74 Crystallization Jobs

Handling of different unit operations like Batch charging, Solvent receiving & Charging, Layer separation, Work up, Distillation & Sparkler filtration, Transfer the reaction mass, Crystallization, Centrifugation, drying, milling, sieving and packing etc. Follow the Instructions as per BMR. Timely completion of Batch as per the Schedule given by department Head / Designee. Raw material cross verification before charging the Batch. To Co-ordinate with QC during batch execution and equipment cleaning to get the analytical report / results. Ensure the cleaning, sanitization as per procedure and recording in document. Follow up of Safety and cGMP during the production. Follow the SOPs during manufacturing process. Good documentation practice & Online entry in BMR and ECR. Updation of usage log, Weighing balance log. Personal hygiene. Prior intimation to Engineering department and QC department for good support. Before handling any raw materials or solvents SDS of respective raw materials should know. Co-ordinate with other production employees for smooth operations. Ensure Data Integrity & Training. Any other work allotted by Head Production / Designee. Desired Candidate Profile 2 -7 years of experience in the chemical manufacturing industry with expertise in Production Planning, Shift Planning, Manpower Handling, Daily Production Planning, Handling, Monitoring & Cross Functional Coordination, Bachelor's degree in Chemistry (B.Sc) or Chemical Engineering (B.Tech/B.E.). Strong understanding of chemical processing techniques and quality control measures Job Types: Full-time, Permanent Pay: ₹350,000.00 - ₹700,000.00 per year Benefits: Food provided Health insurance Leave encashment Provident Fund Application Question(s): What is your Current CTC? Education: Bachelor's (Required) Location: Harohalli, Karnataka (Required) Work Location: In person Application Deadline: 10/08/2025 Expected Start Date: 18/08/2025

The personnel handling this profile will be responsible for performing reactions as per the project requirements. You will document observations in relevant notebooks, follow instructions from the supervisor, and work in a group or individually to accomplish tasks efficiently. Your responsibilities will include performing synthetic chemistry reactions, conducting reaction workups, purifying compounds using column chromatography, crystallization, and re-crystallization techniques. You will operate lab equipment and ensure samples are given for analysis, recording results and updating the supervisor/group leader on synthesis progress. It is vital to record experiment/reaction observations, results, resource utilization, and other related activities in the laboratory or e-notebook promptly and confidentially. You should maintain instruments/equipment by ensuring calibration, preventive maintenance, cleanliness, and reporting breakdowns to maintenance promptly. You must be knowledgeable about the MSDS of handled chemicals, emergency response procedures for spillage, leakage, or fire, and adhere to waste segregation guidelines as per EHS norms. Following EHS and quality system requirements is crucial for individual and lab safety. Attending mandatory trainings, updating training records upon completion, and ensuring confidentiality are also part of your role.,

Key Responsibilities Mandatory skill: Chemical Engineer with 8 to10 years’ experience with Basic level of understanding on the GMP aspects. Interaction with the CFT team for the lab development and the manufacturing facility. Willing to travel to SBPs at different locations. Process volume calculations, capacity calculations. Interaction with the Process R & D for the process understanding and prepare the process engineering input form. Evaluation of the time lines and preparation of Gantt Charts. Interaction with the production team run the projects in the plant with complete safety and quality compliance. Process screening and hazard evaluation Literature search, thorough understanding of MSDS Identification of reactive chemical group/ hazardous reaction chemistry and calculation towards the estimation of hazard potential Proper understanding the reaction chemistry interacting with Process R&D Process Optimization Providing necessary technical inputs during interaction with scientists for process robustness w.r.t. scalability, operability and cost effectiveness; Involving in process optimization with focus on right quality & yield on scale to ensure smooth execution of scale up batches and to be in-line with the project requirements. Safety During Execution Identification of hazards in the process and provide justification for modification of the process w.r.t. safe execution of batches in plant to achieve safe execution of batches. Coordinating with the IPDO and CRA lab team generate the safety data required for the scale up process. Documentation Preparation of PE package, Process hazard analysis, Risk analysis, BPR preparation on need basis. Technical Requirements Good chemical engineering knowledge on unit operation like Reaction , Distillation, Crystallization and Isolation Process engineering knowledge on Mixing, Distillation, Filtration, Drying Thorough process understanding of API Scale up and Technology transfer. Capacity calculations and equipment evaluations. Gantt chart preparation. Mapping of the execution plant/ facility. Coordination for the equipment modifications taking the dummy trials at the plant. Timeline calculation Preparation of PFD , P&ID Utility calculations. Soft Skill Requirement Communication, Time management, Adaptability, Interaction with Marketing team and other CFTs, Understand the customer specifications. Desired Candidate Profile Good chemical engineering knowledge on unit operation like Reaction , Distillation, Crystallization and Isolation Process engineering knowledge on Mixing, Distillation, Filtration, Drying Thorough process understanding of API Scale up and Technology transfer. Capacity calculations and equipment evaluations. Gantt chart preparation Education And Experience B Tech Chemical Engineer with 12 to 15 Years’ Experience.

