224 Spectroscopy Jobs - Page 5

About ThinkBio.Ai ThinkBio.Ai is revolutionizing the biopharmaceutical and healthcare fields with AI-powered resources. Our five specialized teams clinical, science, AI, software, and managed services work together to develop AI-based solutions that are deployed horizontally (data platforms and workflow tools) and vertically (clinical focus areas such as oncology, autoimmune diseases, and cardiology). Our mission is to help our clients find answers to their toughest questions and to accelerate the application of scientific breakthroughs in the clinic. Position Summary: We are seeking a highly motivated individual with expertise in structural biology to join our team as a Postdoctoral Fellow or Scientist, depending on experience level. The position will involve applying structural biology techniques to understand protein-protein interactions, drug-target binding, and disease mechanisms, integrating these insights into computational models. The successful candidate will have a PhD in structural biology, biophysics, biochemistry, or a related field, with a deep understanding of macromolecular structure and function. Fresh PhD graduates will be hired as Postdoctoral Fellows for a two-year term, while candidates with at least two years of postdoctoral fellowship or industry experience will be considered for a Scientist position. : Apply deep domain knowledge in structural biology to characterize macromolecular complexes and understand their roles in disease pathways. Integrate structural insights with multi-omics data (genomics, transcriptomics, proteomics, and metabolomics) to understand molecular mechanisms of disease. Utilize and develop computational tools for structural modeling, molecular dynamics simulations, and ligand docking to complement experimental data. Stay up to date with the latest advancements in structural biology, biophysics, and computational methods to incorporate cutting-edge research into disease modeling efforts. Collaboration & Project Management: Work closely with cross-functional teams, including disease domain experts, computational scientists, and clinicians to enhance translational research efforts. Work with the Scientific Manager to help in project planning, execution, and reporting, ensuring alignment with research objectives. Communicate findings effectively through reports, presentations, and discussions with internal teams and external collaborators. Publish research findings in high-impact, peer-reviewed journals. Present work at scientific conferences, symposia, and internal research meetings. Contribute to grant applications and funding proposals where relevant. Qualifications & Experience: PhD in structural biology, biophysics, biochemistry, or a closely related field. Strong expertise in at least one major structural biology technique (e.g., X-ray crystallography, cryo-electron microscopy (cryo-EM), NMR spectroscopy). Solid understanding of protein structure-function relationships, macromolecular interactions, and their relevance to disease biology. Experience in experimental design, data collection, data processing, and structure determination. Excellent verbal and written communication skills, with the ability to convey complex structural biology concepts clearly. Preferred: Experience with computational structural biology tools (e.g., Rosetta, AlphaFold, molecular dynamics software). Previous experience working in a multidisciplinary research environment. Familiarity with AI/ML approaches in structural biology or drug discovery. Other Considerations: Fresh PhD graduates will be hired as Postdoctoral Fellows for a two-year term with an opportunity for promotion to Scientist based on performance. Candidates with at least two years of postdoctoral experience in structural biology in either academia or industry will be hired as Scientists with opportunities for career advancement. Why Join Us? Work at the cutting edge of structural biology and disease research. Contribute to groundbreaking disease modeling and molecular insights. Collaborate with leading experts in multiple disease domains. Competitive salary, benefits, and career development opportunities. Application Instructions: Interested candidates should submit a cover letter and CV to careers@thinkbioai.com .

University: Delft University of Technology (TU Delft) Country: Netherlands Deadline: 2025-07-22 Fields: Chemical Engineering, Chemistry, Materials Science, Environmental Engineering, Process Engineering Delft University of Technology (TU Delft) invites applications for a postdoctoral position focused on heterogeneous catalysis and high-pressure instrumentation for the catalytic transformation of CO₂ into sustainable aviation fuel (SAF). The successful candidate will join a multidisciplinary team to design and develop advanced reactor–catalyst systems, contributing to the decarbonization of air transport through innovative process engineering. Responsibilities Include – Designing and operating novel high-pressure flow/batch reactor systems. – Developing and synthesizing tailored catalyst materials for targeted hydrocarbon production. – Integrating system components and evaluating process performance under relevant operating conditions. – Conducting comprehensive process analysis to establish a scalable CO₂-to-SAF platform. Requirements – PhD in Chemical Engineering, Chemistry, Materials Science, or a closely related discipline. – Hands-on experience with high-pressure reactor operation and catalyst synthesis. – Proven experience in process development and optimization for gas-phase reaction systems. – Familiarity with analytical techniques for gas and liquid product analysis. – Expertise in material characterization methods (e.g., XRD, surface area analysis, spectroscopy, microscopy). – Strong problem-solving skills and ability to optimize complex reaction processes. – Excellent verbal and written communication skills in English, with a demonstrated publication record. – Ability to work independently and as part of a multidisciplinary team. Application Procedure Interested candidates are invited to apply by 22 July 2025. Please submit your CV and a motivational letter via the application portal at: https://careers.tudelft.nl/job/Delft-Postdoc-in-Heterogeneous-Catalysis-and-High-Pressure-Instrumentation-for-CO%E2%82%82-to-SAF-2628-CD/823591702/ Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee!

