31 Gcms Jobs

Role Overview: As an Organic Chemist - Industrial Postdoc at altM, you will be responsible for designing, synthesizing, and characterizing organic compounds for various applications. Your primary functions will include conducting laboratory experiments, analyzing data, and interpreting results to drive innovation and advance research goals. Key Responsibilities: - Design and execute organic synthesis routes to target compounds. - Perform purification and characterization of organic molecules using analytical techniques such as NMR, HPLC, GC-MS, and IR spectroscopy. - Analyze and interpret experimental data to troubleshoot reactions and optimize synthetic routes. - Collaborate with cross-functional teams to develop innovative solutions and address project challenges. - Maintain accurate records of experimental procedures, results, and observations. - Stay current with literature and technological advancements in organic chemistry to contribute to the development of novel methodologies and technologies. - Adhere to safety protocols and best practices in the laboratory environment. Qualifications Required: - PhD / Master's degree in organic chemistry / related field(s), or evidence of exceptional ability. - 1-2+ years of industrial experience preferred. - Strong theoretical and practical knowledge of organic chemistry principles and techniques. - Hands-on experience with organic synthesis, purification, and characterization methods. - Proficiency in using laboratory equipment and analytical instruments. - Ability to work effectively in a fast-paced research environment and manage multiple projects simultaneously. - Excellent problem-solving skills and attention to detail. - Strong communication and interpersonal skills, with the ability to collaborate effectively in a team setting. - Commitment to safety, compliance, and ethical conduct in scientific research. Additional Details: This is an onsite role and requires physical presence. Please note that the compensation is competitive and negotiable for the right talent.,

The role based in Hyderabad, India, within the Chemistry Solutions department involves supporting the chemistry services team in delivering final compounds to clients by ensuring the testing and enhancing of purity levels as per requirements. This is achieved through effective coordination with a team of analysts. The main responsibilities of this role include building lasting internal client relationships by engaging in technical discussions with clients to understand project requirements. It also involves supporting team members in closing identified gaps to enhance client satisfaction. Additionally, ensuring seamless project execution through effective lab support and planning is crucial. This includes estimating lab requirements, monitoring instrument calibration, reviewing SOPs, and allocating resources based on daily work plans. Efficiency and quality in delivery are paramount, involving the evaluation of solvents/samples for analytical test suitability, approving analytical methods, and ensuring timely delivery of final reports to clients. The role also includes resolving method development issues, coordinating with R&D scientists for analytical queries, and interacting with external clients as needed. Maintaining safety at work is a key aspect, ensuring compliance with lab management practices, safe handling of chemicals and instruments, and successful implementation of new analytical techniques. Upholding data integrity and IP confidentiality is essential, along with developing the morale and skill set of the team through talent selection, knowledge enhancement, mentoring, and coaching. The candidate should possess knowledge of analytical tools and techniques, operational understanding of analytical instruments, documentation processes, safety protocols, IP confidentiality, and data integrity. Additionally, the ability to conduct cost-benefit analyses and optimize solvent usage is required. The ideal candidate will hold a postgraduate degree in Analytical Chemistry or Organic Chemistry with 9-12 years of relevant experience, or a Ph.D. in Analytical Chemistry or Organic Chemistry, or an M. Pharm in Pharmaceutical Analysis with 7-10 years of relevant experience. Advanced knowledge of MS Office and basic knowledge of ChemDraw are preferred. The additional responsibilities, educational qualifications, certifications, and key performance indicators will be discussed during the interview process. The work environment details, specific requirements, and other miscellaneous details will also be communicated accordingly.,

