: Meticulous attention to detail is crucial for accurate testing, documentation, and investigations. Communication and Interpersonal Skills: Ability to effectively communicate with team members, management, and other stakeholders. Problem-solving skills: Ability to identify the root cause of quality issues and implement effective corrective actions.,

You will be responsible for assisting in the collection and testing of raw materials, packaging materials, and finished products following Standard Operating Procedures (SOPs) and regulatory guidelines. Additionally, you will be required to learn and provide support in the basic operation and maintenance of laboratory instruments such as HPLC, UV, pH meter, etc., under supervision. It will be your responsibility to maintain accurate records of test results and lab activities in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You must strictly adhere to GMP, GLP, and safety protocols, and report any deviations or non-conformities to your supervisor. Furthermore, you will participate in training sessions to gain an understanding of Quality Control (QC) procedures, SOPs, and regulatory requirements. This role will provide you with opportunities for continuous learning and development in the field of laboratory testing and compliance.,

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.,

Date: 4 Aug 2025 Location: Bangalore, KA, IN, 560100 Custom Field 1: Development Services Job Description Designation: Research Associate/ Executive/ Analyst, Small Molecule Bioanalytical Research Laboratory, Clinical Development Job Location: Bangalore, India Reporting to: Group Leader of Small Molecule Bioanalytical Laboratory Job Grade: Level 9-I The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngenes 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. The Role The Research Associate/ Executive/ Analyst for the Small Molecule Bioanalytical Laboratory is a technical role responsible for conducting BA/BE studies in the laboratory. Job responsibilities include performing critical method development and validation programs, technical and regulatory compliance of all studies. This role requires an individual with a robust background in pharmaceutics, or other related life sciences, coupled with extensive experience in the bioanalytical field, particularly within small molecule bioanalysis. This role demands an individual with a strong commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecule analysis. The role reports into the Project Leader / Group Leader, Small Molecule Bioanalytical Laboratory and is a full-time position based out of Bangalore, India. Key Responsibilities Of The Role Perform the bioanalytical work including sample processing for method development, method validation and study sample analysis as per the protocol in compliance with SOPs, STPs. Prepare STP, MV protocol and study sample analysis protocol. Coordinate with maintenance department for any problems related to utilities and equipment / instrument (e.g. LC-MS/MS, HPLC, etc) failures. Document data generated, entries in official documents. Ensure all studies adhere to regulatory guidelines and expectations set by GCP/ GLP. Participate in all discussions on project-specific scientific details. Education And Experience Education Masters in Pharmaceutics or other related life sciences from a reputed university. Industry Experience Minimum of 1 years of experience in regulated small molecule bioanalysis Hands-on experience in small molecule regulated bioanalytical experiments People Leadership Experience NA Exposure And Experience Experience with working for a Bioanalytical CRO lab will be an added advantage. Core Competencies Required For The Role Scientific: Brings a creative and an innovative advantage to projects Is curious, eager to learn and make a difference Thinks scientifically and understands the problem statement in assigned programs/assays Publishes posters, papers and articles regularly Technical Conducts/plans experiments without errors and gaps Reports/analyzes data punctually and communicates effectively Troubleshoots and investigates logically (is able to defend the logic behind experimental results) Is able to forecast risks and make mitigation plans ahead of time Has good organizational, project management skills Documentation Records data as per ALCOA++ policy Pays attention to detail Is punctual in responding to QC and QA reports Displays minimal audit finding index Writes clearly and concisely with English skills at >B+ 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 with regard to 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. Pls visit us at https://syngeneintl.com/ to know more about us and what we do. Show more Show less

