144 Medicinal Chemistry Jobs - Page 3

Skill required: Tech for Operations - Artificial Intelligence (AI) Designation: AI/ML Computational Science Sr Manager Qualifications: Any Graduation/Post Graduate Diploma in Management Years of Experience: 16 to 25 years Language - Ability: English(Domestic) - Advanced About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be part of the Technology for Operations team that acts as a trusted advisor and partner to Accenture Operations. The team provides innovative and secure technologies to help clients build an intelligent operating model, driving exceptional results. We work closely with the sales, offering and delivery teams to identify and build innovative solutions.The Tech For Operations (TFO) team provides innovative and secure technologies to help clients build an intelligent operating model, driving exceptional results. Works closely with the sales, offering and delivery teams to identify and build innovative solutions. Major sub deals include AHO(Application Hosting Operations), ISMT (Infrastructure Management), Intelligent AutomationUnderstanding of foundational principles and knowledge of Artificial Intelligence AI including concepts, techniques, and tools in order to use AI effectively. What are we looking for Machine LearningMachine Learning AlgorithmsMicrosoft Azure Machine LearningPython (Programming Language)Python Software DevelopmentAbility to work well in a teamWritten and verbal communicationNumerical abilityResults orientation1 CL6 AI Research Scientists1. Deep Expertise in Machine Learning & AI Theory2. Algorithm Design & Theoretical Innovation3. Data Proficiency & Synthetic Data Generation4. Responsible AI & Ethical Awareness5. Programming & ToolingThe Azure OpenAI Service L100 deck also emphasizes the evolution of tooling from symbolic AI to modern generative models 6.6. Collaboration & CommunicationAI Research Scientists often work in interdisciplinary teams and must:Publish researchPresent at conferencesCollaborate with engineers, product teams, and stakeholders1 CL6 Data ScientistsThis role requires a unique blend of technical and legal fluency. 1Data Scientists must be able to build and evaluate models that power autonomous agentsespecially those involved in legal document analysis, compliance automation, and contract intelligencewhile ensuring these agents adhere to evolving legal standards 2. According to the GenAI Foundation Strategy_12AUG2024, this includes assessing AI use cases Roles and Responsibilities: In this role you are required to identify and assess complex problems for area(s) of responsibility The individual should create solutions in situations in which analysis requires in-depth knowledge of organizational objectives Requires involvement in setting strategic direction to establish near-term goals for area(s) of responsibility Interaction is with senior management levels at a client and/or within Accenture, involving negotiating or influencing on significant matters Should have latitude in decision-making and determination of objectives and approaches to critical assignments Their decisions have a lasting impact on area of responsibility with the potential to impact areas outside of own responsibility Individual manages large teams and/or work efforts (if in an individual contributor role) at a client or within Accenture Please note that this role may require you to work in rotational shifts Qualification Any Graduation,Post Graduate Diploma in Management

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Position Summary Client: Reliable CRO providing CRAMS & Drug Discovery Services Position: Group Leader - Discovery Chemistry (USA, EU & Japan) Reporting to: CEO (India) + Head-Chemistry (USA) Team Handling: 6/8 members Role & responsibilities 1. Fee-for-Service Project Leadership Manage 15-20 concurrent custom synthesis projects (1mg-10g scale) Develop client-specific quotation templates with: 1. Technical feasibility assessments. 2. Competitive pricing strategies. 3. Risk mitigation plans (alternate routes, backup suppliers). Ensure audit-ready documentation for IP-sensitive projects. 2. Winning Quotation Development Craft technically compelling proposals highlighting: 1. Kemio's unique capabilities (e.g., exotic heterocycle expertise). 2. Case studies of similar molecules delivered. 3. Value-add services (free analytical characterization, stability studies). Collaborate with BD team to benchmark against 3 competitor quotes per RFP. 3. Operational Excellence Maintain FFS project dashboard tracking: 1. Resource allocation (FTE hours vs. budget). 2. Critical reagent inventory levels. 3. Client communication logs. Implement rapid response protocol for urgent quote requests (24h turnaround). Recruiter's Contact Details: Dharmesh Sikligar BEST-FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat, India Mobile: 09558802906 Website: www.bestfitrecruitment.co.in

Plan and conduct multi-step organic syntheses to develop novel molecules.Work closely with cross-functional teams, including medicinal chemists,biologists, and analytical scientists to advance drug discovery projects. Required Candidate profile - Experience in medicinal chemistry or CRO environment, preferably in drug discovery, or custom synthesis. - Proficiency in synthetic organic chemistry.

