analytical scientist injectable Jobs in Hyderabad

analytical scientist injectable

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formulation development scientist

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principal scientist 2 - preclinical safety Jobs in Hyderabad

principal scientist 2 - preclinical safety

principal scientist | t-cell immunology Jobs in Hyderabad

principal scientist | t-cell immunology

principal scientist 2 preclinical safety

Novartis India

<div>
 
 Summary
 
 
 
 The Preclinical Safety (PCS) department within the Novartis Biomedical Research - Translational Medicine Unit provides non-clinical safety strategy of products in -discovery, -development and -market, globally, with state-of-the-art regulatory compliance.
 
 
 As a Principal Scientist-2, you will join our PCS team in India to discuss strategies and deliver non-clinical safety deliverables for the products you are globally responsible for. This role also involves development and review of nonclinical scientific submission components (eCTD module 2.4 and 2.6) and other lifecycle management regulatory documents for multiple projects.
 
 
 
 About The Role
 
 
 
 Key Responsibilities
 
 :
 
 
 
 <ul>
 <li>
 Strategy and delivery of PCS deliverables for products under development and in-market.
 </li>
 <li>
 Independently provide PCS inputs in PSURs, DSURs, annual reports, registrations, renewals and label updates for the delegated products.Addresses regulatory queries on delegated products.
 </li>
 <li>
 Conducts literature searches and analyzes relevant non-clinical safety data and decide benefit-risk of new nonclinical information in collaboration with patient safety experts.
 </li>
 <li>
 Contribute to the objectives and deliverables of (Global Project Team) in cross-functional collaboration with other GPT representatives.
 </li>
 <li>
 Evaluates the toxicological profiles of impurities, degradants and assess the specification limits based on ICH guidelines.
 </li>
 <li>
 Provides to nonclinical scientific writing support fo regulatory submission documents such as, IB, IND/CTA, NDA/BLA/MAA and Health Authority briefing books.
 </li>
 <li>
 Organizes nonclinical scientific activities and timelines in collaboration with authors for planned submission to meet strategic objectives of nonclinical submission deliverables.
 </li>
 <li>
 Develop expertise in internal Document management system to facilitate timely completion of projects and meet compliance requirement.
 </li>
 <li>
 Act as a nonclinical scientific liaison to Submissions &amp; Documentation (S&amp;D) vendor supporting nonclinical submission document management.
 </li>
 <li>
 Ensure that all the activities and deliverables are compliant with Novartis animal welfare policies, in-house standard operating procedures, Novartis expert recommendations (where feasible) and all relevant international regulatory guidelines/regulations.
 </li>
 <li>
 Be a team player and support local implementation of Preclinical safety strategies and independently contribute to multidisciplinary project/program goals within the Preclinical safety team. Communication skill is critical to this role in forming strong working relationships with team members and across functional disciplines.
 
 
 </li>
 </ul>
 
 Essential Requirements
 
 
 
 <ul>
 <li>
 PhD in life sciences with 6+ years experiences in drug discovery, drug development and/or life cycle management studies with an exceptional understanding of nonclinical submission writing
 </li>
 <li>
 In-depth knowledge of toxicology and preclinical safety assessment, understanding of drug metabolism and pharmacokinetics / pharmacodynamics, experience working in project teams, and knowledge of drug development and regulatory environment
 </li>
 <li>
 Understanding of GLP principles in nonclinical studies and submission writing.
 </li>
 <li>
 Proficient with full range of techniques used in job and core areas. Working knowledge of tools and processes used in drug design and development.
 </li>
 <li>
 Extensive library research skills and knowledge of problems-solving techniques; publication and presentation experience preferred.
 </li>
 <li>
 Excellent communicators, strong team players and have a high level of logistical/planning ability.Strong written and verbal capabilities in English preferred.
 </li>
 <li>
 Registration and certification with one of the International Toxicology registers.
 
 
 </li>
 </ul>
 
 Desirable Requirement
 
 
 
 <ul>
 <li>
 Animal Models ,Communication Skills, Data Analysis.
 </li>
 <li>
 Ethics ,Laboratory, Problem Solving.
 </li>
 <li>
 Regulatory Compliance.
 </li>
 <li>
 Research.
 </li>
 <li>
 Risk Assessment.
 </li>
 <li>
 Toxicology.
 
