28 Eli Lilly jobs in India
Drug Development Cloud Engineer
Posted today
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Position: Software Engineer I Veeva Quality
Location : Hyderabad, India
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
Position Summary:
At BMS (Bristol Myers Squibb), digital innovation and Information Technology are central to our vision of transforming patients’ lives through science. To accelerate our ability to serve patients around the world, we must unleash the power of technology. We are committed to being at the forefront of transforming the way medicine is made and delivered by harnessing the power of computer and data science, artificial intelligence, and other technologies to promote scientific discovery, faster decision making, and enhanced patient care.
Software Engineer I role is a member of the Veeva Drug Development & Cloud team and is accountable for Veeva Configuration and Operational activities in the various vaults of the BMS Veeva ecosystem. In this role, the individual is primarily responsible for supporting platform updates, enhancements and/or end-user support & access management activities including Architecture, design, and testing. This role does not have any supervisory responsibility, however, may act as a functional mentor to more junior team members.
If you want an exciting and rewarding career that is meaningful, consider joining our diverse team!
Desired Candidate Characteristics:
- Have a strong commitment to a career in technology with a passion for healthcare
- Ability to understand the needs of the business and commitment to deliver the best user experience and adoption
- Able to collaborate across multiple teams
- Excellent communication skills
- Innovative and inquisitive nature to ask questions, offer bold ideas and challenge the status quo
- Agility to learn new tools and processes
Key Responsibilities:
- Supporting a wide range of projects across multiple domain areas, selected candidate’s responsibilities will include:
- Collaborate closely with the Veeva Drug Dev & Quality Cloud team to obtain high level overview knowledge of the Veeva vault platform and various vaults
- Assist in the deployment of the Veeva Vault Platform and general releases including documentation and testing
- System analysis, design, and configuration to meet business requirements
- Contribute to all aspects of testing activities (unit, system, and/or user acceptance testing) of the vault release including script generation, execution, review, and approval
- Deliver on validation documentation required on the various operational activities to ensure maintenance of the system’s validated state
- Provide operational support activities of the Veeva vaults to our global user community, such as maintenance and break-fix releases, security assessments, regulatory risk assessments, incident response, etc.
- Perform periodic user access review of the applications
- Obtain/maintain a Veeva Associate Administrator Level certification
Qualifications & Experience:
- Requires thorough knowledge of the principles and concepts of a discipline and developed knowledge of other related disciplines, typically gained through a university degree and 2-3 years of experience.
- Works within established procedures. Actively participates in troubleshooting of routine problems.
- Makes decisions that impact own work and other groups/teams.
- Works under minimal supervision.
- Does not have any supervisory responsibility, however, may act as a functional mentor to more junior team members.
- Experience in implementing/supporting SaaS (Software as a Service) solutions
- Experience in automated testing tools
- Experience in life science industry with Quality domain knowledge
- Experience in GMP (Good Manufacturing Practice) practices
- Makes decisions while understanding the team's work and how it fits into the broader enterprise.
- May need support from within the team or outside the team when working on broader or complex topics in understanding environment.
- Identifies opportunities to improve and grow, balancing performance feedback and career development
- Applies a continuous improvement mindset in enhancing efficiency, quality and effectiveness or their work outputs.
- Displays understanding of performance metrics driving the team's goals and questions the external environment and its' implication on the goals and strategies.
- Able to review multiple factors of data and can effectively organize information to compare and assess short and long-term implications.
- Can create a well-developed recommendation and sound actions.
- Ideal candidate will also have Veeva Associate Administrator Level (previously called Veeva White Belt) certification.
#HYDIT #LI-Hybrid
Senior Formulation Scientist, Drug Development
Posted 4 days ago
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Job Description
- Design and develop stable, efficacious, and bioavailable drug formulations.
- Conduct pre-formulation studies to understand drug substance properties.
- Select and evaluate appropriate excipients for formulation development.
- Perform formulation optimization studies using DoE methodologies.
- Characterize formulated products using various analytical techniques.
- Develop and validate analytical methods for formulation assessment.
- Plan and execute stability studies according to ICH guidelines.
- Support process development and scale-up activities for manufacturing.
- Troubleshoot formulation and process-related issues.
- Stay abreast of the latest advancements in pharmaceutical formulation science and technology.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 7 years of relevant industry experience in pharmaceutical formulation development.
- Extensive knowledge of various dosage forms (e.g., oral solid, parenteral, topical).
- Proficiency in formulation development techniques and characterization methods.
- Strong understanding of GMP, ICH guidelines, and regulatory submission requirements.
- Experience with drug substance characterization and solid-state properties.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills.
- Ability to work independently and manage multiple projects effectively in a remote setting.
- Experience with biologics formulation is a plus.
Senior Formulation Scientist - Drug Development
Posted 10 days ago
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Responsibilities:
- Design and execute pre-formulation studies to characterize drug substances.
- Develop and optimize formulations for various dosage forms, with a primary focus on oral solids (tablets, capsules).
- Evaluate and select appropriate excipients to achieve desired drug product performance and stability.