Mobile: 93459 12525 Email: hr@vaighaiagro.com Company Website: https://vaighai.in/ Company: Vaighai Chemical Industries Limited Job Location: R.S.No : 32/1 & 32/2 Melakasakudy Village, Nedugadu Commune, Karaikal – 609603 https://maps.google.com/maps?q=10.9610287%2C79.7885898&z=17&hl=en Job Title: Junior Engineer – Process Job Objective: 1. Support the safe and efficient production of Potassium Chlorate (KClO₃). 2. Monitor and maintain process parameters. 3. Ensure adherence to quality and safety standards. Key Responsibilities: 1. Monitor plant operations (electrolysis, crystallization, drying) and maintain key process parameters. 2. Assist in achieving daily and monthly production targets. 3. Coordinate with shift operators and maintenance for smooth operations. 4. Support in start-up, shutdown, and plant cleaning procedures. 5. Identify opportunities for process improvement and assist in trials and optimization. 6. Ensure product quality as per defined specifications (purity, moisture, particle size). 7. Follow safety protocols and use proper PPE at all times. 8. Report any unsafe conditions or process abnormalities immediately. 9. Maintain production logs, shift reports, and material usage records. 10. Assist in troubleshooting and resolving process or equipment issues. Qualifications: 1. Diploma in Chemical Engineering or related field. 2. 0–2 years of experience in a chemical or chlorate manufacturing plant (preferred). 3. Basic understanding of chemical processes and industrial safety practices. 4. Good communication, teamwork, and analytical skills. Working Conditions: 1. Shift-based job (including night shifts). 2. Work in a chemical plant environment with exposure to hazardous chemicals. 3. Strict compliance with safety and environmental regulations required Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Work Location: In person

Job Title: Sales Manager – Process Technology (filtration and drying equipment ) Location: India (Preferred: Mumbai / Pune / Hyderabad ) Department: Process Technology Reports to: General Manager – Process Technology --- About BHS-Sonthofen India Pvt. Ltd.: BHS-Sonthofen is a globally recognized technology leader in mechanical process engineering, offering solutions in mixing, crushing, recycling, filtration, and drying. The Process Technology division specializes in solid-liquid separation and drying equipment, with key applications in the chemical, pharmaceutical, and environmental industries. --- Key Responsibilities: Identify and develop new business opportunities for filter and drying systems in the pharmaceutical and fine chemical sectors across India. Drive the complete sales cycle – from lead generation, technical proposal development, and pricing strategy to negotiation and contract closure. Work closely with internal process engineers and global teams (Germany ) to align on customer requirements and customized solutions. Manage existing client relationships and ensure customer satisfaction through regular follow-ups and support. Attend industry exhibitions, seminars, and customer audits to represent BHS Process Technology solutions. Keep track of market trends, competitor activities, and regulatory requirements in the pharma and chemical space. Coordinate with the project execution and service team to ensure smooth delivery and commissioning of systems. --- Qualifications: Bachelor’s degree in Mechanical / Chemical Engineering or equivalent. A Master’s degree (MBA/PGDM) is a plus. 5–10 years of technical sales experience in capital equipment or process systems for pharmaceutical or chemical industries. Proven experience with filtration, centrifugation, drying, crystallization, or similar unit operations is highly desirable. Ability to read and interpret P&ID, technical drawings, and process flow diagrams. Excellent communication, presentation, and negotiation skills. Willingness to travel extensively across India. --- What We Offer: Opportunity to work with cutting-edge German technology in solid-liquid separation and drying. A collaborative work environment with international exposure. Competitive compensation and performance-linked incentives. Career growth and learning opportunities in a growing market segment.

