123 Spectroscopy Jobs - Page 5

Job Description : Carry out Experiments for process feasibility and optimization. Impurity Synthesis and their Characterization using NMR and Mass Techniques, following proposed ROS. Writing LNB / ELNB and proper documentation. Scale-up of Intermediates and products in Lab in the given timeline. Learning and updating Job related knowledge, like process development, Quality, and regulatory aspects. Carryout Experiments to support Plant for trouble shooting in ongoing products to address OOS and OOT issues. Adhering to SOPs / Guidelines, Safety Norms in Lab and maintain cleanliness of work area. Supporting senior colleagues in Development & Optimization activities. Maintaining personal hygiene, safety, and discipline in the workplace.

Job Title : Senior Scientist Nanomaterials Location: Hyderabad Department: Research & Development Job Type: Full-time Job Summary: We are seeking a highly skilled Senior Scientist with expertise in Nanomaterials to lead cutting-edge research in the development and characterization of novel nanomaterials with a focus on atomic-level interactions. The ideal candidate will possess a PhD in Physics, Materials Science, or a related field, and have extensive experience in both experimental techniques and theoretical modeling in the domains of nanomaterials. This role offers the opportunity to drive innovative research, collaborate with multidisciplinary teams, and contribute to the development of next-generation materials for a variety of technological applications. Key Responsibilities: Lead and conduct research in the development of nanomaterials with a focus on understanding their atomic and subatomic structure and behavior. Design and execute experiments involving the synthesis, characterization, and manipulation of nanomaterials at the atomic scale, utilizing cutting-edge techniques. Investigate the quantum mechanical properties of nanomaterials and their applications in fields such as nanoelectronics, energy storage, and sensing technologies. Collaborate with multidisciplinary teams, including engineers, chemists, and data scientists, to integrate atomic-level insights into practical material designs. Develop simulation models and theoretical frameworks to understand the behavior of materials at the atomic and nanoscale levels. Publish and present research findings in peer-reviewed journals, scientific conferences, and industry seminars. Contribute to grant writing and securing research funding for future projects in nanomaterials and atomic physics. Stay current with the latest advancements in nanotechnology, incorporating new findings into ongoing research efforts. Qualifications: PhD in Materials Science, Nanotechnology, or a closely related field. Minimum of 5 years of post-doctoral research experience in the areas of nanomaterials. Extensive experience in atomic-level characterization techniques and nanomaterial synthesis methods. In-depth understanding of quantum mechanics, atomic interactions, and nanomaterial properties. Strong theoretical background in atomic physics and nanoscale phenomena. Proven track record of publishing in high-impact journals and presenting at international conferences. Experience with modeling software (e.g., COMSOL, Gaussian, VASP, MATLAB, or similar) to simulate nanomaterial behavior at the atomic level. Strong problem-solving, analytical, and communication skills, both written and verbal. Experience in collaborative research and the ability to manage interdisciplinary teams. Preferred Skills: Familiarity with advanced computational methods in quantum mechanics and materials modeling. Knowledge of nanomaterial applications in areas like electronics, energy storage, and biotechnology. Hands-on experience with laser spectroscopy, optical characterization, or electronic properties measurement of nanomaterials. Experience in mentor roles, guiding students and junior researchers in both theoretical and experimental research

Lab Chemist Name:Lab Chemist Role:Chemist Industry:Activated Carbon Plant Location:Udaipur (Rajasthan) Job Type:Full Time Experience:Fresher- 3years Salary:Best in the industry Education:BSC/Diploma(Organic Chemistry) Description: Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. Conferring with scientists and engineers to analyze, interpret, and develop tests. Introducing heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies. Evaluating and ensuring compliance with laboratory safety procedures and standards.