JOB TITLE : Laboratory Analyst DEPARTMENT: CPS QSE Function BASE LOCATION: CPS Plant (Sanand) Job Summary Key roles and responsibilities of this position Provides analytical support to operating unit w.r.t.chemical analysis & Microbiology analysis using internal/external valid & official test methods and international literatures. Provides analytical support to operating unit which mainly includes working in chemical lab as well as in waste water treatment plant (ETP/STP) for water analysis Ensures all the analytical testing programs are executed in accordance with Company and ISO/IEC 17025 requirements. Effective implementation of quality control procedures to ensure products and manufacturing processes are in compliance with Company policies, procedures, practices and standards. Key Duties/Responsibilities Quality Execution- 60% Test and analyse ingredients, intermediates and finished products to ensure compliance with the Company specifications. Perform organoleptic tests & Sensory evaluations of Ingredients and Finshed product beverage bases. Analysis of Ingredients and Finished products using a range of modern techniques like high performance liquid chromatography and spectroscopy. Raw water/process water, Waste water (ETP/STP) sampling and analysis of consent parameters on daily basis. Managing chemical inventory, instrument calibration and analytical data for audit purpose. Also analyse waste water data to indicate improvement opportunities. Responsible to making sure that data is accurately recorded and reported in accordance to company guidelines. Conduct capability a study for testing equipment’s & laboratory processes in accordance with Company as well as ISO/IEC 17025 requirements. Ensure Calibration & preventive maintenance of laboratory instruments is carried out as per schedule and complies with the requirements of ISO/IEC 17025. Participation in internal/external proficiency testing programs in accordance with ISO17025. Identify, classify, and maintain documentation and sensitive information consistent with record handling and retention requirements. Conduct Periodic review of laboratory equipment’s, lab processes to ensure operational fitness in accordance with Company and ISO/IEC requirements. Prepare sampling and testing plan for ingredients, intermediate, finished products, or other materials in order to perform analyses (e.g., chemical, physical, sensory). Genrate data, perform data evaluation and trend analysis to support and risk assessments. Play active role in Laboratory global Network teams and deliver the objectives. Provide support to other parts of the laboratory as require. Management system knowledge of ISO 14001 & ISO 9001 , ISO 17025. Quality Assurance - 40% Ensure products are manufactured as per Company guidelines. Compliance of manufacturing processes with the Company’s quality and food safety requirements. Maintaining ETP/STP/WTP records, conducting trend analysis, graphical representation of results, and communicating the necessary data and record retention in accordance with Company policy and Legal requirements (MPCB Consent). Ensure compliance to quality, food safety and Environmental, safety & Loss Prevention program requirements when conducting analytical/microbiology work and discarding materials (reagents, samples, etc.) to minimize any risks identified. Maintaining appropriate records, communicating the necessary data and record retention in accordance with Company policy and requirements of ISO 9001, ISO/IEC 17025, ISO 22000 and PAS 220. Implement GLP requirements and Laboratory Safety programs. Implement formal corrective actions to avoid issues recurrence. Participate in root cause analysis sessions to solve non-conformances. Perform data audits in order to ensure accuracy of data and analytical processes which may include database queries, statistical process control, correlation studies, notebook review, and/or traceability exercises Participate in the laboratory quality system activities such as internal audits, writing standard operating procedures, and documentation review Record data from analyses or experiments in a computer, log book, or laboratory notebook Organization Impact/Influence This position works with Laboratory Manager and QA Manager and provides support for testing and release of ingredients and finished products and to comply the Laboratory operation requirements as per TCCC and ISO/IEC 17025 Accreditation requirements. The job scope will also involve the interactions with internal and external stake holders as below. Internal Interactions Leadership team, all QA ,Manufacturing and warehouse staff to communicate the decisions related to Quality matters, Material disposition and reporting. Process control and manufacturing team on initiatives to create and achieve Zero defect product quality mind-set. Involve with Laboratory and Quality team to conduct Analytical test method validation and implementation of quality control test procedures. Warehouse and logistics team on incoming ingredient and packaging material identification and disposition activities External Interactions Global CPS Lab community for Laboratory initiatives, receive analytical testing support, problem solving , sharing and implementing of best practises as per company requirements. IQD/APTC/EASC and third party laboratories to coordinate for testing and release. Supplier and vendors: Calibration & Maintenance and Third party service support. Supervisory Responsibilities Coordinate with admin and plant associates to monitor and implement GLP and GMP activities. Coordinate and Supervise Visitor /contractor activities related activities to ensure compliance as per Company requirement. Related Job Requirements/Qualifications Minimum 3-4 years in Quality control /Laboratory in Food / health care or Pharma company as Analyst or similar positions. Good Knowledge of qualitative and quantitative chemical analysis, environment analysis. Knowledge of using advanced analytical instruments, trouble shooting and data interpretation. Through knowledge of Microbiology testing of Treated water, raw water, Commercial sterility of Finished products & Testing of pulp and fruit Juices. Must be proficient and capable to handle and lead problem solving of issues related to microbiological contaminations and testing. Knowledge chemistry to understand composition, structure and properties of ingredients and finished products. Exposure on principles and techniques of basic food science and their application to the beverage industry. Should have experience in analytical processes using instruments such as GC, LC, IC, AA, FTNIR, Particle size analysis, PCR & Rapid microbiology. Should be familiar with accreditation and certification programs such as ISO17025, 9001, FSSC 22000. Good Knowledge of laboratory information management system, SAP functionalities including quality module. Conduct review of scientific or other literature and able to apply develop and implement new analytical test methods. Systematic thinking and problem solving ability. Educational/Skill Requirements M. Sc. Chemistry / Biochemistry/ Analytical Chemistry deg.in food science or equivalent. Language: Good written and oral communication skills in English. Good IT and presentation skills- Microsoft Excel, Power point and Word, Power BI. Experience of LIMS and SAP and system database. Cultural Diversity Able to interact in English and local language internally and externally. No ethnic or cultural differences faced in this job Judgment And Decision Making Key decision maker in determining whether actions are necessary to address quality issues identified as part of analytical monitoring program. Working Conditions Laboratory environment. Use of chemicals and standards under good laboratory practices, Microbiology testing as per microbiology standard requirement & GLP norms. Highly unlikely, it is possible that, this position is subject to hazards and risks associated with normal chemical testing laboratory such as noise, heat stress and hazardous chemical / ingredient exposure conditions. Travel Requirements This position will be primarily based in Gujrat, India with minimum travelling (maximum 5% of work time under normal conditions). Trips include occasional visits or training at other concentrate plants, bottling operations and training centers. Skills Data Compilation; Testing Methods (Inactive); Quality Control (QC); Communication; Recordkeeping; Data Entry; Laboratory Testing; Researching Annual Incentive Reference Value Percentage:8 Annual Incentive reference value is a market-based competitive value for your role. It falls in the middle of the range for your role, indicating performance at target.

