Jobs at 1074 Amgen Technology Pvt Ltd

18 open positions · $10 - $12

Open roles

Study Delivery Associate Associate IS Engineer - Veeva Vault Specialist IS Architect - Platform Specialist Software Engineer - R&D Omics Sr Associate Business Analysis Senior Associate - RWE Application Development Sr Assoc QA - Global Supply Quality Sr Associate Biostatistics Senior Manager, Biostatistical Programming Senior Associate - Clinical Pharmacology

Study Delivery Associate

India - Hyderabad, IndiaFrom $40/yr

Career Category Operations Job Description Role Name: Study Delivery Associate ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. ABOUT THE ROLE Role Description: The Study Delivery Associate provides essential administrative and operational support to clinical trial management activities. This role supports the Study Delivery Team in meeting study timelines, ensuring regulatory compliance, and executing standardized processes related to clinical trial coordination, document and system management. The Study Delivery Associate may also support specialized activities to promote expertise, quality, and consistency across studies. Key responsibilities include maintaining accurate and timely data within clinical systems (e.g., CTMS) and supporting study training and related operational requirements. Roles & Responsibilities: Study Coordination Support the setup and maintenance of study-level trackers, dashboards and timelines. Communicate study progress, timelines and deliverables to the Study Delivery Manager. Assist with tracking and following up on study actions, including risk mitigation actions. Assist with the preparation and record keeping of risk & quality reviews. Ensure completion of study team training and inspection readiness activities to maintain compliance with regulatory requirements. Assist with trial-related events, global site communications, and logistics for investigator meetings Support study start-up activities, including system setup, supplier access management, ICF tracking and document readiness. Support vendor relationships and site engagement strategies. Manage shipment, reconciliation and analysis of biological samples. Coordinate investigational product logistics, ensuring compliance with reconciliation processes. Data & Systems Management Maintain clinical trial systems (e.g., CTMS, study training), ensuring timely and accurate data entry. Support system access requests and access management. Document Preparation Assist with preparing, reviewing and maintaining study documentation, including regulatory submissions, monitoring plans and study guides. Support TMF filing. Process Improvement & Knowledge Sharing Contribute to process improvement and share knowledge & share knowledge and experience. Basic Qualifications and Experience: Bachelor’s degree OR Associate’s degree and 4 years of clinical execution experience OR High school diploma / GED and 6 years of clinical execution experience Preferred Qualifications and Experience: 2 years' work experience in life sciences or medically related field, including 1 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company Experience working on global clinical trials Competencies: Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support Experience with tracking and filing of essential documents such as protocols, informed consent forms, and regulatory submissions to ensure documents are version-controlled and inspection-ready. Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools. Ability to maintain accurate and timely data entry. Skilled in managing clinical trial data flow, investigator documentation, and protocol adherence while ensuring regulatory compliance Cultural sensitivity and collaboration across global teams. Ability to recognize, highlight and resolve issues. Demonstrates curiosity and willingness to take on new tasks. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

10 months agovia common crawlApply ›

Associate IS Engineer - Veeva Vault

India - Hyderabad, IndiaFrom $198/yr

Career Category Information Systems Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do Let’s do this. Let’s change the world. In this vital role you will as Veeva Vault team, you will collaborate with business partners, product owners, developers, and testers to develop release strategies for Amgen’s Veeva Vault PromoMats and Vault MedComm. You will ensure these systems meet business needs and maintain their availability and performance. Your role includes working with product managers, designers, and engineers to create scalable software solutions, automate operations, monitor system health, and respond to incidents to reduce downtime. Roles & Responsibilities: Possesses strong rapid prototyping skills and can quickly translate concepts into working code. Lead day to day operations and maintenance of Amgen’s Amgen’s Vault PromoMats and Vault MedComm and its hosted applications. Stay updated with the latest trends, advancements and standard processes for Veeva Vault Platform ecosystem. Design, develop, and implement applications and modules, including custom reports, SDKs, interfaces, and enhancements. Analyze and understand the functional & technical requirements of applications, solutions and systems, translate them into software architecture and design specifications. Develop and complete unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process while exhibiting expertise in Risk Based Validation methodology. Work closely with multi-functional teams, including product management, design, and QA, to deliver high-quality software on time. Maintain detailed documentation of software designs, code, and development processes. Work on integrating with other systems and platforms to ensure seamless data flow and functionality. Stay up to date on Veeva Vault Features, new releases and standard methodologies around Veeva Platform Governance. Assess and plan for the impact of Veeva changes and releases on collaborators. Assisst to develop and managing communication plans to engage Veeva collaborators and provide clear messaging. Support designing and delivery of training programs, offering ongoing support and coaching. Be part of change impact assessment. What we expect of you Basic Qualifications and Experience: Master's or Bachelor’s degree 2 to 5 years of Computer Science, Information Systems experience or related field Functional Skills: Must-Have Skills: Experience with Amgen’s Vault PromoMats and Vault MedComm, including Veeva configuration settings and custom builds. Strong knowledge of information systems and network technologies. Experience in building configured and custom solutions on Veeva Vault Platform. Experience in managing systems, implementing and validating projects in GxP regulated environments. Extensive expertise in SDLC, including requirements, design, testing, data analysis, creating and managing change controls. Proficiency in programming languages such as Python, JavaScript etc. Solid understanding of software development methodologies, including Agile and Scrum. Experience with version control systems such as Git. Good-to-Have Skills: Familiarity with relational databases (such as MySQL, SQL server, PostgreSQL etc.) Proficiency in programming languages such as Python, JavaScript or other programming languages Outstanding written and verbal communication skills, and ability to translate technical concepts for non-technical audiences. Experience with ETL Tools (Informatica, Databricks). Experience with API integrations such as MuleSoft. Solid understanding & Proficiency in writing SQL queries. Hands on experience on reporting tools such as Tableau, Spotfire & Power BI. Professional Certifications: Veeva Vault Platform Administrator or Equivalent Vault Certification (Preferred) SAFe for Teams (Preferred) Soft Skills: Excellent analytical and solve skills. Strong verbal and written communication skills. Ability to work effectively with global, virtual teams. Team-oriented, with a focus on achieving team goals. Strong presentation and public speaking skills. Work Hours: This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required. Potential Shifts (subject to change based on business requirements): Second Shift: 2:00pm – 10:00pm IST; Third Shift: 10:00 pm – 7:00 am IST. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 weeks agovia common crawlApply ›

