434 Organic Chemistry Jobs - Page 11

Fresher/ Any Graduate Role & responsibilities :- 1. Production - Data analyst 2. Production -MIS 3. Production - Planning 4. Data analyst Experience - 0 t0 3 Years Preferred candidate profile - Any industry Perks and benefits - 3.25 to 3.75

Urgently Hiring Diploma chemical for production department job for pharma industry. Company: Pharma API Industry Designation: Production Trainee (3 shift Job) Salary : 15k - 20K ( depending on your interview performance ) location - Mysore (Nanjangud) **required only Male candidates** If interested kindly share your resume to 7780363938 or Jyotsna@avaniconsulting.com With the below details: 1. Name: 2. Highest Qualification: 3. Passing Year: 4. Percentage marks obtain: 5. If okay with the shift job: 6. If okay with the job location: 7. Current Location: 8. Contact number: 9. Email id:

Role & responsibilities: Core Purpose of the Role: Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner Role Accountabilities: Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipments Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. Ensure that the instrument / equipment is calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately Ensure that they know the MSDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality Preferred candidate profile

E-mail ID - Deepanshu.bhatt1@piind.com Mobile Number - 8696900583 Position Purpose The role holder will be responsible for contributing to the discovery, pre-development, CRAMS, CDMO, in agrochemistry, pharma, fine chemicals adding significant value to the business of PI. The role will carry out literature/patent search, FTO analysis and other KM services in accordance with the project timelines and objectives. The role holder will contribute to generating IP and ensuring its protection. Key Responsibilities Strategic Efficient contribution to the overall success of PI by driving innovation and team performance according to objectives and targets being set by the leadership team Generating and ensuring the security of intellectual property for R&D (filing of patent applications, building and defending the PI patent portfolio, ensuring novelty and patentability) Continuously build knowledge in the area of agro-chemistry, pharma, fine chemicals and KM specific expertise, through active learning, education, advanced trainings and seminars Operational Keep self and team updated on the state of the art in IP management and KM specific tools Carrying KM services like FTO analysis and opinion, novelty search, literature supply and others with appropriate documentation and distribution of results Support competitor intelligence activities Develop and foster positive relationships with other teams and support groups such as chemistry/biology to maximize knowledge sharing and cooperation Comply with all the safety requirements as per the requirement of the role Leading knowledge transfer through presentations, training materials, tips and best practices for collaboration, so as to continually improve the performance of the group People: Act as a committed ambassador of PI Brand Actively imbibing the values and philosophy of PI Industries Ltd. Ensure smooth working by maintaining high level of morale and working ethics

Candidate should be exeprinecd in process development in R&D in API synthesis Candidate with the exeprience of handelling Photo reactor will be prefered . Experience in Vitamin synthesis will be prefered