1. Conduct chemical tests and build improvement methods Prepare test solutions, compounds, and reagents for laboratory personnel to conduct test Analyze organic and inorganic compounds to determine chemical and physical properties, composition, structure, relationships, and reactions, utilizing chromatography, spectroscopy, and spectrophotometry techniques Develop, improve, and customize products, equipment, formulas, processes, and analytical methods Work on model area development as per 5S- organize the work space for efficiency and effectiveness by identifying and storing the items used, maintaining the area and items, and sustaining the new order Compile and analyze test information to determine process or equipment operating efficiency and to diagnose malfunctions Ensure the equipment log is timely filled and regularly update the day to day activity tracker Confer with scientists and engineers to conduct analyses of research projects, interpret test results, or develop nonstandard tests Direct, coordinate, and advise personnel in test procedures for analyzing components and physical properties of materials Induce changes in composition of substances by introducing heat, light, energy, and chemical catalysts for quantitative and qualitative analysis Write technical papers and reports; and prepare standards and specifications for processes, facilities, products, and tests Ensure that materials are labeled properly and used in right quantities; maintain sufficient stock of chemicals and supplies to perform lab experiments Suggest improvements for test procedures to achieve project objectives and work towards development of standard procedures to improve quality and efficiency Ensure health and safety standards are adhered to while performing the tests and ensure that the necessary safety equipment is used during chemical procedures Take initiatives to drive growth for DCBL and ensure sustained growth in line with long-term and short-term objectives of the organization Ensure initiation and sensitization of the employees towards digitization and automation of the processes Focus on utilization of advanced business analytics tools to derive key insights critical for the success of the organization 2. Self/ Team Development Review and monitor performance of team members and provide requisite developmental support/ inputs Recommend training as required for team s development Develop the team and update their knowledge base to cater the organization need Strategize avenues for enhancing employee satisfaction in the function, resulting in high engagement levels of employees

Key Responsibilities: Lead the design, development and validation of new analytical methods for evaluating the quality, safety, nutritional content of Food & Nutra products. Manage & oversee the analytical laboratory operations, including equipment, personnel workflows to ensure accurate and reliable results. Collaborate closely with R&D Quality Assurance, Regulatory teams to ensure analytical method align with product development goals and regulatory requirements. Drive continuous improvement of analytical methodologies to enhance efficiency, accuracy and precision in food & nutra-analysis. Ensure compliance with local and international food safety and quality standards such as FSSAI, FDA or ISO. P Provide technical expertise including chromatography, spectroscopy, mass spectrometry and microbiological testing. Conduct troubleshooting and root cause analysis to resolve analytical issues in food & nutra product analysis. Maintain accurate documentation of analytical procedures, method validation reports and other relevant records. Stay updated with the latest advances in food & nutra-analysis technologies and incorporate cutting edge methods into the labs practices.

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-29-03-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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.

1. Conduct chemical tests and build improvement methods Prepare test solutions, compounds, and reagents for laboratory personnel to conduct test Analyze organic and inorganic compounds to determine chemical and physical properties, composition, structure, relationships, and reactions, utilizing chromatography, spectroscopy, and spectrophotometry techniques Develop, improve, and customize products, equipment, formulas, processes, and analytical methods Work on model area development as per 5S- organize the work space for efficiency and effectiveness by identifying and storing the items used, maintaining the area and items, and sustaining the new order Compile and analyze test information to determine process or equipment operating efficiency and to diagnose malfunctions Ensure the equipment log is timely filled and regularly update the day to day activity tracker Confer with scientists and engineers to conduct analyses of research projects, interpret test results, or develop nonstandard tests Direct, coordinate, and advise personnel in test procedures for analyzing components and physical properties of materials Induce changes in composition of substances by introducing heat, light, energy, and chemical catalysts for quantitative and qualitative analysis Write technical papers and reports; and prepare standards and specifications for processes, facilities, products, and tests Ensure that materials are labeled properly and used in right quantities; maintain sufficient stock of chemicals and supplies to perform lab experiments Suggest improvements for test procedures to achieve project objectives and work towards development of standard procedures to improve quality and efficiency Ensure health and safety standards are adhered to while performing the tests and ensure that the necessary safety equipment is used during chemical procedures Take initiatives to drive growth for DCBL and ensure sustained growth in line with long-term and short-term objectives of the organization Ensure initiation and sensitization of the employees towards digitization and automation of the processes Focus on utilization of advanced business analytics tools to derive key insights critical for the success of the organization 2. Self/ Team Development Review and monitor performance of team members and provide requisite developmental support/ inputs Recommend training as required for teams development Develop the team and update their knowledge base to cater the organization need Strategize avenues for enhancing employee satisfaction in the function, resulting in high engagement levels of employees