Specialist IS Architect - Platform

India - Hyderabad, IndiaFrom $198/yr

Career Category Engineering Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do Let’s do this. Let’s change the world. In this vital role you will be part of the SCRUM development team under the Scaled Agile Framework (SAFe) Medical Data Analytics and Insights Product Team and primarily focus on delivering Analytics capabilities across Global Medical business organization. The selected individual will be responsible for architecting, design and develop integration and data pipelines, analytics solutions and engage with validation engineers, product owner, architects and the members of the development team. This role requires expertise in architecting solution based on Databricks framework, Developing API integrations framework and experience with reporting tools like Tableau, The architect will develop technical solutions using Enterprise Datalake and ETL technology platforms. Additionally, collaboration with various global teams is required to ensure seamless integration and operational excellence. The ideal candidate will have a strong technical background in architecting end-to-end software development lifecycle and be a Scaled Agile practitioner. This role demands the ability to drive and deliver against key organizational strategic initiatives, foster a collaborative environment, and deliver high-quality results in a matrixed organizational structure. The ideal candidate will architect and design solutions and support the implementation of software solutions that meet the unique needs of our medical teams. They will provide day to day operations, data standardization, ad hoc query, reporting, technical support, training, data Roles & Responsibilities: As a Specialist IS Platform Architect Lead the design, aid development, and deployment of advanced data integration solutions for Global Medical teams, enabling actionable insights across diverse business capabilities. Design integrated solutions and analytical summarized dimensional data models and datasets to augment visualization applications and dashboards Aid Development platform team with design, development of backend infrastructure and integrated views using AWS, Databricks notebooks with Python, sql, node.js Drive innovation in data analytics by introducing advanced techniques (e.g., AI, predictive analytics, dynamic storytelling) to highlight trends and opportunities. Drive API based integration capabilities to integrate the Global Medical ecosystem Monitor and enhance the performance of data pipelines, ensuring optimal load times and usability. Ensure data integrity, quality, and compliance with regulatory standards, such as HIPAA and GDPR. Partner with cross-functional teams to understand business requirements and translate them into scalable visualization solutions. Present data insights n solutions to senior leadership, enabling data-driven decision-making across the organization. Train and mentor team members and business users on the effective use of analytics best practices. Establish and monitor KPIs and data load pipelines Drive cross-functional collaboration with engineering, data science, and business teams to streamline workflows and enhance efficiency. Drive the implementation of reusable, scalable frameworks for visualization solutions to support global reporting needs. Support ad-hoc and strategic reporting requests with customized data visualizations tailored to business needs. Technical Expertise & Innovation Stay updated with emerging trends and tools in data and analytics, incorporating innovative solutions into the team's workflows. Advocate for the adoption of cutting-edge tools and methodologies to elevate the organization's visualization capabilities. Collaborate on the development of a centralized data lake and ensure alignment with enterprise architecture standards. An ongoing commitment to learning and staying at the forefront of AI/ML advancements What we expect of you We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications. Basic Qualifications: Doctorate degree / Master's degree / Bachelor's degree and 8 to 13 years of Information Systems experience Technical Expertise in architecting visualization solutions and applications such as Tableau, Power BI, or React js equivalent. Proficiency in integrating data and hands on experience with AWS, SQL, Python, R, or other data analysis programming languages. Strong understanding of medical data models, including Field Medical, Medinfo, and SciComm frameworks. Excellent communication and stakeholder management skills. Strong project management skills, with experience leading cross-functional teams Preferred Qualifications: 8+ years of experience in Architecting, data analytics, visualization, or business intelligence, preferably within the pharmaceutical, life sciences, or healthcare industry. Demonstrated experience in managing global data projects and collaborating with cross-functional teams in a matrixed organization. Advanced certifications in data visualization tools (e.g., Tableau Certified Professional, Microsoft Power BI Certification). Familiarity with cloud platforms such as AWS, Azure, or GCP, and experience in integrating data visualization solutions with cloud-based architectures. Functional Skills: Must-Have Skills: Excellent communication and interpersonal skills, with the ability to convey technical information to non-technical users Ability to work collaboratively with cross-functional teams and manage multiple tasks simultaneously Strong analytical and problem-solving skills to interpret complex data and provide actionable insights Strong skills in analyzing and modeling large datasets, with expertise in creating aggregate data models and enabling ad-hoc reporting. Good-to-Have Skills: Work experience in the biotechnology or pharmaceutical industry. Experience using and adopting Scaled Agile Framework (SAFe) Ability to work effectively in a fast-paced, dynamic environment. An ongoing commitment to learning and staying at the forefront of AI/ML advancements. Professional Certifications SAFe for Teams certification (preferred) Soft Skills: Exceptional collaboration and communication skills. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. Strong ability to inspire and lead teams, fostering collaboration and accountability. Proactive approach to identifying challenges and implementing data-driven solutions effectively. Proven ability to work with cross-functional and multicultural teams to deliver on shared goals. Flexibility to manage evolving priorities in a fast-paced, dynamic environment. Equal opportunity statement Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 months agovia common crawlApply ›

Specialist Software Engineer - R&D Omics

India - Hyderabad, India$10 - $12/yr

Career Category Information Systems Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do Let’s do this. Let’s change the world. In this vital role you will work for Research Informatics and you will be responsible for development and maintenance of software in support of target/biomarker discovery at Amgen. This role requires expertise in code development (e.g. Python, Nextflow, R, etc), some systems administration / application management knowledge, experience with CI/CD processes and cloud computing technologies (e.g. AWS, Google Cloud, etc). Additionally, experience in working withmulti-functionall teams that include software/data engineers, business analysts, architects, cloud infrastructure teams and experience in agile practices, along with effective communication skills are highly desired. Develop software to transform and visualize omics (genomics, proteomics, transcriptomics) data using programming languages such as Python, Java, R. Develop data processing pipelines for large datasets in the cloud (e.g. Nextflow); integrate with other data sources where applicable Collaborate with the other engineering team members to ensure all services are reliable, maintainable, and well-integrated into existing platforms Adhere to best practices for testing and designing reusable code Ensure effective communication between scientific area management, technical staff and vendors to analyze scientific needs and implement informatics solutions in data acquisition, integration and analysis What we expect of you Master’s degree and 4 to 6 years of in Software Development, IT, or related field, OR Bachelor’s degree and 6 to 8 years of in Software Development, IT, or related field, OR Diploma and 10 to 12 years of in Software Development, IT, or related field. Basic Qualifications: Proficiency in code development (Python, R) and the software development lifecycle Experience with Application development (RShiny, Ploty Dash, etc) Proficient with SQL and relational databases (e.g PostgreSQL, MySQL, Oracle, Databricks) Experience with cloud computing platforms and infrastructure Preferred Qualifications: 3+ years of experience in biopharma or life sciences Experience in pipeline development using one or more of the following programming languages (Python, Nextflow, etc) Experience in RESTFul API development e.g flask, MuleSoft Experience with Benchling (LIMS) development Experience with Bioinformatics tools, development and usage Experience with installing software and configuring linux-based systems Experience with AI/ML tools e.g. Sagemaker, LLM Work experience in the biotechnology or pharmaceutical industry. Experience using and adopting Agile Framework Professional Certifications (please mention if the certification is preferred or mandatory for the role): Agile certifications (e.g. SAFe) – (preferred) Cloud Computing (AWS) – (preferred) Soft Skills: Strong learning agility, ability to pick up new technologies used to support early drug discovery data analysis needs Collaborative with good communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

