ResponsibilitiesTo follow the safety rules in the premises according to the company norms. Monitoring of DP, RH and temperature area in their visual inspection Responsible for Operation and Cleaning of Wrap around labeling machine, Autocartonator machine, Online check weigher, track and trace system, Bopp taping machine with weighing balance and PFS machines. Responsible for labeling and packing of products as per BPR. Responsible to perform visual inspection of the products /media filled vials or PFS as per the sop. Responsible for Operation and cleaning of Automatic visual inspection machine and X-RAY inspection machine. Operation and cleaning of visual inspection table and Operation of Lux meter. Responsible to perform the in process checks during operation.Qualification & Experience4 years or more in 2-3 yearsBachelor Degree (BS) - B. Sc./ B.Pharma. - Required Master Degree (MS) M. Sc. - Preferred

ResponsibilitiesThe overall purpose and main responsibilities are listed below: Support HEVA/Medical team in assigned therapy area portfolio to plan and generate robust health economics and value based evidence to maximize the value propositions from both a global and US perspective working within the Market Access tripod Seek opportunities to innovate HEVA/Medical value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA/Medical evidence to ensure reimbursement decisions and optimal access Develop and maintain therapeutic area (TA) expertise People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA/Medical teams across various time zones Performance: (1) Support in the HEVA/Medical evidence generation plan: Develop research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide strategic support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (2) Support execution of approved HEVA/Medical study(s) and manage ongoing study(s) if required: Supports the HEVA/Medical product lead to manage and execute research studies to support the clinical, economic and humanistic value of products (3) Support development of core value dossier (CVD) and Academy of Managed Care Pharmacy (AMCP) dossier and provide strategic directionQualification & ExperienceExperience: 5+ years of experience in Health Economics and Outcomes Research (HEOR) for the pharmaceuticals industry, CRO consultancy or academia. Soft and technical skills: Stakeholder management, writing/communication skills, external engagement and ability to work independently and within a team environment Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies; Understands reimbursement decisions to determine value drivers and how evidence is used in decision making and how it impacts various payers (e.g., providers, patients, health systems); Knowledge of methods and principles of health economics, health technology assessment (HTA) reviews Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree Languages: Excellent knowledge of English language (spoken and written)

ResponsibilitiesSupport the development and maintenance of comprehensive architecture strategies tailored to the needs of managing and transferring clinical trial data, from research and collection to submission. Research and implement innovative data technologies and methodologiesfor Master Data Management and Data Quality (e.g. Reltio, Data Quality checks etc.) Develop and implement data strategies to ensure the accuracy, integrity, and security of clinical data. Provide technical support and guidance to users as needed. Collaborate closely with other DigitalX team members and data professionals to integrate assigned systems or environments with other systems and workflows, ensuring a smooth and controlled flow of data. Support designing scalable architectures to track and maintainproduct data and associated automated jobs. Oversee and support development of APIs, interfaces, and middleware solutions for seamless communication and data exchange between clinical software systems and databases. Lead or take part in projects related to system upgrades, migrations, or new implementations. Liaise with software vendors and service providers to address issues, manage licenses, and support negotiate contracts. Actively participate in or lead Agile activities, including backlog grooming, using Azure DevOps Services. Stay updated on industry guidelines (e.g. IDMP compliance) and advancements to recommend and implement new tools and practices. Responsible for Data Quality (DQ) business rules implementation, DQ Analysis, and DQ Remediation activities. Identify, document and track DQ violations and defects, work with development, data lake teams to resolve issues. Assistorganizations stay ahead of data trends and discover new ways to useproduct data.Quaification & ExperienceBachelor of Science degree in Computer Science, Information Systems, Data Science, or a related field. Minimum of 5 years of relevant experience working in Master Data Management solutions and Data Quality framework within a healthcare industry. Deep understanding of clinical data systems, as well as related environments and tools. Proficient in Reltio data model configuration (Entity types, attributes), matching rules, operational values and survivorship rules, relationships, User Interface, and hierarchies.