As a member of the Toshvin Analytical team, you will have the opportunity to contribute to our mission of providing top-quality services to our clients and supporting business growth. We are a group of skilled professionals seeking individuals who are enthusiastic, driven, and dedicated to join us in our journey towards success. If you envision a fulfilling career with a prominent instrumentation company in India, Toshvin Analytical welcomes you to apply for the position of Application Sales. In this role, you will report to the Senior General Manager and be based in Baroda. The ideal candidate should possess a minimum of 5 years of hands-on experience in GCMS & GCHS and/or GC-MS/MS, along with a Master's degree in Chemistry or M. Pharma. Proficiency in local and global regulations, particularly in the pharma and food markets, is highly desirable. Your primary responsibilities will include providing support to the sales team in promoting GC-HS, GC-MS, GC-MS/MS, System GC, etc., developing solutions and product presentations for customers, engaging in technical discussions, and staying informed about the latest applications in chromatography and MS products. To excel in this role, you should demonstrate excellent English communication skills, both written and verbal, effective presentation abilities, a willingness to travel extensively, and a strong aptitude for continuous learning. Additionally, a sound understanding of applications related to the food, pharma, and environment industries, as well as knowledge of sample preparation techniques for various testing purposes, will be advantageous. If you are ready to embark on a challenging yet rewarding career in the field of analytical instrumentation and sales, we encourage you to submit your CV to careers@toshvin.com and be a part of our dynamic team at Toshvin Analytical.,

As a GCMS/MS Trainee at FARE Labs, you will be involved in advanced training focused on Gas Chromatography-Mass Spectrometry (GC-MS) and various sample matrices. GC-MS is a powerful analytical technique that combines the separation capabilities of gas chromatography with the identification and quantification strengths of mass spectrometry. It is widely used in fields such as environmental analysis, food safety, and forensic science due to its sensitivity, specificity, and ability to analyze complex mixtures. Your main objectives will include gaining a comprehensive understanding of GC-MS principles using national/international standard methods, acquiring practical skills for operating GC-MS systems, and familiarizing yourself with data analysis and interpretation techniques. Throughout the training, you will cover various aspects such as instrumentation, GC-MS method development, practical applications through hands-on training, data analysis, and troubleshooting common issues related to GC-MS systems. Responsibilities in this role will include strict adherence to safety protocols to prevent accidents, active participation in all training sessions and practical exercises, respect for laboratory equipment and facilities, collaboration with fellow participants, and maintaining integrity and accuracy in all testing procedures and documentation. To excel in this position, you are expected to demonstrate a commitment to the training program by attending all scheduled sessions, completing assignments, and actively participating in practical exercises. Compliance with health and safety regulations, including wearing appropriate personal protective equipment and adhering to safety protocols, is essential. A signed commitment agreement and proof of immunizations may be required before the start of the program. If you are passionate about advancing your skills in GC-MS and are committed to learning in a dynamic training environment, please email us at trainings@farelabs.com to express your interest and learn more about this exciting opportunity.,

The Sensory Analyst is responsible for conducting sensory and physical evaluations of finished goods to ensure compliance with quality standards. Your role will involve analysis, documentation, and coordination with relevant departments to maintain product integrity and support the quality control system. You will be responsible for conducting sensory analysis of finished goods (FG) from Mixing & Blending and Production, performing physical evaluations of products per quality requirements, and analyzing and reporting customer complaint samples. Additionally, you will coordinate with Production & Formulation (P&F) teams for sample collection and result reporting, maintain records for all sensory analysis activities, and ensure proper storage and labeling of final product samples. In terms of quality system implementation and compliance, you will support the implementation of quality systems and good laboratory practices, ensure compliance with safety, environmental, statutory, and procedural requirements, maintain QC records and reports, and assist in audits and compliance activities. You will also be responsible for performing calibration and performance verification of lab instruments, validating test methods, and conducting analysis for residue and heavy metals in finished goods, semi-finished goods, and additives. Your role will also involve conducting investigations related to customer complaints on finished goods, participating in developmental work using techniques such as GC, HPLC, AAS, and GC-MS, and performing recurring analysis for customer returns and complaints. Furthermore, you will ensure compliance with 5S practices in the lab, calibrate and maintain glassware, adhere to good laboratory practices (GLP) and safety protocols, and focus on achieving key performance indicators such as adherence to audits and compliance standards, first-time quality targets for FG/SFG, on-time in full (OTIF) compliance for quality checks, reduction in customer complaints, and continuous employee development and engagement in quality initiatives. To qualify for this role, you should have a Bachelor's/Masters degree in Food Technology, Chemistry, Microbiology, or a related field, along with a minimum of 5 years of experience in sensory analysis, quality control, or a related function in the food or pharmaceutical industry. Additionally, you should possess strong sensory evaluation and analytical skills, experience with lab instruments (GC, HPLC, AAS, GC-MS), knowledge of quality control procedures, compliance, and documentation, attention to detail, problem-solving abilities, communication skills, and proficiency in data entry and report generation.,