 
 </li>
 </ul>
 Commitment to Diversity &amp; Inclusion: :
 
 
 
 We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
 
 
 
 Why Novartis: Our purpose is to reimagine medicine to improve and extend people&rsquo;s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our
 
 
 people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture
 
 
 You&rsquo;ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards
 
 
 
 Commitment To Diversity And Inclusion
 
 
 
 Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
 
 
 Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network.
 
 
 
 Why Novartis:
 
 Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
 
 
 
 Benefits and Rewards:
 
 Read our handbook to learn about all the ways we&rsquo;ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
</div>

Principal Scientist 2 - Preclinical Safety

PI Health Sciences Ltd

<div>
 
 
 
 Role - Research Scientist - In Vitro ADME
 
 
 
 
 
 
 
 
 Educational Qualifications
 
 
 <ul>
 <li>
 Master&rsquo;s degree in pharmacology, Biochemistry, Pharmaceutical Sciences, or related discipline.
 </li>
 <li>
 5&ndash;7 years of direct experience in an in-vitro ADME laboratory (pharma/biotech/CRO).
 </li>
 </ul>
 
 
 
 
 
 
 Purpose:
 
 
 
 
 To generate high-quality, reproducible in-vitro ADME data that supports medicinal chemistry and discovery biology teams in optimizing molecular properties. The role ensures robust ADME assay execution, scientific interpretation, innovation in assay methodologies, and effective cross-functional collaboration to accelerate hit-to-lead and lead optimization programs.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 
 
 A. Strategic Responsibilities
 
 
 <ul>
 <li>
 Provide strategic ADME insights to Medicinal Chemistry and Biology for compound prioritization.
 </li>
 <li>
 Influence project direction by interpreting trends in clearance, permeability, solubility, DDI risk, and transporter interactions.
 </li>
 <li>
 Contribute to defining the ADME package for hit-to-lead, lead optimization, and early preclinical milestones.
 </li>
 <li>
 Identify and introduce emerging ADME assay technologies, automation opportunities, and predictive tools (e.g., IVIVE, ADMET modelling).
 </li>
 <li>
 Support long-term capability building of the DMPK platform.
 </li>
 </ul>
 
 
 
 
 
 B. Operational Responsibilities
 
 
 <ul>
 <li>
 Independently design, execute, and troubleshoot in-vitro ADME assays such as metabolic stability, plasma stability, protein binding, CYP inhibition/induction, phenotyping, PAMPA, Caco-2, MDCK, transporter assays, solubility, and DDI workflows.
 </li>
 <li>
 Analyse and interpret LC-MS/MS data to calculate intrinsic clearance, permeability coefficients, efflux ratios, enzyme contributions, and stability parameters.
 </li>
 <li>
 Maintain meticulous documentation through ELNs, assay worksheets, and technical reports.
 </li>
 <li>
 Coordinate with cross-functional teams for sample management, study timelines, and data delivery.
 </li>
 <li>
 Maintain lab infrastructure including LC-MS/MS, automation systems (TECAN), incubators, and cell culture platforms.
 </li>
 <li>
 Support assay validation, SOP drafting, and continuous improvement initiatives.
 </li>
 </ul>
 
 
 
 
 
 C. Financial Responsibilities
 
 
 <ul>
 <li>
 Optimize usage of consumables, enzymes, reagents, plates, and solvents to minimize assay costs.
 </li>
 <li>
 Ensure efficient LC-MS/MS run scheduling to maximize instrument throughput and reduce operational overheads.
 </li>
 <li>
 Contribute to budgeting for ADME assays, method development projects, and instrument maintenance needs.
 </li>
 <li>
 Avoid repeat experiments through strong assay robustness and error-free execution.
 </li>
 </ul>
 
 
 
 
 