Job Title: Process Engineer - Peptides Location: Hyderabad, Telangana, India Job Summary: We are seeking a highly motivated and experienced Process Engineer with a strong background in peptide process development, scale-up, and technology transfer. This critical role will support our business, ensuring the efficient and robust development and manufacturing of peptide molecules from lab to commercial scale. The successful candidate will leverage their expertise in downstream techniques, process optimization, and problem-solving to drive project success and contribute significantly to our clients' drug development pipelines. Key Responsibilities: Lead and execute process engineering activities for peptide molecules, including process development, scale-up, and technology transfer (R&D to pilot/commercial manufacturing). Apply in-depth knowledge of downstream techniques: preparative HPLC (ion exchange, reverse phase, normal phase), lyophilization, tangential flow filtration, nano filtration, and micron filtration. Conduct process understanding studies, generate data for unit operations (reaction, distillation, extraction, crystallization, filtration, drying), and assess process scalability. Evaluate and select plant facilities, propose modifications, and ensure timely completion of plant modifications for commercial scale, including CAPEX evaluation. Identify hardware requirements for commercial scale based on lab, kilo lab, and pilot plant data. Re-engineer difficult or hazardous unit operations using safety studies data (DSC/TGA/Reaction Calorimeter) and conduct HAZOP and risk analysis. Perform particle characterization studies (PVM, FBRM) to assess process parameter impact on morphology, particle size, and distribution; support powder processing for desired PSD. Manage batch planning, scheduling, and execution at commercial scale, including troubleshooting for timely technology transfer and delivery. Monitor pre-validation and validation batches; implement learnings/recommendations. Drive time cycle reduction and debottlenecking initiatives for peptide molecules (SPPS, purification, lyophilization). Coordinate effectively with cross-functional teams (R&D, Analytical, QA, RA, CMCQA, Production, Safety) for smooth operations and project delivery. Prepare and review technical documents: Part-C (EHS Package), PED (Process Engineering Document), technology transfer checklists, and exothermic reaction assessment reports. Contribute to capacity enhancement and cost improvement projects by optimizing processes and reducing raw material consumption. Provide technical services, process troubleshooting, and root cause investigation with robust CAPA implementation. Evaluate Request for Proposals (RFPs) and contribute to facility upgradation based on production requirements. Required Skills & Experience: Bachelor's or Master's degree in Chemical Engineering or a related field. Minimum of 3 - 8 years of hands-on operational experience in process engineering within the pharmaceutical industry. Proven expertise in peptide process development, scale-up, and technology transfer, demonstrated by successful projects involving complex peptide molecules

As a Project & Process Engineer at our Chemical manufacturing company located in Dombivli East, MIDC Phase 2, you will be responsible for a variety of key tasks. Your main duties will include process engineering and commissioning for new plants, encompassing both Brownfield and Greenfield projects. You will also conduct HAZOP sessions and prepare corresponding reports. In this role, you will be involved in the preparation of essential documents such as P&ID, PFD, and plant layouts for new projects and improvement initiatives. Additionally, you will be responsible for creating equipment lists and modifying P&IDs as necessary based on the project progress. Your expertise will be utilized in basic and detailed Engineering processes, where you will demonstrate competency in generating Design Basis, BFDs, PFDs, P&IDs, and various Process Calculations. This will involve activities like preparing, evaluating, and implementing Material & Energy Balances, as well as line sizing calculations, pump hydraulic calculations, and pump selections. Furthermore, you will contribute to the development of line lists, equipment lists, and instrument lists. Your role will also encompass participation in different unit operations such as distillation, liquid-liquid extraction, steam stripping, filtration, drying, crystallization, evaporation, and scrubbing processes. As part of your responsibilities, you will be involved in the preparation of Instrument Process Data sheets, Process Data Sheets for Pumps & Storage Tanks, Utility calculations, Utility Distribution Diagrams, and Piping Layouts. Your expertise in DCS safety, Heat Exchanger Design calculations, Pump Calculations, Cooling tower calculations, and Breather Valve calculations will be crucial for the successful completion of projects. Your thorough understanding of utility requirements for the plant will also play a vital role in ensuring efficient operations. If you are looking to join a dynamic team and contribute to the growth of our organization, we welcome your application for this challenging role. Regards, HR Darshanaa Indo Amines Limited www.indoaminesltd.com,

