procurement manager - research & development Jobs in Hyderabad India

procurement manager - research & development

analytical scientist Jobs in Hyderabad India

analytical scientist

formulation development scientist Jobs in Hyderabad India

formulation development scientist

junior chemist (r&d-agro) Jobs in Hyderabad India

junior chemist (r&d-agro)

principal scientist - pathology Jobs in Hyderabad India

principal scientist - pathology

scientist pharmaceutical development

Sandoz India Pvt Ltd

<div>
 
 Job Description
 
 
 
 
 Your Key Responsibilities:
 
 
 
 
 Your Responsibilities Include, But Not Limited To
 
 
 
 <ul>
 <li>
 Independently plan, organize, perform and document scientific experiments /GMP testing /manufacturing plant activities under minimal supervision; handle several activities at a time
 </li>
 <li>
 -Take over responsibility for and utilize special tools /equipment or specialized facilities as an expert; schedule and perform maintenance and qualification of instruments / equipment -Proactively identify conflict situations and contribute to solutions
 </li>
 <li>
 -Work according to appropriate standards for quality, ethics, health, safety, environment protection, and information security; lead initiatives to ensure continuous improvement. Documentation of raw data, evaluate and interpret results; propose and actively support the design of next experiments.
 </li>
 <li>
 Review and verify raw data generated by others; approval of tests / experiments performed by others. Write protocols, scientific reports or lab procedures based on templates or SOPs under minimal supervision. For technical development units: Develop new methods or optimize existing methods/processes (lab or plant); contribute to development and implementation of new technologies
 </li>
 <li>
 -For GMP units: ensure compliance to cGMP -For technology-focused roles: Perform information and literature searches under minimal guidance. Actively foster knowledge exchange.
 </li>
 <li>
 Train and coach associate scientists, technicians, temporary employees and employees under training / education -For project-focused role: Participate in function-specific sub teams and fulfill assigned project tasks and responsibilities under supervision -Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.
 </li>
 <li>
 Contributes to some cost center goals and objectives -Design, plan and perform / supervise scientific experiments and contribute to project related scientific /technical activities under minimal supervision (e.g., interpret and report results, generate and evaluate data, draw relevant conclusions, optimize existing methods / processes).
 </li>
 <li>
 Establish innovative solutions for verification and control of critical quality attributes, critical material attributes or critical process parameter in cooperation with other colleagues. Establish control procedures and specifications and review test procedures. Generate scientific documents to hand over to internal and / or external partners (e.g., MST, TechOps, authorities, external companies) and support generation of international registration documents under minimal supervision.
 </li>
 <li>
 If assigned this task, maintenance of infrastructure / equipment and required investments (e.g. system ownership) -Generate lab procedures or SOP&rsquo;s, generate protocols and reports -Lead technical meetings during product development at the local level as well as on the level of SDC network -Report and present scientific /technical results internally and contribute to publications, presentations and patents.
 
 
 </li>
 </ul>
 
 Essential Requirements
 
 
 
 What you&rsquo;ll bring to the role:
 
 
 <ul>
 <li>
 M Pharm with 2-5 years' experience or PhD with 1-3 years' experience
 </li>
 <li>
 Functional Breadth.
 </li>
 <li>
 Operations Management and Execution.
 </li>
 <li>
 Collaborating across boundaries.
 
 
 </li>
 </ul>
 
 Skills
 
 
 
 <ul>
 <li>
 Environment.
 </li>
 <li>
 Experiments Design.
 </li>
 <li>
 Health And Safety (Ehs).
 </li>
 <li>
 Laboratory Equipment.
 </li>
 <li>
 Manufacturing Process.
 </li>
 <li>
 Materials Science.
 </li>
 <li>
 Process Simulation.
 </li>
 <li>
 Project Management.
 </li>
 <li>
 Sop (Standard Operating Procedure).
 </li>
 <li>
 Technical Writing.
 
 
 </li>
 </ul>
 Why Sandoz?
 
 
 Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!
 