This role is responsible for executing chemicals reactions to synthesize required quantities of molecules / compounds as per client specifications using efficient route and techniques. Responsibilities Set-up and execute reactions for synthesis of target molecules/ compounds: Understand the project requirements as specified by the client, the synthetic route Understand and discuss the MSDS (Material Safety Data Sheet) with team members Identify and mitigate any potential safety risk with the help of supervisor Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage and minimum wastage Ensure parallel execution of multiple reactions Monitor the reaction by observing progress by using analytical techniques Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality Analyze analytical data, evaluate and interpret results from the synthesis and report Meet productivity benchmarks on number of reactions / number of steps / number of compounds / quality / compounds purity / project timelines Ensure safety at work through enforcement of good laboratory practices: Follow safety and quality systems in the labs Maintenance and usage of equipment/apparatus/instruments as per SOPs and general housekeeping norms Maintain records, data integrity and IP confidentiality: Document reactions executed, research findings/ observations accurately in lab notr books as per client requirements to ensure data integrity Maintain strict IP confidentiality and adhere to all related policies To prepare final reports as required Ensure high morale and skill development of team: Improve knowledge of organic chemistry (particularly synthesis) / Analytical techniques etc. through ono on one discussions with supervisor/ regular classroom trainings/ project trainings/ further education programs etc. Functional/ Technical Skills Knowledge of Chemistry & Execution Knowledge of Safety Protocols Knowledge of IP & Confidentiality and Data Integrity Ability to conduct cost benefit analysis and optimum usage of resources Required Educational Qualification & Relevant experience Msc (Organic/ Medicinal Chemistry) with 1 - 5 years of relevant experience Additional Requirements Candidates with their research publications in leading journals would be preferred Additional Responsibilities: Educational qualifications preferred Required Certification/s: Required Training/s: Required work experience Industry: Role: Years of experience: Key Performance Indicators: Required Competencies: Required Skills: Work Environment Details: Specific requirements Other details Learn more about our end-to-end capabilities This website uses cookies to improve your experience while you navigate through the website. Out of these, the cookies that are categorized as necessary are stored on your browser as they are essential for the working of basic functionalities of the ... Necessary Necessary Always Enabled Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information. Non-necessary Non-necessary Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. It is mandatory to procure user consent prior to running these cookies on your website.

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. : Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.

Responsibilities: Perform chemistry reactions & record data follow lab safety practices work for novel chemistry targets working with team spirit Office cab/shuttle Health insurance Annual bonus Provident fund

Consulting with patients to understand their symptoms and health concerns. Diagnosing and treating acute illnesses, such as bacterial and viral infections, as well as chronic diseases and conditions, such as hypertension, heart disease, or diabetes. Prescribing or administering medication, therapy, and other specialized medical care to treat or prevent illness, disease, or injury. Explaining procedures and discussing test results or prescribed treatments with patients. Monitoring patients' conditions and progress, and re-evaluating treatments, as necessary. Providing health and wellness advice to patients, including diet, physical activity, hygiene, and disease prevention. Immunizing patients against preventable diseases. Maintaining detailed notes of appointments with patients, including comments, tests, and/or treatments prescribed, and test results. Referring patients to other medical specialists, when necessary. Providing support and advice to patients receiving long-term care.