You will be a Quality Assurance & Analytical Chemist at FMC, where your primary responsibility will be to provide daily analysis support by developing, validating, and applying various modern analytical technologies and approaches for the development and commercialization of agricultural products. You will ensure that FMC quality standards and good laboratory practices are implemented at the Toller site by conducting cross-checks and on-site audits as per business needs. Your role will involve knowing, understanding, and practicing all aspects of laboratory safety and industrial hygiene protocols, developing, validating, and implementing methods for qualitative and quantitative analysis, conducting routine and non-routine analysis, collecting data, generating summaries and reports, supporting investigations of quality incidents, and operating and maintaining various analytical instrumentation. You will work closely with synthetic chemists and engineers to provide structure determinations and analytical results as requested, manage the quality of active ingredients and intermediates with contract manufacturers, review MOA and analytical Teck pack, and perform other tasks assigned by the line manager. To be successful in this role, you should have a Master's degree or above in chemistry/biochemistry or equivalent experience, along with 10+ years of experience and a minimum of 8 years in analytical development/quality control positions. You should have experience with method development and troubleshooting using various lab instruments/techniques and a track record of delivering quality results on time. Strong interpersonal, problem-solving, and troubleshooting skills are essential, along with good written and oral communication and coordination capabilities with different stakeholders. Familiarity with computers and software packages from various instrument manufacturers is also desirable. If you are a motivated leader with a strong technical background and a passion for safety and efficiency, we invite you to apply for this dynamic role and become a part of our team at FMC.,

You are seeking an Assistant General Manager- Research & Development position at an Indian Pharmaceutical MNC located in Thane, Maharashtra. As the Associate General Manager, you will lead the Analytical Method Validation team, overseeing validation activities for various dosage forms and managing a team of 15+ scientists. Your responsibilities include ensuring regulatory compliance, driving quality and efficiency, and fostering collaboration with R&D, Regulatory, and Plant QA/QC teams. Your key responsibilities will involve providing leadership for analytical method validation across different formulations, overseeing RM and PM characterization, managing method validation projects in alignment with regulatory guidelines, and serving as a subject matter expert for analytical lifecycle management. You will also be responsible for interactions with internal regulatory teams, reviewing DMF documentation, defining product specifications and analytical methods, ensuring audit readiness, and providing support to various cross-functional units. To excel in this role, you should hold a degree in Analytical Chemistry or related scientific discipline, possess extensive experience with analytical instrumentation, have knowledge of international regulatory guidelines, understand QMS principles and GLP practices, demonstrate strong leadership skills, and exhibit excellent communication and project execution capabilities. Additionally, you should be willing to work in shifts if required and be open to travel to external sites as needed. If you meet the qualifications and are interested in this opportunity, please share your CV at pooja.j@domniclewis.com.,

You will be responsible for setting up an analytical facility to test Battery Materials, raw materials, and in-process samples as necessary. Ensuring all testing is done to Zero Error standards and guaranteeing defect-free product delivery. You will establish and maintain Quality Assurance Systems to achieve world-class product delivery and zero customer complaints. Adherence to IMS procedures and documentation is crucial for this role. Your essential qualifications should include hands-on experience in chemical and instrumental analysis, with the ability to handle hygroscopic/hazardous materials. Proficiency in Glove box operations, Ion chromatography, GC-MS, ICP-MS, etc. Good analytical skills are required along with experience in root cause analysis. Leadership qualities are necessary to coach and develop high-performance teams. A strong understanding of Chemistry and operational issues is expected. The educational requirement for this position is an M. Sc in Analytical/Inorganic Chemistry preferred, or equivalent, with practical experience in chemical analysis. You should have a total of 8 to 12 years of experience in chemical/instrumental analysis, data interpretation, and troubleshooting. Experience in handling hygroscopic/hazardous materials (3-5 years) is essential, with an added advantage of experience in a large and leading chemical complex. Desirable experience in battery material testing is a plus. In summary, you will be leading the analytical testing facility for Battery Materials, ensuring high-quality standards, and continuous improvement in product delivery.,