- Perform laboratory experiments to investigate solubility enhancement, bioavailability improvement, and controlled/sustained release profiles.
- Utilize analytical techniques (e.g., HPLC, UV-Vis, dissolution testing) for characterization and quality control of formulations.
- Prepare comprehensive study protocols, reports, and technical documentation for regulatory submissions.
- Troubleshoot formulation-related challenges and implement effective solutions.
- Collaborate with analytical development, process development, and regulatory affairs teams.
- Stay abreast of the latest advancements in formulation technologies and industry best practices.
- Mentor junior scientists and contribute to the scientific growth of the R&D department.
- Ensure compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines.
- Participate in cross-functional project team meetings and contribute to strategic decision-making.
- Master's or Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related discipline.
- Minimum of 5-7 years of hands-on experience in pharmaceutical formulation development, with a focus on oral dosage forms.
- Proven expertise in formulation design, excipient selection, and drug product characterization.
- Proficiency in analytical methods for drug substance and drug product characterization.
- Strong understanding of physicochemical properties, biopharmaceutics, and pharmacokinetics.
- Experience with various dosage form manufacturing processes and equipment.
- Knowledge of regulatory requirements for drug development (e.g., ICH guidelines).
- Excellent problem-solving, analytical, and critical-thinking skills.
- Strong written and verbal communication skills, with the ability to present scientific data effectively.
- Ability to work independently and collaboratively in a fast-paced R&D environment.
- Experience with pre-formulation studies and solid-state characterization techniques.
Senior Formulation Scientist, Drug Development
Posted 15 days ago
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Job Description
Key Responsibilities:
- Design and develop robust formulations for various dosage forms (e.g., oral solids, injectables, topical).
- Conduct pre-formulation studies to characterize drug substances and excipients.
- Optimize formulations to achieve desired physicochemical properties, bioavailability, and stability.
- Plan and execute formulation development experiments, including scale-up and technology transfer.
- Develop and validate analytical methods for the characterization of drug products.
- Prepare detailed technical reports, formulation development protocols, and regulatory submission documents.
- Collaborate with cross-functional teams including R&D, analytical development, DMPK, and regulatory affairs.
- Troubleshoot formulation-related issues and provide solutions to manufacturing challenges.
- Stay abreast of scientific advancements, new technologies, and regulatory guidelines in pharmaceutical formulation.
- Manage project timelines and resources effectively.
- Mentor junior scientists and contribute to their professional development.
- Conduct literature searches and patent reviews related to formulation development.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 5-7 years of hands-on experience in pharmaceutical formulation development.
- Proven expertise in developing various dosage forms and understanding of drug delivery systems.
- In-depth knowledge of excipient functionality, compatibility, and selection.
- Experience with analytical techniques used for characterizing drug products (e.g., HPLC, DSC, XRPD).
- Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements (e.g., ICH guidelines).
- Excellent problem-solving, analytical, and critical-thinking skills.
- Strong written and verbal communication skills, with the ability to present complex data clearly.
- Proficiency in scientific literature databases and formulation software.
- Ability to work effectively in a collaborative, cross-functional team environment.
- Experience with stability studies and data interpretation.
- Demonstrated ability to manage projects and meet deadlines.
Lead Formulation Scientist - Drug Development
Posted 17 days ago
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Job Description
Key Responsibilities:
- Lead the design, development, and optimization of oral solid dosage forms (tablets, capsules) and potentially other dosage forms (e.g., injectables, topicals).
- Conduct pre-formulation studies to understand drug substance characteristics relevant to formulation development.
- Develop scientifically sound formulation strategies to improve drug solubility, bioavailability, and patient compliance.
- Perform experiments to evaluate excipient compatibility, drug-excipient interactions, and critical process parameters.
- Oversee the scale-up of laboratory-scale formulations to pilot and commercial manufacturing processes.
- Develop and validate analytical methods for characterizing formulated products.
- Ensure all formulation activities comply with Good Manufacturing Practices (GMP) and regulatory guidelines.
- Collaborate with analytical development teams to ensure product quality and stability.
- Provide technical guidance and mentorship to junior formulation scientists and technicians.
- Prepare comprehensive development reports, regulatory submission documents (e.g., IND, NDA sections), and scientific presentations.
- Stay current with advancements in formulation science, drug delivery technologies, and pharmaceutical manufacturing.
- Troubleshoot formulation and manufacturing issues, providing scientific expertise for resolution.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 7 years of progressive experience in pharmaceutical formulation development.
- Proven expertise in oral solid dosage form development, including tablet and capsule manufacturing.
- Strong understanding of drug substance characterization, excipient functionality, and manufacturing processes.
- Experience with pre-formulation techniques, solubility enhancement, and controlled/sustained release technologies.
- Familiarity with analytical techniques used for drug product characterization (e.g., HPLC, dissolution testing, DSC).
- Knowledge of GMP regulations and experience preparing regulatory documentation.
- Excellent problem-solving, critical thinking, and experimental design skills.