Jr. Process Development Scientist POSITION PURPOSE: The Jr. Process Development Scientist with some supervision from the Chemical Development Lead focuses on the route scouting and Chemical Process Development of Bayers existing and pipeline crop protective agents. Collaborates with all internal and external functional teams. The job holders ensure all the experimental work is done following the highest safety standards and document the generated data in the Electronic Lab Notebook. The applicant will have an excellent practical and theoretical understanding of synthetic organic chemistry or a relevant technology and can design and execute high-quality, thoughtful experimentation while making significant contributions both independently and as a team member. The candidate will work within an interdisciplinary and cross-divisional team in the Crop Protection Innovation organisation. TASKS AND RESPONSIBILITIES: Conduct process chemistry research as an individual contributor, which includes, but is not limited to, research on inventing new synthetic routes and associated manufacturing processes that turn the molecules into agrochemical solutions Conduct experiments for route scouting, process optimization, safety evaluation, high throughput screening and chemo/biocatalytic reaction discovery and optimization. Invent synthetic routes and develop safe, robust, and cost-effective processes to manufacture Crop Protection Agents developing the synthetic routes Contribute to the Chemical Development Process by conducting laboratory experiments by own hand and providing experimental results, technical updates, documentation, data interpretation, recommendations for process optimization, etc. With the help of the Process Engineer optimize unit operations Investigate optimization, generate safety and process engineering data required for scale-up of chemical reactions This is a highly practical role where you will be working in the R&D laboratories to generate new synthetic routes and assist in the design, planning and execution of multi-step experimental studies guided by risk assessment to deliver safe, efficient, robust manufacturing processes. Collaborate within project teams by working closely with analytical chemists, process engineers, pilot plant team and project managers within the Crop Protection Innovation organization. Staying up to date with the latest advancements in chemistry and technologies. Find opportunities to use these technologies in solving process development challenges Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs. Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices. KEY WORKING RELATIONS: Internal Crop Protection Innovation Team Analytical Chemist from Pilot Plant Team AIM Production Team AIM Analytical team at Vapi External Coordinate with various vendors and engineers for instrument installation/maintenance activities WHO YOU ARE: M.Sc/M.Pharm in Organic Chemistry with 0-3 years experience designing and performing experiments in a laboratory setting to meet project timelines and objectives. Comprehensive and state-of-the-art knowledge of modern synthetic methodologies as well as a basic understanding of organic reaction mechanisms and retrosynthesis. Strong understanding of small molecule analysis including chromatographic and spectroscopic techniques and structure elucidation by NMR and Mass Spectroscopy is required Embraces ambitious goals and drives progress with urgency. Consistently seeking opportunities to acquire knowledge, develop skills, and share insights. Possesses a strong willingness to learn and grow through challenging experiences, actively engaging in giving and receiving constructive feedback to foster continuous improvement. Effectively interacts with diverse teams across functions, cultivating strong working relationships with both internal and external collaborators to enhance overall performance Ability to work in the shifts Location: India : Gujarat : Vapi Division: Crop Science Reference Code: 841765

Industrial PhD Researcher POSITION PURPOSE: We are seeking a highly motivated Industrial PhD Researcher to join our Crop Protection Innovation, AgChem Manufacturing Solution Process Development Team. The candidate will be enrolled on the PhD program with one of the top research institutes in India. This position offers a unique opportunity to conduct doctoral research at the intersection of academia and industry, focusing on both basic and applied organic chemistry. The successful candidate will gain hands-on experience in industrial chemistry practices, preparing them for leadership roles in process development and innovation. TASKS AND RESPONSIBILITIES: Conduct research projects that address real-world industrial challenges, focusing on developing innovative solutions that can be directly implemented on an industrial scale. Work closely with both academic supervisors and industry mentors to ensure the research aligns with both scholarly standards and industrial objectives. Conduct laboratory experiments independently, and accurately document experiments and results in the Electronic Lab Notebook (ELN). Stay updated about the latest advancements in chemistry and technology through literature review, attending conferences and participating in training sessions. Adhere to Environmental, Health and Safety (EHS) protocols, actively participating in discussions to improve EHS practices. Prepare research reports, presentations, and publications summarizing findings and their industrial impact in peer-reviewed journals. KEY WORKING RELATIONS: Internal Crop Protection Innovation Team Pilot Plant Team External Institutes and Universities External PhD Guide WHO YOU ARE: M.Sc. in Organic Chemistry having exceptional academic grades from a reputable Indian University/Institute with intent to pursue an Industrial PhD. Knowledgeable in modern synthetic methodologies and organic reaction mechanisms, with familiarity in chromatographic and spectroscopic techniques (NMR, IR, HPLC, GC and Mass Spectroscopy). Courageous to work on difficult chemistry assignments, examples, total synthesis of complex natural products, enantioselective catalysis and other methodology development. Eager to learn process development skills like process optimization, analytical instruments handling, process engineering data generation, thermal safety data generation and interpretation, and scaling up processes in pilot plant and on commercial scale. Independently planning and executing multi-step synthesis of complex compounds. Consistently seeking opportunities to acquire knowledge, develop skills, and share insights. Possesses a strong willingness to learn and grow through challenging experiences, actively engaging in giving and receiving constructive feedback to foster continuous improvement. Location: India : Gujarat : Vapi Division: Crop Science Reference Code: 841769