Join us and contribute to the discovery of medicines that will impact lives! Aganitha is accelerating drug discovery and development for Biopharma and Biotech R&D with in silico solutions leveraging Computational Biology & Chemistry, High throughput Sciences, AI, ML, HPC, Cloud, Data, and DevOps. In silico solutions are transforming the biopharma and biotech industries. Our cross-domain science and technology team of experts embark upon and industrialize this transformation. We continually expand our world-class multi-disciplinary team in Genomics, AI, and Cloud computing, accelerating drug discovery and development. What drives us is the joy of working in an innovation-rich, research-powered startup bridging multiple disciplines to bring medicines faster for human use. We are working with several innovative Biopharma companies and expanding our client base globally. Read about how and what solutions we build. Aganitha, which means countless or limitless in Sanskrit, serves as a reminder and inspiration about the limitless potential in each one of us. Come join us to bring out your best and be limitless! Key Responsibilities: - Engage and co-innovate with R&D teams of our Biopharma clients, and collaborate with a team of Biologists, Medicinal Chemists, Computational Chemists, Computational Biologists, Data Scientists, Data Engineers, and Web Developers to create the next generation of innovative computational solutions for drug discovery and development. - Lead architecture initiatives from inception to completion - Design and oversee implementation of solutions for BioPharma R&D - Manage Engineering teams using Agile methodologies - Enhance reuse with platforms, frameworks, and libraries - Collaborate with business users to create architecture in alignment with a business need - Drive scope definition, requirements analysis, functional and technical design, application build, product configuration, unit testing, and production deployment and ensure delivered solutions meet/perform to technical and functional/non-functional requirements. - Champion the adoption of reusable architecture assets to improve efficiency - Produce documentation to aid in the understanding of existing architecture solutions - Advise our technical teams to optimize the recommended product suite in defining, building, and deploying end-to-end solutions - Lead the translation of the clients business requirements into systems design - Drive the development of prototypes and technology demonstrators within microservice architecture, cloud-native solutions - Design and document system installation and upgrade guides, specifications, and related standards and guide technical team, application specialists - Design application user guides, document common workflows, prepare training materials and conduct or participate in knowledge-sharing sessions with technical teams - Design future state reference architectures that will provide a template for teams to achieve security, scalability, reliability, and maintainability - Design and implement optimal deployment strategies and custom interfaces for integration with customer systems and technologies - Help customers tackle thorny technical issues by collaborating to create smart, efficient, and effective solutions - Work closely with customers on the installation, configuration, and update/maintenance of on-premises or cloud-hosted installations of our scientific computing and enterprise software applications - Collaborate with product managers, developers, and scientists, to improve the deployment, support, and configuration of our applications Desired Skills / Expertise: - Big data engineering with distributed computing frameworks - Cloud and DevOps automation - App dev with modern tech stacks of Python, ReactJS, and fit-for-purpose database technologies - Experience in directing/building solutions leveraging Machine learning (ML) and AI (Deep learning) - Excellent communication skills with a desire to work in multidisciplinary teams Educational Qualifications: - Bachelors / Masters / Ph.D. in Computer Science or related technical field,

Roles and Responsibilities To perform product lifecycle management tasks for externally supplied products and own production products like evaluation of change controls, deviations, temperature excursions, stability data, process validation documents from Product quality point of view. Handling of problem-solving cases for products (includes both analytical and formulation related changes which have impact on product quality). Overall product quality evaluation and provide input during suppliers meetings. Follow up with suppliers and/or other stakeholders for documents related to changes for externally supplied products. E.g., possible impurities in API and finished products risk assessment in line with updated guidelines. Requesting, follow-up and tracking of Product Quality Review (PQRs) related data. Preparation and evaluation of Product Quality Review (PQRs) for externally supplied products, related coordination and follow-up with suppliers and other stakeholders. Writing of Product Quality Review (PQRs) for own production products and ensure its timely approval. Preparation and review of other documents related to Product Quality Review (PQRs). Responsible for planning stability studies, writing and/or review of stability protocols, reports and preparation of technical documents in CTD format. Co-ordinate and follow up stability studies at CROs/CQC. Writing and/or reviewing of process validation, technology transfer, study batch documentation for own products. Write/check/review pharmaceutical documents as per regulatory requirements. Candidate having knowledge of theoretical and/or possible Physico-chemical risks for products based on appropriate available data (E.g., evaluation of synthesis route of API, excipients, packaging materials details etc.) will be an added advantage. Write documents into Orion s IT systems. Preparation and maintenance of lists/documents/records and archiving at appropriate place. Co-ordination with other departments / partners. Achievements of responsibilities within the agreed timelines. To assist the overall working of Indian Pharmaceutical team. Other possible tasks appointed by Supervisors. Note: We do not have own laboratories in India! Primary Skills (essential) Minimum 4 years experience in Formulation R&D or API R&D activities in global Pharma industry Knowledge of organic chemistry/ Pharmaceutical medicinal chemistry/ synthetic chemistry will be an added advantage Ability to analyze the impact of change on Nitrosamine and/or other relevant physico-chemical risks assessment, if possible. Confirmed knowledge of EU requirements and ICH guidelines Candidate having interest and/or experience in pharmaceuticals documentation or any relevant pharmaceutical formulation / manufacturing related documentation will be preferred. Practical development skills from the laboratory to the production scale concerning different types of formulations (tablets, capsules, liquids, etc.) will be considered as an added advantage. Fluency in oral and written English Task oriented with learning attitude and Teamwork skills Confirmed skills of Microsoft Office are essential This job offers An excellent opportunity to work in an inspiring and important role in the area of Pharmaceuticals Great opportunity to become part of the wholly owned subsidiary of globally operating Orion Group Possibility to utilize your own strengths with the support of professionals Flexible, high spirit working environment where your skills are appreciated Good work-life balance Clear, transparent processes and responsible supervisors are our benefits to the personnel Education Bachelors/masters degree in pharmacy from a reputed College/University or Masters degree in chemistry from a reputed College/University At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life. Please visit our website to find further information about our values and Orion as an employer https: / / www.orion.fi / en / careers / orion-as-an-employer / . How to apply and additional information Please fill Candidate Information Form on https: / / forms.gle / o9BhfmhigBcyp5fy7 & email your CV to recruitmentindia@orion.fi Required documents: CV/Resume Application deadline: 31.07.2025