Division Department Sub Department 1 Job Purpose Develop, optimise and execute the process for APIs to ensure on time implementation within budget Key Accountabilities (1/6) Develop API process in lab by literature survey, API intermediate characterization to ensure the quality and on time implementation Carry out literature survey and route selection for assigned project Prepare and execute development strategy for the assigned project Maintain record book of experiments carried out in lab, results received from the ADL Optimize process parameters to achieve process robustness for ensuring successful completion of lab trial and lab confirmatory batches with optimised costs Support creation of new IP assets for the company by performing experiments related to innovations like new process and polymorphs Maintain and calibrate the instruments in lab as per calibration schedule Follow individual safety procedures while working in lab by following GLP Follow the green chemistry approach while conducting experiments Key Accountabilities (2/6) Prepare development report and MPG on the basis of development work (carried out in lab) in order to successfully transfer the technology in plant Prepare tech Transfer documents like MPG, pre requisite, solubility chart, development report in coordination with ROC based on process developed in lab Coordinate with manufacturing units for carrying out pilot, pre-validation and validation batches under the supervision of group leader Key Accountabilities (3/6) Conduct QbD study, carryover study, impurity (genotoxic) identification / synthesis / characterization to achieve regulatory compliance and minimize the deficiencies in the DMF filling Perform QBD studies by conducting QBD experiments in coordination with QBD team Conduct impurity profile and carryover studies, impurity (genotoxic) identification / synthesis / characterization. Key Accountabilities (4/6) Support procurement in identifying and finalising the vendors for key raw materials by performing vendor qualification to achieve on time implementation Carry out experiments required for vendor qualification on receipt of material Compare and derive trend data for shortlisting vendors by comparing materials received Key Accountabilities (5/6) Ensure compliance of checklist for stage gate and milestone meetings to complete the project within time Carry out the listed activities in the stagegate and milestone checklists within time Key Accountabilities (6/6) Major Challenges Delay in getting analytical results from ADL causes delay in the overall development of project 2. Re-conducting experiments in cases of incorrect quality raw material being received from procurement (due to rejections). Bring to the notice of group leader in such cases. 3. Rework as more experiments need to be performed due to changing requirements for product development. Key Interactions (1/2) Manufacturing, SCM and ADL for receiving samples and delivering results (frequently) QA and QC for quality related procedures (frequently) IP for inputs regarding literature (need basis) ROC for documentation support (frequently) Safety for safety information (frequently) Engineering for machine maintenance (need basis) Key Interactions (2/2) Vendors and suppliers for raw materials and instruments, equipment (need based) Dimensions (1/2) Process development for 4 projects (last year) Execution of process on plant for 1 project (last year) Dimensions (2/2) Key Decisions (1/2) Use of Specific reagents, solvents, reaction condition Key Decisions (2/2) Route selection for development (to GL) Specific vendor for raw materials, instruments and equipment (to SCM) Education Qualification Educational qualifications: M. Sc. Organic Chemistry Relevant Work Experience 3-5 yrs in process R&D

Role & responsibilities Perform lab experiments as per experiments planning in consultation with senior Write the lab note book properly at time of performing experiment Discuss the experiment observation with senior Wear proper PPE while handling chemicals and performing experiments Submit the sample to analytical as per experiment requirement and planning Collect the test report from analytical lab Maintain the project documents and file properly Maintain the lab chemicals as per hazards and compatibility data, study the MSDS sheet Maintain the raw materials, solvents stock and store it properly Maintain the lab glassware and stock Clean and maintain work place area