JOB DESCRIPTION Job Title: Executive or Senior Executive Job Location: Bangalore Job Grade: Level 9 (9 I or 9 II) About Syngene: Syngene ( www.syngeneintl.com ) is an innovation led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards 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: The candidate shall be r esponsible to perform the development, validation, and routine testing of bioassay/ELISA for Large Molecules (LMs), especially Monoclonal antibodies (mAbs) and other LMs. The candidate shall be responsible for method development, validation, and stability testing drug substance/drug product. The candidate shall be willing to work in shifts. Role Accountabilities: Shall develop and validate cell based assays and binding assays (ELISA), SEC and CGE especially for monoclonal antibodies (mAbs), etc. Shall troubleshoot the problems for these methods. Must have strong knowledge of the development of cell based bioassays for Monoclonal antibodies. Experience in Qualification and Validation of cell based bioassays Shall have experience on Good documentation/laboratory practices such as ALCOA+ Broad knowledge on analysis of cell based assays to derive relative potency software s (such as Softmax Pro and PLA) Basic cell culture technics and hands on experience in maintaining of mammalian cells. Must have experience in handling various cell lines (adherent and suspension cell lines). Preparation of Mammalian cell banks for Bioassays. Experience in handling of primary and continuous cell lines like Revival, maintenance, cell bank preparation, and cryopreservation Shall prepare the raw datasheets, protocols, reports, and SOPs Handling of QMS (Incidents, deviations, Out of Specifications, change controls, etc.) for GMP activities 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/GMP/Safety and as per the procedure defined in the internal standard operation procedure Must have good hold on MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Experience in developing and validating SEC, CGE methods is an added advantage especially for monoclonal antibodies (mAb) is an added advantage Experience in calibration and qualification of HPLC, UPLC, GC, and other QC laboratory instruments is added advantage Good communication and e mail writing skills are required since the candidate needs to communicate with clients/external users situated overseas Commitment to safety Behavioral Skills Good Interpersonal skills Self time management Good Team player Polite/Good Communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 2 6 years Skills and Capabilities: Development, validation, and routine testing of Bioassay /ELISA, SEC, CGE for Monoclonal antibodies (mAbs) and other Large molecules Qualification and validation of cell based bioassays Able to follow instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Experience in developing and validating SEC, CGE and HPLC methods for mAbs is an added advantage Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+ Good knowledge of MS office (word, excel, ppt) and E mail writing skills Education M. Pharm/ M. Tech/ M.Sc. / B.Sc. (Biotechnology/Biochemistry) with 2 6 years experience in GMP environment (QC)

- Perform daily activities for failure analysis (FA) for advanced technology nodes collaborating with different FA labs - Develop a Failure analysis ecosystem in India for various materials, applications and defects collaborating with Apple labs across geographies - Conduct physical fault isolation using various FA tools - Develop comprehensive FA methodologies for failures on metals, plastics, polymers, glass and other types of raw materials - Prepare technical reports / presentations summarizing failure analysis findings recommend improvements in production processes - Analyzing experimental data to provide in-depth understanding of design features manufacturing process nuances - Researching innovative technology to understand root causes of different types of cosmetic defects, reliability and dimensional failures on different components - Providing process improvement direction to multi-disciplinary teams to improve product quality, reliability, part cosmetics, bonding performance of components. - Interacting with a diverse and passionate group of team members to communicate results and provide clear and first principles driven direction based on failure analysis - Tackle new challenges everyday both technical and logistical, where your contributions will drive improvements to the product. - Manage Quality functions for some metal processing like billet manufacturing, extrusion etc Minimum Qualifications Minimum Qualifications 8+ years of expertise in failure analysis methodology to identify root cause Ability to make clear and concise slides/ presentations through Keynote, Excel, etc. Demonstrate an unwavering passion for engineering products with exceptional reliability Expertise in Failure Analysis techniques (Optical Microscopy, FTIR, X-ray/CT, Scanning Electron Microscopy/Energy Dispersive Spectroscopy, EBSD etc.), and the ability to use failure analysis methodology to derive a root cause of failure Bachelor s degree in engineering (mechanical, materials, etc.). MS/ME or PhD in Mechanical, Metallurgical Engineering with industry experience preferred Key Qualifications Key Qualifications Preferred Qualifications Preferred Qualifications Excellent written and verbal communication skills for audiences ranging from technicians to senior executives Experience in spirited collaboration between multidisciplinary teams of engineers and scientists to solve complex electromechanical / mechanical design challenges Ability to travel internationally without restriction Collaborative attitude and ability to cross-functionally work effectively Education Experience Education Experience Additional Requirements Additional Requirements More