Jun 16, 2025via common crawlApply ›

Sr Associate Business Analysis

India - Hyderabad, IndiaFrom $198/yr

Career Category Operations Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Senior Associate, R&D Business Analysis Team What you will do In this role, you will be an experienced individual contributor within the R&D Business Analysis Team, supporting enterprise analytics and workforce transformation initiatives through hands-on data analysis, modeling, and insight generation. You will work under the guidance of Managers and Senior Managers while building strong analytical, financial, and business acumen. You will contribute to analytics delivery across the value journey, including development of resource, financial, and capability baselines; analytics data packs; business cases; and value confirmation and realization. You will also collaborate with Technology partners to support automation and continuous improvement efforts, contributing to the development of sustainable analytics platforms that enable ongoing transformation. The ideal candidate will demonstrate their analytical skills to challenge the status quo, drive continuous improvement, and embed digital ways of working into our end-to-end processes Objectives of this Role Support deliverables for workforce strategy: Support financial and data analyses across baselining, business case development, value confirmation, value extraction and value realization. Collaborate with cross-functional global teams to ensure accurate analytics and insights delivery operating in the "following-the-sun" model Activity-Based Cost Analysis: Support analyses of total workforce spend and allocation. Recommend strategic cost-saving initiatives and optimizations based on analysis findings Vendor Analysis: Support the evaluation of vendor performance and impact on organizational efficiency. Develop strategies for vendor optimization and cost management Opportunity Analysis: Support identifying and prioritizing areas of opportunity across the organization. Collaborate with cross-functional teams to implement organizational improvements System Updates & Scenario Modeling: Build and optimize data and financial models that support key processes across the value journey of our transformation. Help ensure central systems and scenario modeling tools are updated with accurate data and assumptions. Support development of new modeling tools to enhance predictive capabilities External Market Analysis: Support the analysis of external market trends and their impact on workforce strategy. Provide strategic recommendations based on market insights to drive organizational competitiveness Job Responsibilities: Support BAT Managers with hands-on data gathering, modeling, and business case development Build and maintain detailed resource, financial, and capability baselines for initiatives and functions Conduct analyses for value confirmation and support tracking of value realization Assist with variance analysis, deviation management, and value reconciliation against approved cases Analyze workforce and financial data to identify areas of opportunity and optimization Build and optimize data and financial models across the value journey Support updates to central systems and scenario modeling tools with accurate data and assumptions Lead and facilitate information collection efforts, including stakeholder interviews and data validation Collaborate with global, cross-functional teams operating in a “follow-the-sun” model Partner with Finance and planning teams to understand impacts to budgets and long-range What we expect of you We are all different, yet we all use our unique contributions to serve patients. The Senior Associate is an experienced individual contributor who delivers high-quality financial and analytical insights, supports data-driven decision-making, and partners effectively across R&D and enterprise functions. Basic Qualifications Master’s degree OR Bachelor’s degree and 4–7 years of Data Analytics, Science & Technology Management, or Finance experience OR Proficiency in financial modeling (Excel), data analytics, and business intelligence tools Passion for data exploration, visualization, and building analytical narratives Intellectual curiosity with the ability to learn new tools, concepts, and methods Experience working in highly collaborative, cross-functional environments Working knowledge of financial data, metrics, and systems Key Responsibilities Deliver high-quality financial and business analysis to support R&D planning, budgeting, forecasting, and decision-making Develop analytical insights that inform business cases, workforce strategy, and resource optimization Partner with cross-functional stakeholders to translate business questions into structured analytical solutions Contribute to continuous improvement, standardization, and automation of analytics and reporting Ensure accuracy, integrity, and confidentiality of financial and workforce data Preferred Qualifications Advanced Excel and financial modeling skills Experience in budgeting, forecasting, and strategic planning Understanding of how business decisions impact financial statements (P&L, Balance Sheet, Cash Flow) Experience with Oracle Hyperion/EPM, SAP, Anaplan Experience with PowerBI, Tableau, Alteryx, Databricks, or similar analytics tools Familiarity with SQL or Python and exposure to AWS services (e.g., S3, Redshift) Prior multinational or global corporate experience Soft Skills Strong analytical, problem-solving, and critical-thinking skills Clear written and verbal communication High integrity and ethical standards Ability to manage multiple priorities in a dynamic environment Collaborative and adaptable mindset What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 months agovia common crawlApply ›

Senior Associate - RWE Application Development

India - Hyderabad, IndiaFrom $198/yr

Career Category Clinical Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Sr Associate Biostatistical Programming What you will do Let’s do this. Let’s change the world. In this vital role you will Enhance and support existing R Shiny applications with a focus on front-end improvements Provide support for the Atlas web-based application from the OHDSI community Develop and implement web solutions using HTML, CSS, and JavaScript Collaborate with stakeholders to understand their requirements and translate them into technical solutions Participate in continuous integration and continuous deployment (CI/CD) processes Manage and optimize data workflows to support efficient data processing and analysis Maintain clear and effective communication with team members and stakeholders Provide technical solutions to programming problems within CfOR Lead and develop technical programming and process improvement initiatives within CfOR Represent the programming function and participate in multidisciplinary project team meetings Project manage all programming activities, according to agreed resource and timeline plans Ensure all programming activities on the project adhere to departmental standards Provide input to and participate in intra-departmental and CfOR meetings Stay updated with R programming trends and integrate new technologies as needed Establish coding standards and best practices for R package and R Shiny development Optimize performance and refactor code to enhance efficiency and reliability Validation and testing software tools. What we expect of you We are all different, yet we all use our unique contributions to serve patients. This crucial role involves generating Real-World Evidence (RWE) to support Amgen products throughout the drug development lifecycle. This individual contributor programming role will collaborate with teams across multiple time zones to fulfill requests, clarify requirements, escalate issues, and deliver high-quality results. The Senior Statistical Programmer will report to a locally based Manager. The Senior Statistical Programmer will be responsible for hands-on programming and results delivery. Additionally, they will be responsible for enhancing existing R Shiny applications and providing support for the Atlas web-based application from the OHDSI community. The ideal candidate should possess a bachelor’s degree and have at least four years of relevant career experience in full stack development. Proficiency in R and R Shiny is required, along with a strong working knowledge of HTML, CSS, and JavaScript programming. The successful candidate will demonstrate scientific and technical excellence, exceptional oral and written communication skills, problem-solving abilities, and meticulous attention to detail. The ability to work effectively within a large, globally distributed team is essential. Basic Qualifications: Bachelor's degree with 5-8 Years in Computer Science, Information Technology, or a related field Preferred Qualifications: Master’s degree in Computer Science, Information Technology or other relevant scientific subject Training or experience using the Observational Medical Outcomes Partnership (OMOP) common data model Experience working with the OHDSI community and supporting Shiny applications Familiarity with Real-World Evidence and its applications in observational studies Experience: Developing and maintaining web applications using R Shiny Supporting and enhancing web-based applications in a collaborative environment Collaborating with multi-functional teams to deliver technical solutions that meet user requirements Key Competencies Required: Proficient in R and R Shiny (Basic) Required: HTML (Intermediate) Required: CSS (Intermediate) Required: JavaScript (Intermediate) Preferred: Python (Basic) Git workflows using version control Continuous Integration and Continuous Deployment (CI/CD) Excellent verbal and written communication skills in English Ability to have efficient exchanges with colleagues across geographical locations Agile project management Real-world data (RWD) including insurance claims databases, electronic medical records and patient registries; for example, MarketScan, Optum, PharMetrics, Flatiron, Medicare OMOP common data model Scientific / technical excellence Oral and written communication, documentation skills Leadership Innovation Teamwork Problem solving Attention to detail Learning attitude What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. We have a tool called Atlas which is Java based application R Shiny programming Java Programming is a priority for this role It is an IC role and he or she will be supporting two different teams We used to build the Shiny dashboard using R programming. Statistical is not required and it is a developer role He / she will be maintaining the existing application Atlas It is a redefining the application . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