Job Title: Laboratory Chemist- Special Process Job Description: The Laboratory Chemist will be responsible for conducting chemical analyses and tests to ensure the quality and compliance of surface treatment processes used in aerospace applications. The role involves developing, optimizing, and monitoring chemical processes and materials to enhance performance and safety. The chemist will work closely with engineering and production teams to troubleshoot issues and improve methodology. Responsibilities include preparing lab samples, performing experiments, documenting results, and ensuring adherence to industry regulations and standards. Additionally, the Laboratory Chemist will be tasked with maintaining laboratory equipment, managing inventory of chemicals, and training junior staff. Key Responsibilities: - Conduct chemical analyses and experiments to develop and optimize surface treatment processes. - Analyze and interpret results, preparing comprehensive reports and documentation. - Collaborate with production and engineering teams to resolve technical issues and improve product quality. - Ensure compliance with safety regulations and environmental standards in laboratory practices. - Maintain laboratory equipment and chemical inventories, ensuring proper storage and handling of hazardous materials. - Perform routine and non-routine testing, and develop standard operating procedures (SOPs) for laboratory operations. - Train and mentor junior lab staff on best practices and safety protocols. Skills and Tools Required: - Bachelors or Masters degree in Chemistry, Chemical Engineering, or a related field. - Strong understanding of Laboratory testings, Periodic testings, chemical analysis techniques, including spectroscopy and titration. - Experience with surface treatment processes such as anodizing, plating, and Paint coatings is preferred. - Familiarity with standards in the aerospace industry, such as ASTM,AMS, ISO,NADCAP and Major Primes. - Proficiency in using laboratory software for data analysis and reporting. - Strong attention to detail and critical thinking skills for problem-solving. - Excellent communication and teamwork abilities to collaborate effectively with cross-functional teams. - Adept at multitasking and managing time efficiently in a high-paced environment. - Knowledge of safety protocols and hazard management in a laboratory setting.

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-28-06-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 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.

Job Title: Service Engineer Department: Customer Support Location: Delhi About Inkarp Instruments Services Inkarp Instruments is a trusted name in delivering high-quality laboratory, analytical, scientific, and research instrumentation across various sectors including healthcare, pharmaceuticals, academia, and industrial R&D. With a focus on excellence in service and technical support, we aim to empower scientific progress through precision and reliability. Job Summary We are seeking a motivated and skilled Service Engineer to join our Technical Services team. The role involves installation, calibration, maintenance, troubleshooting, and repair of a wide range of laboratory, analytical, and scientific instruments. The position also includes execution and management of Annual Maintenance Contracts (AMC), ensuring high standards of service and customer satisfaction. Key Responsibilities  Installation & Commissioning: Set up and install scientific instruments at customer sites, ensuring full operational readiness.  Preventive & Corrective Maintenance: Perform scheduled maintenance and attend breakdown calls for instruments under warranty or AMC.  Troubleshooting & Repairs: Diagnose and resolve technical issues efficiently, both remotely and on-site.  AMC Execution: o Carry out service activities for instruments under AMC contracts, including scheduled visits, preventive checks, and emergency support. o Maintain and update AMC service logs, renewal status, and customer communication. o Coordinate with the service coordinator/manager to ensure timely and complete AMC delivery.  Calibration & Validation: Conduct calibration and support IQ/OQ/PQ documentation as per industry and regulatory requirements.  Customer Support: Provide technical assistance and training to end-users for optimal instrument operation and longevity.  Documentation: Maintain accurate and timely service reports, AMC logs, and instrument history records.  Sales Support (Optional): Identify opportunities for AMC renewals, spares, and upgrades during service visits and communicate with the sales team.  Compliance: Ensure all service activities are carried out in line with safety, quality, and regulatory standards. Required Qualifications & Skills  Education: Diploma / B.E. / B.Tech in Electronics, Instrumentation, Biomedical Engineering, or related field.  Experience: 1–5 years in servicing laboratory or scientific instruments, including AMC execution.  Technical Skills: Strong technical troubleshooting, hands-on maintenance, and documentation skills; knowledge of electrical, mechanical, and software systems related to lab instruments.  Soft Skills: Good communication, interpersonal skills, customer focus, and ability to work independently.  Travel: Willingness to travel extensively to customer sites as needed. Preferred Qualifications  Familiarity with AMC management practices and reporting.  Experience with instruments from global OEMs in spectroscopy, chromatography, microscopy, etc.  Understanding of service CRM systems and ERP tools.  Knowledge of quality standards like ISO, GLP, GMP, NABL. What We Offer  Competitive compensation and travel allowances.  Opportunities for professional growth and training.  Exposure to advanced lab and analytical technologies.  Supportive work environment with a focus on service excellence.

University: Istituto Italiano di Tecnologia (IIT) and Politecnico di Milano Country: Italy Deadline: 2025-09-10 Fields: Physics, Materials Science, Electrical Engineering, Nanotechnology, Optical Engineering The Istituto Italiano di Tecnologia (IIT) and Politecnico di Milano invite applications for Postdoctoral and PhD positions in the field of Nano-Optics. These positions are part of an internationally recognized research group led by Professor Antonio Ambrosio, focusing on advanced topics such as structured light, 2D materials, metasurfaces, and light–matter interactions at the nanoscale. Available Positions Postdoctoral Position – Research focus: Nano-Optics Innovation through Metasurfaces and Light Structuring – Responsibilities: Design and fabrication of metasurfaces, investigation of ultrafast optical control, and study of polaritonic responses in van der Waals materials – Location: IIT – CNST, Milan – Application deadline: 2025-09-10 – Application link: https://lnkd.in/dqQhSGxC PhD Position #1 – Research focus: Tailoring Light–Matter Interactions via Structured Light – Responsibilities: Study of complex optical beams and their interaction with anisotropic and 2D materials, unveiling novel photonic phenomena – Required skills: Optical setup design, metasurface fabrication, FDTD simulations – Location: Politecnico di Milano – PhD in Physics – Application link: https://lnkd.in/dA–_WZJ PhD Position #2 – Research focus: Light–Matter Interaction at the Nanoscale in 2D Materials – Responsibilities: Engineering and imaging of polaritons in van der Waals materials using advanced nano-imaging and nano-spectroscopy techniques – Required skills: 2D materials synthesis, nano-optics, numerical modeling – Location: Politecnico di Milano – PhD in Physics – Application link: https://lnkd.in/dA–_WZJ Requirements – A strong academic background in physics, materials science, electrical engineering, nanotechnology, or a related field – Relevant laboratory and/or computational skills as described per position – Motivation and ability to work in an interdisciplinary, international environment Additional Information – International applicants are encouraged to apply – Support is available for relocation and research stays abroad – These positions were advertised by Professor Antonio Ambrosio on LinkedIn For further details and to submit your application, please refer to the respective links above. Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register