 
 With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
 
 
 Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!
 
 
 Join us!
</div>

Scientist - Pharmaceutical Development

PI Health Sciences Ltd

<div>
 
 
 Job Title: Research Scientist / Senior Research Scientist &ndash; Process R&amp;D
 
 
 
 
 Department:
 
 R&amp;D &ndash; Process Development
 
 
 
 Industry:
 
 CDMO / API
 
 
 
 
 
 
 Purpose of the Role:
 
 
 
 To lead and execute the development, optimization, and scale-up of robust, cost-effective, and regulatory-compliant chemical processes for Active Pharmaceutical Ingredients (APIs) and intermediates, ensuring smooth technology transfer from lab to kilo lab and manufacturing.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 1. Strategic Responsibilities
 
 
 <ul>
 <li>
 Drive innovation by designing synthetic routes that align with project timelines and regulatory requirements.
 </li>
 <li>
 Contribute to technology differentiation strategies that enhance the CDMO&rsquo;s scientific credibility and client value proposition.
 </li>
 <li>
 Collaborate with cross-functional teams (Analytical, QA/QC, and Regulatory) to support integrated drug development solutions.
 </li>
 </ul>
 
 
 2. Operational Responsibilities
 
 
 <ul>
 <li>
 Perform route scouting and literature searches, and develop robust and scalable chemical processes using QbD principles.
 </li>
 <li>
 Conduct laboratory experiments for reaction optimization, impurity profiling, and process safety assessment.
 </li>
 <li>
 Prepare and review technical reports, SOPs, and technology transfer documents.
 </li>
 <li>
 Ensure compliance with GMP/GLP and EHS standards during lab-scale and pilot-scale operations.
 </li>
 <li>
 Participate in troubleshooting during scale-up or commercial production batches and provide technical support during client audits.
 </li>
 </ul>
 
 
 3. Financial Responsibilities
 
 
 <ul>
 <li>
 Optimize process economics by reducing cycle time, yield improvement, and minimizing raw material costs.
 </li>
 <li>
 Support cost estimation activities during project proposals or client RFQs by providing technical insights.
 </li>
 </ul>
 
 
 4. People &amp; Collaboration Responsibilities
 
 
 <ul>
 <li>
 Guide junior team members on experimental planning, data interpretation, and documentation best practices.
 </li>
 <li>
 Promote a culture of safety, learning, and innovation within the team.
 </li>
 <li>
 Work closely with program management and business development to align project goals with customer expectations.
 </li>
 </ul>
 
 
 
 
 
 Qualifications &amp; Experience
 
 
 <ul>
 <li>
 M.Sc. (Organic Chemistry) / PhD
 </li>
 <li>
 3&ndash;7 years of experience in Process R&amp;D, preferably in CDMO organizations
 </li>
 <li>
 Hands-on expertise in synthesis, scale-up, impurity profiling, and technology transfer
 </li>
 <li>
 Familiarity with analytical techniques (HPLC, GC, NMR) and regulatory documentation
 </li>
 </ul>
 
 
</div>

Research Scientist

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 non-supervisory role involves conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) utilizing suitable methods. The Scientist will enhance the laboratory's scientific proficiency and work ethic by offering extensive technical support and knowledge. Proficient in numerous common laboratory techniques, the Scientist is capable of providing valuable observations and insights into challenging projects. The individual in this role will furnish technical aid to the Verification Program by executing analytical tests and preparing comprehensive summary reports.
 
 
 
 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&rsquo;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.
 