Date: 3 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Dedicated Centre Job Description Functional or Technical skills Job Role : Analytical Chemistry-Analyst (NPD) Department : Analytical - BGRC Job Location : Bangalore 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 companys 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 at all times. 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 This role involves method development, method validation, method transfer and R&D stability studies by using laboratory instruments like Ultra performance liquid chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, Particulate matter analysis using Malvern, PAMAS, HIAC and other relevant instrumentation techniques. etc. Role Accountabilities Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Must have experience in handling HPLC, UPLC (Empower-3 software), GC, UV Visible spectrophotometer balances, Potentiometer, and stability chambers, Particulate matter analysis techniques. Shall have experience on Good documentation/laboratory practices such as ALCOA+. Experience in calibration and qualification of various analytical instruments HPLC, UPLC, GC, and other QC laboratory instruments Shall prepare and review the raw data sheets, instrument operating procedures, and standard operating procedures Shall have good experience in handling of QMS (such as incidents, Out of Specifications, Deviations, and Change control). Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards/Chemicals/Reagents/Consumables/Spares etc., required for the projects Shall adhere to the procedure of GxP/Safety and as per the procedure defined in the internal standard operation procedure Shall operate the MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Must possess good communication and e-mail etiquettes. Behavioural Skills Good Interpersonal skills Self-time management Good team player Good communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience Specific requirements for this role 0-6 years Skills And Capabilities Hands-on HPLC, UPLC/UHPLC, CG, UV-visible spectrophotometer, Potentiometer, Particulate matter analysis techniques and QC other analytical instruments Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+. Able to follow work instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Good knowledge of MS-office (word, excel, ppt) Education M. Pharm/ M. Tech/ M.Sc. / B.Tech., B.Sc. (Analytical chemistry/Chemistry) 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 with regard to 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. Show more Show less

Position Overview We are seeking a dedicated and skilled Organic Chemist to join our dynamic team in Jaipur. This full-time position offers an exciting opportunity to contribute to innovative projects in the field of organic chemistry. The ideal candidate will possess a strong foundation in organic chemistry principles and methodologies, along with practical experience in quality assurance and testing. If you are passionate about advancing your career in a collaborative environment, we encourage you to apply. Key Responsibilities Conduct research and experiments in organic chemistry to develop new products and processes. Perform quality assurance (QA) analysis and testing to ensure compliance with industry standards. Utilize various QC tools and techniques to monitor and improve product quality. Develop and optimize analytical methods using techniques such as Gas Chromatography (GC), High-Performance Liquid Chromatography (HPLC), and UV Spectrophotometry. Document and report findings, ensuring accurate record-keeping and adherence to regulatory requirements. Collaborate with cross-functional teams to support product development and troubleshooting efforts. Stay updated with the latest advancements in organic chemistry and related fields. Qualifications The successful candidate will possess the following qualifications: Bachelor's or Master's degree in Organic Chemistry or a related field. 1 to 5 years of relevant work experience in a laboratory setting. Strong knowledge of organic chemistry principles and laboratory techniques. Proficiency in QA analysis, QA testing, and the use of QC tools. Hands-on experience with GC, HPLC, and UV spectrophotometer. Excellent problem-solving skills and attention to detail. Ability to work independently and as part of a team in a fast-paced environment. Strong communication skills, both written and verbal. This position is based in Jaipur and follows a day schedule with an on-site work mode. We are looking to fill one position, and the annual salary for this role is 4,50,000. If you meet the qualifications and are eager to make a significant impact in the field of organic chemistry, we invite you to submit your application.