ResponsibilitiesPrioritizes, and performs the day-to-day operations of Clinical Transparency or Public Disclosure, ensuring the timely completion, review and approval of registration, updates and results disclosure activities or public disclosure strategy plans and public disclosure tracking mechanisms for studies and assets conducted globally. Makes appropriate decisions regarding the applicability and timing of clinical transparency or public disclosure activities according to national laws, regulations, industry guidance and corporate position. Manages the review and approval process for Clinical Transparency (clinical trial registrations, updates and results disclosures) and related documents (plain language and redacted documents) or public disclosure strategy plans and public disclosure tracking mechanisms, including communication with partner companies or collaborators. Facilitates periodic review of active registrations or public disclosure strategy plans to ensure records are updated or verified as required. Uses appropriate problem solving to determine escalation of issues to management.Qualification & ExperienceBachelor’s Degree, or equivalent experience required. Proficient organizational skills and high attention to detail. Self-directed and motivated, with ability to work without significant direct supervision, asking questions when necessary. Ability to manage multiple tasks and readily switch activities to accommodate priority needs. Proficient computer skills, including experience with MSWord and Excel. Healthcare professional background preferred.2 years pharmaceutical industry experience in writing content for Clinical Transparency purposes. Clinical trials experience including study management, statistics, medical writing and / or data management preferred. Working knowledge of clinical drug development and clinical trial protocols preferred.

ResponsibilitiesPrioritizes, and performs the day-to-day operations of Clinical Transparency or Public Disclosure, ensuring the timely completion, review and approval of registration, updates and results disclosure activities or public disclosure strategy plans and public disclosure tracking mechanisms for studies and assets conducted globally. Makes appropriate decisions regarding the applicability and timing of clinical transparency or public disclosure activities according to national laws, regulations, industry guidance and corporate position. Manages the review and approval process for Clinical Transparency (clinical trial registrations, updates and results disclosures) and related documents (plain language and redacted documents) or public disclosure strategy plans and public disclosure tracking mechanisms, including communication with partner companies or collaborators. Facilitates periodic review of active registrations or public disclosure strategy plans to ensure records are updated or verified as required. Uses appropriate problem solving to determine escalation of issues to management. Addresses inquiries related to clinical transparency and related documents or public disclosure activities. Interacts and collaborates across various departments and management levels within Astellas to ensure open and effective communication. Provides feedback to clinical transparency or public disclosure leadership resulting from new and updated transparency requirements. Ensures compliance with evolving clinical transparency or public disclosure requirements, including retrospective review and work as necessary. Contributes toward the continuous improvement of global clinical transparency or public disclosure processes, procedures, and standards. Establishes and maintains global working relationships.Qualification & ExpeirenceBachelor’s Degree, or equivalent experience required. Proficient organizational skills and high attention to detail. Self-directed and motivated, with ability to work without significant direct supervision, asking questions when necessary. Ability to manage multiple tasks and readily switch activities to accommodate priority needs. Proficient computer skills, including experience with MSWord and Excel. Healthcare professional background preferred. Preferred Qualifications 2 years pharmaceutical industry experience in writing content for Clinical Transparency purposes. Clinical trials experience including study management, statistics, medical writing and / or data management preferred. Working knowledge of clinical drug development and clinical trial protocols preferred.

Responsibilities The employee leads technical aspects of drug substance manufacturing including process optimization, technical transfers and development of the technical agenda. This position requires comprehensive knowledge of the pharmaceutical industry, Good Manufacturing Practices (GMP), regulatory requirements, and the essential role scientists play in making medicine and creating real-world solutions. The successful candidate should have a proven track record of driving technical agendas and influence externally in the peptide space.Qualification & ExperiencePh.D. in scientific disciplines of Biochemistry, Chemistry, or related fields, or equivalent industry experience /Ph.D + Post Doc in Chemistry (focusing more Peptide chemistry) with 12+ years