 D. People Responsibilities
 
 
 <ul>
 <li>
 Mentor junior team members on ADME assay execution, data analysis, and instrument handling.
 </li>
 <li>
 Foster a culture of scientific rigor, collaboration, and knowledge sharing across the discovery teams.
 </li>
 <li>
 Provide training on new assays, safety practices, LC-MS/MS operations, and automation tools.
 </li>
 <li>
 Demonstrate collaboration with Medicinal Chemistry, Biology, and PK/PD teams by ensuring timely delivery of ADME insights.
 </li>
 </ul>
 
 
 
 
 
 E. Risk &amp; Compliance Responsibilities
 
 
 <ul>
 <li>
 Ensure adherence to internal SOPs, quality standards, and audit requirements.
 </li>
 <li>
 Follow all safety guidelines related to chemical handling, biohazards, waste disposal, and lab operations.
 </li>
 <li>
 Conduct periodic instrument checks, calibration, and preventive maintenance to avoid operational risks.
 </li>
 <li>
 Maintain strict data integrity (ALCOA+), traceability, and documentation discipline.
 </li>
 <li>
 Flag scientific, operational, or compliance risks (e.g., assay drift, QC failures) proactively.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 3. Behavioural Competencies
 
 
 
 (Aligned with PI Industries / PIHS leadership attributes&mdash;Curious, Creative, Courageous, Caring)
 
 
 
 1. Scientific Curiosity
 
 
 <ul>
 <li>
 Continuously explores new techniques, ADME tools, predictive modelling, and literature.
 </li>
 </ul>
 
 
 2. Collaboration &amp; Cross-Functional Partnership
 
 
 <ul>
 <li>
 Works seamlessly with Chemistry, Biology, Toxicology, and PK/PD teams.
 </li>
 <li>
 Communicates data clearly, proactively, and purposefully.
 </li>
 </ul>
 
 
 3. Problem-Solving &amp; Analytical Thinking
 
 
 <ul>
 <li>
 Identifies root causes in assay performance issues and proposes smart solutions.
 </li>
 </ul>
 
 
 4. Planning &amp; Execution Discipline
 
 
 <ul>
 <li>
 Delivers consistent, high-quality data within agreed timelines.
 </li>
 <li>
 Manages workload in a fast-paced discovery environment.
 </li>
 </ul>
 
 
 5. Ownership &amp; Accountability
 
 
 <ul>
 <li>
 Takes responsibility for experiment design, execution, reporting, and data integrity.
 </li>
 </ul>
 
 
 6. Innovation Orientation
 
 
 <ul>
 <li>
 Suggests process improvements, new assays, automation enhancements, and efficiency tools.
 </li>
 </ul>
 
 
 7. Compliance Mindset
 
 
 <ul>
 <li>
 Adheres to SOPs, safety standards, documentation rules, and audit expectations.
 </li>
 </ul>
 
 
</div>

Pharmacologist

Microsoft

<div>
 
 Overview
 
 
 
 We are seeking a passionate and technically skilled Data Scientist II to join the Commerce &ndash; Platforms, Data, and Experiences (PDX) team. This team plays a pivotal role in shaping Microsoft&rsquo;s commerce data strategy, building scalable data platforms, and delivering actionable ML driven insights that drive business transformation across the ecosystem.
 
 
 As a Data Scientist II in PDX, you will work at the intersection of data engineering, data processing, and machine learning to solve complex business problems. You will collaborate with cross-functional teams to design experiments, build predictive models, and develop scalable solutions that enhance decision-making and customer experiences by producing descriptive, diagnostic, predictive and prescriptive insights.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Design and implement advanced analytics solutions to support commerce data platform initiatives including analytics based on Machine Learning Models.
 </li>
 <li>
 Partner with engineering and product teams to define data requirements and ensure high-quality data pipelines.
 </li>
 <li>
 Conduct exploratory data analysis, feature engineering, and model evaluation using structured and unstructured datasets.
 </li>
 <li>
 Ensure the models built are operable, scalable, extensible and performant.
 </li>
 <li>
 Develop dashboards, visualizations, and storytelling artifacts to communicate insights to stakeholders.
 </li>
 <li>
 Lead experimentation efforts to evaluate new features, forecasting, data quality and anomaly detection systems.
 </li>
 <li>
 Build extensible solutions on LLM models to improve productivity of engineers across the commerce organization.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s or Master&rsquo;s degree in Computer Science, Statistics, Mathematics, or related field.
 </li>
 <li>
 2+ years of experience in data science, analytics, or applied machine learning.
 </li>
 <li>
 Proficiency in Python, SQL, and ML frameworks (e.g., Scikit-learn, TensorFlow, PyTorch).
 </li>
 <li>
 Experience with cloud platforms (Azure preferred) and big data technologies.
 </li>
 <li>
 Strong understanding of statistical modeling, predictive analytics, and experimentation design.
 </li>
 <li>
 Excellent communication and stakeholder management skills.
 </li>
 <li>
 Demonstrated experience leveraging AI tools and technologies to enhance engineering effectiveness, coupled with a strong curiosity and commitment to continuous learning in the field of Artificial Intelligence.
 