- Strong leadership, project management, and communication abilities.
- Ability to work effectively in a cross-functional team environment.
- Experience with statistical analysis and design of experiments (DoE) is a plus.
Senior Formulation Scientist - Drug Development
Posted 18 days ago
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Job Description
Senior Formulation Scientist - Drug Development
Posted 18 days ago
Job Viewed
Job Description
Key Responsibilities:
- Lead the design, development, and optimization of novel drug formulations for various dosage forms (e.g., tablets, capsules, injectables, topicals).
- Conduct pre-formulation studies to characterize drug substances and excipients.
- Develop and validate robust formulation and manufacturing processes.
- Perform stability studies and interpret data to assess product shelf-life.
- Troubleshoot formulation-related issues and propose effective solutions.
- Collaborate closely with analytical development, DMPK, and manufacturing teams.
- Prepare scientific reports, technical documentation, and contribute to regulatory submissions (e.g., IND, NDA).
- Stay abreast of the latest advancements in formulation science and pharmaceutical technology.
- Supervise and mentor junior scientists and research associates.
- Manage project timelines and deliverables effectively.
- Ensure adherence to cGMP guidelines and quality standards throughout the development process.
- Evaluate new excipients and drug delivery technologies.
Qualifications:
- Master's degree or Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 5 years of experience in pharmaceutical formulation development.
- Hands-on experience with various dosage forms and formulation techniques.
- Proficiency in pre-formulation characterization and drug delivery systems.
- Strong understanding of physical chemistry, materials science, and analytical techniques.
- Experience with scale-up and technology transfer activities.
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong written and verbal communication skills, with the ability to present scientific data.
- Knowledge of regulatory requirements (e.g., FDA, EMA) related to drug product development.
- Experience in a hybrid work environment is beneficial.
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Remote Clinical Research Scientist - Drug Development
Posted 12 days ago
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Lead Research Scientist - Oncology Drug Development
Posted 15 days ago
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Job Description
Key responsibilities include:
- Designing and overseeing preclinical research strategies for oncology therapeutics.
- Leading a team of scientists in hypothesis-driven research and experimental design.
- Analyzing and interpreting complex biological data to guide project direction.
- Developing and validating in vitro and in vivo models for drug efficacy and safety testing.
- Collaborating closely with cross-functional teams including medicinal chemistry, DMPK, and translational science.
- Identifying and evaluating external research collaborations and technologies.
- Staying abreast of the latest scientific advancements and competitive landscape in oncology.
- Preparing and presenting research findings at internal meetings and external scientific conferences.
- Contributing to the preparation of regulatory documents and patent applications.
- Mentoring and guiding junior researchers.
The successful candidate will hold a Ph.D. in Molecular Biology, Pharmacology, Biochemistry, or a related field, with a minimum of 7 years of post-doctoral or industry experience in cancer research and drug discovery. A strong publication record and proven success in leading research projects from discovery to preclinical development are essential. Expertise in cancer genomics, immunology, or specific signaling pathways relevant to oncology is highly desirable. Excellent analytical, problem-solving, and communication skills are paramount for this remote role, requiring the ability to collaborate effectively across geographical boundaries. This is a unique opportunity to significantly contribute to the development of life-saving cancer treatments within a dynamic and forward-thinking organization.
Senior Clinical Research Scientist - Remote Drug Development
Posted today
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The ideal candidate will possess a strong scientific background, with a proven track record in pharmaceutical research and development. You will be adept at translating scientific findings into actionable clinical research plans and communicating complex scientific information effectively to diverse audiences, including regulatory agencies, investigators, and internal stakeholders. This role demands excellent analytical, problem-solving, and critical thinking skills.
Key responsibilities include providing scientific leadership for clinical development programs, authoring study protocols and clinical study reports, and interpreting clinical data to assess drug efficacy and safety. You will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and medical affairs, to ensure successful trial execution. Staying abreast of the latest scientific advancements and regulatory changes in the pharmaceutical industry is essential.
We are looking for a self-motivated and results-oriented individual who can work independently and manage multiple projects concurrently in a remote setting. Excellent written and verbal communication skills are paramount. This is an exceptional opportunity to contribute to the development of life-saving medicines and advance your career in pharmaceutical research from anywhere.
**Responsibilities:***
- Design and develop clinical trial protocols for new drug candidates.
- Oversee the conduct of clinical trials, ensuring adherence to protocols and regulations.
- Analyze and interpret clinical trial data to assess safety and efficacy.
- Author study reports, manuscripts, and regulatory submission documents.
- Collaborate with internal and external stakeholders on clinical development strategies.
- Provide scientific expertise and guidance to project teams.
- Stay current with scientific literature and regulatory guidelines.
- Ph.D. or M.D. in a relevant life science discipline.
- Minimum 8 years of experience in clinical research within the pharmaceutical industry.
- Demonstrated experience in designing and managing Phase I-IV clinical trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Strong analytical and statistical interpretation skills.
- Excellent written and verbal communication abilities.
- Proven ability to work effectively in a remote, collaborative environment.