Job Description Roles and Responsibilities: Lab Business set up as per testing requests, tender & contracts with customers, Marketing as per Testing facility available in lab, Man power adjustment, Authorisation of SOP, Method Development & Method Validation, Standard Regulation comply with as per norms, Training program arrangement-Plan & impart Technical & Quality related Training to the staffs, evaluate & maintain, Authorisation of Test Reports, Take action for the purchase of consumables, spares of Instruments, chemicals, CRMs, Standards etc., Monitoring & supervising overall activity of the designed lab Experience/ Knowledge Have proper knowledge of water/ waste water/ Textile & Dye/ Chemicals analysis for wet lab Parameters, Spectroscopy parameters, heavy Metals & alloys analysis/ Chromatography testing. Have skills for method development, verification & validation. Have management skills for lab development. Have proper complete knowledge for analytical Instrument like; GC/GC-MS/HPLC/LC-MS/ICP/UVVIS etc. handling/ Calibration/ trouble shooting. Have proper documentation knowledge for Quality standard document

Company Description BacAlt is dedicated to converting post-harvest waste into value-added biopolymers applicable in various industries such as textile, skincare, wound care, and agriculture. Our innovative approach addresses sustainability by transforming waste into useful products. Located in Bengaluru, BacAlt strives to contribute to a more sustainable future by leveraging cutting-edge technology and research. Job Title : Analytical Scientist C Department : R&D Department Reporting to : Head of Polymer Science Location : Bangalore Qualification : Master's degree in Analytical Chemistry with 3-4 years of industrial experience. Experience in Pharmaceutical industry desirable. Job Type : Full-Time Salary Range. : 4.8 - 7.2 LPA Key Responsibilities · Develop and validate analytical methods for various instruments, including: HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, Particle Size Analyser, Dynamic light scattering, Kinematic & Dynamic Viscosity Measurement, Dissolution and Disintegration Testing. · Responsible for wet analysis in lab such as LOD, Karl fisher, bloom testing, kinematic viscosity, moisture analyser, calibration of balance, titration method and plan out other testing methods as well after discussion with head of dept. · Plan out stability study of raw materials, intermediates as well as finished products with desired temperature and humidity conditions. · Conduct testing as per established protocols and procedures for formulations, Active Pharmaceutical Ingredients (APIs), and excipients. · Possess comprehensive knowledge of instrumental analysis, method development, sample preparation, and interpretation of results clearly and concisely. · Record and report experimental data, ensuring accuracy and compliance with standard operating procedures (SOPs) and Good Laboratory Practices (GLP). · Assist in laboratory and equipment maintenance adhering to GMP requirements. · To initiate an incident, deviation, change control, out of specification (OOS), out of trend (OOT), out of change (OOC) or corrective and preventive action (CAPA) in consultation with the department head. · Strong analytical and problem-solving abilities to address complex issues in analytical chemistry. · Adherence to safe laboratory practices and waste disposal protocols in line with company policies. Behavioural Attributes · Demonstrates personal commitment to the team and values individual differences to support shared goals. · Self-disciplined to drive assigned experiments and achieve desired results. · Aptitude to learn and grow, building a better understanding of analytical chemistry work, SOPs, protocols, and GLP processes. · Willingness to take on tasks beyond the listed responsibilities as per team requirements. . Ability to work effectively within a team, demonstrating flexibility and resourcefulness to meet targets with minimal supervision. Ensure all laboratory activities comply with BacAlt Biosciences internal policies and procedures.

Role - Peptide Characterization/Advance Characterization Using HRMS/LC-HRMS/LC/MS Level - Team Lead Position at Mid / Senior level role Key Responsibility: Handing LC-HRMS, Characterization of Peptides for Small molecules, API in Analytical R&D Job Profile:- Leading Characterization of peptides and small molecules with Liquid Chromatography and High-resolution mass spectrometry (LC-HRMS, LC-MS/MS) for structural elucidation, impurities profiling. Managing a team of Peptide / Protein characterization (HRMS) Method development and impurity profiling of Peptides/Proteins and Impurities characterization using HRMS. Spectroscopy (UV-Visible, Circular Dichroism, Spectrofluorometer), Capillary Electrophoresis, and analytical method development, method validation. Impurities profiling & characterization of peptides impurities, small molecules with LC-HRMS and tandem mass spectrometry . Knowledge of liquid chromatography, ionization, mass spectrometry fundamentals, general analytical chemistry is must for characterization of small and large molecules. Method development and method validation for characterization of peptides on spectroscopy (UV-Visible, CD, Fluorescence, etc) and capillary electrophoresis instruments. Qualifications PhD in Analytical chemistry or Analytical Method development with relevant experience. 9 - 20 years experience in High-resolution mass spectrometry (LC-HRMS, LC-MS/MS) etc. Strong Expertise in LC-HRMS method development is an imp criteria. Strong organizational, critical thinking and communications skills. Attention to detail and good judgement. Candidate with relevant exp can share profiles on rashmi.gupta@biocon.com Kindly mention below details while sharin g CV:- Current CTC? Have you handled LC-HRMS ? if yes, how much exp you have? Are you handling Advance Characterisation/ Peptide Characterisation ? Are you PhD or not? Notice Period? Ready to work in Bangalore (onsite) ? (5 Days working)

Role Description This is a full-time on-site role for a Postdoctoral Fellow (upto 3 years) in Cancer Biology or Solution NMR Spectroscopy based in Kharagpur. The Postdoctoral Fellow will be responsible for conducting research in their specialized area, collaborating with other researchers, writing papers, and presenting findings at conferences. Qualifications Strong background in Cancer Biology or Solution NMR Spectroscopy Experience in conducting research and writing scientific papers Ability to work collaboratively in a team Excellent analytical and problem-solving skills PhD in a relevant field (Cancer Biology, Biochemistry, Biophysics, etc.) Experience with lab techniques and equipment related to the field Strong communication and presentation skills