Role & responsibilities Handson crystallization and synthesis lab work Use of instrumentation (FTIR, UVVis, HPLC, NMR) Preferred candidate profile 2-3 Yrs in Crystallization or Synthesis in Lab area

Date: 11 Jul 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services Job Description Job Title: Research Associate Trainee Job Location: Hyderabad/Bangalore Department: Discovery Chemistry 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 Role Accountabilities Attend training on environment, health, and safety (EHS) measures. Follow environment, health, and safety (EHS) requirements always in the workplace ensuring individual and lab/plant safety 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. Leadership Capabilities Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Specific requirements for this role Experience – 0-3 Years Education – MSc General/Organic 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.

As a Technical Sales Engineer at JordProxa, you will play a crucial role in supporting the sales process to create business opportunities. Working under the guidance of the Technical Sales Manager, your primary responsibility will involve assisting in the development of proposals that effectively showcase the benefits of JordProxa's crystallisation, evaporation, and related plants to potential customers. Your contribution will ensure that proposals are comprehensive in technical details and accurate in cost estimates. Your duties and responsibilities will include reviewing client specifications and bid requirements to identify key technical and commercial aspects that need to be addressed in proposals. Collaborating with the Technical Sales Manager and Technologists, you will help in creating process designs and equipment layouts for various project inquiries. Additionally, you will actively engage with customers to understand their requirements and provide technical insights to support the sales process. Furthermore, you will be involved in estimating project costs using established procedures and templates, obtaining vendor quotes as needed, and maintaining price databases. Staying updated on new technologies relevant to JordProxa's product portfolio and market trends will be essential, as you collaborate with the Sales and R&D teams to align technology with market demands. Your role will also entail contributing to process improvements and optimization initiatives to enhance the efficiency and accuracy of proposal preparation. Moreover, you will play a part in transitioning projects to the Operations team once they are secured. To excel in this position, you should hold an undergraduate degree in Process or Chemical Engineering with 3-5 years of experience in designing process plants. Familiarity with crystallization and evaporation plant design, operation, or commissioning will be advantageous. Strong written communication skills, experience in integrated process systems design, and proficiency in technical document review are essential. Additionally, knowledge of chemical/process design and simulation software, along with proficiency in Microsoft Office applications, is required. A proactive attitude towards business development, a focus on quality, and a commitment to providing value to the company and clients are key attributes for success in this role.,

Job Description Job Description – Technical Sales Engineer As the Technical Sales Engineer, reporting to Technical Sales Manager, you will support the sales process to generate business opportunities for JordProxa. A key part of this role will be assisting in the preparation proposals that present a compelling and logical case to customers for purchasing crystallisation, evaporation and other related plants from JordProxa. You will provide technical support in the sales process, ensuring that proposals contain sufficient technical detail and that cost estimates are accurate. Duties And Responsibilities Proposal Development and Technical Support: Review client specifications and bid requirements to identify areas of technical and commercial concern that should be addressed in our estimate and proposal. Support the preparation of proposals, ensuring they effectively communicate the value proposition and technical benefits of JordProxa’s solutions. Work closely with Technical Sales Manager and Technologists to develop process designs (including mass balance and preliminary equipment designs) for PFS / Budget level enquiries. Work closely with Technical Sales Manager and Proposal Manager in the preparation of tender bids and firm proposals for major projects Customer Engagement And Sales Support Work closely with customers to define requirements and provide preliminary technical insights. Meet and collaborate frequently with other members of the sales team to ensure proposals are tailored to customer requirements and align with the agreed sales strategy. Estimates Assist in preparing estimates using agreed processes and templates for firm, budget, and feasibility offers. Obtain vendor quotes where necessary and help develop and maintain price data bases R&D And Process Improvements Stay informed about new technologies relevant to JordProxa’s product portfolio and market trends. Participate in discussions with the Sales and R&D teams to align technology with market needs. Seek to enhance the speed and accuracy of proposal preparation through optimization and process improvement initiatives. Operations & Customer Follow-Up Participate in the process of handing over the project to the Operations team once a Job is won Skills And Experience Undergraduate degree in Process / Chemical Engineering 3-5 years of experience in designing process plants. Experience with crystallization and evaporation plant design, operation, or commissioning is beneficial. Ability to prepare well-written and compelling technical documents. Experience in the design of integrated process systems. Proficiency in reviewing PFDs, P&IDs, plant GA drawings, and 3D designs. A proactive and positive attitude focused on business development and supporting fellow staff throughout pre-award and execution phases. Knowledge of chemical/process design and simulation software. Proficiency in Microsoft Office programs such as Excel, PowerPoint, and Word. Focus on quality and provision of value to the Company and our clients