4 months agovia common crawlApply ›

Sr Assoc QA - Global Supply Quality

India - Hyderabad, IndiaFrom $198/yr

Career Category Quality Job Description Description Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people’s lives. We are seeking a highly motivated individual for our Global Supply Quality (GSQ) team. This is an incredibly exciting opportunity to join a team of quality professionals. HOW MIGHT YOU DEFY IMAGINATION? You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role. Live What you will do The Sr. Associate QA position is responsible for the Quality oversight of Amgen’s alliance partnerships and external supply portfolio management. This position is responsible for being an integral quality member of the Amgen cross-functional External Supply and Business Development teams that includes but is not limited to Amgen Contract & Development Manufacturing, Process Development, Supply Chain, and Business Development. Responsibilities: Working independently, the individual will be responsible for, but not limited to the following: Perform QA Contact role for partners to ensure adherence to quality agreements, identifying performance improvement opportunities Perform Partner/Client assessments for Change Control and Deviation records Perform Quality tasks in support of Partnership Alliance Quality in accordance with Quality Agreements (i.e. document revisions, document redactions, support partner audits) May perform QA responsibilities associated with Portfolio Strategy Execution, such as supporting Due Diligence activities Work closely with all relevant stakeholders for the end-to-end process and ensure compliance to GMP/GDP. Prepare, review and approve SOPs and other GMP/GDP documentation in compliance with corporate and regulatory requirements, to ensure alignment with procedures, current Good Manufacturing Practices (cGMP) and other applicable regulations Collaborate with external suppliers and partners Understand and incorporate risk management strategy into the overall external supply lifecycle Support in tactical activities related to internal/external audits and inspections Take part in operational improvement initiatives, programs, and projects Develop solutions that are thorough, practical, and consistent with functional objectives Ownership of business metrics, performance assessments, and other key documents to inform the health of external supplier and partner relationships. Work under minimal supervision in line with Amgen Values and Leadership Attributes. Win What we expect of you: Education and Experiences: We are all different, yet we all use our unique contributions to serve patients. The quality professional we seek is a strong leader with these qualifications: Bachelor’s degree in science or engineering and 2+ years of professional experience in related fields. Understanding of GMP/GDP requirements. Familiarity with raw material compendial testing Experience overseeing quality of suppliers or external parties Strong technical writing skills. Strong experience in Alliance Management Preferred Qualifications Strong continuous improvement mindset and lean practices experience. Understanding of end-to-end supply chain business processes. Experience in project management across multiple departments and geographies. Quick process understanding, insight and visualizing. Strong analytical and problem-solving skills. Independent self-starter, able to work autonomously, under pressure and in teams. GMP/GDP knowledge and understanding of pharmaceutical regulations. Energetic, detail oriented, highly motivated with a “can do” outlook. Change management skills. Ability to communicate across all levels of the organization. Effective written and verbal communication skills. Experience with Microsoft Office Tools including Excel, Word, and PowerPoint. Ability to multi-task and prioritize . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 months agovia common crawlApply ›

Sr Associate Biostatistics

India - Hyderabad, IndiaFrom $10/yr

Career Category Clinical Development Job Description Job Description Job Description HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission -to serve patients - drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together - researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Biostatistics Sr Associate What you will do Let’s do this. Let’s change the world. Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN) playing a key role in integrated delivery and functional leadership. As a Biostatistics Senior Associate, you will provide hands-on statistical expertise to clinical studies across the drug development lifecycle. You will author and review statistical documents, perform data analyses, and collaborate cross-functionally to ensure scientific rigor, regulatory compliance, and timely delivery of study outputs. This role provides an opportunity to gain breadth across statistical deliverables while developing depth in clinical trial methodology, programming, and cross-functional teamwork. Responsibilities: Author and provide statistical contributions to Statistical Analysis Plans (SAPs), Table/Figure/Listing (TFL) shells, randomization specifications, submission data file specifications (SDTM/ADaM), and other key study-related documentation. Conduct and document statistical analyses for clinical trials, including primary and secondary endpoint analyses, exploratory analyses, and dose-level review support. Perform and document quality control (QC) of datasets and outputs to ensure accuracy, consistency, and compliance with CDISC standards. Participate in Clinical Study Team (CST) meetings to provide statistical input and represent Biostatistics. Collaborate with programming colleagues to ensure timely delivery of study outputs. Contribute to clinical publications, study reports, and regulatory submissions. Support the review of deliverables from external suppliers for quality. Stay abreast of new methodologies, tools, and regulatory guidelines in statistical practice. Ensure that statistical sections of the Trial Master File (TMF) are maintained and up to date. Adhere to Amgen’s policies, SOPs, and relevant controlled documents, and support audits as needed. This position is currently located at Amgen India (Hyderabad). Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a strategic Biostatistics leader with a passion for tech-enabled transformation. Basic Qualifications: Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with 2 years post-graduate experience as a statistician in the pharmaceutical industry or medical research, OR Doctoral degree in Statistics/Biostatistics (or related subject with high statistical content) with 1 year post-graduate experience. Competency in statistical programming (SAS or R). Experience applying statistical methods in the analysis and conduct of clinical trials. Ability to clearly communicate in English, both written and oral. Preferred Skills: Master’s degree with 4+ years post-graduate experience, or Doctorate with 2+ years. Prior leadership of at least 1 study/project with minimal oversight. Experience authoring protocols, SAPs, and reviewing CSRs. Familiarity with CDISC standards (SDTM, ADaM). Experience with AI/automation tools to drive efficiency. Strong understanding of drug development and statistical applications across the clinical lifecycle. Thrive What you can expect of us As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being. Vast opportunities to learn and develop within our global organization Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

8 months agovia common crawlApply ›

Senior Manager, Biostatistical Programming

India - Hyderabad, IndiaFrom $10/yr

Career Category Clinical Job Description Senior Manager, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Senior Manager, Biostatistical Programming What you will do Let’s do this. Let’s change the world. Amgen is expanding its Global Statistical Programming (GSP) capabilities, with Amgen India (AIN) playing a key role in supporting integrated delivery across regions. As a Senior Manager of Biostatistical Programming (Programming Execution Lead), you will partner with the Global Programming Lead (GPL) and lead an offshore team of Study Lead Programmers (SLP) and Study Programmers (SP) to ensure successful execution of end-to-end programming activities for products within or across therapeutic areas. Together with the GPL, this Senior Manager will be accountable and responsible for Global Statistical Programming study results and drug approval submission activities for the assigned product areas. Key Responsibilities: Accountable and responsible for ensuring successful execution and delivery of Global Statistical Programming milestone analysis deliverables and regulatory submission packages for a product, or group of Amgen products, being supported by the offshore programming team. Work with GPL to ensure successful implementation of programming strategies, such as functional standards and industry requirements for the assigned product globally. Plan and monitor progress of projects and address issues accordingly. Provide GSP product level input to developing and managing resource plans and budgets for GSP. Efficiently and effectively monitor and utilize assigned staff at product level according to priorities. Lead and/or participate in departmental process improvement initiatives and cross-functional working groups. Assist in study and system audits and inspections by internal and external bodies. Develop, review, and implement Policies, SOPs and other controlled documents affecting GSP globally. Provide hands-on support to the assigned product areas as required. Provide coaching and mentoring to local programming staff. Provide input into career development plans for all staff on assigned projects This position will be located at Amgen India (Hyderabad). Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a results-oriented, tech-forward programming leader with deep expertise in clinical trial operations and digital transformation. Basic Qualifications: BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects, with at least 8 years of statistical programming experience in clinical development environment. Strong technical, communication, and leadership skills Ability to lead and manage programmers in successful and timely completion of all programming activities for a study or multiple studies from end to end Experience developing a successful offshore statistical programming team Flexibility and desire to work across different time-zones Advanced analysis and reporting skills in SAS (including SAS/STAT, Macro, Graph, SQL, etc.) Prior regulatory submission experience for drug approval Thorough understanding and experience with data quality and compliance checks Experience in software development (e.g., gathering user requirements, creating technical specifications, developing code, creating, and driving test plans) Experience working effectively in a globally dispersed team environment with cross-cultural partners Prior staff development leadership and project management experience Excellent oral and written English communication skills Ability to effectively perform complex statistical programming and related tasks Preferred Skills: MSc or higher degree in statistics, biostatistics, mathematics, or related quantitative or scientific subjects Familiarity with open-source programming tools (e.g., R, Python), automation platforms, and emerging technologies in statistical programming Thrive What you can expect of us As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being. Vast opportunities to learn and move up and across our global organization Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 months agovia common crawlApply ›