Join our team and contribute to the discovery of medicines that will impact lives! Located in Hyderabad, India, Aganitha is dedicated to accelerating drug discovery and development for Biopharma and Biotech R&D through innovative in silico solutions. Our team leverages Computational Biology & Chemistry, High throughput Sciences, AI, ML, HPC, Cloud, Data, and DevOps to drive advancements in the industry. In silico solutions have revolutionized the biopharma and biotech sectors, and our team of experts is at the forefront of this transformation. We are constantly expanding our multi-disciplinary team in Genomics, AI, and Cloud computing to accelerate drug discovery and development. Our passion lies in working in an innovation-rich, research-powered startup that bridges various disciplines to bring medicines to market faster. Collaborating with innovative Biopharma companies globally, we are committed to pushing boundaries and making a difference. As a part of our team, your key responsibilities will include engaging and co-innovating with R&D teams of our Biopharma clients, leading architecture initiatives, designing and overseeing implementation of solutions for BioPharma R&D, managing Engineering teams, enhancing reuse with platforms and frameworks, collaborating with business users, driving scope definition, and ensuring delivered solutions meet technical and functional requirements. Desired skills and expertise for this position include experience in big data engineering, cloud and DevOps automation, application development with modern tech stacks, and proficiency in Machine Learning and AI. Excellent communication skills and the ability to work in multidisciplinary teams are also essential. We are seeking individuals with educational qualifications such as a Bachelors, Masters, or Ph.D. in Computer Science or a related technical field to join our dynamic team at Aganitha. If you are passionate about making a difference in drug discovery and development, we invite you to join us in our mission to bring out your best and be limitless!,

We are seeking a highly motivated and experienced Study Director to oversee chemical characterization studies within our research and development team. The ideal candidate will have a strong background in analytical chemistry, extensive knowledge of chemical characterization techniques, and a proven track record in managing complex projects. This position offers a competitive salary and benefits package, along with opportunities for professional growth and development. If you are passionate about advancing scientific research and thrive in a collaborative environment, we encourage you to apply. Roles and Responsibilities 1. Oversee and manage chemical characterization studies from initiation to completion, ensuring adherence to regulatory standards and internal protocols. 2. Design study plans and methodologies that are scientifically sound and aligned with project objectives, including the selection of appropriate analytical techniques and equipment. 3. Coordinate with cross-functional teams, including project managers, chemists, and quality assurance personnel, to ensure effective study execution and communication. 4. Review and approve study protocols, analytical methods, and reports to ensure accuracy, compliance, and scientific integrity. 5. Provide technical expertise and guidance related to chemical characterization, including the interpretation of analytical data and results. 6. Ensure that all studies are conducted in compliance with Good Laboratory Practice (GLP) and other relevant regulations. 7. Manage study budgets and timelines, identifying potential risks and implementing mitigation strategies to ensure successful project delivery. 8. Train and mentor staff on appropriate methodologies and regulatory requirements related to chemical characterization studies. 9. Participate in project meetings, presenting study findings and progress updates to stakeholders, and incorporating feedback into study design and implementation. 10. Maintain up-to-date knowledge of industry trends, emerging technologies, and regulatory changes affecting chemical characterization and related fields. 11. Facilitate communication with regulatory agencies as needed, providing data and documentation to support submissions and inquiries. 12. Contribute to the continuous improvement of departmental processes and methodologies, ensuring best practices are followed in study design and execution.