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are seeking a dynamic and experienced Scientist in Process Engineering in Active Pharmaceutical Ingredient (API) development with proven expertise in scaling up or down technologies to meet production demands. Proficient in Process and Chemical Engineering, adept at troubleshooting complex projects, facilitating technology transfer, and optimizing operations. Roles & Responsibilities ' Need to have detailed knowledge on Continuous manufacturing process development including batch unit operations. Summarize literature survey for relevant processes and technologies, Basic knowledge on green chmistry principles, Preparation of RMC sheets for respective projects. Hands on experience on different types of pumps, flow reactors and appilications. Knowledge on using of PAT tools for flow process developement. Scientific understanding for screening molecules in Flow and process development and scale up from laboratory to commercial scale (Scale up Correlation for all unit operations). Data analysis and drawing inferences/outcomes with minimum guidence. Understand feasibility process, define process variables and responses in collaboration with R&D for DoE studies to understand design space to meet critical quality attributes (CQAs) . Conduct scale-up and what-if studies with minimal guidance. ELN documentation as per SOP Draft the process for scale up i.e. Kilo lab, CPP and T&V batches in coordination with CFTs Evaluate and establish processes for recovery of solvent and product. Coordinate with vendors, SCM, engineering team and stores for spares & consumables which are required for day to day and projects activities. Generate safety data under supervision of safety experts using related tools like RC1/DSC/TSU/ARC/MIE etc. Generate sufficient data using lab-scale prototypes of downstream equipments Prepare equipment requirements based on the campaign plan with minimal guidance. Track modification and ensure facility suitability and readiness. Knowledge on Continuous& Batch crystallization process development,filtration and drying. Knowledge on down stream unit operations like Liquid liquid extractions. Execute Scale up batches ( Kilo lab/Pilot plant/commercial plant) batches to verify design space and study scale-dependent parameters, and share observations and suggestions for process/equipment modifications Execute T&V campaign and support in related activities with minimal guidance Support troubleshooting activities in case of issues in scale up/validation batches with minimal guidance Support draft investigation reports Support work towards DMF filing and addressing regulatory queries related to Process Engineering Should be aware of process validation & other general GMP & GLP aspects Maintain process documentation. ' Be familiar with IP landscape & other published literature related to product Qualifications Educational qualification: MSc. Chemistry/Organic Chemistry Minimum work experience: 3 to 7years of experience with scale up & tech transfer of Active Pharmaceutical Ingredients (API) Skills & attributes: Technical Skills Process Optimization and Development . Data Analysis and Interpretation Quality by Design (QbD) Knowledge of Flow Chemistry/ Continuous Manufacturing Knowledge of Organic Chemistry and Retrosynthesis and Knowledge of Computational Tools (SciFinder, Synthia, etc.) Impurity Synthesis and Structure Confirmation Knowledge on documentation for TT and Scale up Execution Collaboration & Communication with Cross-Functional Teams Behavioural Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Date: 8 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services 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 always 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 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 solving 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 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 Syngene’s productivity expectations (# of compounds/month and # of steps/month) 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 Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience Up to 5 years Skills And Capabilities Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms Candidate should be capable of solving synthetic problems independently Should be excellent in purification and analytical interpretation skills. Familiar with operations of relevant apparatus - instrument / equipment. Education M.Sc in general or organic chemistry