We are actively looking for credible team members who would be primarily responsible for: 1. Testing of battery materials in Coin / Pouch cell configurations 2. Benchmarking of properties / performance with expected standards 3. Improvements to existing cell performances 4. Setup / maintenance of battery performance lab Essential Knowledge of battery materials cathode, anode, electrolyte Hands-on experience with assembly and testing of Li ion cells (coin & pouch type) Electrochemical methods cyclic voltammetry, impedance spectroscopy, charge / discharge cycling Chemical analysis, Thermal analysis, spectrophotometry, etc. Inorganic synthesis, especially oxides, phosphates, silicates of alkali and transition metals. Educational Requirements : Candidates holding a Ph.D. in Electrochemistry/Inorganic Chemistry/ Physical Chemistry or MSc. with experience of Li/Na ion batteries will be preferred. Skills and Expertise: Good analytical ability and having exposure to root cause analysis Proper understanding of Chemistry and operational issues Require innovative approaches for research/analysis for new lab Good communication skills and team building approach Adequate understanding with cross functional departments.

Plan, coordinate, and direct QC and Application development activities, to support manufacturing and RD in timely delivery of results / products to customers. To ensure analytical / testing protocols are developed for all planned products. Monitoring laboratory data and metrics on a regular basis to ensure that appropriate investigation, corrective action, and/or escalation is conducted. Drive investigation in case of non-conforming laboratory test results. Identify training needs and arrange for training. To ensure adequate testing facility is available at all times. To ensure plan timely calibration / maintenance of all the equipment and instruments. To provide hands on leadership and management of day-to-day quality interactions within the manufacturing group and QC group. Obtain ISO and other specific certifications for the lab. Skills and academic qualifications Functional Skills Functional Skills Required - Lab management Knowledge of battery materials cathode, anode, electrolyte Hands-on experience with assembly and testing of Li ion cells (coin pouch type) Electrochemical methods cyclic voltammetry, impedance spectroscopy, charge / disc Technical Skills required - Inorganic synthesis, especially oxides, phosphates, silicates of alkali and transition metals. Chemical analysis, Thermal analysis, spectrophotometry, etc.

TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industrys broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in RD generates a steady flow of APIs, enabling timely introduction of new products to market. How you ll spend your day Excellent communication and with hands on experience. Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets. Troubleshooting/OOS investigations during validations. Having a good knowledge of HPLC, IR, UV, KF Titrator, Halogen Moisture analyzer, Polarimeter and wet analysis Having good knowledge of HPLC trouble shooting. Sound knowledge of Organic Chemistry Spectroscopy. Having a good knowledge of HPLC Method development of API/RM/KSM and SM using various detector like Mass, IR, CAD, ELSD, UV-PDA and UV. Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques. Data interpretation by NMR, Mass Spectrometer, DSC, TGA FTIR Having a sound knowledge of Analytical method validation. Hands on experience of various Analytical Instruments-Coulometer, FT-IR, UV, Karl Fisher, Halogen Moisture Analyzer etc., >sound knowledge of Organic Chemistry Spectroscopy. Your experience and qualifications MSc (Organic chemistry/Analytical chemistry) 4- 7 year