 
 </li>
 </ul>
 This position will be open for a minimum of 5 days, with applications accepted on an ongoing basis until the position is filled.
 
 
 Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance with religious accommodations and/or a reasonable accommodation due to a disability during the application process, read more about
 
 requesting accommodations.
 
</div>

Data Science Engineer

US Pharmacopeia

<div>
 
 Description
 
 
 
 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&mdash;regardless of background&mdash;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
 
 
 
 This is a professional, highly technical, non-supervisory position that supports the food ingredients program unit team (PUT) within USP&rsquo;s Global Science and Standards Division (GSSD). The incumbent reports to a local management position at the India site as well as functionally reporting to a management position in the Foods PUT in the US. The incumbent will support the development and technical stewardship of Food Chemicals Codex (FCC) standards, other scientific products, outreach and awareness (in India, US, and internationally), and internal strategic initiatives. These activities require the ability to identify and critically evaluate published information on chemical analysis of food ingredients, regulatory and safety reviews of foods, and data and supplier documents to support development of standards and guidance documents. The successful candidate may develop proposals, coordinate, and lead specific technical studies related to food analysis. The incumbent may present technical talks to academics, the food industry, and regulators to advocate for the work of the program, to solicit feedback, and to support program goals related to awareness and capacity building. The incumbent will work collaboratively with industry stakeholders, the Food Ingredients Expert Committee, the PUT, and other USP program units and departments.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 
 The Sr. Scientist I/II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Provide scientific expertise to USP&rsquo;s Foods PUT with a focus on identifying, developing, and supporting food standards and other fit-for-purpose solutions.
 </li>
 <li>
 Perform critical evaluation of technical data related to food quality and purity including working closely with internal and external laboratories on analytical method development, validation, and data analysis.
 </li>
 <li>
 Works with USP staff, the USP Food Ingredient Expert Committee (FI EC), subcommittees (SC), and Expert panels (EP), external stakeholders as related to Food Ingredient monograph and RS development.
 </li>
 <li>
 Supports in the preparation of data packages and briefing materials to present to the FI EC and other expert bodies; manages projects appropriately and ensures impeccable work-product delivery.
 </li>
 <li>
 Foster collaboration and communication with other USP program units and departments,
 </li>
 <li>
 Keep abreast of global trends and developments in related scientific fields and share learnings with managers and colleagues.
 </li>
 <li>
 Communicate effectively with stakeholders from industry, academia, scientific organizations, and regulatory agencies.
 </li>
 <li>
 Assist and guide Expert Committees and related expert bodies to support the development of FCC standards and other program products.
 </li>
 <li>
 Performs other related duties in support of the Foods Program Unit as assigned.
 