Senior Associate - Clinical Pharmacology

India - Hyderabad, IndiaFrom $198/yr

Career Category Clinical Development Job Description The department of Clinical Pharmacology, Modeling and Simulation (CPMS) within Amgen is dedicated to the development of novel, effective, and safe medicines. We are seeking a highly experienced Senior Associate to join the CPMS group. The successful candidate will contribute to Amgen’s multimodality development portfolio by conducting formal clinical pharmacology data analyses, summarizing pharmacokinetic/pharmacodynamic (PK/PD) data and results in clinical study report documents, performing quality control, reviewing PK/PD datasets, and adhering to applicable regulatory guidance (ie, good clinical practices [GCP]). In addition, the successful candidate will possess good written and oral communication skills, the ability to work well in teams, and will demonstrate technical aptitude and a strong work ethic. The individual will also be responsible for review and compliance with all applicable SOPs, business practices and company policies. The primary core responsibilities of the Senior Associate will include: Execution of formal PK/PD data analysis and report writing for clinical studies with a strong emphasis on quality and meeting timelines Perform quality control of analyses and outputs (ie, tables, figures, listings, and reports) to ensure accuracy and consistency in accordance with standard processes Review and create standardized datasets supporting clinical pharmacology analyses Work closely with CPMS data analysts and other team members, effectively communicate with project team representatives and actively participate/collaborate cross functionally Basic Qualifications Bachelor’s degree with 5-9 Years of total experience and 3 years of relevant experience in clinical pharmacology data analysis with an emphasis on non-compartmental analysis Preferred Qualifications Bachelor’s or Master’s degree in Pharmacy preferred, but can also be in related fields such as biology, chemistry, or biochemistry. Following skills are required: good understanding of clinical pharmacology and pharmacokinetic/pharmacodynamic concepts experience in conducting non-compartmental analysis experience working with clinical pharmacology datasets and report writing experience in working with Phoenix analysis software and with standardized analysis datasets (ADaM) Familiar with the drug development process, regulatory guidelines (including Good Clinical Practices), analysis methodology, and clinical pharmacology studies Skilled in using Microsoft Office software (ie, Word, Excel, PowerPoint) Able to work under tight deadlines Strong analytical, writing, communication, organization, and teamwork skills . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 months agovia common crawlApply ›

Biostatistics Sr Associate – Data Visualization

India - Hyderabad, IndiaFrom $10/yr

Career Category Clinical Development Job Description HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission -to serve patients - drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together - researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. Biostatistics Sr Associate What you will do Let’s do this. Let’s change the world. Amgen is expanding its global Biostatistics capabilities, with Amgen India playing a key role in integrated delivery and functional leadership. As a Biostatistics Senior Associate, you will provide hands-on statistical expertise to clinical studies across the drug development lifecycle. You will author and review statistical documents, perform data analyses, and collaborate cross-functionally to ensure scientific rigor, regulatory compliance, and timely delivery of study outputs. This role provides an opportunity to gain breadth across statistical deliverables while developing depth in clinical trial methodology, programming, and cross-functional teamwork. Responsibilities: Apply biostatistical methods to analyze and interpret clinical trial data Develop and maintain statistical programming solutions using R for data analysis, reporting, and automation Collaborate with cross-functional teams to ensure timely delivery of study outputs Support study teams with regulatory submission deliverables following industry standards such as CDISC (SDTM, ADaM) where applicable Stay abreast of new methodologies, tools, and regulatory guidelines in statistical practice Build automated workflows and reproducible reporting pipelines to improve efficiency and quality of statistical outputs Contribute to process improvements and innovative technologies that optimize statistical programming and reporting workflows Ensure compliance with regulatory requirements and internal quality standards Assist in reviewing Amgen policies, SOPs, and controlled documents to ensure compliance This position is currently located at Amgen India (Hyderabad). Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a strategic Biostatistics leader with a passion for tech-enabled transformation. Basic Qualifications: Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with 4 years post-graduate experience as a statistician in the pharmaceutical industry or medical research, OR Doctoral degree in Statistics/Biostatistics (or related subject with high statistical content) with 2 year post-graduate experience. Competency in statistical programming (R/Python). Experience with R Shiny or interactive reporting tools Experience applying statistical methods in the analysis and conduct of clinical trials. Ability to clearly communicate in English, both written and oral. Preferred Skills: Master’s degree with 6+ years post-graduate experience, or Doctorate with 4+ years. Prior leadership of at least 1 study/project with minimal oversight. Experience authoring protocols, SAPs, and reviewing CSRs. Familiarity with CDISC standards (SDTM, ADaM). Experience with AI/automation tools to drive efficiency. Strong understanding of drug development and statistical applications across the clinical lifecycle. Thrive What you can expect of us As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being. Vast opportunities to learn and develop within our global organization Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

4 months agovia common crawlApply ›

Sr. Associate, Marketing Operations

India - Hyderabad, IndiaFrom $40/yr

Career Category Marketing Job Description Role Name: Sr Associate, Marketing Operations Department Name: Global Device Strategy Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. ABOUT THE ROLE Role Description: The Global Customer Capabilities & Innovation organization strives to bring new ways of working to better support our patients and customers. The Device Strategy team’s purpose is to empower patients with a simple, seamless injection experience. This position will achieve this purpose through development and enhancement of patient & HCP-focused educational materials for Amgen’s drug delivery devices throughout the product lifecycle. The Senior Associate will manage the development of educational materials across various brands and devices. This role will partner with other GDS team members to deliver educational messages to the right stakeholders in the right medium across key moments that matter. The successful candidate will lead several initiatives to enhance the injection experience that will positively impact patients, their healthcare teams, and Amgen brands. Roles & Responsibilities: Content Development: Coordinate with GDS team members and agencies to produce high-quality marketing materials, including digital content, print collateral, and video assets. Manage material changes due to product label updates and continuous improvement initiatives. Prep materials for MAC Review in Veeva. Project Management: Oversee project timelines, budgets, and deliverables, ensuring campaigns are executed on time and within scope. Agency Management: Manage key projects with external agencies and vendors to ensure high-quality deliverables and adherence to timelines. Performance Analysis: Track, analyze, and report on key performance indicators (KPIs) for campaigns, making data-driven recommendations for optimization. Generate and maintain a monthly metrics dashboard with insights on key areas of focus for the device(s). Basic Qualifications and Experience: Doctorate degree and 1 year of Marketing and/or business experience in a role aligned with a Marketing/Sales commercial organization Or Master’s degree and 3 years of Marketing and/or business experience in a role aligned with a Marketing/Sales commercial organization Or Bachelor’s degree and 5 years of Marketing and/or business experience in a role aligned with a Marketing/Sales commercial organization Functional Skills: Required Skills: Strong marketing acumen with an understanding of marketing strategy, market research, and tactical plan development. Experience working with advertising agencies to develop and produce engaging creative. Excellent written and verbal communication skills. Experience marketing directly to consumers, with a preference for pharmaceutical or regulated consumer goods or services. Exceptional attention to detail and accuracy in all deliverables. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., Teams, Smartsheet). Preferred Skills: Experience with drug delivery devices, such as: pre-filled syringes, auto-injector pens, lyophilized reconstitution kits, and/or infusion pumps. Translating market research insights into effective campaigns or programs. Experience working in a multinational environment with global teams. Understanding and fulfillment of compliance and data privacy requirements. Soft Skills: Strong organizational, prioritization and time-management skills. Strong bias for action and ability to handle multiple priorities in a fast-paced environment. High degree of professionalism and interpersonal skills. Strong problem-solving abilities and adaptability to changing priorities. Collaborative mindset and ability to build positive relationships across diverse teams. Consistently operates in compliance to the Amgen Code of Conduct. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