JOB DESCRIPTION Job Role: Lab Analyst Job Role ID: SECTION I: BASIC INFORMATION ABOUT THE JOB ROLE Job Role Variant: Lab Analyst Manager Job Position: Job Position ID: Value Stream: Asset Operations Job Family: Manufacturing Sub-Job Family: Trainee Grade/Level: Location: SECTION II: PURPOSE OF THE ROLE To assist with various laboratory activities ensuring quality, safety, and compliance of Refinery, Petrochemical, Polymer, Elastomer, Polyester, New Energy products through meticulous testing and management of laboratory operations under the guidance of experienced lab personnel while ensuring accurate analysis, testing, and quality control of various products SECTION III: KEY RESPONSIBILITIES AND ACCOUNTABILITIES OF THE ROLE Responsibilities Laboratory Operations Assist in the collection and preparation of samples from various stages of production process including proper labelling, documentation, and sample handling and ensure integrity of samples for analysis. Perform routine tests and experiments on samples using laboratory instruments and equipments including chromatography, spectroscopy, titration and other analytical methods Record and document test results, observations and experimental data in raw data book, process register and in individual raw data book. Update analysed result in LIMS and inform supervisor to review and validate LIMS results. Detect exceptions or deviations in test results and highlight / report to concern Assist in the calibration, validation and maintenance of laboratory equipment and instruments to ensure validity of test results. Dispose left over samples safely as per laboratory practices and procedures. Conduct inspection of received routine samples and distribution of samples as per type of analysis to the different sections of the laboratory. Proactively communicate to shift in charge for any abnormal samples or non-receipt of routine sample as per schedule. Workplace Safety, Audit & Compliance Adhere to laboratory safety protocols and guidelines at all times and ensure personnel as well the safety of assets Handle hazardous materials / chemical with outmost care and dispose as per the set guidelines/ protocols Keep self familiarized with the industry regulations, standards and protocols and ensure all lab activities comply with these requirements Policies, Processes and Procedures Conduct day to day activities in compliance with all relevant policies, processes, standard operating procedures (SOPs) and instructions so that work is carried out in a controlled and consistent manner. Keep self abreast with leading practices & trends in the industry and contribute in continuous improvement of systems, processes and procedures through LEAN six sigma methodology, DMAIC analysis, 5S adherence, QCC, Kaizen, etc. SECTION IV: SUCCESS METRICS (TOP 3-5 KPI's) Compliance to ISO 17025 Quality Management System Quality audit score Zero Penalty due to Non-Compliance of Health & Safety Regulations Reliability of reported results Awareness of LIMS and SAP-QM Awareness various standards and compliances (e.g. ISO 9001, ISO 18001, ISO 45001, AS9100D) SECTION V: OPERATING NETWORK Internal: Supervisor/ Manager, Lab Team, Quality Control/ Quality Assurance Team, Production Team, Research and Development Team, Health and Safety Team External: NA SECTION VI: KNOWLEDGE AND COMPETENCIES Education Qualifications Bachelors of Science (Chemistry) or Master of Science (Chemistry); M.Sc. Candidates will be preferred. Experience (Must Have & Good to Have) 0-2 years in QA/QC discipline Functional / Behavioral competencies required to execute the role FUNCTIONAL COMPETENCIES SECTION VII: CAREER MOVEMENTS Feeder Roles: Possible Next Role Movement: Lab Analyst

TechnoS is hiring a dynamic Sales Manager. The role involves networking, driving sales, building customer relationships, and expanding market presence. The ideal candidate should have experience in sales, tenders, strong communication

Validate & optimize R&D, support manufacturing, scale-up & QC. PhD (2+ yrs)/MS (5+ yrs) in pharma preferred. Expertise in safety, distillation, GC/DoE. Send CV to shivam@lykora.in or call 9845098759.

The Position will be responsible for assisting in analytical method development of assigned project within given timeframe as per safety and environmental rules. Raw materials and finished products analysis. Generating Certificate of Analysis (COA) and compiling supporting documents. Pro-activeness to trouble shoots any complexity during analysis. Strategic Responsibilities To understand the analytical scope of the project assigned. Inputs in planning of analytical support to R&D and Kilo and Pilot Plant. To ensure proper maintenance of laboratory instruments or equipment s. Timely calibration of assigned instruments. Proper house- keeping and use of PPE s. Use relevant MSDS for safe handling and disposals of toxic chemicals. Operational Responsibilities Analytical Method Development on GC, HPLC and Wet analysis. Analytical Method Validation / Verification/Evaluations on GC, HPLC and Wet analysis. Routine analysis and Standard Test Procedure (STP) preparation. Characterization of various compounds by UV-Vis., FT-IR, DSC, FT-NMR and Mass (LC-MS/GC-MS) Spectroscopy. Preparation of Reference Standard/Working Reference Standard, Calibration solutions and Calibration of Instruments. Elemental Characterisation by CHNS Analyser and Elemental impurities analysis by ICP-OES and MS. On-line data logging into Analytical Lab. note books/ LIMS System at ADL. Analysis support to KL/PP and commercial site method transfer. Financial Responsibilities Contribute to budget proposals. Contribute to budgetary controls within the area of responsibility. People Responsibilities Utilization of all available sources for skill up-gradation. Actively participation in problem solving sessions/ training programs. Coordination and communication with interdepartmental team members. Time management. Education Qualification Master/Doctorate in Analytical /Organic Chemistry from a reputed University / Institute. Work Experience 2-6 Industrial Experience. Industry to be Hired from Agro Chemicals/Fine chemicals/ Pharma-API and Specialty chemicals. Functional Competencies Analytical Skills Practical Experience on HPLC /GC Understanding of HSE Data Management Analytical data interpretation

