Urwah Admin

Amgen

<p><strong>Live</strong></p> <p><strong>What you will do</strong></p> <p>Let s do this. Let s change the world. In this vital role, you will manage country-specific regulatory affairs for Amgen's molecules, coordinate and implement regulatory submissions, ensure compliance with corporate and local requirements and lead documentation for local submissions under Senior Manager's guidance :</p> <ul> <li> <p>Ensures regulatory submissions are made on time and meet Amgen s corporate and local regulatory requirements</p> </li> <li> <p>Reviews promotional and non-promotional materials.</p> </li> <li> <p>Exchanges regulatory information and intelligence with other regulatory colleagues and cross functional teams on an ongoing basis and provides advice on local regulatory considerations/regulations in a timely manner.</p> </li> <li> <p>Partners with International Regulatory Leads (IRLs) and Global Regulatory Leads (GRLs) to support the regulatory development, registration, and lifecycle management of all Amgen molecules.</p></li> <li> <p>Partners with peers to ensure consistency on procedures.</p> </li> </ul> <p><strong>Win</strong></p> <p><strong>What we expect of you</strong></p> <p>We are all different, yet we all use our unique contributions to serve patients. The Regulatory Affairs professional we seek is a teammate with these qualifications.</p> <p><strong>Basic Qualifications:</strong></p> <ul> <li> <p>Bachelor`s degree in Pharmaceutical Science</p> </li> <li> <p>Working with policies, procedures and SOP s.</p> </li> <li> <p>Comprehensive understanding of regulatory activities and how they impact other projects and/or processes.</p> </li> <li> <p>Knowledge of the Gulf legislation and regulations</p> </li> <li> <p>Understanding of regulatory activities and how they impact other projects and/or processes</p> </li> <li> <p>Understanding of drug development</p> </li> <li> <p>Demonstrate ability to work in teams</p> </li> <li> <p>Ability to understand and communicate scientific/clinical information</p> </li> </ul> <p><strong>Preferred Qualifications:</strong></p> <ul> <li> <p>Regulatory experience of the Gulf Markets</p> </li> <li> <p>Knowledge of regional countries legislation and regulations relating to medicinal products in the Gulf Markets.</p> </li> <li> <p>Experience interacting with regulatory agency in the Gulf markets</p> </li> </ul> <p><strong>Thrive</strong></p> <p><strong>What you can expect of us</strong></p> <p>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.</p> <p>In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p> <p><strong>Apply now</strong></p> <p><strong>for a career that defies imagination</strong></p> <p>Objects in your future are closer than they appear. Join us.</p>

Associate Regulatory Affairs

<div><p><b>HOW MIGHT YOU DEFY IMAGINATION?</b></p><p>
If you feel like you&rsquo;re part of something bigger, it&rsquo;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&rsquo;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&rsquo;s time for a career you can be proud of. Join us.</p><p></p><p><b>
Biostatistics Manager</b></p><p><b>
What you will do</b></p><p>
Let&rsquo;s do this. Let&rsquo;s change the world.</p><p>
Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN) playing a key role in integrated delivery and functional leadership. As a Biostatistics Manager, you will provide technical expertise and support the execution of statistical deliverables for clinical studies. Operating under guidance, this role contributes through accurate implementation of statistical analyses and ensures adherence to CfDA and regulatory standards.</p><p></p><p><b>
Responsibilities:</b></p><ul><li><b>
Provide statistical contributions, review, and quality control of study design documents, including Key Design Elements (KDE) and protocols</b></li><li>
Serve as the GBS lead on the Clinical Study Team leadership team to execute clinical trials according to the protocol, performing risk assessments and ensuring quality data collection and alignment between data collection and study objectives</li><li>
Oversee statistical contributions to key design elements, protocols, randomization specifications, statistical analysis plans, tables, figures and listing shells, submission data file specifications, and other key study-related documentation</li><li><b>
Collaborate cross-functionally to deliver robust, valid and scientifically rigorous analysis results in Table, Figure and Listings (TFLs), Flash Memos (FM), Clinical Study Reports (CSRs), clinical publications, and other communications</b></li><li><b>
Ensure statistics sections of the TMF are maintained and up-to-date</b></li><li>
Communicate effectively with internal and external stakeholders regarding study-specific findings, analysis, and insights</li><li>
Contributes to defining signal detection threshold</li><li>
Manages self and collaborates closely with peers to ensure timely and quality deliverables</li><li>
Reviews deliverables from external suppliers for quality</li><li>
Staying abreast of the latest developments in the field of statistics in drug development and contribute to scientific advances in the field</li><li>
Assisting in the review of Amgen Policies, SOPs, and other controlled documents</li><li>
Contributing to process improvement initiatives and operational efficiencies.</li><li>
Manage self and other resources according to priorities</li><li>
Knowledgeable of developments in the field of statistics in drug development (innovative trial design) and Amgen&rsquo;s statistical policies, procedures and strategies.</li><li>
Assist with the development and implementation of technology that utilizes AI to streamline statisticians' work.</li></ul><p></p><p>
This position is currently located at Amgen India (Hyderabad).</p><p></p><p><b>
Win</b></p><p><b>
What we expect of you</b></p><p>
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.</p><p></p><p>
Basic Qualifications:</p><ul><li>
MSc or PhD in Statistics, Biostatistics, or related field.</li><li>
~4&ndash;5 years relevant industry experience.</li><li>
Proven ability to apply statistical methods in clinical development.</li></ul><p></p><p>
Preferred Skills:</p><ul><li>
Doctorate degree in Statistics/Biostatistics</li><li><b>
Experience in machine learning, real world data analytics, electronic health record data analysis, clinical trial simulation or related applications</b></li><li>
Life-cycle drug development experience</li><li>
Experience working effectively in a globally dispersed team environment with cross-cultural partners.</li></ul><p></p><p><b>
Thrive</b></p><p><b>
What you can expect of us</b></p><p>
As we work to develop treatments that take care of others, so we work to care for our teammates&rsquo; professional and personal growth and well-being.</p><ul><li>
Vast opportunities to learn and develop within our global organization</li><li>
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul></div>