As a Project & Process Engineer at our Chemical manufacturing company in Dombivli East, MIDC Phase 2, you will be responsible for various key tasks related to process engineering and commissioning for both Brownfield and Greenfield projects. This includes conducting HAZOP sessions, preparing HAZOP reports, and creating P&ID, PFD, and plant layouts for new projects and improvement projects. You will play a crucial role in preparing equipment lists, modifying P&IDs as per the built, and engaging in basic & detailed Engineering (Process). Your competency will be vital in generating Design Basis, BFDs, PFDs, P&IDs, and conducting Process Calculations. Additionally, you will be involved in Material & Energy Balance evaluation, PFD & P&ID implementation, line sizing calculations, pump hydraulic calculations, and pump selection. Your responsibilities will also encompass the preparation of line lists, equipment lists, and instrument lists. You will be engaged in various unit operations such as distillation, liquid-liquid extraction, steam stripping, filtration, drying, crystallization, evaporation, and scrubbing. Furthermore, you will be tasked with creating Instrument Process Data sheets and Process Data Sheets for pumps & storage tanks. Your role will involve utility calculations, Utility Distribution Diagram & Piping Layout, DCS safety considerations, and the design calculations for Heat Exchangers, Pumps, Cooling towers, and Breather Valves. Understanding the utility requirements for the plant and ensuring efficient utility distribution will be essential aspects of your responsibilities. If you are passionate about engineering, possess a strong understanding of chemical manufacturing processes, and are eager to contribute to the success of our company, we look forward to having you on board. Regards, HR Darshanaa Indo Amines Limited www.indoaminesltd.com,

As a Polymorph Screening Scientist at Morepen Proprietary Drug Research Pvt Ltd. (MPDRPL), your primary responsibility will be to lead the screening and selection of solid forms for drug candidates. You will play a crucial role in improving the physicochemical properties of active pharmaceutical ingredients (APIs) by overseeing polymorph screening activities. It is essential to identify the most stable and bioavailable forms of drug substances for regulatory submissions. Collaborating with cross-functional teams, you will mentor junior scientists and drive advancements in solid-state drug discovery. Your key responsibilities will include overseeing the screening of potential polymorphs, solvates, and hydrates for APIs, interpreting and analyzing solid-state data, scaling up identified novel polymorphs, collaborating with various teams to align polymorph selection with drug formulation strategies, preparing regulatory-compliant data for filings, troubleshooting any issues related to polymorph stability, and ensuring accurate documentation and reporting of experimental protocols and findings. The deliverables expected from you include the identification and characterization of stable polymorphs and crystal forms for drug candidates, detailed screening reports, regulatory-compliant data for solid-state forms, and methodologies for high-throughput screening, scaleup, and solid-state characterization. To qualify for this role, you should hold a Ph.D. in Pharmaceutical Sciences, Solid state Chemistry, Chemistry, or a related field, with a focus on solid-state chemistry or materials science. Alternatively, a Master's degree with equivalent experience will be considered. You should have a minimum of 6+ years of industry experience in solid-state chemistry, polymorph screening, or pharmaceutical development and proven expertise in solid-state characterization techniques and polymorph screening methods. Proficiency in solid-state characterization methods, high-throughput screening techniques, and knowledge of computational techniques for polymorph prediction are essential technical skills required for this role. In addition to technical skills, you should possess excellent problem-solving, troubleshooting, and decision-making skills. Effective communication skills, both written and verbal, are crucial for presenting complex data to diverse audiences. Being detail-oriented with strong organizational and documentation skills will contribute to your success in this role at MPDRPL.,