This project is based in the neonatal intensive care unit. It recruits neonates (later preterm and term) who are at risk of acute kidney injury and monitors them using a near-infrared spectroscopy device (NIRS). The machine is attached to the neonate and the readings are recorded and stored. Other demographic and clinical data variables are documented. All neonates enrolled in the study are followed up at 3, 6 and 12 months for kidney function parameters. Project Research Scientist-1 (Non Medical) Position Starting: 15th March, 2025 No. of Vacancy: one Preferred Qualifications: First class post graduate degree including integrated PG degrees Second class postgraduate degree including integrated PG degrees with PhD Basic computer operating skills Salary: 56,000 +16,800 HRA (total 72,800 pm) Language : English, Kannada, Hindi Preferable Tamil, Telugu Experience: At least 1 year experience of working in a biomedical research project Last Day for Receiving Application: 10th March, 2025 Roles and Responsibilities: To ensure all eligible neonates are included in the study To ensure complete data collection of all neonates recruited in the study. To maintain the research documents of every enrolled subject. Data entry of all the data related to the study To communicate with families during the hospital stay, and at discharge and liaise between the research team and the patient s families To communicate with families and liaise with them to ensure follow-up during the first year after discharge To support families with getting appointments for follow-up and the investigations to be done at follow-up To support timely report submission to ICMR and IEC. To maintain the documents and bills related to the expenses of the study Interested candidates may send their Resume to: The Principal Investigator ICMR NIRSneo Project

Purpose of Position To monitor the plating chemical preparation, Chemical monitoring and maintenance, Chemical indent, conducting experiment etc. Ensure Plating chemistries are analysed, Monitored and controlled on regular basis in plating plant Specific Responsibilities Ensure that the Quality policy is understood, implemented, and practiced at all levels in the plating department. Establish and maintain documented procedures for the identification of chemicals at all stages in the plating department. Establish and maintain a documented procedure for process control in the plating department. Conduct a monthly review of trends in the plating chemicals and initiate corrective action for major deviations in the chemistry. Establish and maintain a documented procedure for handling, storage, preservation, and labeling of chemicals in the plating department. Maintain and control inventory of plating chemicals and safety equipment in the plating department. Ensure proper housekeeping and disposal of used chemical containers in the plant. Prepare a monthly statement of chemical consumption in-plant. Ensure Gold/Silver accountability norms are fixed and reported every month. Develop and maintain SOPs, WIs, and formats required for the lab. Participate in the goal-setting process for the department and strive for excellence. Maintain housekeeping standards and ensure safety measures. Specific Authorities: In charge of the Lab Authorized to analyze the plating baths and make chemical additions Authorized to update the Lab records Lab analytical chemicals ordering in Coupa Preparation and modification of the Lab and Chemicals storage & handling procedures (QMS/EHS) Authorized to operate ICP Lab and Chemical safety Draw chemicals from Main Chemical stores Gold addition to bath in the presence of Finance, WH, and Plating Manager or their representative Addition of Silver Potassium Cyanide. Skill Sets & Competencies Electroplating Process Knowledge : Understanding the fundamentals and practical aspects of electroplating. Chemistry Preparation : Skills in preparing and handling chemical solutions for plating. Process Parameters : Knowledge of factors influencing plating quality such as temperature, current density, and solution composition. Analytical Techniques : Proficiency in techniques including Atomic Absorption Spectroscopy (AAS), Inductively Coupled Plasma (ICP), pH measurement, turbidity measurement, conductivity measurement, Oxidation-Reduction Potential (ORP) measurement, wet analysis, and gravimetric analysis. Plating Experimentation : Experience with Hull Cell testing for evaluating plating quality. Troubleshooting : Ability to diagnose and resolve issues in the plating process. Plating Quality Requirements : Understanding quality standards and requirements for plating. Chemical Handling and Safety : Knowledge of proper handling, storage, and safety procedures for chemicals. 5S Housekeeping Technique : Familiarity with this technique for organizing and maintaining a clean workspace. SAP Exposure : Experience using SAP software for process management and reporting. Gold Accountability : Understanding of gold-related processes such as gold assay, variance, and stock reporting (advantageous). Performance Monitoring and Reporting : Skills in monitoring, controlling, and improving plating processes and chemicals. Process Validation and Revalidation : Experience with validating and revalidating electroplating processes. Basic Computer Skills : Proficiency in MS Office and other basic computer applications. QMS and System Requirements : Understanding of Quality Management Systems (QMS) and requirements specific to the plating area. IATF 16949 Compliance : Knowledge of and ability to execute requirements of the IATF 16949 standard for automotive quality management. EHS Compliance : Adherence to Environmental, Health, and Safety regulations