Specializations : Physical Chemistry / Analytical Chemistry / Organic and Medicinal Chemistry / Inorganic and Materials Chemistry Designations Available: Assistant Professor, Associate Professor, and Professor Desired Skillset: Applicants should preferably hold a Ph.D. in the relevant subject from reputed Institutions. Should have sufficient experience in Teaching, Industry & Research with reputed Institutions. Should have research papers published in International / National Journals. Should have books published and Scholars awarded / currently working for. Applicants with patents registered / consultancy works carried out will be given preference. Exposure in handling high-value funded projects will be an added advantage Preferred Qualifications: Ph.D. in relevant streams with good academic records Areas of Specialization: Physical Chemistry Analytical Chemistry Organic and Medicinal Chemistry Inorganic and Materials Chemistry Responsibilities: Academics: Classroom presentation Laboratory Instructions Development Learning of Resource Materials & Laboratory Development Student Assessment & Evaluation including Examination work of University. Participation in Co-curricular & extracurricular activities Student s guidance, counseling & helping in their personal, ethical, moral, and overall character development Keeping abreast of new knowledge and skills, help to generate new knowledge and help dissemination of such knowledge through books, publications, seminars, handouts, etc Continuing Education Activities Self-development through upgrading qualifications, Experience & Professional activities Research Consultancy: Research development activities & Research guidance Industry sponsored projects Providing consultancy and testing services Promotion of industry-institution interaction and R & D Academic / Administration: Academic and Administrative management of the institution Policy planning, monitoring & evaluation, and promotional activities; both at the department level and institution level Design and development of a new programme. Preparing projects for funding in areas of R&D work, laboratory development, modernization, expansion, etc Administration both at departmental & institutional levels Development, administration, and management at Institutional levels Monitoring and evaluation of academic and research activities Participation in policy planning at the Regional / National level for the Development of Technical Education Helping mobilization of resources for the Institution Develop, update and maintain MIS Plan and implement Staff Development activities, conduct Performance Appraisal Maintain Accountability Extension / Industrial Connectivity Interaction with Industry and Society Participation in Community services Providing R&D support and consultancy services to Industry and other user agencies Providing non-formal modes of education for the benefit of the Community Promotion of Entrepreneurship and Job rotation Dissemination of knowledge Providing Technical support in areas of social relevance Apart from the above duties, any other relevant work is assigned by the Dean of the respective schools

As a Medicinal Chemist, you will be instrumental in the development, synthesis, and enhancement of innovative drug candidates. Your role will call for a blend of scientific proficiency, analytical thinking, and practical laboratory experience to lead drug discovery projects from initial identification to advanced optimization and preclinical phases. Working in close collaboration with diverse teams, you will contribute towards the creation of cutting-edge therapeutics to meet the gaps in medical treatment. Your primary responsibilities will include: - Designing and synthesizing novel small molecules aimed at specific disease targets. - Strategizing and executing pioneering methodologies in drug discovery autonomously or in partnership. - Leveraging Structure-Activity Relationships (SAR) and Structure-Property Relationships (SPR) to refine efficacy, specificity, and pharmacokinetic characteristics. - Engaging with computational chemists, biologists, and pharmacologists to prioritize new chemical entities for synthesis and evaluation. - Conducting comprehensive literature assessments to adopt novel synthetic strategies and technologies. - Participating in the development of patent applications, technical documents, and scientific publications. - Employing computational models to anticipate the performance of new drugs and facilitate the design of fresh compounds. - Keeping abreast of evolving trends in AI-driven drug discovery and advancements in medicinal chemistry. To qualify for this role, you should possess: - A Ph.D. in Organic Chemistry or a related discipline. - Extensive industry experience spanning 10-13 years within Life Sciences, R&D, CRO, biotech, or pharmaceutical sectors. - Profound expertise in synthetic organic chemistry, medicinal chemistry, and chemical biology. - Proficiency in contemporary synthetic techniques, purification methodologies, and analytical tools such as NMR, LC-MS, and HPLC. - Demonstrated achievements in lead optimization and preclinical drug discovery. - Familiarity with pharmaceutical industry standards and regulatory landscapes. - Knowledge of AI-driven drug discovery techniques would be advantageous. - Exceptional problem-solving abilities, scientific ingenuity, and a fervor for innovation. - Strong communication and teamwork skills to thrive in a multidisciplinary environment.,

Role Requirements: Ph.D. degree and or post-Doctoral research with a minimum of 3 years of CRO experience with excellent communication skills is preferred. The candidate should manage a team of 7-12 FTEs and capable of designing scheme, troubleshoot, problem solve independently, and execute high-profile project. The person should be flexible working shifts as per the organizational policy. The candidate should be excellent in cross functional teamwork and excellent in customer engagement. Technical/functional Skills: The candidate should have excellent knowledge of modern synthetic methodology including asymmetric synthesis, heterocyclic chemistry, catalysis and the reaction mechanism is expected. Should be expert in synthetic problem solving/troubleshooting skills. Excellent communication skills including face to face and virtual interactions with team and clients. Must have exceptional Presentation skills. The candidate should maintain an accurate scientific notebook, draft concise written reports for publications. Managerial Skills: Expertise in handling multiple collaborations. Demonstrated in handling a team size of 7-12 FTEs Worked effectively with interdisciplinary teams. Efficient Lab management skills The Leader must demonstrate the essential qualities of People Management. Giving & receiving performance-enhancing feedback Setting clear performance expectations Conducting challenging performance conversations Coaching individuals toward improved performance Delegating tasks Creating accountability Lead the change