 
 <ul>
 <li>
 Conducts verification projects (Dietary Supplements/Dietary Ingredients) by performing individual analytical tests such as HPLC, GC,Dissolution, ICP-MS, ICP-OES, and wet analysis as assigned by the Team Leader
 </li>
 <li>
 Completes projects within designated timelines and priorities.
 </li>
 <li>
 Demonstrates a robust scientific approach to laboratory analysis.
 </li>
 <li>
 Regularly utilizes personal experience, academic training, and technical insights, including emerging sciences, to address complex technical issues within the laboratory.
 </li>
 <li>
 Compiles project reports and responds to QA observations.
 </li>
 <li>
 Executes all testing and data analysis with precision, minimizing errors.
 </li>
 <li>
 Shows a strong commitment to continuous learning and personal development.
 </li>
 <li>
 Proposes and implements new approaches or processes to enhance laboratory operations.
 </li>
 <li>
 Influences project direction positively by aligning own work with the overall direction of laboratory projects.
 </li>
 <li>
 Assists with additional testing programs and laboratory maintenance tasks as required.
 </li>
 <li>
 Ensures compliance with Good Laboratory Practices (GLP) and safety systems in the laboratory.
 </li>
 <li>
 Maintains equipment calibration according to the schedule.
 </li>
 <li>
 Coordinates the procurement of chemicals, columns, glassware, etc., in advance, in coordination with lab operations and the purchase department, considering project deadlines.
 </li>
 <li>
 Adheres to US Pharmacopeia (USP) mission, policies, and procedures.
 </li>
 <li>
 Cultivates positive relationships with Quality Assurance (QA), Human Resources (HR), Purchase, Accounting, IT, and other departments.
 </li>
 <li>
 Participates actively in the preparation and planning for ISO-9001 &amp; ISO-17025 certification/recertification, including taking an active role in internal QA and external audits and addressing audit issues promptly.
 </li>
 <li>
 Supports Global Public Health (GPH), Reference Standard Laboratory (RSL), and other departmental teams as required for analytical testing, review, execution, and approval
 
 
 </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>
 Master&rsquo;s degree in pharmacy or Analytical chemistry.
 </li>
 <li>
 Minimum 1 to 3 years with relevant laboratory experience.
 </li>
 <li>
 Previous engagement in a high-volume pharmaceutical manufacturing QC laboratory or a contract pharmaceutical analytical testing laboratory, specifically pertaining to pharmaceutical dosage forms such as oral and liquid
 </li>
 <li>
 Strong preference for candidates with expertise in HPLC operation using Empower software, as well as proficiency in dissolution analysis
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 Proficiency in leading projects to completion with a high level of scientific expertise, including extensive knowledge of pharmaceutical testing requirements and test protocols encompassing compendial methods (USP, BP, EP, etc.). Preference for expertise in GC operation with Empower software, as well as proficiency in ICP-OES, ICP-MS and LC-MS with troubleshooting abilities. Additionally, adept in operating and troubleshooting other related analytical instrumentation (IR, KF, UV,Ion chromatography,wet analysis etc). Exceptional communication and presentation skills, both verbal and written, with a preference for candidates experienced in the pharmaceutical industry. Familiarity with ICH guidelines and FDA regulations, along with experience in compendial procedures and compliance, is highly desired. Proficiency in Electronic Laboratory Note book(ELN) is also preferred. Demonstrates a personal commitment to ensuring timely delivery of high-quality work and possesses the skills to anticipate, troubleshoot, and resolve technical challenges
 
 
 
 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 &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Scientist I, Verification Program

Novartis India

<div>
 
 Summary
 
 
 
 Plan and perform scientific experiments (or pilot plant processes) for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures in collaboration within a multifunctional project team coordinated by a Project leader. Contribute to maintenance of lab instruments/infrastructure.
 
 
 
 About The Role
 
 
 
 
 Your responsibilities include, but are not limited to:
 
 
 