Eastern Naphtha-Chem Pvt Ltd is India's leading manufacturer of Beta Naphthol, Naphthalene, Sodium Sulfite, and other naphthalene series industrial chemicals Role & responsibilities Primary responsibility for all all aspects of production, yield and quality targets for beta naphthol plant. Production planning, targets fulfilment and production activities as per SOPs. Oversight and guidance of supervisors / shift in charge and operating personnel. Overall responsibility for production including capacity/ utilization/ OEE/ etc, raw material consumption ratios improvement, energy and electricity usage optimization, breakdown maintenance and resolution, regular maintenance plan development and implementation, etc. Collaboration with R&D Team for plant improvement initiatives Identification of recurrent equipment breakdowns, and preventive maintenance and coordinating with maintenance personnel to complete the jobs safely & effectively. Optimization of manpower planning Training of personnel Development of systematic protocol for each chemical unit process within plant including preparation of SOPs, BMSs, Protocols, reports, etc. Preparation, maintenance, and refinement of daily and monthly reporting systems and MIS. Key responsibility includes accurate estimation of plant raw material input ratios. Responsibility for quality control within plant Preferred candidate profile Education: BSc/ MSc in Chemistry or BTech/ MTech in Chemical Engineering Experience: >20 years in Chemicals/ Process Industry Functional Area: Production, Plant Operations and Maintenance, Operations Improvement Experience in production in dye/ organic intermediates (preferably unit processes like sulfonations, distillations, alkali fusions, carboxylations, solvent recovery and handling, etc.)

Date: 8 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services Job Description Designation: Associate Scientist – 8-I Job Location: Bangalore Department: DDS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Key Responsibilities Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipment 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’s are 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 Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality Prepare SOPs/IOPs/EOPs/OCPs when any new lab activity is identified or existing one requires updating Any other lab responsibilities as indicated by the EHSQ team member/ supervisor / group leader. Understanding and demonstrating responsibility for safety of self & colleagues by following all safety protocols provided by Syngene Adherence to all environment, health, and safety (EHS) policies & standards always in the workplace Wearing all PPE as required. Adherence to all procedures related to Syngene’ s data integrity policies Compliance to Syngene’ s quality standards at all times. For running independent project(s) in the areas of immuno-oncology For driving the assigned project with full commitment, To champion the biology of project, establish all assays, models required to drive the project and work in collaboration with team members within the domain, across different domains and across department To take active participation in running experiments, compiling the data in required format and prepare study reports To train and mentor other scientists in a timely manner To work in a collaborative fashion with research scientists from various disciplines Educational Qualification: MSc (Chemical Sciences). Experience: 4.5 - 8 Years Required Skills Should be familiar with concepts of chemical synthesis Familiar with operations of relevant apparatus - instrument / equipment. Good Knowledge of analytical techniques and analytical data interpretation. Good communication skills Behavioral Skills: Good communication skills, good presentation skills, hardworking, sincere and a team player. Must demonstrate integrity and take accountability of their work 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 about 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.

Date: 7 Jul 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services Job Description Job Title: Research Associate Trainee Job Location: Hyderabad/Bangalore Department: Discovery Chemistry 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 Role Accountabilities Attend training on environment, health, and safety (EHS) measures. Follow environment, health, and safety (EHS) requirements always in the workplace ensuring individual and lab/plant safety 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. Leadership Capabilities Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Specific requirements for this role Experience – 0-3 Years Education – MSc General/Organic 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.

Description The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities (small molecules and peptides) through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Senior Scientist I has the following responsibilities: Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules & peptides. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Execute small molecule synthesis and, solid-phase and solution-phase peptide synthesis with a focus on quality. Perform peptide modification techniques, including cyclization, disulfide bridge formation, stapling, and derivatization. Support in characterization of peptides by utilizing advanced characterization techniques such as LCMS, HPLC, and NMR to ensure peptide quality and accuracy. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab. Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: M Sc (Organic Chemistry) from a reputed university with minimum 11-13 years of industrial experience in API Process R&D/CDMO/CRO (OR) Ph.D (Full Time) in Synthetic Organic Chemistry from a reputed group with 7-10 years of post doctoral and/or industrial research experience in API Process R&D/CDMO/CRO. Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of Small Molecule APIs/ NCEs on lab scale and production. Experience in handling automated peptide synthesizers and purification processes is highly desirable. Proven ability for adoption of QMS and documentation procedure Adherence to lab safety guidelines Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions, solid phase and complex peptide synthesis and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Good practical, documentation & presentation skills. Attention to detail, stratregic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