5 months agovia common crawlApply ›

Pharmacovigilance Operations Senior Manager

India - Hyderabad, IndiaFrom $10/yr

Career Category Safety Job Description The Pharmacovigilance Operations Senior Manager provides strategic leadership and operational oversight of the global safety system and associated data mart to ensure accurate, compliant, and timely safety data analytics and reporting. This role is accountable for driving system performance, data integrity, inspection readiness, and regulatory compliance while advancing adoption of automation, artificial intelligence (AI), and innovative technologies across the pharmacovigilance ecosystem. Operating with a high degree of autonomy, the Senior Manager partners closely with Pharmacovigilance stakeholders to deliver scalable, future-ready solutions that enhance efficiency, insight generation, and regulatory confidence. Key Responsibilities Global Safety Systems & Data Governance Provide leadership and oversight for changes, enhancements, and configurations of the global safety system and associated data mart. Own data integrity, consistency, and reliability standards for safety data used in analytics, regulatory submissions, and decision-making. Oversee system configurations, including reporting rules, product and study setup, and integration points. Direct and govern User Acceptance Testing (UAT) activities to ensure validated, inspection-ready system changes. Partner with Safety Technology and Managed Services to optimize system performance, support models, and service delivery. Safety Data Outputs & Regulatory Reporting Own the strategy, prioritization and delivery of safety data outputs supporting: Periodic safety reporting (e.g., PADER, PSUR, DSUR), Signal detection and safety surveillance & Regulatory inquiries, audits, and inspections Ensure timely, high-quality delivery of automated and scheduled safety reports. Establish quality oversight, peer review standards, and continuous improvement for safety data outputs. Lead the definition and implementation of reporting solutions, including: User-defined reports, Query By Example (QBE) & Optimized search strategies aligned with global standards Translate business requirements into scalable, compliant reporting solutions. Study Start-Up & Systems Integration Provide strategic oversight for study start-up and integration activities, including: EDC–Safety Database integrations (e.g., RAVE/Veeva to LSMV/Argus) Review and approval of Mapping Specifications Worksheets (MSWs) UAT planning, execution, and documentation Ensure integrations meet regulatory, validation, and data quality expectations. Automation, AI & Innovation Leadership Define and drive the roadmap for automation, AI, and advanced analytics within pharmacovigilance operations. Lead the evaluation, implementation, and validation of innovative technologies, including: AI-assisted case processing, Signal detection and analytics solutions & Reporting and workflow automation Partner cross-functionally to pilot and operationalize new capabilities while ensuring compliance, data integrity, and inspection readiness. Monitor emerging technologies, industry trends, and regulatory expectations related to AI in pharmacovigilance. Establish governance, documentation, and change management frameworks to ensure sustainable and compliant adoption of innovation. Training, Process Excellence & Capability Building Lead the development and delivery of training for safety systems, reporting tools, and associated processes. Drive process standardization and continuous improvement through SOPs, work instructions and user documentation. Mentor and develop team members, strengthening technical depth and leadership capability. Compliance & Inspection Readiness Execute activities delegated by the Qualified Person for Pharmacovigilance (QPPV) as defined in the PV System Master File. Maintain a continuous state of inspection readiness across systems, data, and processes. Serve as a primary representative for: Health Authority inspections, Internal and external audits Own audit responses and remediation activities within scope of responsibility. Knowledge, Skills, and Experience Technical & Functional Expertise Deep expertise in pharmacovigilance safety systems, preferably ArisGlobal LifeSphere. Strong experience with reporting and analytics platforms (e.g., Cognos, Spotfire, Tableau). Working knowledge of Oracle databases, Oracle Developer, and programming languages (e.g., Python, PL/SQL). Solid understanding of data warehousing, analytics, and data mining techniques. Proven experience with SDLC, system validation, and regulated development standards. Regulatory & Domain Expertise Strong understanding of global pharmacovigilance regulations and safety reporting requirements. In-depth knowledge of clinical trial and pharmacovigilance operational processes. Experience supporting regulatory inspections and internal audits in a leadership capacity. Ability to interpret and apply aggregate safety data and analytics to regulatory and business decisions. Leadership & Professional Skills Proven ability to lead complex, cross-functional initiatives with minimal oversight. Strong strategic thinking, prioritization, and execution skills. Decisive problem-solver with sound judgment and escalation instincts. Executive-level written and verbal communication skills. Demonstrated ability to influence, build partnerships, and lead through change. Experience Pharmaceutical industry and/or health authority experience required. Prior experience supporting pharmacovigilance systems, safety data analytics, or regulatory reporting strongly preferred. Case management experience is strongly preferred. Education Doctorate degree OR Master’s degree and 3 years of directly related experience OR Bachelor’s degree and 5 years of directly related experience OR Associate’s degree and 10 years of directly related experience OR High school diploma / GED and 12 years of directly related experience . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

10 months agovia common crawlApply ›

Artwork Strategist - Global Artwork

India - Hyderabad, IndiaFrom $198/yr

Career Category Supply Chain Job Description Why this role matters Every artwork change sits at the intersection of multiple requirements – Regulatory, technical elements, Supply Chain, packaging and business. As an Artwork Strategist, you help ensure those requirements come together correctly before artwork is executed. Your judgement and ability to identify issues early will directly contribute to compliant, timely and right-first-time artwork delivery, supporting Amgen products and patients around the world. What you will do As an Artwork Strategist, you will play a pivotal role in translating Amgen's labelling and implementation strategies into artwork projects that are ready for successful implementation by the artwork executional team. Sitting at the intersection of Regulatory, Supply Chain, Packaging and Artwork, you will ensure that the strategy for implementing product launches and labelling variations is sound and that the information provided to our Artwork Designers and Reviewers is accurate, complete and ready for execution. This is not simply an artwork coordination role. You will be expected to connect the dots, ask the right questions, challenge where something does not look right and proactively drive issues to resolution. You will support products and markets globally and work with a broad network of colleagues across Amgen. Your key responsibilities You will: Participate in artwork implementation strategies for product launches, labelling variations and lifecycle changes, ensuring regulatory and Supply Chain implementation requirements are correctly translated into artwork execution. Assess artwork readiness, ensuring Designers and Reviewers receive accurate, complete and consistent inputs before artwork activities begin. Bring together and reconcile inputs from multiple functions, including Regulatory Operations, Supply Chain Project Management, Packaging Engineering, Master Data Management, Serialization and HFE-ID. Identify missing, conflicting or unclear requirements and proactively work with stakeholders to resolve them before they impact artwork execution. Manage and prioritize multiple artwork projects, ensuring activities progress in time to achieve required artwork start dates and business milestones. Support artwork projects through the applicable stages, including test artworks, mock-ups and master artworks, ensuring the agreed implementation strategy is maintained throughout execution. Apply your understanding of packaging sites, packaging lines, regulatory requirements and Supply Chain processes when assessing artwork implementation approaches. Support product launches and labelling variations across global regions, whilst maintaining sufficient cross-regional knowledge to provide effective back-up when required. Represent Global Artwork in cross-functional projects and contribute to improvements in artwork processes, systems and automation. What we are looking for You will thrive in this role if you enjoy working in a complex environment where there is not always a straightforward answer. We are looking for someone who can absorb information from several sources, understand how the pieces fit together and recognize when something is missing or inconsistent. You are comfortable speaking up, constructively challenging assumptions and influencing stakeholders to reach the right outcome. You will bring: A relevant degree or equivalent professional experience in Supply Chain, Life Sciences, Engineering, Packaging, Pharmaceutical Operations or a related field. Strong critical-thinking and problem-solving skills. Excellent organizational and priority-setting capabilities, with the ability to manage multiple activities and changing business needs. Strong communication and stakeholder-management skills. Confidence working independently and taking ownership for progressing issues to resolution. The ability to collaborate effectively across functions, cultures and geographies. Fluent written and spoken English. Preferred experience 9+ years of experience in one or more of the following would be advantageous: Pharmaceutical, biotechnology or another regulated industry. Pharmaceutical labelling variations and lifecycle management. Pharmaceutical packaging, packaging operations or packaging lines. Regulatory, Supply Chain, Packaging Engineering or Manufacturing. Artwork or labelling operations. GMP-regulated environments. Product launches and lifecycle changes. Artwork systems, digital workflows or automation. Working within a global organization. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 weeks agovia common crawlApply ›