 <ul>
 <li>
 Meet quality, quantity and timelines in all assigned projects; Perform and document scientific experiments; Plan &amp; organize scientific experiments under minimal guidance from more experienced team members. Seeks proactively for support and coaching from Project Leader, Scientific Expert or other team members during the whole process if necessary.
 </li>
 <li>
 Provide documentation of raw data. Evaluate and Contribute to interpretation and report results under minimal guidance from more experienced team members. Propose and provide input for the design of next experiments. Optimize existing methods (lab or plant) or contribute to new method development and reproduce published methods and develop more efficient ones.
 </li>
 <li>
 Generate lab procedures, reports and/or instructions and/or SOP&rsquo;s. Actively transfer procedures/instructions to pilot plant or production, including troubleshooting, process steering controls etc. Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team member.
 </li>
 <li>
 Keep record of and manage chemicals, intermediates, excipients and solvents within own area of responsibility.
 </li>
 <li>
 Collaborate with other team members to facilitate deliveries of DS and/or DP. Act as mentors for new joinees.
 </li>
 <li>
 Utilize special tools/equipment&rsquo;s and/or specialized facilities e.g., containment/sterile labs. Evaluate new lab equipment. Schedule and perform routine maintenance and calibration of lab instruments/equipment &amp; contribute to maintenance of infrastructure/equipment.
 </li>
 <li>
 Actively participate in project teams/meetings/networks. Actively contributes to team goals.
 </li>
 <li>
 Ensure all own activities are aligned with overall drug development process. Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC &amp; Novartis Guidelines ;Strategic and scientific contribution to Networks, target achievements according to net-work charter and annual objectives
 
 
 </li>
 </ul>
 
 What You&rsquo;ll Bring To The Role
 
 
 
 <ul>
 <li>
 PhD on technical subject with relevant experience. or Master of Science with 4+ years of relevant experience Fluency in English language.
 </li>
 <li>
 Awareness for safe handling of chemicals, potentially dangerous materials and equipment. Broad theoretical and scientific knowledge in the relevant area (e.g. manufacturing, analytical, pharmaceutical).
 </li>
 <li>
 Skilled scientist with expertise in trace level quantification of GTI/ Nitrosamines/Nitrites or similar impurities using LC-UV/FID, Ion chromatography and LCMS.
 </li>
 <li>
 Experience on dealing OOS/OOE and deviations involving above mentioned analytical techniques.
 </li>
 <li>
 Proficient with laboratory and/or technical tools. Good knowledge of software and computer tools.
 </li>
 <li>
 Good documentation skills.
 
 
 </li>
 </ul>
 
 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
 
 
 
 Join our Novartis Network:
 
 Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
 
 
 
 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>

Expert Science and Technology (Nitrosamine/Nitrite)

Dr. Reddy's Laboratories

<div>
 
 Dr. Reddy&rsquo;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&rsquo;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 &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; 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 &ndash; 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&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; 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 Analytical Specialist in Active Pharmaceutical Ingredient (API) MSc business for employing advanced analytical techniques to characterize and elucidate the structure and properties of various materials at a molecular and atomic level. You will play a crucial role in driving research and development initiatives by providing in-depth insights into complex materials through the application of cutting-edge analytical methodologies.
 
 
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 &bull; You will be responsible for working on new product development, addressing regulatory deficiency queries, and leveraging filings. Your role involves ensuring the qualification of reference/working standards, developing analytical methods, conducting validations, and transferring methods to QC.
 
 
 &bull; You will be responsible for developing and validating analytical methods, preparing method development and validation reports, and conducting online sample analysis for product development. Your role includes compiling forced degradation studies and identifying unknown impurities.
 
 
 &bull; You will compile stability data for completed projects, analyse product strategy, efficiency, and cross-functional issues in Analytical Research and Development (AR&amp;D). Your role involves visualizing developmental needs, understanding process scalability, and ensuring the procurement of necessary laboratory supplies.
 
 
 &bull; You will be responsible for maintaining lab equipment according to Good Laboratory Practices (GLP), investigating abnormal results in collaboration with group leaders, and ensuring calibration of instruments as per the schedule. Your role includes adhering to safety and environmental protocols, keeping the work area clean, and maintaining well-organized documentation.
 
 
 &bull; You will be responsible to employ advanced analytical techniques such as spectroscopy Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet- Visible Spectroscopy (UV-Vis), mass spectrometry, Gas chromatography (GC), high-performance liquid chromatography HPLC), electron microscopy transmission electron microscope (TEM) and the scanning electron microscope (SEM), X-ray diffraction, and other specialized techniques to analyse and characterize materials.
 