As a Quality Control & Quality Assurance Manager at our Tarapur plant, you will report to the Regional Senior QFS Manager with a dotted line to the Plant Manager. Your role involves overseeing QC & QA routine activities to achieve departmental targets. You will be responsible for various quality control activities including approving/rejecting pre-shipment samples, raw materials, in-process, and finished goods. Implementing quality control procedures, setting quality standards, and conducting vendor audits are key aspects of your role. Managing customer complaints, collaborating with different departments to resolve issues, and ensuring departmental performance aligns with targets and budgets are also part of your responsibilities. You will develop new testing methods when necessary, establish testing and inspection procedures, and manage QA executives" duties. Additionally, you will be involved in preparing and modifying SOPs for ISO, HACCP, and HALAL, ensuring proper specifications of materials, and conducting quality, food safety, and HALAL audits. Leading ISO 9001:2015 and food safety system management reviews, maintaining safe working conditions during QA activities, minimizing waste generation, coordinating with third-party laboratories, and ensuring compliance with various standards including ISO 9001:2015, HACCP, FSSC 22000, HALAL, and Kosher are crucial aspects of your role. You will also be responsible for staff management, training subordinates, and continual improvement of quality management systems. To qualify for this role, you should hold a University Degree in Chemistry with a minimum of 10 years of experience in a reputed flavor, fragrance, speciality chemicals, aroma chemical, pharma, or chemical company. Strong leadership, problem-solving, and analytical skills, along with knowledge of ISO 9001:2015 and FSSC22000, are essential. Fluency in Marathi, English, and Hindi, both written and spoken, is required, along with proficiency in MS Office. At ADM, diversity, equity, inclusion, and belonging are fundamental principles driving our innovation and growth. We are committed to fostering a diverse workforce and inclusive work environments where every colleague feels valued, contributes meaningfully, and can develop their career. To learn more about our dedication to advancing diversity, equity, inclusion, and belonging, visit our website. ADM is dedicated to unlocking the power of nature to provide global access to nutrition. With a focus on sustainability, innovation, and a wide range of ingredients and solutions, we lead in human and animal nutrition, as well as agricultural origination and processing. Join us in enriching lives worldwide by exploring more at www.adm.com.,

As a Senior Manager in the Research and Development department at Gujarat Fluorochemicals Limited, you will play a crucial role in leading a team to drive innovation and growth. Your main responsibilities will include conducting thorough literature surveys, identifying viable and non-infringing routes for commercializing fluoro-specialty molecules, developing and standardizing industrial processes, and meeting cost targets within specified timelines. Additionally, you will be expected to discover and develop new products, prepare various reports, and scale up lab processes to commercial levels. To excel in this role, you must have strong leadership skills to manage a team of scientists and chemists, possess in-depth knowledge of synthetic and analytical methods, and demonstrate proficiency in interpreting analytical data from various sources such as UV, IR, NMR, GC, GCMS, HPLC, LCMS, and MS. Familiarity with GLP, GMP, IMS guidelines, as well as an understanding of literature and patents, will be essential. Moreover, you should be adept at meeting customer requirements and have a good command of SAP and IMS systems. Ideally, you should hold a Master's or Ph.D. degree in Organic Chemistry and have accumulated 12-13 years of relevant experience in R&D, with a preference for candidates with a background in Fluoropolymers. Your total experience should fall within the range of 12-15 years, with specific expertise in Fluorospecialties. If you are a proactive and results-driven professional with a passion for research and development, we encourage you to apply for this challenging and rewarding opportunity at Gujarat Fluorochemicals Limited.,

As a Senior Manager in Research and Development at a reputed Chemical Manufacturing Company located in Vadodara, Gujarat, your primary responsibilities will include conducting Organic Synthesis with a strong background in analytical tools. You will be tasked with Route Scouting, focusing on cost reduction strategies, and effectively leading and managing teams of chemists. Your role will require hands-on experience in a Good Laboratory Practice (GLP) environment, along with the ability to work with analytical instruments such as NMR, GCMS, and IR for accurate data interpretation. Proficiency in the basics of Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC) is essential for this position. This position demands a candidate with a minimum qualification of M. Sc in Organic Chemistry, preferably holding a Ph.D., and possessing a substantial experience of 10-15 years in the field. The salary range for this role is between 16.00 to 20.00 Lacs per annum. If you meet the specified qualifications and have the requisite experience, we encourage you to apply for this full-time, permanent position by visiting our website at https://www.crownhrservices.com/job-opening. For further inquiries, you can contact us via mobile at 8511522332. As part of the benefits package, you will be entitled to Provident Fund contributions. The work schedule will be during day shifts, and the work location is in person at our facility in Vadodara, Gujarat.,