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compliance and safety requirements. Review of laboratory data, instrument logbook and reports wherever applicable. Initiation of departmental CCRs and tracking the progress to execute the proposed changes through QMS system. Preparation of TAP (Transfer of Analytical Procedures) protocol and Report for various sites. Procuring respective samples and Impurities accordingly. Planning and executing the assigned TAP projects to various sites. Preparation, maintenance and archival of regulatory submission documentation like SOP, protocols, reports for method development and validation. Job Responsibilities Prepares working plan for assigned projects and provides timeline to Deputy Manager. Develops stability indicative analytical methods for drug substance and finished product Responsible for all activities in Analytical Development, including cGLP, documentation and implementation of departmental quality systems. Responsible for protocol preparation, planning, execution, review and report preparation of various analytical method validation parameters. Ensures analytical methods validation is conducted according to approved validation protocol in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Responsible for method verifications and publishing of analytical methods Maintenance and archival of analytical method validation documents. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. Raising Change control for various analytical activities (Method SOP and department SOPs)by QMS trackwise To prepare General, Operation and Calibration Standard Operating Procedures. Responsible for initiation, execution and completion of technology transfer and collaborative validation activities of analytical methods to and / or from other departments of Apotex wherever applicable. Responsible for technology transfer and Transfer of analytical procedures activity to support the supervisor. Communicating the requirements for the Leaders and within the team members for effective cGLP procedures and departmental quality systems to achieve all outcomes. With guidance of scientists, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. To participate in the mandatory trainings to execute the day to day job responsibilities. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Practice and up-gradation of knowledge with respect to cGMP. Performs all work in accordance with all established regulatory and compliance and safety requirements. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Work as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education A graduate/post graduate in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, spectrophotometer and dissolution apparatus, wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge on preparation and review of various documents like SOPs, Formats, Protocols, Reports, analytical data, investigation and deviation reports. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities Should possess troubleshooting knowledge on Instruments and analysis. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 3-4 years experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Purpose Statement: Handle high pressure reactions at R&D lab operations, compile data and ensure adherence to safety and incorporate best laboratory housekeeping practices. - Responsible for the availability of raw materials, catalysts and instrument spares as per high pressure lab requirements. -To analyze quality results and discuss the experimentation plan and parameters with Research Incharge. - Understand the safety aspects of all reactions, chemicals and catalysts to be used in high pressure reactions. - Ensure the proper setup ( compatibility of autoclave, high pressure addition pumps, thermostats etc) as planned. - Carry out reaction process as per the provided plan, get the analysis done for raw materials, catalysts , in process reaction intermediates and product. - Record all observations and give suggestions for improvement. - Report any breakdown, abnormal functioning of instruments in high pressure lab. - Ensure proper housekeeping of the lab. - Maintain highest safety practices while working by using required PPEs (Personal protective equipment). - Maintain the log sheets of all the experiments regularly with critical observations and feed the data into Electronic Lab Notebook (ELN). - Ensure working in lab as per SOP's provided. - Maintain stock of all the chemicals, catalysts and instrument spares required as per 5'S' (sort, set-in-order, shine, standardize, sustain) - After reaction completion, decontaminate the autoclave/instruments properly. - To ensure proper and complete recovery/quenching of catalysts after reaction. - To ensure proper and safe storage of catalysts and maintain its record. - Segregate effluents as per the lab system. - To undergo trainings as per schedule. Experience 2-7 Years. Qualification M.Sc Organic Chemistry or equivalent. Certifications/Trainings Analytical & Waste Treatment, Process Safety training, Process Development training preferred

Role & responsibilities 1. Good knowledge of synthetic organic chemistry. 2. Performing literature searches for the molecules that reaction is being carried out and understanding of the chemistries Strong skills in designing, optimizing, and scaling up synthetic chemical processes. 3. Plan and conduct experiments for chemical synthesis, ensuring the process can be reproduced and scaled up efficiently. 4. Design scalable synthetic processes that avoid patent infringement, especially for API (Active Pharmaceutical Ingredients) development. 5. Improve processes to make them industrially feasible, reduce costs, and enhance efficiency for existing products. 6. Validate synthetic processes at both laboratory and production plant scales. 7. Plant support for trial & validation batches. And troubleshooting of plant concerns. 8. Literature survey through various scientific databases. 9. Interpretation of NMR (Nuclear Magnetic Resonance), IR (Infrared Spectroscopy), MS (Mass Spectrometry), XRPD(X-Ray Powder Diffraction)and chromatography data 10. Knowledge of scale-up processes, and familiarity with Good Manufacturing Practices (GMP) and ICH-guideline. 11. Hands-on experience with bench-scale and pilot-scale synthesis is essential. Skilled in preparing detailed reports, presentations and technical documents like SOPs, process development reports, costing sheets, and technology transfer documents. Preferred candidate profile M.Sc/ M. Pharm/ Ph.D in Pharmacy Interested Candidates can share their resumes on shikha.mishra@walterbushnell.com