 
 </li>
 </ul>
 
 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
 
 
 <ul>
 <li>
 Senior Scientist I: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 7-10 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 11-13 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted.
 </li>
 <li>
 Senior Scientist II: Ph.D. in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 10-13 years or MS in Food Science, Food Chemistry, Food Technology, Analytical Chemistry or allied field and 13-15 years, respectively, of relevant experience. An equivalent combination of experience and education may be substituted
 </li>
 <li>
 Candidates must have experience related to food safety, food quality, or analytical chemistry as well as outstanding written and verbal communication skills in English.
 </li>
 <li>
 Ability to review, analyze, and interpret and report on data from various analytical tests such as from HPLC, GC, LC/MS, GC/MS, IR, Raman, UV-Vis, NMR, ICP-MS, AA, etc.
 </li>
 <li>
 Experience in developing, validating, using, or evaluating food analytical methods
 </li>
 <li>
 Ability to communicate effectively and diplomatically with technical and non-technical stakeholders
 </li>
 <li>
 Experience in working directly in or with the food industry, such as experience with food quality systems, regulatory affairs, and supply chain management
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Ability to manage and prioritize multiple concurrent, complex projects with minimal direction and a history of successful timely project management
 </li>
 <li>
 Experience applying food regulations from local or international regulatory bodies, and collaborating with scientific standards organizations is a plus
 </li>
 <li>
 Ability to rapidly and expertly assess complex technical issues in a fast-paced environment
 </li>
 <li>
 Ability to embrace change. Adaptable, willing to learn, strong interpersonal and technical presentation skills; strong knowledge of MS Office and related products.
 </li>
 <li>
 Ability to operate independently where appropriate, yet understands when to escalate issues and how to establish effective working relationships
 </li>
 <li>
 Ability to work well with diverse employees and customers in a cooperative and friendly manner
 </li>
 <li>
 Able work flexible hours when needed
 
 
 </li>
 </ul>
 
 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.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Senior Scientist I /Senior Scientist II, Documentary Standards ( Foods)

Tredence Inc.

<div>
 
 
 About the Company
 
 
 
 
 
 
 Tredence focuses on last-mile delivery of powerful insights into profitable actions by uniting its strengths in business analytics, data science and software engineering. The largest companies across industries are engaging with us and deploying their prediction and optimization solutions at scale. Head quartered in the San Francisco Bay Area, we serve clients in the US, Canada, Europe, and South East Asia.
 
 
 We are seeking an experienced data scientist who apart from the required mathematical and statistical expertise also possesses the natural curiosity and creative mind to ask questions, connect the dots, and uncover opportunities that lie hidden with the ultimate goal of realizing the data&rsquo;s full potential.
 
 
 
 
 
 
 About the Role
 
 
 
 
 
 <ol>
 <li>
 Strong in Agile, architecture reviews, CI/CD, and DevOps processes.
 </li>
 <li>
 9 to 14 yrs years of experience leading software delivery teams across Java, React, and GenAI domains.
 </li>
 </ol>
 
 
 
 
 
 Responsibilities
 
 
 
 
 
 <ul>
 <li>
 Proven experience in project execution
 </li>
 <li>
 Stakeholder communication
 </li>
 <li>
 People management
 </li>
 <li>
 Ability to guide teams technically while driving delivery excellence and process efficiency
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 
 
 
 <ul>
 <li>
 PMP/CSM certification preferred
 </li>
 </ul>
 
 
 
 
 
 Required Skills
 
 
 
 
 
 <ul>
 <li>
 Experience in Java
 </li>
 <li>
 Experience in React
 </li>
 <li>
 Experience in GenAI domains
 </li>
 <li>
 Strong Agile skills
 </li>
 <li>
 Architecture reviews
 </li>
 <li>
 CI/CD processes
 </li>
 <li>
 DevOps processes
 </li>
 </ul>
 
 
 
 
 
 Preferred Skills
 
 
 
 
 
 <ul>
 <li>
 PMP certification
 </li>
 <li>
 CSM certification
 </li>
 </ul>
 
 
 
 
 Tredence is an equal opportunity employer. We celebrate and support diversity and are committed to creating an inclusive environment for all employees. Visit our website for more details: https://www.tredence.com/
 
 
 
</div>

Engineering Manager – JAVA

<div>
 
 Description
 
 
 
 
 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&mdash;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.
 
 
 
 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?
 
 
 
 In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.
 