As a Quality Assurance & Analytical Chemist at FMC, you will be part of a team dedicated to providing innovative solutions for agriculture, contributing to the productivity and resilience of farmers" land. With a focus on science and technology, you will play a vital role in developing new herbicide, insecticide, and fungicide active ingredients, product formulations, and pioneering technologies that benefit both farmers and the environment. Your responsibilities will include: - Ensuring laboratory safety and industrial hygiene protocols are followed at all times. - Developing, validating, and implementing qualitative and quantitative analysis methods to meet business needs. - Conducting routine and non-routine analysis to support project quality and timing requirements. - Collecting data, generating summaries, and preparing reports. - Collaborating with tech leaders to investigate quality incidents and implement corrective actions. - Operating and maintaining various analytical instruments (HPLC, GC, IC, MS, Titrator, FTIR) to provide accurate data. - Collaborating with chemists and engineers to provide analytical results and structure determinations. - Managing the quality of active ingredients and intermediates with contract manufacturers. - Supporting changes in processes, equipment, and materials through QAR coordination. - Reviewing MOA and analytical Teck pack for improvement suggestions. - Performing other tasks as assigned by the line manager. The ideal candidate will have: - A Master's degree or above in chemistry/biochemistry or equivalent experience. - 10+ years of experience with a minimum of 8 years in analytical development/quality control. - Proficiency in method development and troubleshooting with various lab instruments/techniques. - A track record of delivering quality results on time. - Strong interpersonal skills, problem-solving abilities, and communication skills. - Familiarity with computer software packages from different instrument manufacturers. If you are a motivated leader with a technical background and a commitment to safety and efficiency, we invite you to apply for this role and become a valuable part of our team at FMC.,

The Chemist role involves performing standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. As a Chemist, you will contribute by conducting laboratory testing, including qualitative and quantitative chemical and physical analysis of raw materials, finished products, and stability samples. You will be responsible for preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation such as HPLC, FTIR, UV-Visible spectrophotometer, and reviewing product certificates of analysis for accuracy and conformance. Additionally, you will perform routine calibration and performance verification of lab equipment and instrumentation, provide input on Standard Operating Procedures (SOPs), Test Methods, and laboratory documents, and participate in investigations, address Out of Specifications (OOS), resolve deviations, and implement Corrective and Preventive Actions (CAPA) under general supervision. Adhering strictly to current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) is essential, including detailing data in lab notebooks and following cGMP guidelines. You will interpret test results, compare them with determined standards and limits, and analyze records for trend verification under supervision while maintaining a safe, clean, and efficient laboratory environment. This role does not have any supervisory responsibilities but requires the ability to adapt as the external environment and organization evolve. To be successful in this position, you should have the ability to complete testing according to established methods, demonstrate basic proficiency in lab instrumentation and multiple test methods, solve problems and carry out responsibilities under supervision, coordinate workload effectively, demonstrate strong customer and results orientation, interact effectively at all levels with sensitivity to diversity, and function as a team member. The ideal candidate will possess a Bachelor/Master of Science in Chemistry, Biochemistry, or related scientific fields, or equivalent experience, along with knowledge of LC/MS and GC/MS, previous cGMP regulation and compliance knowledge, nutraceutical or pharmaceutical laboratory work experience, and knowledge in ISO17025 Lab Management. Join us for this exceptional opportunity to contribute to world-class research and shape the future of nutritional science!,

As an Analyst reporting directly to the Department Head - Chemistry, you will be responsible for providing technical support and analysis within the Testing Laboratory. With over 1 to 5 years of laboratory testing experience, you will demonstrate the ability to handle complex roles and duties independently. Your background and understanding of Chemistry are mandatory for this role. Experience with instruments such as Gas Chromatography (GC/MS) is required to perform analytical tests effectively. Your essential duties and responsibilities will include participating in general lab duties, ensuring compliance with GMP, SOPs, and current test methods, writing SOPs, and performing analytical tests using GC and other laboratory instruments. You will also be responsible for documentation, sample preparation, interdepartmental coordination, supply ordering, assisting with instrumentation training and maintenance, and accurate reporting in lab books. This is a full-time position with benefits such as cell phone reimbursement, health insurance, leave encashment, and provident fund. You will be working day shifts with opportunities for performance bonuses and yearly bonuses. The ability to commute or relocate to Mohali, Punjab is preferred. A Bachelor's degree is preferred for this role, and at least 1 year of experience with GC is also preferred. If you are looking for a challenging opportunity where you can utilize your chemistry background and analytical skills, and work in a dynamic testing laboratory environment, this Analyst position may be the right fit for you.,