Position: Subject Matter Expert (Chemistry) Role Type: Solution Author Employment Type: Contract-Based Location: Remote Shift Timing: Early Morning Shift – 4:00 AM to 1:00 PM (IST) Note: Fresh graduates are welcome to apply. If you are currently employed full-time elsewhere, please do not apply. This role demands full dedication and consistent availability. Only apply if you are actively seeking new opportunities or pursuing higher education, and can commit to working 8 hours each day. Overview: Endeavor Academy, a reputed EdTech service provider, is hiring Chemistry Subject Matter Experts for early morning shifts. The SME will be responsible for authoring detailed, high-quality academic solutions, resolving student queries, and contributing to assessment content across various subfields of chemistry. Key Responsibilities: Solution Authoring Create clear, accurate, and step-by-step solutions to academic problems from topics such as: Physical Chemistry (Thermodynamics, Equilibrium, Kinetics, Electrochemistry) Organic Chemistry (Nomenclature, Mechanisms, Reactions, Functional Groups) Inorganic Chemistry (Periodic Table, Chemical Bonding, Coordination Compounds) Analytical Chemistry (Titrations, Spectroscopy, Chromatography) Ensure academic alignment with prescribed curricula and content standards. Doubt Resolution Respond to academic doubts and queries posted by students via the platform. Deliver concept-driven, easy-to-understand responses within expected timelines. Assessment Support Create and review assessment questions and solutions. Grade and provide feedback on student responses where required. Portal Interaction Utilize the designated platform for submission and progress tracking. Ensure quality, formatting, and timely submission of solutions. Content Accuracy Maintain high accuracy in all academic content. Revise or update existing content as per academic changes or feedback. Qualifications: Bachelor’s or Master’s degree in Chemistry or related fields. Strong command over core chemistry concepts across disciplines. Good written English communication skills. Prior experience in teaching, tutoring, or content creation is a plus. Key Skills & Attributes: High attention to detail and accuracy. Strong problem-solving and analytical skills. Time management and ability to meet tight deadlines. Passion for education and simplifying complex topics. Why Join Us? Competitive compensation based on content quality and volume. Remote working opportunity with a fixed early morning shift. Be part of a dynamic team making an impact in digital education. Continuous learning and professional development. Application Process: Interested candidates should submit their updated resume and any sample academic content (if available) to hr@endeavoracademy.co.in Shortlisted candidates may be required to complete a subject-specific test as part of the selection process.

Job Title: Laboratory Chemist- Special Process Job Description The Laboratory Chemist will be responsible for conducting chemical analyses and tests to ensure the quality and compliance of surface treatment processes used in aerospace applications. The role involves developing, optimizing, and monitoring chemical processes and materials to enhance performance and safety. The chemist will work closely with engineering and production teams to troubleshoot issues and improve methodology. Responsibilities include preparing lab samples, performing experiments, documenting results, and ensuring adherence to industry regulations and standards. Additionally, the Laboratory Chemist will be tasked with maintaining laboratory equipment, managing inventory of chemicals, and training junior staff. Key Responsibilities Conduct chemical analyses and experiments to develop and optimize surface treatment processes. Analyze and interpret results, preparing comprehensive reports and documentation. Collaborate with production and engineering teams to resolve technical issues and improve product quality. Ensure compliance with safety regulations and environmental standards in laboratory practices. Maintain laboratory equipment and chemical inventories, ensuring proper storage and handling of hazardous materials. Perform routine and non-routine testing, and develop standard operating procedures (SOPs) for laboratory operations. Train and mentor junior lab staff on best practices and safety protocols. Skills And Tools Required Bachelor's or Masters degree in Chemistry, Chemical Engineering, or a related field. Strong understanding of Laboratory testings, Periodic testings, chemical analysis techniques, including spectroscopy and titration. Experience with surface treatment processes such as anodizing, plating, and Paint coatings is preferred. Familiarity with standards in the aerospace industry, such as ASTM,AMS, ISO,NADCAP and Major Primes. Proficiency in using laboratory software for data analysis and reporting. Strong attention to detail and critical thinking skills for problem-solving. Excellent communication and teamwork abilities to collaborate effectively with cross-functional teams. Adept at multitasking and managing time efficiently in a high-paced environment. Knowledge of safety protocols and hazard management in a laboratory setting.

Analytical R&D Analyst I - TAPI Job Details | Teva Pharmaceuticals Find a Career With Purpose at Teva Search by Postal Code Area of Interest Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Analytical R&D Analyst I - TAPI Jun 18, 2025 Greater Noida, India, 201306 Who we are 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 R&D 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 years Already Working @TEVA? Teva s Equal Employment Opportunity Commitment

Morepen Proprietary Drug Research Pvt Ltd (MPDRPL) , a leading pharmaceutical research and development organization, is seeking a talented and motivated Medicinal Chemist to join our innovative team. With a commitment to excellence and the advancement of healthcare, we are dedicated to discovering and developing breakthrough therapeutic solutions that improve patient outcomes worldwide. Roles & Responsibilities : Design and synthesize novel small molecule compounds with potential therapeutic applications Conduct structure-activity relationship (SAR) studies to optimize lead compounds for potency, selectivity, and drug-like properties Perform multi-step organic synthesis of pharmaceutical intermediates and active pharmaceutical ingredients (APIs) Analyze and interpret analytical data (NMR, MS, HPLC) to confirm compound identity and purity Maintain detailed laboratory notebooks and prepare comprehensive reports on synthetic methods and compound characterization Stay current with scientific literature and emerging trends in medicinal chemistry and drug discovery Support patent applications and intellectual property documentation Ensure compliance with laboratory safety protocols and MPDRPL Environmental Health Safety (EHS) guidelines Knowledge & Experience : Master's degree (M.Sc.) or Bachelor's degree (B.Sc.) in Organic Chemistry, Medicinal Chemistry, or related field 1-4 years of hands-on experience in medicinal chemistry, pharmaceutical research, or related chemical synthesis roles Strong foundation in organic synthesis, reaction mechanisms, and synthetic methodology Experience with modern analytical techniques including NMR spectroscopy, mass spectrometry, and chromatography Knowledge of structure-activity relationships (SAR) and drug design principles Familiarity with chemical databases, literature searching, and computational chemistry tools Understanding of pharmaceutical development processes and regulatory requirements Excellent problem-solving skills and ability to work independently as well as in team environments Strong communication skills and ability to present scientific data effectively Preferred Qualifications: Experience with parallel synthesis and library design Knowledge of ADMET properties and their optimization Familiarity with fragment-based drug discovery approaches Experience with process chemistry and scale-up activities Publications in peer-reviewed journals or patent applications Why Join us: Opportunity to work on cutting-edge drug discovery projects with significant therapeutic potential Access to state-of-the-art laboratory facilities and advanced analytical instrumentation Collaborative research environment with opportunities for professional growth and skill development Competitive compensation package with performance-based incentives Comprehensive benefits including health insurance, retirement plans, and professional development support Mentorship opportunities with senior scientists and exposure to diverse therapeutic areas Contribution to meaningful research that directly impacts patient health and well-being Application Process: To apply, please submit your resume and a cover letter highlighting your relevant experience and research interests to jobs@morepenpdr.com We are an equal opportunity employer committed to fostering an inclusive and diverse workplace environment.