Qualifications: Masters degree in Pharmaceutical Sciences (M. Pharm) or Chemistry (M.Sc) with 4-6 years of hands-on experience. Proficiency in analytical techniques such as HPLC, UV spectroscopy, DSC, Dissolution testing, with expertise in developing analytical methods for drug substances, reference standards (RS), and impurities. Experience in soft gel analysis preferred. Proactive problem solver with a strong ability to identify issues and propose effective solutions. Team-oriented with experience collaborating across functional teams. Strong documentation skills and effective communication abilities. Capable of working independently with minimal supervision. Roles and Responsibilities: Perform laboratory activities adhering to Pharmaceutical GLP/GMP and internal guidelines, ensuring safety and reliability. Conduct analytical testing of dosage forms, focusing on Assay, dissolution, related substances, and other specified tests, particularly for soft gelatin capsules. Perform analytical testing for dosage forms involved in stability studies. Independently execute tasks following in-house SOPs and good documentation practices. Travel to SPIs other locations, customer sites, or contract manufacturing units as needed for method transfer activities. Meet defined priorities, scope, timelines, and deliverables consistently

The Bloom Energy Mumbai team is seeking a highly motivated Engineer to support its Fuel Cell Materials Engineering development team. The Stack Engineer will be an integral part of an interdisciplinary team to improve the performance and manufacturability of current and future fuel cell stack Technologies. Hiring a Stack engineer to support Bloom Energy servers Engineering and field failures analysis, conduct detailed root cause investigation and develop test plans to investigate the root cause. Roles and Responsibilities: Support all engineering development Fuel cell systems analysis in identifying various failure modes. Support investigation of Fuel cell Systems performance failure issues during field operating conditions and develop a failure pareto. Support Bloom Energy future product engineering/field HB data analysis. Interface with testing team to timely execute stack tests and ensure all required documentation are completed. Analysis of test data and provide recommendations for mitigating the root causes with the team support. Apply statistical techniques to analyze production and/or field data to learn about product performance, reliability. Apply techniques like 8Ds, 5whys to investigate the root cause. Present clear reports to the team on the deep dive analysis. Develop and execute new test protocols to Turn-on/off failure modes and performance issues. Perform meticulous and careful post-mortem analysis of test articles to investigate the root cause and apply extensive knowledge of materials characterization techniques to gain insight into various failures modes. Support material characterization activities as and when required. Must be willing to do Hands-on data analysis and failure analysis activities. Key Skills Required: Fundamental Knowledge on fuel cell technology, electrochemistry. Demonstrate good failure analysis and Root cause analysis skills. Strong drive for results and continuous improvement. Good knowledge on materials characterization techniques (SEM, EDS, XRD), and electrochemical diagnostics such as electrochemical impedance spectroscopy (EIS) preferred. Very strong written, verbal, and interpersonal communication skills. Ability to work independently and effectively within cross-functional teams, in a fluid and fast-paced environment. Knowledge of impedance analysis is additionally preferred skill. Knowledge on writing VB scripts and excel based macros is added advantage. Knowledge on writing Python scripts is added advantage.

Process Development: Contributing to the development of scalable processes for API Manufacturing. You may work on process optimization to improve yield, selectivity, and purity of the target molecules. Laboratory Work: Conducting hands-on experiments in the laboratory to synthesize and analyze API samples. You will be familiar with various laboratory techniques, such as organic synthesis, purification, and analytical methods Problem-Solving and Troubleshooting: Identifying and troubleshooting issues that arise during API synthesis or analysis and proposing effective solutions. Analytical Characterization: Analyzing and characterizing API samples using techniques such as HPLC, GC, NMR, and IR spectroscopy. You will be responsible for interpreting analytical data and ensuring the quality and consistency of the APIs. Data Analysis and Documentation: Recording experimental data accurately and maintaining comprehensive lab notebooks. You will also be involved in writing technical reports and documentation related to your research and development work. Regulatory Compliance: Adhering to relevant regulatory guidelines and ensuring that API Development activities are conducted in compliance with Good Laboratory Practice (GLP) and other regulatory requirements. Safety and Environmental Practices: Following proper safety protocols in the laboratory and adhering to environmental practices to minimize the impact of chemical processes.