As the General Manager - R&D at Gujarat Fluorochemicals Limited, you will play a crucial role in leading a team to drive the research and development efforts of the organization. Your primary responsibilities will include conducting literature surveys, identifying innovative and cost-effective processes for fluoro-specialty molecules, developing new products, and ensuring the scalability of lab processes to commercial levels. You will be tasked with managing a team of scientists and chemists to facilitate new product and process development while enhancing existing products. A deep understanding of synthetic and analytical methods, along with proficiency in interpreting data from various analytical techniques, such as UV, IR, NMR, GC, GCMS, HPLC, LCMS, and MS, will be essential for success in this role. Your educational background should include a Ph.D. in Organic Chemistry, coupled with a minimum of 15-18 years of experience in R&D, with at least 8 years in a leadership position. Familiarity with GLP, GMP, IMS guidelines, as well as expertise in understanding literature/patents, customer requirements, and proficiency in SAP & IMS will be crucial for this role. If you are a dynamic and experienced professional with a passion for innovation and a track record of success in the field of Fluorospecialities, we invite you to apply for this challenging opportunity as the General Manager - R&D at Gujarat Fluorochemicals Limited.,

Walk In Drive For Quality Control In Formulation Division @ MSN Formulation Unit -II , Kothur . Department :- Quality Control Formulations Experience:- 2 to 8 Years Skills :- Formulation QC - HPLC | GC | GC MS | LIMS | LCMS | ICPMS | Dissolution | IP/FP | Stability | Method Validation | Method Development | Method Transfer | E&L | | Proficiency with Equipment | Method Development & Optimization | Understanding of Regulations | Data Analysis | Testing and Inspection | Process Improvement | Regulatory Compliance | Equipment Maintenance | Training and Support | Root-cause analysis | Method development and validation | (OSD & Injectables) | USFDA | Regulatory Approvals Division :- Formulation Interview Date:-30-08-2025 - Saturday Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur, MSN Unit -V R K Puram. Venue Location :- MSN Laboratories Pvt Ltd| Formulation Unit -2 | Kothur | Sy. No 1277&1319 -1324| Nandigama|Rangareddy| Telangana - 509216 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

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

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

You are seeking a Senior Chemist with experience in handling GC-MS and HPLC instruments. As a Senior Chemist, you will be responsible for conducting analytical chemistry experiments, data analysis, and reporting results. This is a full-time position with benefits including paid sick time, paid time off, and a performance bonus. The work schedule is during the day shift. The ideal candidate should have a Bachelor's degree in Chemistry or a related field. A minimum of 1 year of experience in analytical chemistry is preferred. This position is located in Bangalore City, Karnataka. Candidates should be able to reliably commute to the work location or be willing to relocate before starting work.,

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

As a candidate for this position, you should hold a B.Sc. or M.Sc. degree in Chemistry. With 2-3 years of experience in the Fragrance industry, you are expected to be well-versed in all laboratory processes and procedures. Previous experience working with Gas Chromatography Mass Spectrometry (GCMS) is essential for this role. Additionally, proficiency in Microsoft Office, particularly Excel, is required to efficiently carry out the responsibilities of this position.,