We are looking for both junior and senior scientists to join our team and contribute to the development of our novel mRNA-based vaccines and therapeutics. The ideal candidates will have experience in nucleic acid delivery systems, particularly focusing on lipid or polymer-based formulations, and will work on advancing our platform for efficient, long-term mRNA stability and delivery. The role will involve formulation discovery, microfluidics, particle size analysis, and nucleic acid quantification in a collaborative, fast-paced environment. Key Responsibilities: Design, develop, and optimize lipid nanoparticle (LNP) or polymeric formulations for nucleic acid delivery (RNA or DNA), with a focus on mRNA. Conduct microfluidics experiments to synthesize, encapsulate, and characterize lipid or polymeric nanoparticles. Perform formulation characterization, including particle size and zeta potential measurements, pKa determination, and viscosity assessments. Quantify nucleic acids using RiboGreen, NanoDrop spectrophotometry, and other relevant techniques. Utilize gel electrophoresis for nucleic acid and protein analysis (including Western blotting). Implement and refine nanoparticle purification techniques, such as ultrafiltration and tangential flow filtration (TFF). Conduct cell-culture experiments, including transfection of immortalized cell lines with nucleic acids or nucleic acid formulations. Set up and conduct high-throughput in vitro screening assays for evaluating formulation effectiveness. Support the setup and automation of laboratory protocols, including lab automation equipment setup and programming. Participate in animal studies to evaluate drug or vaccine delivery formulations. Collaborate with cross-functional teams to troubleshoot and solve technical challenges in formulation and characterization. Contribute to the continuous improvement of experimental techniques and methodologies. Qualifications: MSc or PhD in Life Sciences, Chemistry, Biophysics, Chemical Engineering, or a related discipline, with substantial experience in nucleic acid delivery or adjacent delivery modalities. Proven track record of successful project execution in nucleic acid delivery, formulation, or related fields. Solid experience in lipid or polymer-based drug delivery, ideally for mRNA or nucleic acids. Familiarity with microfluidics techniques for nanoparticle synthesis and characterization. Experience with nanoparticle characterization techniques, including size analysis, zeta potential, viscosity, and pKa determination. Expertise in nucleic acid quantification techniques such as RiboGreen assays, NanoDrop spectrophotometry, and gel electrophoresis. Experience with cell-based assays (e.g., reporter assays, ELISA) and transfection of nucleic acids. Experience with high-throughput screening methods and assay automation is desirable. Strong analytical and problem-solving skills with the ability to independently interpret experimental data and troubleshoot technical issues. Excellent communication skills, both written and verbal, with the ability to present scientific findings clearly and effectively. A collaborative mindset and ability to work in interdisciplinary teams. Self-motivated with a strong desire to rapidly learn and master new experimental techniques. Desired Experience (Not Required for All Candidates): Experience with formulation purification techniques, such as ultrafiltration and TFF. Experience in animal studies related to nucleic acid delivery. Familiarity with lab automation or the programming of lab automation systems. What We Offer: Competitive compensation. Comprehensive health insurance with coverage options for immediate family (including pre-existing conditions). A collaborative, multidisciplinary work environment focused on tackling innovative challenges in mRNA delivery and therapeutics. Opportunities for professional growth and contribution to groundbreaking biotechnology advancements. PopVax is committed to creating an inclusive, diverse environment and is proud to be an equal-opportunity employer. We encourage individuals from all backgrounds to apply.

Job Responsibilities Support customers with on-site installation, implementation, maintenance, and repair of instruments like HPLC, TEA Product line, etc. Install and optimize hardware/software and configurations at customer sites to ensure flawless operation. Diagnose and resolve product performance issues promptly. Perform maintenance and repairs efficiently, advising customers on preventive measures to ensure efficient product performance. Deliver fully coordinated solutions, including peripherals, communications, operating systems, and application software. Train other field engineers and customers in the solutions to ensure successful implementation. Achieve assigned spares and service revenue targets, ensuring payment collections for transactions with the assigned customer base. Report all service activities, including service reports, weekly updates, and expense statements, to maintain clear communication. Follow company policies on attendance, travel, safety, and technology use to ensure disciplined operation. Job Requirements Bachelor's degree in Engineering or a related field, or equivalent experience. Proven experience in field service or a related technical role. Strong problem-solving skills and the ability to diagnose and resolve technical issues. Excellent communication skills, both verbal and written. Ability to train and mentor peers and customers. Willingness to travel extensively to customer sites.

As a Quality Control and Assurance Manager, your main responsibility will be to manage and supervise QC and QA operations to ensure alignment with industry standards and company SOPs. You will be in charge of performing and overseeing analytical testing using advanced laboratory instruments such as AAS, HPLC, and Titration. Your role will also involve ensuring that quality standards are maintained throughout all production stages. Additionally, you will conduct internal and external audits, ensuring the timely implementation of corrective and preventive actions (CAPA) and maintaining documentation in compliance with regulatory requirements. As a leader in the QC/QA team, you will also provide guidance and mentorship to team members. To be successful in this role, you should hold a B.Sc/M.Sc in Chemistry or a related field and have a minimum of 8-12 years of experience in Quality Control & Assurance within the chemical or related industries. Sound knowledge of various analytical techniques and instrument handling is essential, along with proven experience in audit preparation and compliance. Strong communication, leadership, and problem-solving skills are crucial for this position. Candidates who can join immediately will be given preference. This is a full-time, permanent position with benefits including health insurance, paid sick time, and Provident Fund. The work location is in Khanna, Punjab, therefore, reliable commuting or planning to relocate before starting work is preferred. The ideal candidate should have at least 9 years of experience in chemical testing. If you meet the candidate requirements and are ready to take on this challenging role, we encourage you to apply and be a part of our dynamic team.,