Artwork Designer - Global Artwork

India - Hyderabad, IndiaFrom $198/yr

Career Category Supply Chain Job Description Job Summary We are seeking a talented Artwork Designer with a strong mindset for process improvements to join our team. As an Artwork Designer, you will be responsible for creating and/or reviewing right-first-time artworks, both created manually or automatically, and providing technical support for daily execution as required. In addition, you will be supporting the Artwork team with artwork readiness by creating and/or reviewing artwork (brand) templates, design templates and review of artwork print proofs, and artwork generated by Amgen partners. Key Responsibilities: Artwork Design in compliance with Amgen’s Standard Operating Procedures: Design right-first-time artworks, both manually or automatically, for all Amgen products and in different stages of development (test, mock-up, masters). Design artwork templates (design and brand templates). Artwork Review in compliance with Amgen’s Standard Operating Procedures: Review artworks, both manually or automatically, for all Amgen products and in different stages of development (test, mock-up, masters). Review templates: technical layout templates (TLTs), design templates, brand templates Review Supplier Print Proofs. Review and approve Artworks created by Amgen partners Assess non right-first-time artworks and perform root cause analysis on a subset of those artworks based on the criticality of the error. Collaborate with cross-functional teams to incorporate feedback and revisions into design iterations, as needed. Provide technical support to the artwork team and Amgen’s outsource service providers. Collaborate with printer suppliers to ensure their technical requirements are met and incorporated into our artworks to ensure print readiness with the highest quality standards. Represent artwork team and contribute to cross-functional projects, as needed. Provide input to optimize artwork processes, and support continuous process and quality improvements. Participate in team meetings. Basic Qualifications: Master’s degree in graphic design, fine arts, or related field undefined Bachelor’s degree in graphic design & 2-4 years of Packaging/Labeling experience in a GMP environment. Proven experience as an Artwork Designer in a highly regulated industry / cGMP pharmaceutical industry. Proficiency in graphic design software such as Adobe Creative Suite (Photoshop, Illustrator, InDesign) and other relevant tools. Solid understanding of design and packaging principles. Experience with print production processes and knowledge of prepress requirements. Preferred Qualifications: Bachelor’s Degree in Graphic Arts, Packaging or Life Sciences. 2 + years Packaging /Labeling experience with a focus on artwork creation. 2 + years of relevant work experience in a highly regulated industry / cGMP pharmaceutical industry. Experience with Microsoft Office software (Excel, Word, Power Point), visual tools (e.g. Tableau, PowerBI, Google Charts), and Document Management System (e.g VEEVA vault). Skills: Excellent communication skills and the ability to present and articulate design concepts effectively. Strong attention to detail. Ability to work independently as well as collaboratively in a fast-paced environment. Creative thinking and problem-solving skills. Flexibility to adapt to changing priorities and project requirements. Demonstrate sound judgement and decision-making abilities. Continuous improvement mindset. Self-motivated individual who demonstrates willingness to learn and be receptive to change. Great interpersonal and communication skills. Ability to uphold a sense of personal accountability. Experience with pharmaceutical labeling regulations. Proven track record of partnering with other departments to deliver on common objectives. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 weeks agovia common crawlApply ›

Artwork Reviewer - Global Artwork

India - Hyderabad, IndiaFrom $198/yr

Career Category Supply Chain Job Description Job Summary We are seeking a talented Artwork Reviewer who is willing to grow and develop their career within our team. As an Artwork Reviewer, you will be responsible for reviewing artworks, both created manually or automatically, for all Amgen products in any stage of development (test, Mock-up, master), as well as reviewing artwork (brand) templates, design templates, supplier print proofs, and artwork generated by Amgen partners. Key Responsibilities: Artwork Review in compliance with Amgen’s Standard Operating Procedures: Review artworks, both manually or automatically, for all Amgen products and in different stages of development (test, mock-up, masters). Review templates: technical layout templates (TLTs), design templates, brand templates Review Supplier Print Proofs. Review and approve Artworks created by Amgen partners Provide input to optimize artwork processes, and support continuous process and quality improvements. Participate in team meetings. Basic Qualifications: Bachelor’s degree in graphic design & 1-2 years of Packaging/Labeling experience in a GMP environment. Proficiency in graphic design software such as Adobe Creative Suite (Photoshop, Illustrator, InDesign) and other relevant tools. Solid understanding of design principles withing pharma industry. Knowledge of print production processes and prepress requirements. Preferred Qualifications: Some relevant work experience in a highly regulated industry / cGMP pharmaceutical industry. Experience with Microsoft Office software (Excel, Word, Power Point), visual tools (e.g. Tableau, PowerBI, Google Charts), and Document Management System (e.g VEEVA vault). Skills: Excellent communication skills and the ability to present and articulate design concepts effectively. Strong attention to detail. Ability to work independently as well as collaboratively in a fast-paced environment. Creative thinking and problem-solving skills. Flexibility to adapt to changing priorities and project requirements. Demonstrate sound judgement. Continuous improvement mindset. Self-motivated individual who demonstrates willingness to learn and be receptive to change. Great interpersonal and communication skills. Ability to uphold a sense of personal accountability. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 weeks agovia common crawlApply ›