Job title : Chemistry Scientist Job location : Bangalore Core Purpose of the Role: Personnel handling this profile will be responsible for conducting reactions and delivering final compounds within a fast turnaround time, meeting the specific requirements of both the project and Syngene. The candidate should be capable of independently designing the synthetic scheme for any target and solve chemistry problems. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene. Role Accountabilities: Expected to design a synthetic scheme for any given target and to be proactive in identifying rate limiting steps along with the mitigation strategy. The candidate should be well versed in using literature search engines and predictive synthesis tools Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipments Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. The candidate should be capable of meeting Syngenes productivity expectations (# of compounds/month, # of steps/month and productivity index of around 1.5) without compromising on safety and quality. The candidate should be capable of synthesizing the final compounds at a faster turnaround time. The candidate should have excellent analytical interpretation and purification skills. Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms. Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety. Attend all mandatory trainings and update training records as and when trainings are completed. Always ensure confidentiality. Specific requirements for this role Experience : 2.5-10 years Skills and Capabilities: Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms. Should be capable of designing synthetic schemes and troubleshooting synthesis problems independently. Should be excellent in purification and analytical interpretation skills. Familiar with operations of relevant apparatus - instrument / equipment. Education: M.Sc. in organic chemistry

Roles and Responsibilities Conduct process research and development activities to improve existing processes or develop new ones. Develop and implement reaction conditions for organic synthesis reactions to achieve desired product yields and purities.

Role & responsibilities ED Chemist Salary - 3.2 to 4.2 LPA

Oversee batch manufacturing & processing * Ensure chemical quality & safety standards met * Coordinate production schedules & resources allocation Log Sheet Verification: Regularly check and verify log Health insurance Annual bonus

Oversee batch manufacturing & processing * Ensure chemical quality & safety standards met * Coordinate production schedules & resources allocation Log Sheet Verification: Regularly check and verify log Health insurance Annual bonus

Assist in formulation and blending of cosmetic products Perform in-process and finished product quality checks Maintain lab and production records as per SOPs Ensure adherence to GMP and safety protocols Support production team in shift operation Required Candidate profile ONLY MALE candidates B.Sc./M.Sc. in Chemistry/related field 0–3 years of experience in a cosmetics/chemical manufacturing environment Willingness to work in rotational shifts Perks and benefits pf, meal, accomodation

Group Leader -HP API Lab Ph.D. in organic chemistry (post-doc is preferable) from reputed institutions in India/overseas Lead end-to-end synthesis and scale-up of HP APIs. Ensure containment and EHS compliance. Drive cross-functional collaboration for successful tech transfer and scale up

About Us:. Soul AI is a pioneering company founded by IIT Bombay and IIM Ahmedabad alumni, with a strong founding team from IITs, NITs, and BITS. We specialize in delivering high-quality human-curated data, AI-first scaled operations services, and more. Based in SF and Hyderabad, we are a young, fast-moving team on a mission to build AI for Good, driving innovation and positive societal impact.. We are looking for an experienced Chemistry SME to develop educational content for high school students. This is a remote, flexible opportunity where you can work on cutting-edge AI projects, applying your domain knowledge to refine AI’s understanding and performance.. Key Responsibilities. Annotate and evaluate AI-generated Chemistry content aligned with K12 curriculum standards.. Ensure accurate and accessible explanations of topics like organic chemistry, stoichiometry, and thermodynamics.. Design prompts and assess AI responses for clarity, depth, and educational value.. Provide feedback to enhance the AI’s scientific accuracy and teaching style.. Collaborate with AI teams to reflect best practices in K12 Chemistry education.. Required Qualifications:. PhD in Chemistry, Education, or a related field.. Strong knowledge of Chemistry.. Experience in content creation or teaching Chemistry is a plus.. Familiarity with online teaching tools and educational platforms.. Why join us?. Competitive pay.. Fully remote and flexible work schedule.. Opportunity to contribute to the advancement of AI technology.. Join us to play a vital role in shaping the future of AI through high-quality training and data solutions!. Show more Show less

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

Chemveda is hiring for Ph.D Chemistry Freshers for our Discovery Chemistry Team Qualification - Ph.D Chemistry (2024,2025 passed outs) Department - Discovery Synthesis Position Name - Senior Research Associate Work Location - Hyderabad Key Skills and Competencies: Experience in Organic Synthesis/Multi-step Synthesis Handling reactions from mg to KG scale. Sound Knowledge of isolation, separation & purification techniques. Experience in characterization and identification of Organic molecules using spectroscopy techniques like NMR, IR, LCMS, HPLC. Positive and confident individual with strong work ethics. Team player and good communication skills Interested candidates can share their profiles with ramasatish.uppuluri@chemvedals.com or Whatsapp - 9100490347