Job Description: As a Lab Chemist / Scientist, you will be responsible for analyzing environmental (Water, Waste Water, Soil) and food samples. Your main duties will include maintaining documents in compliance with NABL & ISOI 7025 standards. Additionally, you will need to have knowledge about the uncertainty principle and hands-on experience in handling various equipment, especially UV spectrometers. Experience in handling an Instrumentation laboratory (GC-MS, ICP-OES) will be considered an added advantage. Your role will also involve analyzing results by calculating the quantity of elements in a sample and interpreting analytical data. Qualifications required for this position include a BSc / M.Sc / PhD in Chemistry or Biochemistry. The ideal candidate should have 0 to 5 years of relevant experience. This position is based in Chennai (Ayapakkam) and there are 3 vacancies available. The salary for this role is not a constraint for the right candidates, and bachelor accommodation will be provided for outstation individuals. If you meet the requirements for this role and are interested in joining our team, we encourage you to apply now. --- As an Oil & Gas professional, your responsibilities will include interpreting data to identify key performance indicators and trends, creating company reports and documentation that offer key data insights, and ensuring accuracy and consistency in reporting. Qualifications required for this position include Any Degree with 1 to 3 years of relevant experience. In addition to these responsibilities, you must be proficient in typing documents with a flexible typing speed and have knowledge of Excel, Word, and PPT. You will also be required to maintain documents as per NABL & ISO17025 standards. This role has 1 vacancy available and the salary is not a constraint for the right candidate. Bachelor accommodation will be provided for outstation individuals. If you believe you are the right fit for this role, we encourage you to apply now.,

As the Lead Specialist GOE CAL at dsm-firmenich in Mumbai, you play a crucial role in bridging the gap between taste, texture, and health through innovative ingredients and solutions. Diversity, Equity & Inclusion is at the core of our values, ensuring equal access to opportunities, a sense of belonging, and authenticity celebrated across the organization. Your responsibilities include planning and conducting analytical techniques such as GC-MS, LC-MS for flavors, perfumes, and natural products, contributing to method development and the team's technical growth. You will manage analytical instruments, lab operations, ensure SOP compliance, accurate documentation, and collaborate closely with cross-functional teams to provide effective analytical support. Utilizing your expertise in gas chromatography and mass spectrometry, you will conduct volatile compound analysis, prepare analytical reports, and serve as a subject matter expert in analytical/flavor chemistry. Your problem-solving mindset, drive for innovation, and strong sense of ownership will be essential in delivering meaningful results and collaborating within diverse teams. We offer a supportive and empowering environment that encourages personal growth, a crucial role in projects, and the opportunity to build your brand. If you hold an MSc. with 5+ years or Ph.D. with 2+ years of experience in analytical chemistry, possess hands-on experience in method development, and demonstrate knowledge of ISO 17025:2017 standards, we invite you to apply online via our career portal. Join our global and collaborative team at dsm-firmenich, where innovating in nutrition, health, and beauty is at the heart of what we do. With a diverse workforce and a commitment to progress, we aim to create essential solutions for life, desirable products for consumers, and a more sustainable future for the planet.,

The Chemist role involves performing standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. As a Chemist, you will contribute by conducting laboratory testing, preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation, reviewing product certificates of analysis, maintaining Certificates of Analysis (C of A) files, and providing input on Standard Operating Procedures (SOPs), Test Methods, and laboratory documents. You will also participate in investigations, address Out of Specifications (OOS), resolve deviations, and implement CAPA with general supervision while strictly adhering to current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Key responsibilities include interpreting test results, maintaining a safe, clean, and efficient laboratory environment, and ensuring routine calibration and performance verification of lab equipment and instrumentation. Although there are no supervisory responsibilities, you should possess the ability to adapt as the external environment and organization evolve. Successful candidates will demonstrate the ability to complete testing according to established methods, proficiency in lab instrumentation and multiple test methods, problem-solving skills, and the capacity to coordinate workload effectively. The ideal candidate will hold a Bachelor/Master of Science in Chemistry, Biochemistry, or related scientific fields, or equivalent experience. Additionally, knowledge of LC/MS and GC/MS, previous cGMP regulation and compliance knowledge, nutraceutical or pharmaceutical laboratory work experience, and familiarity with ISO17025 Lab Management are preferred. Join us in this exceptional opportunity to contribute to world-class research and shape the future of nutritional science.,

Hands on skill and Knowledge of LCMS, HPLC, UHPLC, GC, GCMS, Wet chemical Understanding of analytical chemistry, discussion with synthesis, plant, PE laboratory analysis of samples in time., Ensure that laboratory work is carried out in a safe manner Required Candidate profile Analytical Research & analytical method development for organic molecules. Method validation. Method transfer. Stability studies. GLP. GDP, Building Problem Solving, Customer Centricity, Analysis