Preferred candidate profile: PhD (Organic chemistry / Medicinal chemistry) with 5 -6 years of experience in antibody drug conjugates (ADC) development Roles & Responsibilities: Must have hands on experience in linker- payload synthesis and overall understanding of ADC. Should be able to design and execute synthesis of complex drug linkers and ADC payloads. Should have proficiency in characterization and analysis of synthesized molecules using analytical techniques such as HPLC, LC-MS and NMR. Thorough understanding of linker chemistry and latest development in the space. Efficient employment of structure-based drug design principles and integrate with other experimental data collected in the design of new linkers. Mentor and manage team members for high performance and scientific growth. Collaborate with project team members and communicate progress against goals in a multidisciplinary setting: chemistry, antibody engineering, biology, pharmacology, DMPK, and external collaborators. Accurate documentation of experiment and maintaining a well-organized laboratory notebook (LNB). Understanding of systems and process related to safety, health, and environment (SHE).

Job Role: Discovery Chemistry Scientist Job location: Bangalore Job grade: 7-II/6-I 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 Key Responsibilities: Supervise the subordinates for timely completion of assigned projects. Responsible for periodic reports updating to both internal and external clients Ensure the optimum resource utilization and cost efficiency Responsible for project planning and execution Ensure the implementation of regulatory compliances Troubleshoot the problem areas of project(s) Responsible for clear individual derivable Possess the knowledge and exposure to environment, health, and safety (EHS) practices Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety Attend training on environment, health, and safety (EHS) measures imparted company Behavioral Skills: Strong commitment to exceptional customer experience, and a high level of dedication Excellent speaking-listening-writing skills, attention to details, proactive self-starter Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Exceptional influencing and leadership skills. Enthusiasm, motivation, and persuasive ability in a team and cross-functional environment. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience: 2-8 years Education: Ph. D in organic chemistry / Medicinal chemistry from reputed universities in India / abroad. Skills and Capabilities: Candidate should have a experience in drug discovery from pharmaceutical or biotech industry. Excellent understanding of the concepts of drug discovery, preferably having prior experience of progressing a project from hit identification to lead optimization. Has prior experience working with a cross-functional team, comprising assay biologists, Structural biologists, DMPK scientists, computational chemists, and safety pharmacologists. Familiarity with molecular modelling concepts and tools is desirable. Strong knowledge of data analysis (SAR/SPR) and informatics tools. Familiarity with cGMP and regulatory knowledge. Strong Client communication and presentation skills. Extensive knowledge and experience in synthesis planning, synthetic methods and use of modern chromatographic and analytical tools. Behavioral / Managerial skills: Proven ability to lead and motivate the teams. Excellent written and verbal communication skills. A team player / works well in multi-discipline teams Builds strong plans to provide clarity for others, and utilizes time management tools and capabilities. Equal Opportunity Employer: It s 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.

Prolim is seeking an Application Engineer, Advanced, in the field of computational chemistry and multiscale modeling. You are an enthusiastic team player with a computational background in biology, chemistry, or physics. As part of Simcenter CULGIs dynamic and multidisciplinary team, you will support the customer to achieve their objectives. You will be responsible for the day-to-day execution of individual projects, executing simulation tasks ensuring quality results, reporting on their progress, and delivering successful and valuable solutions to the customer. You will interact with the customer to support the management of their expectations. Responsibilities Interfaces with customers during the execution of the projects Provides information to the development team to improve our software solutions Writes/updates scripts to support and enhance the creation of simulation tasks Proactively communicates the status on all projects Apply appropriate tools to analyze, identify, and resolve technical problems Required Knowledge/Skills, Education, and Experience A B.Tech Biotechnology/Chemistry , MSc Biotechnology /Chemistry / Ph.D. degree in computational science in either biology or chemistry Ability to work on multiple projects simultaneously Ability to communicate complex technical concepts clearly and effectively Problem-solving and reasoning skills Excellent written, verbal, and interpersonal communication skills Preferred Knowledge/Skills, Education, and Experience Previous role as RD engineer is a plus Commercial or professional industrial experience is a plus. Having experience in multiscale modeling and/or computational chemistry is a plus