 
 &bull; You will be responsible for trouble shooting for products from lab development stage to plant scale up using various analytical techniques.
 
 
 &bull; You will be Supporting complex generic projects by generating knowledge of Reference listed Drug (RLD) through reverse engineering and develop strategy to prove pharmaceutical sameness.
 
 
 &bull; You will be responsible for Coaching, Mentoring and training the scientists and members of the team.
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 MS in Pharmaceutical Analysis/Post Graduation in Pharma/Physics
 
 
 
 Minimum work experience:
 
 5-10 years of experience
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 &bull; Hands on experience in Reverse Engineering of drug products
 
 
 &bull; Experience in Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet- Visible Spectroscopy (UV-Vis).
 
 
 &bull; Knowledge on Morphology Analysis, Image Analysis and Optical Microscopy.
 
 
 &bull; Understanding and experience on Gas chromatography (GC) or high-performance liquid chromatography HPLC) method development and method validations.
 
 
 &bull; Hands on experience in liquid chromatography mass spectrometry (LCMS)/ liquid chromatography-high resolution mass spectrometry (LC-HRMS)
 
 
 &bull; Experience in electron microscopy, Transmission Electron Microscope (TEM) and the Scanning Electron Microscope (SEM)
 
 
 &bull; Knowledge on competitive strategies for technology innovation and Analytical Equipment.
 
 
 &bull; Proficiency in data analysis, interpretation, and statistical tools.
 
 
 
 
 
 
 
 Behavioral Skills
 
 
 
 &bull; Excellent communication and interpersonal skills.
 
 
 &bull; Ability to work with cross functional teams.
 
 
 &bull; Strong analytical and problem-solving abilities.
 
 
 &bull; Leadership skills to motivate and mentor the team.
 
 
 
 
 
 
 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) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;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&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; 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&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;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&rsquo;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/#!/
 
 
</div>

Analytical Scientist

Azurity Pharmaceuticals

<div>
 Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company&rsquo;s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
 
 
 Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
 
 
 
 Job Responsibilities
 
 
 
 <ul>
 <li>
 Design, conduct and or supervise formulation development, process development, process optimization, scale up and manufacturing of product.
 </li>
 <li>
 Prepare and review documents such as batch records, Batch Packaging Records, Product Development reports, SOPs, Stability protocols, Raw material specifications, Packaging material specifications and In-process/ Finished product specifications, labelling and stability loading.
 </li>
 <li>
 Review of test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals.
 </li>
 <li>
 Schedule experiments and prioritize assignments to meet project objectives and deadline.
 </li>
 <li>
 Maintain laboratory equipment and follow company safety standards.
 </li>
 <li>
 Conduct laboratory experiments and prepare reports with conclusions and recommendations.
 </li>
 <li>
 Follow current laboratory procedure and develop new laboratory procedures or improvise existing procedures to meet project objectives.
 </li>
 <li>
 Identify and manage the potential risks within complex projects in a timely fashion.
 </li>
 <li>
 Record accurate and complete experimental methods and results in compliance with good documentation practices.
 </li>
 <li>
 Act as primary scientific contact to external collaborators.
 </li>
 <li>
 Check and manage inventories of supplies and raw materials.
 </li>
 <li>
 Ensure completion of all the training on time.
 
 
 </li>
 </ul>
 
 Qualifications And Education Requirements
 
 
 
 <ul>
 <li>
 M. Pharm or Ph.D. in Pharmacy with minimum industrial experience of 3 to 6years in pharmaceutical development and scale-up of products.
 </li>
 <li>
 Preferred area of expertise is oral dosage forms precisely in Modified Release/ extended release/ targeted release/immediate release solid/Suspensions/Solutions.
 </li>
 <li>
 Global Product Development Experience with markets like US/EU/China/ROW.
 </li>
 <li>
 Experience of developing branded and differentiated products &ndash; 505(b)(2) category would be preferred.
 </li>
 <li>
 Experience of working with CROs/CDMOs would be preferred.
 </li>
 <li>
 Should be well versed with Microsoft office applications.
 