Date: 28 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services Job Title: In-vitro Bioanalytical Scientist Job Location: Bangalore 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 companys 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 at all times ? 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 ? Client facing, scientific leadership role your main responsibility will be to provide expert DMPK support to multidisciplinary integrated Drug Discovery projects ? Defining and implementing the DMPK strategy to expedite project progression. ? Participate in various capability building projects as per business requirements ? The candidate will be responsible for providing input into the design of experimental protocols and Bioanalytical procedures for the analysis of drug candidates in biological samples ? Should deliver scientific presentation in departmental journal club and write official Project reports Role Accountabilities ? Plan and supervise routine Bioanalytical work flow to ensure deliverables/ productivity, along with verification of analytical study data for its accuracy and integrity. ? Mentor and supervise fellow scientists for method development and troubleshooting for routine as well as critical Bioanalytical work ? The candidate should be able to troubleshoot LC-MS/MS based bioanalytical methods and he should play key role in evaluation/interpretation of bioanalytical results. ? 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 Leadership Capabilities ? People management ? Strong communication skills ? Team building ? Good communication ? Strong problem solving attitude ? Reasonable Interpersonal skills Syngene Values All employees will consistently demonstrate alignment with our core values ? Excellence ? Integrity ? Professionalism Accountabilities As a Syngene Leader (only For Leadership Hires) ? Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safetyled activities. ? Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. ? Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Experience Minimum 10-15 years of relevant industry Demonstrated Capability ? Collaboration ? Leading Team ? Bioanalytical Excellence Education M. Pharm in Pharmaceutical sciences, Pharmaceutical Analysis with, Minimum 10 years of experience in handling ADME assays and HPLC and LCMS/MS Or Fresh Ph D in similar disciplines 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 with regard to 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. Show more Show less

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.

Perform the analysis by using Analytical Balance Microbalance,pH meter, Conductivity, KF, Autotitrator, Halogen Moisture, UV, IR and Hot air Oven. Etc. HPLC and GC Instrumental analysis. Release ofRaw Materials ,packing materials, In process IntermediateBulk and finished products as per SLA. SAP activities, Labware LIMS activities like LIMS masters preparation and reviewand Approvals. LIMS Ticketsand Audit Trails observations towards closure Reporting of on-line incidents, OOS, OOT as per prescribed format and SOP toQA andhelping in investigating of root cause along with immediate superior Qualifications M. Sc Chemistry

We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performing the PM. To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP. To attend the breakdown's and close notification or order of the instrument /equipment after the Completion of breakdown maintenance. To be a part of investigating the incidence related to instrument Responsible for the maintaining of required spares for all instruments in warehouse. To get the quotations for the required spares and services for the maintenance of the instruments. To generate the purchase requisitions for the required spares and services. To perform the PM in the given frequency within the given period. Adhering to the allotted shift schedule with right time. If any changes prior permission shall be taken from Group leader. Qualifications Educational qualification: An B.Tech. or any Degree in Instrumentation, Mechanical, Electronics, Electrical. Required Work experience : 3 to 6 years Skills & attributes: Technical Skills Hands-on Experience on maintenance of Waters HPLC (Arc, e2695), Agilent HPLC (1200, 1260 Infinity), Agilent GC-HSS (7890, 8890, 7897, G1888), Dissolution Testers (Electrolab, Sotax), Metrohm Titrators. Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). Basic knowledge in SAP usage Behavioural skills Prioritizes effective communication and demonstrates a performance-oriented mind-set. Effective verbal and written communication skills. Performance-oriented approach, consistently striving for high standards. Demonstrates flexibility in working shifts and a clear understanding of team dynamics.