About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and optimize Route of Synthesis (RoS) for novel medicinal drugs. Synthesize and purify medicinal compounds using advanced laboratory techniques. Conduct laboratory experiments to test the efficacy and safety of synthesized compounds. Analyse data from various analytical techniques to assess compound quality and properties. Improve the physicochemical properties of existing drugs to enhance performance and stability. Collaborate with other scientists and departments to advance drug development projects. Follow strict health and safety guidelines to ensure a safe working environment. Review and interpret the structure and purity of chemical compounds using modern analytical tools. Knowledge & Experience Bachelors in Medicinal Chemistry with Masters in Medicinal Chemistry, Organic Chemistry, or a related field. With M.Sc. (2 to 4 years of Experience) At least 2 years of hands-on experience in chemical synthesis within a pharmaceutical or biotech setting. Proficiency in modern synthetic techniques and analytical methods (e.g., NMR, HPLC, MS). strong problem-solving skills and the ability to design efficient synthetic routes. Excellent laboratory skills, including safe handling of chemicals and operation of laboratory equipment. Ability to work collaboratively in a team-oriented environment. Excellent written and verbal communication skills. Detail-oriented with strong organizational skills. Commitment to continuous learning and staying current with scientific advancements. Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans .

Qualification B.Pharm and M.Pharm with at least 55% or equivalent grade with NET/SLET/PhD Eligibility Criteria Assistant Professor : Fresher or 2 years of Teaching experience Associate Professor : Minimum of 8 years of Teaching with at least 5 years at the Assistant Professor level. Minimum 7 Research publication Guided students for research projects Professor : At least 10 years of Teaching with at least 5 years at the Associate Professor level. Minimum 10 Research publication Leadership roles in academic or research institutions Roles and Responsibility 1 ) Provide case studies, group discussions, laboratory experiments, pharmaceutical formulations, practical exercises, and field visits to create an engaging learning experience for students. 2) Publish research papers in national and international pharmacy journals, and present findings at pharmaceutical conferences and seminars. 3) Teach a variety of pharmacy subjects such as Pharmacology, Pharmaceutical Chemistry, Medicinal Chemistry, Clinical Pharmacy, Pharmaceutical Analysis and Pharmacognosy. 4) Participate in departmental meetings, curriculum review processes, and assist with the development of new programs or courses in the pharmacy department. 5) Serve on university or faculty-level committees for academic and administrative purposes, including research committees, examination boards, or curriculum committees within the pharmacy department. Skills Guiding and Advising Learners Participatory Instructional Methods Evaluation and Constructive Guidance Optimal Time Management and Scheduling Research Approaches and Techniques

Advanced Synthetic Strategy Development : Lead the design and implementation of complex multi-step synthetic routes, including the development of innovative methodologies for challenging organic transformations. Utilize critical thinking and advanced technical and analytical skills to independently address and resolve complex challenges in synthetic chemistry and assay development. Propose and implement innovative research strategies, actively contributing to scientific publications, patents, and presentations at conferences. Ensure meticulous documentation of experimental procedures and results, preparing detailed reports that contribute to knowledge sharing within the organization and compliance with regulatory standards. Identify opportunities for operational efficiency and process improvements within the lab, leading initiatives that enhance research productivity and effectiveness. Adherence to safety regulations, quality assurance, and environmental standards, leading efforts to maintain a safe and compliant laboratory environment. Team Leadership and Development : Mentor and train team members, fostering a collaborative environment while ensuring the team meets productivity targets and maintains high-quality standards in research outputs. Work effectively with other departments (such as ADL, QA, EHS, SCM) to align research efforts with organizational goals, driving synergistic outcomes across projects. Comprehensive Project Management : Act as a primary point of contact for clients, managing communications, providing technical expertise, and ensuring the delivery of project milestones and quality results. Oversee and coordinate multiple research projects, ensuring timely delivery and alignment with strategic objectives while collaborating closely with cross-functional teams. Qualifications PhD/Post Doc. in Organic Chemistry /Medicinal Chemistry

" Jubilant Biosys is looking for Research Associate - Discovery Chemistry - Bengaluru location Experience: 3-5 Years Qualification: M.Sc. (Organic/ General/ Industrial Chemistry) M. Pharm (Medicinal Chemistry ) Design and plan synthetic routes for target molecules. Execute multi-step organic synthesis reactions, handling milligram to gram scale reactions. Characterize organic compounds using spectroscopic and related techniques. Perform literature searches using scientific databases (e.g., SciFinder). Solve synthetic challenges and troubleshoot issues. Maintain accurate records, including electronic laboratory notebooks (eLNB) and data integrity. ",