Role & responsibilities Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipments Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. Ensure that the instrument / equipment is calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately Ensure that they know the MSDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality

Job Summary We are seeking a seasoned professional to lead process development initiatives for new chemical entities and drive cost optimization for existing molecules. This role involves supervising a team of scientists, ensuring efficient execution of experiments, and delivering high-impact projects. The ideal candidate will possess deep expertise in organic chemistry and demonstrate proficiency in managing hazardous reactions safely. Job Responsibilities Leadprocess developmentfor new molecules and cost optimization of existing ones. Supervise and mentor a team of scientists, ensuring daily execution of experiments and effective project delivery. Allocate projects, provide technical guidance, and facilitate decision-making within the team. Apply deep knowledge oforganic chemistryand managehazardous reactionssafely. Coordinate with thepilot plantfor process demonstrations, scale-up, and validation. Collaborate with theBusiness Teamto communicate project progress, challenges, and solutions. Review and approve process outlines and technical documentation for commercialization. Investigate batch failures and implement corrective actions. Prepare and enforceSOPs, ensuring team compliance and training. MaintainGLP-compliant documentationand ensure lab safety and organization. Foster effectiveinter- and intra-departmental communication. Promote adigital and automation mindsetto enhance productivity The Person Qualifications: M.Sc./Ph.D. in Organic Chemistry or related discipline Proven leadership experience of 6-8 years in process development and team management. Strong expertise in hazardous chemical handling and safety protocols. Excellent communication, documentation, and project coordination skills. Experience in pilot plant operations and scale-up processes. Familiarity with digital tools and ERP systems for R&D efficiency

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.

ROLE SUMMARY Chemical Kinetic modeling, Understanding mass transport in biological systems. Complete understanding and hands on experiences on using different tools for convolution and deconvolution. Duration: 6 to 12 months ROLE RESPONSIBILITIES Collaborates with the research team to design, implement, validate or refine kinetic models. Performs modeling in support of and in collaboration with formulation and analytical development team. Participates in conduct of laboratory experiments where necessary to delineate reaction mechanisms. Selects and applies appropriate kinetic models to represent reaction systems. Uses appropriate software programs (MATLAB, Ansys ChemKin, Python or others as needed) to perform regression analysis and predictive simulations using kinetic models. QUALIFICATIONS BASIC QUALIFICATIONS M.Sc or Ph.D in physical chemistry, organic chemistry, Biophysics or chemical engineering PREFERRED QUALIFICATIONS Postdoc fellowship with experiences in anyone following area, Experience in studying the mechanism of degradation of small molecules or proteins in solution phase. Experience in kinetic modelling and deconvolution of reaction mechanisms Experience in studying mass transport phenomenon in chemical or biological systems. Ability to adopt reaction models to human biological systems OTHER INFORMATION Internship Expectations Good team player and interested apply skills in pharmaceutical development. Strong foundation in chemical kinetics, thermodynamics, and reaction mechanisms to organic chemicals or biomolecules Strong background in calculus & programming tools Internship Outcomes Develop solutions to commonly faced challenges in pharmaceutical product development. Understand application of predictive methods and data mining/machine learning tools in pharmaceutical systems Work Location Assignment: Hybrid Support Services #LI-PFE

The Store Keeper is responsible for maintaining accurate inventory records, overseeing the receipt and storage of goods, and ensuring that materials are available when needed Receive and inspect incoming goods and ensure that they conform to the purchase order or other specifications Maintain accurate inventory records, including tracking stock levels, documenting stock movements, and conducting regular physical inventory counts Maintain a clean and organized warehouse or storeroom, ensuring that all materials are stored in a safe and accessible manner