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 an Analytical Scientist in our team, you will be responsible for developing and validating robust HPLC methods for the characterization and quantification of biological products such as monoclonal antibodies and recombinant proteins. Your role will involve performing method optimization, robustness studies, and transfer protocols following ICH guidelines. You will also be conducting routine and stability testing by analyzing in-process, release, and stability samples using various techniques including HPLC/UPLC, Capillary and Gel Electrophoresis, UV spectrophotometric methods, Host Cell DNA quantification, and immunoassays like HCP ELISA. In addition, you will be in charge of operating and maintaining analytical instruments such as HPLC, electrophoresis systems, spectrophotometers, and ELISA readers, ensuring their proper calibration, troubleshooting, and performance verification. Your responsibilities will also include preparing and reviewing SOPs, STPs, protocols, reports, and analytical records to comply with regulatory requirements. You will need to maintain accurate documentation in laboratory notebooks and electronic systems. Furthermore, you will participate in internal and external audits and provide analytical data to support regulatory submissions. Collaboration with cross-functional teams including R&D, Quality Control, and Regulatory Affairs will be essential in supporting product development and lifecycle management. You will offer technical support during investigations, deviations, and CAPAs, as well as train junior analysts and new team members on analytical techniques and laboratory practices. To excel in this role, you should hold an M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or a related life sciences discipline, along with 4-8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA-based techniques is required, as well as familiarity with regulatory guidelines such as ICH, FDA, and EMA, and quality systems. Key skills for this position include strong analytical and problem-solving abilities, attention to detail and data integrity, excellent documentation and communication skills, proficiency in software tools like Empower, Chromeleon, SoftMax Pro, and the capability to manage multiple projects and meet deadlines.,

Job Summary Are you passionate about solving customer problems, offering Technical solutions and building deeper business relationships that help drive growth for industry leading Consumer Products customers Joining science and creativity, we are an international collective of thinkers who partner with customers to bring scents, tastes, experiences, ingredients and solutions for products the world craves. If you are skilled at solving complex problems with elegant technical solutions, and have a collaborative approach to exceeding customer expectations, you could be our next Application Specialist! Your Focus As a part of our Application Development team, you will be responsible to work across functions to develop and support products and processes. The role will see you providing technical and functional leadership opportunities and will play a key part in supporting our evolving industry and customer base. The role is based in Hyderabad, India and will report to the Regional Application Leader Grain Processing. How You Will Contribute Involve with hands on work at bench and pilot scales. Design, develop, execute, and contribute innovatively to the development of enzyme and yeast products and processes across scale, analyze and interpret data using statistics to make a sound recommendation for specific projects. Collaborate closely with the application scientist to advance the solution while creating and maintaining an up-to-date project data, both at lab and pilot scale. Objectively support the analysis of customer and project samples using physical, bio/chemical and functional assay. Manage the day-to-day lab activities while upholding to the highest standards of Occupational Health and Safety. Interact with cross functional teams including R&D, sales, marketing, legal, procurement and engineering. What You Will Need To Be Successful Master`s degree (with 3+ years of Industry experience) or a PhD degree in Biochemistry, Biotechnology, Bio Engineering, Agriculture Engineering or a related area. Strong knowledge and experience of industrial scale fermentation, preferably in the grain based ethanol manufacturing. Experience in executing experiments across scales (Lab-Pilot-Commercial) to assess the performance of enzymes and/or yeast meeting project timelines. Experience with analytical techniques relevant to monitoring the biotechnological process (Proximate, HPLC, GC, Biochemical assay, Viscometry, PSD, micro-DSC, Etc). Proficiency with statistical analysis software such as JMP, SPC, excel, etc., for generating scientific report with objective inferences. Excellent verbal and written communication skills Strong team player with the ability to deliver results in a fast-paced environment. Willingness to travel upto 20% across ASPAC, including to customer commercial facilities. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more Show more Show less

The role involves synthesizing and purifying assigned molecules and conducting experiments. You will be responsible for the process development activities of the assigned molecule, as well as supporting the scaling up of developed processes in pilot plants and large-scale manufacturing processes. Additionally, you will provide complete support for Tech Transfer activities by closely collaborating with cross-functional teams. Your role will also include adding value to processes through innovation. It is essential to understand and analyze reports received from the Analytical department, including NMR, Mass Spectrum, IR, HPLC, GC, etc. You will partner with the Analytical Development Laboratory (ADL) to process samples for analysis as per the requirement.,