GeneTech- ATS GeneTech Private Limited is looking for Biochemist to join our dynamic team and embark on a rewarding career journey Research: Conduct laboratory experiments and studies to investigate biochemical processes, including metabolism, cellular signaling, and genetic expression Analysis: Analyze and interpret data from experiments, using various techniques such as spectroscopy, chromatography, and molecular biology methods Hypothesis Testing: Develop and test hypotheses to understand the molecular and chemical basis of biological phenomena Publication: Prepare and publish research findings in scientific journals, contributing to the advancement of knowledge in the field Teaching and Education: Educate and mentor students and junior researchers in biochemistry, often in an academic or research institution Collaboration: Collaborate with other scientists, researchers, and interdisciplinary teams to address complex biological questions Instrumentation: Use and maintain laboratory equipment and instruments to carry out experiments effectively

The Process Development Scientist-I 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 member of a team The candidate will work within an interdisciplinary and cross-divisional team in the Crop Protection Innovation organization, 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

Our purpose at Avient Corporation is to be an innovator of materials solutions that help our customers succeed, while enabling a sustainable world. Innovation goes far beyond materials science; it s powered by the passion, creativity, and diverse expertise of 9,000 professionals worldwide. Whether you re a finance wizard, a tech enthusiast, an operational powerhouse, an HR changemaker, or a trailblazer in materials development, you ll find your place at Avient. Join our global team and help shape the future with sustainable solutions that transform possibilities into realities. Your unique perspective could be the key to our next breakthrough! Job Summary We are seeking an experienced R&D Engineer/Chemist from a polymer & colour sciences background interested in advancing their career within Avient s Corporate Technology Group. The R&D scientist is responsible for identifying and innovating new technologies for color matching techniques, devices, and color rendering. In addition, the scientist must possess a good understanding of pigment/dye chemistries and their suitability for applications with engineering polymers. Successful candidates will be creative and impactful within a team environment. Essential Functions Conduct work in a safe, respectful and ethical manner Drive innovation that enriches Avient s intellectual property portfolio Take responsibility for colour and spectroscopy expertise as a core member of colour system digitization project Evaluate, connect, correlate, and maintain data in current colour system and digital platform Refine, aggregate, and organize current colorant database Interact with data scientists, data analysts and IT to drive development of colour matching interface Conduct test on new equipment for implementation of digital platform Write work instruction and organize training for colour, device, digital platform, interfaces, etc. Coach and train commercial and technical teams to use device & digital platform, and trouble shoot Work with cross business unit and collaborate with colour specialists within Avient Other duties as based on need at time #LI-GM1 Education and Experience MSc (PhD Preferred) in Colour Science, Organic Chemistry, or Polymer Science Possess significant experience in color matching for plastics resins and in management of colorant database Good understanding of masterbatch production process, including mixing, extrusion and palletization. Strong knowledge of regulatory requirements for plastics resins by applications and industries Strong skills in the scientific method and use of design of experiments for data-driven research Experience analytical characterization techniques for rheological, mechanical and, thermal properties of polymers Experience with quality control methods, part & product approval processes and engagement with OEMs & customers is desirable. Additional Qualifications Use of statistical software (StatEase, Minitab, SigmaPro or similar) for executing DOEs Strong competencies in using Microsoft Word for documentation and report writing Strong competencies in use of Microsoft Excel, PowerPoint and Project Greenbelt (or higher) in Six Sigma DMAIC or Lean Six Sigma for continuous improvement We believe that all of our global employees are leaders and that the six most important behaviors for driving our strategy and culture are the same no matter if an employee is a leader of self, a leader of others, or a leader of the business.By playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient s strategic goals, to meet our customer needs, and to accomplish your career goals. At Avient, we believe a wide variety of thoughts, ideas and backgrounds gives us the creativity to be successful in a rapidly changing world. In support of this, we stress equality of opportunity for all qualified individuals in accordance with applicable laws. Decisions on hiring, promotion, development, compensation or advancement are based solely on a person s qualifications, abilities, experience and performance. Avient is an equal opportunity employer. We maintain a policy of non-discrimination in providing equal employment to all qualified employees and candidates regardless of race, sex, sexual orientation, gender identity, age, color, religion, national origin, disability, genetic information, protected veteran s status, or other legally protected classification in accordance with applicable federal, state and local law. If you need an accommodation because of a disability to complete an online application, please contact the Avient.