 
 
 The Scientist III Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Carry out literature search related to assigned projects using various scientific data bases.
 </li>
 <li>
 Design synthetic routes for the target molecules and prepare project proposals with tentative cost estimates
 </li>
 <li>
 Procure key raw materials and reagents required for the project
 </li>
 <li>
 Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds
 </li>
 <li>
 Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems.
 </li>
 <li>
 Troubleshooting synthesis and purification issues
 </li>
 <li>
 Contributing effectively towards more challenging and complex projects through innovative methodologies
 </li>
 <li>
 Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions
 </li>
 <li>
 Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc.
 </li>
 <li>
 Produce quality materials as per customer requirement
 </li>
 <li>
 Packaging of synthesized compounds
 </li>
 <li>
 Plan, execute and complete the projects as per the timelines
 </li>
 <li>
 Document all experiments conducted as per QMS guidelines.
 </li>
 <li>
 Responsible to ensure the calibrations of the equipment as per the schedule
 </li>
 <li>
 Periodic check of the assigned equipment to ensure its working condition
 </li>
 <li>
 Work on any other assigned tasks/ lab management activities/ organizational initiatives
 </li>
 <li>
 Conversant with lab safety norms and strictly follow them.
 </li>
 <li>
 Communicate within the team and cross functional teams
 </li>
 <li>
 Learn and practice Diversity, Equity, Inclusion &amp; Belonging culture
 
 
 </li>
 </ul>
 
 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
 
 
 <ul>
 <li>
 Scientist III &ndash; Ph.D. (Full Time) in Synthetic Organic Chemistry from a reputed group with minimum 1-3 years post-doctoral/ industrial experience in API Process R&amp;D/CDMO/CRO
 
 
 </li>
 </ul>
 (Or)
 
 
 <ul>
 <li>
 M Sc (Organic Chemistry) from a reputed university with minimum 6-8 years of industrial experience in API Process R&amp;D/CDMO/CRO
 </li>
 <li>
 Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis.
 </li>
 <li>
 Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs.
 </li>
 <li>
 Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale and production.
 </li>
 <li>
 Proven ability for adoption of QMS and documentation procedure.
 </li>
 <li>
 Adherence to lab safety guidelines.
 </li>
 <li>
 Excellent troubleshooting skills in synthesis and purification of target compounds.
 </li>
 <li>
 Should possess good verbal and written communication skills.
 </li>
 <li>
 Should possess good organizational, communication, and interpersonal skills.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Extensive knowledge on wide range of organic reactions and hands on experience in handling various sensitive chemicals/reagents.
 </li>
 <li>
 Experience in flow chemistry applications in process development
 </li>
 <li>
 Track record of patents/ publications in synthetic organic chemistry/ process development.
 </li>
 <li>
 Should have exposure to GMP/GLP environment and documentation procedures.
 </li>
 <li>
 Good practical, documentation &amp; presentation skills.
 </li>
 <li>
 Attention to detail, stratregic thinking and problem-solving skills.
 </li>
 <li>
 Demonstrated ability to work both independently and as a member of a team with a passion for quality
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 No
 
 
 
 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 &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Scientist III, Synthetics Laboratory

Golden Opportunities

<div>
 
 Job Description
 
 
 
 Define, build, and lead a team of Data Scientists and Data analysts Discover areas in operations that can be automated through machine learning Demonstrate through technical knowledge on Statistical modeling, Probability and Decision theory, Operations Research techniques and other quantitative modeling techniques Understand the business reality behind large sets of data and develop meaningful solutions comprising of analytical solutions Work closely with internal stakeholders and align them with respect to your focus area Innovate by adapting new modeling techniques and procedures Implementing and operating stable, scalable data flow solutions from production systems into end-user facing applications/reports.
 
 
 
 Skills Required
 
 
 
 RoleData Scientist
 
 
 Industry TypeIT/ Computers - Software]
 
 
 Functional AreaIT-Software
 
 
 Required Education
 
 
 Employment TypeFull Time, Permanent
 
 
 Key Skills
 
 
 <ul>
 <li>
 DATA SCIENCE
 </li>
 <li>
 MACHINE LEARNING
 
 
 </li>
 </ul>
 Other Information
 
 
 Job CodeGO/JC/1384/2025
 
 
 Recruiter NameRamya V
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Data Scientist - GO/JC/1384/2025

Explore 124+ Principal scientist 2 preclinical safety in Hyderabad this December. Find roles across top companies and apply now to boost your career.