Description The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist I/II has the following responsibilities: Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: M Sc (Organic Chemistry) from a reputed university with minimum 1-6 years of industrial experience in API Process R&D/CDMO/CRO Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale and production. Proven ability for adoption of QMS and documentation procedure Adherence to lab safety guidelines Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Good practical, documentation & presentation skills. Attention to detail, strategic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

Department: Biology – DST Location: Shameerpet About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels. Key Responsibilities : To work on structural biology projects starting with X-ray crystallography. involved in protein crystallization, co-crystallization and crystal soaks with different compounds, data collection at local diffractometers and synchrotrons Data processing, structure determination, and validation. Experience/Qualification: PhD with 0-2 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): Good communication skills Should possess good team management skills.

Date: 2 Jul 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services 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 notebooks. 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 equipment’s 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

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities (small molecules and peptides) through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Senior Scientist I Has The Following Responsibilities Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules & peptides. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Execute small molecule synthesis and, solid-phase and solution-phase peptide synthesis with a focus on quality. Perform peptide modification techniques, including cyclization, disulfide bridge formation, stapling, and derivatization. Support in characterization of peptides by utilizing advanced characterization techniques such as LCMS, HPLC, and NMR to ensure peptide quality and accuracy. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab. Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience M Sc (Organic Chemistry) from a reputed university with minimum 11-13 years of industrial experience in API Process R&D/CDMO/CRO (OR) Ph.D (Full Time) in Synthetic Organic Chemistry from a reputed group with 7-10 years of post doctoral and/or industrial research experience in API Process R&D/CDMO/CRO. Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of Small Molecule APIs/ NCEs on lab scale and production. Experience in handling automated peptide synthesizers and purification processes is highly desirable. Proven ability for adoption of QMS and documentation procedure Adherence to lab safety guidelines Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions, solid phase and complex peptide synthesis and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Good practical, documentation & presentation skills. Attention to detail, stratregic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist I/II Has The Following Responsibilities Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience M Sc (Organic Chemistry) from a reputed university with minimum 1-6 years of industrial experience in API Process R&D/CDMO/CRO Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale and production. Proven ability for adoption of QMS and documentation procedure Adherence to lab safety guidelines Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Good practical, documentation & presentation skills. Attention to detail, strategic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time

Description The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist III/IV has the following responsibilities: Carry out literature search related to assigned projects using various scientific data base. Design synthetic routes for the target small molecules. Prepare project proposals with tentative cost estimates. Perform synthesis & isolation of pharmaceutical analytical impurities, reference standards and degradation impurity standards. Procure key raw materials and reagents required for the project Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Troubleshooting synthesis and purification issues independently Contributing effectively towards more challenging and complex projects through innovative methodologies Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc. Produce quality materials as per customer requirement Packaging of synthesized compounds Plan, execute and complete the projects as per the timelines Document all experiments conducted as per QMS guidelines. Responsible for preparation of SOPs, Protocols, reports etc. as per the need Responsible for review the records and documents Responsible to ensure the calibrations of the equipment as per the schedule Periodic check of the assigned equipment to ensure its working condition Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Work on any other assigned tasks/ lab management activities. Conversant with lab safety norms and strictly follow them. Communicate within the team and cross functional teams Learn and practice Diversity, Equity, Inclusion & Belonging culture. Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: Scientist III/IV – M Sc (Organic Chemistry) from a reputed university with minimum 6-10 years of industrial experience in Pharmaceutical Process R&D or CRAMS or CRO set up (Or) Ph.D (Full Time) in Synthetic Organic Chemistry from a reputed group with minimum 1-7 years post-doctoral/industrial research experience in organic synthesis Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis. Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs. Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale. Excellent troubleshooting skills in synthesis and purification of target compounds. Should possess good verbal and written communication skills. Should possess good organizational, communication, and interpersonal skills. Additional Desired Preferences Extensive knowledge on wide range of organic reactions, and hands on experience in handling various sensitive chemicals/reagents. Track record of patents/ publications in synthetic organic chemistry/ process development. Should have exposure to GMP/GLP environment and documentation procedures. Have good practical, documentation & presentation skills. Attention to detail, strategic thinking and problem-solving skills. Demonstrated ability to work both independently and as a member of a team with a passion for quality Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.