Conduct chemical analysis of plant materials to identify active compounds and assess their properties. Research and develop new plant-derived chemicals. Use advanced analytical techniques (e.g., chromatography, spectroscopy, and mass spectrometry) to separate, identify, and quantify chemical components of plant samples. Conduct experiments to synthesize plant-based chemicals and assess their effectiveness in various applications. Ensure compliance with regulatory standards in product development and testing. Collaborate with other scientists, researchers, and engineers to optimize the extraction and formulation of plant-derived chemicals. Prepare detailed reports and presentations on research findings and experimental results. Maintain accurate lab records, including data, protocols, and experimental results. Job Type: Full-time Pay: ₹22,000.00 - ₹35,338.77 per month Benefits: Health insurance Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Apply now » Analytical R&D Analyst I - TAPI Date: Jun 18, 2025 Location: Greater Noida, India, 201306 Company: Teva Pharmaceuticals Job Id: 62433 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's 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 R&D 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 years Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Job Role : Analytical Chemistry-Analyst (NPD) Department : Analytical - BGRC Job Location : Bangalore About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to 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: This role involves method development, method validation, method transfer and R&D stability studies by using laboratory instruments like Ultra performance liquid chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, Particulate matter analysis using Malvern, PAMAS, HIAC and other relevant instrumentation techniques. etc. Role Accountabilities: Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Must have experience in handling HPLC, UPLC (Empower-3 software), GC, UV Visible spectrophotometer balances, Potentiometer, and stability chambers, Particulate matter analysis techniques. Shall have experience on Good documentation/laboratory practices such as ALCOA+. Experience in calibration and qualification of various analytical instruments HPLC, UPLC, GC, and other QC laboratory instruments Shall prepare and review the raw data sheets, instrument operating procedures, and standard operating procedures Shall have good experience in handling of QMS (such as incidents, Out of Specifications, Deviations, and Change control). Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards / Chemicals / Reagents / Consumables / Spares etc., required for the projects Shall adhere to the procedure of GxP/Safety and as per the procedure defined in the internal standard operation procedure Shall operate the MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Must possess good communication and e-mail etiquettes. Behavioural Skills Good Interpersonal skills Self-time management Good team player Good communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 1-6 years Skills and Capabilities: Hands-on HPLC, UPLC/UHPLC, CG, UV-visible spectrophotometer, Potentiometer, Particulate matter analysis techniques and QC other analytical instruments Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+. Able to follow work instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Good knowledge of MS-office (word, excel, ppt) Education M. Pharm/ M. Tech/ M.Sc. / B.Tech., B.Sc. (Analytical chemistry/Chemistry) Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's 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 R&D 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 years Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

We are looking for a meticulous and detail-oriented Trainee/Chemist to contribute to our quality control and assurance processes at Synnat Pharma Private Limited, a leading API manufacturer. This role is crucial in ensuring that our raw materials, in-process materials, and finished products meet stringent quality standards. The ideal candidate will possess a foundational understanding of Good Laboratory Practices (GLP) and GMP guidelines, applying these principles to meticulously execute sampling procedures and conduct thorough data analysis. As a Trainee/Chemist, you will collaborate with cross-functional teams, contributing to the maintenance of laboratory standards and adherence to compliance requirements. Your contributions will be instrumental in upholding the integrity of our manufacturing processes and ensuring the delivery of high-quality pharmaceutical products. This is an excellent opportunity for a motivated individual to gain hands-on experience in the pharmaceutical industry and develop a strong foundation in quality control and assurance. Job Details: Industry: Active Pharmaceutical Ingredient (API) Manufacturer Department: Quality Control / Quality Assurance Role: Trainee / Chemist Location: Visakhapatnam Compensation: 1.5 – 2.0 LPA Experience: 0 – 1 year Qualification: Bachelor's or Master's degree in Chemistry, Pharmacy, or a related field Responsibilities: Raw Material Sampling and Analysis Perform sampling of raw materials as per defined procedures, ensuring representative collection. Conduct visual inspections to detect contamination or degradation. Prepare samples using wet chemistry and instrumental techniques. Accurately record sampling activities in laboratory notebooks/e-systems. Compare results to pre-defined specifications and escalate deviations. Maintain hygiene and safety standards in the sampling area. In-Process and Finished Product Sampling Collect in-process material samples during manufacturing as per sampling plans. Conduct routine testing to monitor key process parameters. Sample finished API products before QC release. Document sampling with detailed reports (sample ID, date, process stage). Collaborate with production and QA to address discrepancies. Ensure all activities align with GMP and regulatory norms. Laboratory Operations and Compliance Follow GLP principles to ensure traceability and data integrity. Maintain detailed records for analyses, calibrations, and maintenance. Prepare and standardize reagents as per lab SOPs. Assist during audits and promptly address observations. Adhere to lab safety protocols and use PPE consistently. Support method development and validation activities. Data Analysis and Reporting Analyze data from techniques like chromatography, spectroscopy, and titrimetry. Interpret results, identify trends, and flag potential issues. Prepare summary reports including tables, graphs, and conclusions. Review and verify analytical data for accuracy. Share test results with QA, Production, and Regulatory teams. Maintain secure and accessible databases for analytical data. General Expectations and Past Experiences: Possess a Bachelor's or Master’s degree in Chemistry, Pharmacy, or a related scientific field. Foundational understanding of GLP and GMP principles. Skilled in wet chemistry and basic analytical techniques. Strong analytical and observational skills to interpret data. Effective communication and ability to work in team environments. Proficient in MS Office (Excel, Word, PowerPoint) for reporting. Highly detail-oriented, quality-focused, and eager to learn. Show more Show less