Business Performance Manager Supply Chain AXP

India - Hyderabad, IndiaFrom $12/yr

Career Category Supply Chain Job Description Manager, Business Performance - Amgen External Planning Role Summary The Manager, Business Performance drives strategic improvements to AXP processes and ways of working, while delivering data-driven insights across the organization. The role helps shape AXP's digital strategy and enables smarter planning and supply chains across internal and external manufacturing through analytics, AI, and technology. The Manager owns improvements to the AXP Process Framework across Plan, Source, Make, Deliver, and Enable. In partnership with the Business Delivery Office (BDO) and Amgen Digital and Technology teams, the role standardizes workflows, identifies process gaps, and advances digital transformation. The role works with Global, Regional, and Site Supply Chain teams, Global Distribution, Contract Quality Management, Operations Finance, Global Planning, and AXP Regional Hubs. It supports performance visibility across commercial and pre-commercial supply, integrated business planning, operational excellence, digital adoption, and compliance. Roles and Responsibilities Improve and Govern AXP Processes · Own and improve the AXP Process Framework across Plan, Source, Make, Deliver, and Enable. · Standardize end-to-end workflows, roles, and handoffs across functions, regions, and sites. · Identify process gaps, risks, duplication, and unclear handoffs; maintain process maps, RACI matrices, work instructions, job aids, and guidance documents. · Work with AXP Compliance and the BDO to manage changes to SOPs and approved documents. · Apply Lean Business Systems and Operational Excellence methods to improve processes and ways of working. Lead Continuous Improvement and Automation · Use process analysis and value stream mapping to identify and prioritize continuous improvement, automation, and quick-win projects. · Develop business justifications that define expected benefits, ROI, cost avoidance, and cost savings. · Track project outcomes and confirm whether expected benefits are achieved. Advance Digital Transformation and Smart Supply Chains · Help shape and deliver AXP's digital strategy and transformation initiatives. · Identify practical uses of data, analytics, AI, and automation to improve internal and external manufacturing, planning, and supply chain processes. · Partner with Amgen Digital and Technology teams to define business needs and develop scalable solutions. · Translate business needs into system and reporting requirements; support implementation, adoption, and ongoing monitoring of solutions. Monitor Business and Financial Performance · Track AXP Supply Chain and Finance metrics with Operations Finance and Global Planning. · Maintain and improve KPI dashboards, reporting tools, and metric definitions; analyze performance across commercial and pre-commercial supply. · Identify important trends, variances, risks, and KPIs requiring immediate attention; share insights and coordinate follow-up actions with the appropriate owners. · Support visibility of agreed measures, including cost to serve, productivity, capacity, inventory, logistics, and financial plan or forecast variances. · Support Quarterly Business Reviews (QBRs), Integrated Business Planning (IBP), and forward 12-quarter strategy discussions. · Present data and analysis clearly to support business decisions. Partner Across AXP and Global Functions · Align priorities with the AXP Supply Execution Manager and BDO Manager. · Partner with Global, Regional, and Site Supply Chain teams, Global Distribution, Contract Quality Management, Operations Finance, Global Planning, and AXP Regional Hubs. · Support integrated processes and systems across regions and functions, working effectively across the US, Europe, and JAPAC time zones. Lead Projects and Develop Team Capability · Lead cross-functional projects and manage multiple priorities with minimal direction. · Advise leaders on options, risks, and solutions for complex issues. · Coach and develop team members; support capability building, succession planning, and engagement. · Promote accountability, collaboration, and continuous improvement. Tools and Systems Familiarity with modern supply chain and business performance tools is preferred: · Supply chain and enterprise planning: SAP S/4HANA, Kinaxis RapidResponse, or other enterprise planning systems. · Process mapping: iGrafx, Microsoft Visio, or Lucidchart. · Analytics and reporting: Tableau or similar business intelligence tools. · Process management: process monitoring, process governance, and controlled documentation. Basic Qualifications Candidates must meet one of the following education and experience requirements: · Doctorate degree and at least 3 years of Supply Chain, Business Analytics, or Operations experience; or · Master's degree and at least 8 years of relevant experience; or · Bachelor's degree and at least 10 years of relevant experience. In addition, candidates must have at least 2 years of experience directly managing or leading projects or programs. Preferred Qualifications · Experience leading cross-functional process standardization or improvement initiatives. · Lean Six Sigma experience; Green Belt certification preferred. · Strong analytical mindset and experience using data to identify business opportunities. · Experience applying analytics, AI, or automation to supply chain processes. · Ability to identify quick wins and develop business justifications, including ROI, cost avoidance, and cost savings. · Experience in pharmaceutical or biotech supply chains and GMP-regulated environments. · Understanding of internal and external manufacturing, including CMO/CDMO operations. · Experience with KPI dashboards, performance reporting, or KPI governance. · Experience supporting QBRs, IBP, or Long-Range Strategy cycles. · Strong project management, communication, presentation, and financial skills, including cost to serve, productivity, and capacity. Soft Skills · Growth mindset and willingness to learn, adapt, and improve. · Uses sound judgment and is willing to take calculated risks to move work forward. · Flexible and effective when collaborating across global time zones. · Seeks feedback, reflects on it, and applies it to improve performance. · Strong stakeholder management and relationship-building skills. · Constructive, accountable, and patient-focused attitude. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 weeks agovia common crawlApply ›

Business Analyst/Transformation - Process Intelligence

India - Hyderabad, IndiaFrom $13/yr

Career Category Information Systems Job Description Live What you will do Process Intelligence is a data-driven approach to creating process transparency by using advanced process analysis capabilities to uncover how end-to-end processes are actually executed, highlighting gaps between expectation and reality. In this vital role you will be accountable for executing the Results Delivery Office (RDO) Process Intelligence strategy and supporting our enterprise transformation programs aligned with the company’s most critical initiatives. Roles & Responsibilities: Drive initiatives to maximize business value from process intelligence deployments (current-state understanding, automation/redesign opportunities, and value capture monitoring). Understand and map end-to-end business processes, underlying systems, and data; identify performance gaps and improvement opportunities. Develop and maintain a knowledge repository of process insights derived from process mining and other process analysis tools; ensure appropriate process documentation and controls. Manage project work across multiple initiatives and process scopes; coordinate activities and information flow between process owners, analysts, IT, and RDO. Create visualization dashboards to present actionable insights and track key metrics, milestones, ROI and/or benefits. Win What we expect of you Basic Qualifications: Master’s OR Bachelor's degree and 7 to 13 years of Business Performance, Continuous Improvement, or Project Management experience Technical Skills: Must Have Skills: Process analysis, visualization, and improvement experience; proficiency with one or more process mining tools (e.g., Celonis, Signavio). Experience processing, filtering, and presenting large data extracted from multiple source systems. Data reporting experience (e.g. Tableau, Power BI). Strong project management capabilities partnering with both business and IT. Good to Have Skills: Coding knowledge (e.g., SQL, Python, YAML). Strong understanding of SAP ECC and S/4 HANA table structures; knowledge of system data structures and database management. Experience deploying AI and automation solutions (e.g., RPA). Broad business process knowledge, including biopharmaceutical-specific processes. Soft Skills: Must Have Skills: Accountability and autonomy to prioritize workload, operate independently, and deliver high-quality outputs. Strong problem solving and decision making; able to tackle ambiguity, apply risk-appropriate decisions, and escalate timely. Effective communication; distil complex information and tailor messages to audience. Teamwork and influencing skills; build strong cross-functional relationships. Good to Have Skills: Comfortable working in a start-up or build environment as we expand into new areas within the company. Continuous improvement mindset; nurture a culture of process transparency and performance improvement. Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

2 weeks agovia common crawlApply ›

1074 Amgen Technology Pvt Ltd office locations

India - Hyderabad, India

Track 1074 Amgen Technology Pvt Ltd in your pipeline

Get AI-powered resume tailoring for 1074 Amgen Technology Pvt Ltd roles, application tracking, and company research tools. Sign up free.

Open roles

Study Delivery Associate

Associate IS Engineer - Veeva Vault

Specialist IS Architect - Platform

Specialist Software Engineer - R&amp;D Omics

Sr Associate Business Analysis

Senior Associate - RWE Application Development

Sr Assoc QA - Global Supply Quality

Sr Associate Biostatistics

Senior Manager, Biostatistical Programming

Senior Associate - Clinical Pharmacology

Biostatistics Sr Associate – Data Visualization

Sr. Associate, Marketing Operations

Pharmacovigilance Operations Senior Manager

Artwork Strategist - Global Artwork

Artwork Designer - Global Artwork

Artwork Reviewer - Global Artwork

Business Performance Manager Supply Chain AXP

Business Analyst/Transformation - Process Intelligence

1074 Amgen Technology Pvt Ltd office locations

Track 1074 Amgen Technology Pvt Ltd in your pipeline

Specialist Software Engineer - R&D Omics