 
 </li>
 </ul>
 By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.
</div>

Formulation Development Scientist

Hetero

<div>
 Job Description:
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Brand Leadership &amp; Strategic Influence:
 </li>
 <li>
 Independently lead brand and portfolio strategy development, ensuring strong positioning and differentiation in key markets.
 </li>
 <li>
 Guide and influence affiliate marketing teams and senior leadership, who in turn drive country-level planning and execution.
 </li>
 <li>
 Act as a regional brand custodian, ensuring consistent messaging and brand identity across markets.
 </li>
 <li>
 Market &amp; Competitive Intelligence:
 </li>
 <li>
 Conduct in-depth analysis of market trends, competitive landscape, and customer insights to refine brand strategies.
 </li>
 <li>
 Provide strategic recommendations to affiliates and leadership based on data-driven insights.
 </li>
 <li>
 Product Launches &amp; Lifecycle Management:
 </li>
 <li>
 Lead regional launch planning and develop strategic frameworks for new product introductions, market penetration and growth
 </li>
 <li>
 Collaborate with emerging market, regional and country regulatory, medical affairs, and sales teams to ensure in-time launch and effective go-to-market strategies.
 </li>
 <li>
 Support local affiliates in implementing best practices for product lifecycle management.
 </li>
 <li>
 Stakeholder Engagement &amp; Cross-Functional Collaboration:
 </li>
 <li>
 Act as a strategic advisor to senior leadership, providing insights on brand growth opportunities and challenges.
 </li>
 <li>
 Work closely with regional and emerging functions (Medical, Market Access, Commercial Excellence, Regulatory) to align marketing initiatives.
 </li>
 <li>
 Partner with affiliate marketing teams to ensure effective adaptation of regional strategies to local market needs including including Promo material development, managing conferences, meetings, scientific symposia, and CMEs.
 </li>
 <li>
 Engage with KOLs, healthcare professionals, and stakeholders to drive product advocacy.
 </li>
 <li>
 Performance Monitoring &amp; Best Practice Sharing:
 </li>
 <li>
 Define and track key performance indicators (KPIs) to measure the success of marketing initiatives.
 </li>
 <li>
 Identify best practices from high-performing markets and facilitate knowledge-sharing across affiliates.
 
 
 </li>
 </ul>
 Additional Skills:
 
 
 <ul>
 <li>
 Strong ability to work independently, yet effectively influence and guide affiliate marketing teams and senior leadership.
 </li>
 <li>
 Expertise in brand strategy development and execution in the field of Critical Care (anti-infective, anti-fungal, immunosuppressants), Hepatitis and HIV.
 </li>
 <li>
 Strong analytical and strategic thinking capabilities to interpret complex market data and provide actionable recommendations.
 </li>
 <li>
 Excellent communication, storytelling, and stakeholder engagement skills to align and inspire cross-functional teams.
 </li>
 <li>
 Understanding of Southeast Asian pharmaceutical markets, including regulatory landscapes and market access dynamics (desirable not mandatory).
 
 
 </li>
 </ul>
 This is an individual contributor role, requiring the ability to influence and guide affiliate marketing teams and senior leadership in countries. The role does not directly manage country-level planning and execution but provides strategic direction to ensure alignment with regional and emerging market priorities.
 
 
 <ul>
 <li>
 Education:
 </li>
 <li>
 Undergraduate or Master&rsquo;s degree in Life Sciences, Pharmacy, Marketing, or Business Administration.
 </li>
 <li>
 Experience:
 </li>
 <li>
 At least 10+ years of experience in the Pharmaceutical Industry, with a minimum of 7-8 years in marketing.
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 International marketing experience is desirable, particularly in brand strategy, new launches, and cross-market collaboration.
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Senior Manager International Marketing - Emerging Markets

Explore 177+ Scientist pharmaceutical development in Hyderabad India this November. Find roles across top companies and apply now to boost your career.