Our purpose at Avient Corporation is to be an innovator of materials solutions that help our customers succeed, while enabling a sustainable world. Innovation goes far beyond materials science; it’s powered by the passion, creativity, and diverse expertise of 9,000 professionals worldwide. Whether you’re a finance wizard, a tech enthusiast, an operational powerhouse, an HR changemaker, or a trailblazer in materials development, you’ll find your place at Avient. Join our global team and help shape the future with sustainable solutions that transform possibilities into realities. Your unique perspective could be the key to our next breakthrough! Job Summary We are seeking an experienced R&D Engineer/Chemist from a polymer & colour sciences background interested in advancing their career within Avient’s Corporate Technology Group. The R&D scientist is responsible for identifying and innovating new technologies for color matching techniques, devices, and color rendering. In addition, the scientist must possess a good understanding of pigment/dye chemistries and their suitability for applications with engineering polymers. Successful candidates will be creative and impactful within a team environment. Essential Functions Conduct work in a safe, respectful and ethical manner Drive innovation that enriches Avient’s intellectual property portfolio Take responsibility for colour and spectroscopy expertise as a core member of colour system digitization project Evaluate, connect, correlate, and maintain data in current colour system and digital platform Refine, aggregate, and organize current colorant database Interact with data scientists, data analysts and IT to drive development of colour matching interface Conduct test on new equipment for implementation of digital platform Write work instruction and organize training for colour, device, digital platform, interfaces, etc. Coach and train commercial and technical teams to use device & digital platform, and trouble shoot Work with cross business unit and collaborate with colour specialists within Avient Other duties as based on need at time Education And Experience MSc (PhD Preferred) in Colour Science, Organic Chemistry, or Polymer Science Possess significant experience in color matching for plastics resins and in management of colorant database Good understanding of masterbatch production process, including mixing, extrusion and palletization. Strong knowledge of regulatory requirements for plastics resins by applications and industries Strong skills in the scientific method and use of design of experiments for data-driven research Experience analytical characterization techniques for rheological, mechanical and, thermal properties of polymers Experience with quality control methods, part & product approval processes and engagement with OEMs & customers is desirable. Additional Qualifications Use of statistical software (StatEase, Minitab, SigmaPro or similar) for executing DOEs Strong competencies in using Microsoft Word for documentation and report writing Strong competencies in use of Microsoft Excel, PowerPoint and Project Greenbelt (or higher) in Six Sigma DMAIC or Lean Six Sigma for continuous improvement We believe that all of our global employees are leaders and that the six most important behaviors for driving our strategy and culture are the same no matter if an employee is a leader of self, a leader of others, or a leader of the business.By playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient’s strategic goals, to meet our customer needs, and to accomplish your career goals. At Avient, we believe a wide variety of thoughts, ideas and backgrounds gives us the creativity to be successful in a rapidly changing world. In support of this, we stress equality of opportunity for all qualified individuals in accordance with applicable laws. Decisions on hiring, promotion, development, compensation or advancement are based solely on a person’s qualifications, abilities, experience and performance. Avient is an equal opportunity employer. We maintain a policy of non-discrimination in providing equal employment to all qualified employees and candidates regardless of race, sex, sexual orientation, gender identity, age, color, religion, national origin, disability, genetic information, protected veteran’s status, or other legally protected classification in accordance with applicable federal, state and local law. If you need an accommodation because of a disability to complete an online application, please contact the Avient. Show more Show less

This Job is based in Australia One of Australia’s leading research & teaching universities Vibrant campus life with a strong sense of community & inclusion Enjoy a career that makes a difference by collaborating & learning from the best At UNSW, we pride ourselves on being a workplace where the best people come to do their best work. The School of Materials Science and Engineering is one of the top ranked Materials programs in the Asia- Pacific regions and strongly positioned in every facet of materials science and engineering. It offers undergraduate programs in Materials Science and Engineering (Honours), as well as a number of combined degree programs with Chemical Engineering, Biomedical Engineering and Commerce. The Postdoctoral Fellow is expected to contribute towards the research effort of UNSW and the School of Materials Science and Engineering and to develop their research expertise through the pursuit of defined projects relevant to their particular field of research. This position will carry out research in an industry sponsored project over four years, requiring skills in high-temperature materials, process metallurgy, materials selection, and materials characterisation. This project will be conducted in collaboration with a key industry partner and other researchers and academics based at UNSW, Monash and Deakin. As part of the School’s academic staff, the Postdoctoral Fellow will also be expected to contribute to lab management and engagement and leadership in the institution. About The Role $110K - $117K plus 17% superannuation and annual leave loading Fixed Term – 4 years Full-time (35 hours per week) The role of Postdoctoral Fellow reports to Professor Sophie Primig and has no direct reports. The Postdoctoral Fellow will also work closely with Professor Jianqiang Zhang and Emeritus Professor David Young. Specific Responsibilities For This Role Include Develop understanding of Aluminium process metallurgy from bauxite, via alumina to Aluminium products. Develop new sustainable processing routes for bauxite and alumina in collaboration with our industry partner. Carry out experimental work on high temperature materials in our process and physical metallurgy labs (e.g., isothermal and cyclic thermal treatments under steam or controlled gas atmospheres, scale growth kinetics, direct reduction, arc melting etc.). Prepare microscopy samples using various metallography techniques. Carry out advanced microscopy including state-of-the-art methods of scanning electron microscopy, X-ray diffraction and related. Carry out FactSage simulations to underpin experimental results. Address materials selection problems based on literature surveys and using the Ansys Granta materials selection software. Closely collaborate with industrial partners, researchers and academics at UNSW, Monash and Deakin. Prepare presentations and progress reports for our industrial partner. Prepare publications for submission to leading journals and conferences of the field. Liaise with the related School academic and technical staff on research progress, lab management and leadership. Other duties as assigned in consultation with the supervisor. Align with and actively demonstrate the Code of Conduct and Values. Cooperate with all health and safety policies and procedures of the university and take all reasonable care to ensure that your actions or omissions do not impact on the health and safety of yourself or others. About The Successful Applicant To be successful in this role you will have: A PhD in Materials Science and Engineering or a related discipline and/or relevant work experience. Strong track record of research in Process Metallurgy, with particular focus on high temperature materials, phase transformations, characterisation techniques, and basic computational skills. Experience in advanced characterisation techniques (scanning electron microscopy, X-ray diffraction). Knowledge of those techniques and willingness to gain skills in other related techniques (e.g., energy dispersive spectroscopy). Experience in hot corrosion testing. Demonstrated experience in computational tools such as FactSage. Experience or interests in applied research at the interface of science, engineering and technology. Excellent interpersonal skills and the ability to work in a team environment, with industrial partners and with academic collaborators. Excellent written and verbal communication skills. Demonstrated ability to present research findings as evidenced by presentations at conferences and other venues. Strong organisational skills including the ability to prioritise a range of tasks and meet deadlines. An understanding of and commitment to UNSW’s aims, objectives and values in action, together with relevant policies and guidelines. Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training. You should systematically address the selection criteria listed within the position description in your application. Please apply online - applications will not be accepted if sent to the contact listed. Contact : Sophie Primig E: s.primig@unsw.edu.au Applications close: July 2nd, 2025 Find Out More About Working At UNSW At Www.unsw.edu.au UNSW is committed to equity diversity and inclusion. Applications from women, people of culturally and linguistically diverse backgrounds, those living with disabilities, members of the LGBTIQ+ community; and people of Aboriginal and Torres Strait Islander descent, are encouraged. UNSW provides workplace adjustments for people with disability, and access to flexible work options for eligible staff. The University reserves the right not to proceed with any appointment. Show more Show less