Job Description: We are seeking a highly motivated and skilled Medicinal Chemist with the industrial experience of 2 to 5 years to join our dynamic research and development team in Bengaluru. The candidate will be responsible for the design, synthesis, and characterization of novel chemical entities (NCEs) in accordance with client specifications and internal guidelines, contributing significantly to our drug discovery programs. Key Responsibilities: Synthesize and characterize novel NCEs efficiently and independently, adhering to client specifications. Apply broad knowledge of modern organic chemistry and synthetic methodologies to complex chemical problems. Execute various synthetic reactions, including but not limited to: heterocyclic chemistry, metal-catalyzed reactions, air/moisture-sensitive reactions, and hydrogenations, carrying out multi-step synthesis as required. Utilize a wide range of techniques for synthesis and purification, including chromatographic methods (e.g., MPLC, HPLC). Perform spectroscopic characterization of novel compounds using techniques such as NMR, LCMS, HPLC, and IR. Maintain accurate and up-to-date Lab Note Books in accordance with client specifications and internal guidelines. Generate final reports and other scientific documents as needed. Demonstrate a strong understanding of systems and processes pertaining to safety, health, and environmental regulations. Strictly adhere to EHS (Environmental, Health, and Safety) guidelines, maintaining a zero-tolerance policy for non-compliance. Required Candidate Profile: Education: M.Sc. in Organic Chemistry or Chemistry. Experience: 2 to 5 years of experience in Synthetic Chemistry (Small Scale). Interview Details (Walk-in Drive): Date: 5 th July'25 Time: 9:00 AM to 3:00 PM Interview Venues: Bengaluru: Aurigene Pharmaceutical Services Ltd. 39-40 Hosur Road KIADB Industrial Area, Phase 2, Electronic City, Bengaluru, Karnataka 560100 Hyderabad: Aurigene Pharmaceutical Services Ltd. Bollarum Road, Jaya Prakash Narayan Nagar, Miyapur, Telangana 500049, India Mandatory Documents to Carry for Interview: Your latest resume. Last three months' salary slips. Salary revision letter (if applicable). 3 Passport-size photographs. Note: The final job posting location will be Bengaluru, regardless of the interview location.

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 Job Purpose: Responsible for handling large groups for Synthetic Chemistry projects catering to multiple clients. Key Responsibilities: Scientific Responsibilities: Overall understanding of the project / projects. Designing feasible synthetic routes for the targets. Proactively identify and escalate potential issues Maintain contingency plans and rapidly resolve the problems as they arise, if required, in consultation with the stakeholders. Discussion of project progress with the client through teleconferences/video conferences as per requirement Providing periodical reports on a need basis and submitting a comprehensive final report upon completion of the project. Responsible for the overall development of the reporting team leaders. Administrative Responsibilities: Project & resource management monitor day-to-day progress and ensure deadlines are met. Interface with the business development team. Partner with global customers and internal teams to ensure a coordinated approach from project initiation through to successful close out. Responsible for overall maintenance of system, infrastructure / instruments in the lab Educational Qualification: Ph. D. /PDF in Organic /Medicinal Chemistry or relevant field. M. Sc. in Organic/Medicinal Chemistry Technical / functional Skills: Possess a very high scientific capability. Knowledge of route scouting. Expert in synthetic organic chemistry from small scale to medium scale. Sound knowledge of Process safety and hazard evaluation. Excellent cGMP and regulatory knowledge. Strong knowledge of Data analysis software. Strong Client communication skills. Cross-departmental interaction. Experience: Minimum 0-1years of experience for Ph. D. / Minimum 12 years for M. Sc. Behavioral Skills: Sound interpersonal skills. Good Team skills Time Management skills Strong system thinking and trouble shooting ability. Sound leadership Equal Opportunity Employer:

" Jubilant Biosys is looking for Senior Research Associate - Discovery Chemistry - Bengaluru location Experience: 5-7Years Qualification: M.Sc. (Organic/ General/ Industrial Chemistry) M. Pharm (Medicinal Chemistry ) Design and plan synthetic routes for target molecules. Execute multi-step organic synthesis reactions, handling milligram to gram scale reactions. Characterize organic compounds using spectroscopic and related techniques. Perform literature searches using scientific databases (e.g., SciFinder). Solve synthetic challenges and troubleshoot issues. Maintain accurate records, including electronic laboratory notebooks (eLNB) and data integrity. ",

" Jubilant Biosys is looking for Research Associate - Discovery Chemistry - Bengaluru location Experience: 1-3Years Qualification: M.Sc. (Organic/ General/ Industrial Chemistry) M. Pharm (Medicinal Chemistry ) Design and plan synthetic routes for target molecules. Execute multi-step organic synthesis reactions, handling milligram to gram scale reactions. Characterize organic compounds using spectroscopic and related techniques. Perform literature searches using scientific databases (e.g., SciFinder). Solve synthetic challenges and troubleshoot issues. Maintain accurate records, including electronic laboratory notebooks (eLNB) and data integrity. ",