ResponsbilitiesMaintain and effectively communicate deep scientific knowledge: Engage in continuous learning to maintain the highest level of technical expertise within oncology. This will enable the MSL to answer deep scientific questions and be sought after by their customers based on peer-credible knowledge and expertise. As a result, the MSL will establish themselves as a reliable, trusted resource of unbiased, accurate, up-to-date medical and scientific knowledge. Excel at customer engagement and support medical/scientific information needs of scientific experts: Through the application of emotional intelligence and a deep understanding of their customers, the MSL will act as one of the primary interfaces between Lilly medical and scientific experts to deliver the best-in-class customer experiences. Core to the role is to answer customer questions by providing deep and advanced disease state and product information. Additionally, the MSL will connect scientific experts with other Lilly resources or internal business partners as appropriate and identify possible collaborative research or external collaborations. Strategic vision and leadership: Synthesize complex data and effectively communicate meaningful clinical insights and unanswered customer questions they receive from scientific experts to Lilly medical and cross-functional teams. The MSL will use creative problem-solving skills and utilize internal resources effectively to execute upon solutions. The MSL will use a principle-based approach to make decisions independently or escalate them appropriately. They cultivate internal networks and collaborate effectively across functions with an active contribution to medical planning and strategy in Lilly India. Territory ownership: The MSL will be expected to demonstrate strategic analysis, planning, and prioritization to maximize efficiency. They will implement and evaluate a strategic territory plan prioritizing core MSL activities and take personal accountability for results. The MSL will execute the role in a compliant manner, adhering to all governing internal and external requirements, procedures, and laws, demonstrating good judgment at all times.

ResponsibilitiesPerform all activities in compliance with GxP requirements. Follow quality and safety requirements in accordance with organizational policies, procedures, and regulatory guidelines. Ensure technical outputs align with Global Training Curricula for instrument operation, material handling, and certifications related to Quality Operations, Manufacturing, and EHS.  Analytical Development and Troubleshooting Troubleshoot analytical issues related to methods and instrumentation. Develop and validate analytical methods using LC-MS, GCMS and ICP-MS for E&L work flow and Nitrosamine work flow support. Develop GTI impurity methods using LC-MS and GC-MS. Assess existing data packages, evaluate feasibility, and recommend remediation where needed. Has strong knowledge of USP, PQRI, and BPOG guidelines for SUS and MUS systems, along with expertise in writing non-laboratory, paper-based assessment reports for packaging commodities. Documentation, Governance, and Review Work with Quality Assurance and cross-functional teams to support consistent and disciplined execution of the LIR/ER/CAPA quality system, ensuring assigned tasks are complete and thorough. Maintain compliance with local and corporate procedures and keep all data packages audit-ready and transferable. Ensure formal milestone reports receive appropriate GT and ELT review to support decision-making. Qualification & ExperienceQualification: Master's in chemistry/pharmacy/Ph.D Type of Experience: Brings 5–7 years of experience in Analytical Research and Development, with strong expertise in nitrosamine workflow support and extractables and leachable studies. Demonstrates hands-on proficiency in HPLC, GC, GCHS, and LCMS within GMP environments, supported by strong data interpretation and technical report-writing skills.

ResponsibilitiesCompilation and update of drug dossiers with focus on the clinical part in close alignment with the therapy field director Provide answers to authorities on registration related medical/pharmacological questions in close alignment with the director of the respective therapy field and with drug regulatory Support of drug development projects Participation in audits: support of therapy field leader with respect to therapy field relevant documents Supportive function in risk management, in particular concerning medico-regulatory topics: Provide support in the development, maintenance and updating of documents related to risk management deliverables Participation in cross-functional teams for medical-regulatory aspects Authorship of assessments concerning product development issues, in analysis of clinical data and in defining the medical evidence needed for driving or improving product development processes in close collaboration with the therapy field director Planning and support of medico-scientific activities related to generation of clinical evidence (studies) in close alignment with the respective director and Clinical Research Assessment of potentially relevant Literature within the frame of the literature vigilance processQualification & ExperienceUniversity degree in Medicine, Pharmacy, natural science, medical engineering or related science EXPERIENCE AND REQUIRED SKILLS: At least 5 years of Regulatory Medical writing work experience, preferably in a comparable position within health care or pharmaceutic or medical technology companies or research institutions Knowledge of relevant regulations for drugs Competence in the direct compilation of medical and scientific documents, and in the coordination and collection of contributions from various people/departments Experience in conducting systemic and process-oriented searches in medical and scientific databases

ResponsibilitiesResponsible for overseeing the day-to-day operations of a pharmacy, ensuring compliance with regulations, managing staff, and maintaining inventory. also play a crucial role in providing excellent customer service and ensuring the safe and effective dispensing of medications Qualification & ExperienceBachelor degree / Masters in Pharmacy Previous experience as pharmacy manager Strong knowledge strong pharmaceutical knowledge, excellent leadership and communication skills, and a deep understanding of pharmacy operations and regulations Excellent communication and patient care skills