Study Statistician

<div><p><b>ABOUT AMGEN</b></p><p>
Amgen harnesses the best of biology and technology to fight the world&rsquo;s toughest diseases, and make people&rsquo;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&rsquo;s known today.</p><p><b>
ABOUT THE ROLE</b></p><p>
Role Description:</p><p>
Let&rsquo;s do this. Let&rsquo;s change the world. We are seeking a strategic sourcing professional who thrives in ambiguity, can think long term, and has the discipline to deliver near-term results.</p><p>
You will serve as the Global Strategic Sourcing Manager and report to the India Indirect Lead. In this role, you will drive sourcing strategy and execution for Software, with a focus on Data Analytics and AI platforms. This includes developing and executing sourcing roadmaps, designing and leading negotiations, building supplier partnerships, and ensuring Amgen secures the right solutions at the best value while managing risk and enabling innovation.</p><p>
Your responsibilities will center on analyzing internal demand, market dynamics, and supplier capabilities to design sourcing strategies that achieve cost efficiency, supply resilience, and innovation. As a strategic sourcing leader, you will partner closely with business stakeholders to align procurement activities with Amgen&rsquo;s digital and enterprise-wide priorities</p><p>
.<b>Roles &amp; Responsibilities:</b></p><ul><li>
Strategic Sourcing Leadership</li><li>
Lead the end-to-end sourcing strategy for Software and AI/Data Analytics platforms.</li><li>
Drive sourcing initiatives that balance innovation, compliance, governance, and cost efficiency.</li><li>
Design and manage RFPs, supplier evaluations, negotiations, and contracting processes.</li><li>
Develop multi-year sourcing roadmaps that anticipate enterprise growth, regulatory needs, and evolving market capabilities.</li><li>
Identify and onboard emerging suppliers in analytics, AI, and predictive modeling to responsibly incorporate innovation.</li></ul><p><b>
Leadership</b></p><ul><li>
Partner with Digital, IT, Data Science, and R&amp;D leaders to align sourcing strategies with Amgen&rsquo;s technology and business roadmaps.</li><li>
Act as a trusted advisor, ensuring sourcing outcomes directly support business objectives.</li><li>
Facilitate cross-functional collaboration and guide stakeholder decision-making during complex sourcing projects.</li><li>
Ensure sourcing decisions adhere to regulatory, cybersecurity, and privacy requirements.</li><li>
Manage supplier performance through scorecards, SLAs, and business reviews.</li><li>
Partner with Legal, Compliance, and Cybersecurity teams to ensure robust contracting and risk mitigation.</li><li>
Leverage spend analytics, benchmarks, and market intelligence to drive cost savings and uncover new value.</li><li>
Deliver measurable improvements in cost efficiency, speed to market, and supplier innovation.</li><li>
Support continuous improvement in sourcing processes and tools to increase agility and impact.</li></ul><p><b>
Functional Skills:</b></p><p><b>
Must-Have Skills:</b></p><ul><li>
Deep expertise in strategic sourcing processes (RFPs, negotiations, supplier evaluations, contracting).</li><li>
Strong understanding of analytics and AI/ML software procurement, including cloud ecosystems (AWS, Azure, GCP, Databricks, Snowflake).</li><li>
Familiarity with procurement platforms (e.g., Ariba) and ERP/analytics tools.</li><li>
Strong analytical and organizational skills with ability to manage large-scale, complex sourcing projects</li></ul><p><b>
Good-to-Have Skills:</b></p><ul><li>
Experience in software/technology sourcing at a global scale.</li><li>
Financial and legal acumen to navigate complex agreements.</li><li>
Ability to evaluate supplier innovation and align sourcing with future business needs.</li><li>
Understanding of AI ethics, governance, and compliance frameworks.</li></ul><p></p><p><b>
Soft Skills:</b></p><ul><li>
Strong verbal and written communication skills.</li></ul><ul><li>
Ability to influence stakeholders and manage change.</li><li>
High initiative, self-motivation, and ability to navigate ambiguity.</li><li>
Comfortable working with global, virtual, and cross-functional teams.</li><li>
Strong negotiation and relationship management skills.</li></ul><p></p><p><b>
Basic Qualifications:</b></p><p>
Master&rsquo;s degree and 9+ years of total experience</p><p>
OR</p><p>
Bachelor&rsquo;s degree and 11+ years of total experience</p><p>
AND</p><p>
6+ Years of Sourcing experience</p><p></p><p>
EQUAL OPPORTUNITY STATEMENT</p><p>
Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p></div>

Strategic Sourcing - Technology, Cross Category

<div><p><b>Join Amgen&rsquo;s Mission of Serving Patients</b></p><p>
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.</p><p>
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. As a member of the Amgen team, you&rsquo;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.</p><p>
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&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p>
Overview</p><p>
We are seeking a highly experienced and motivated Senior Data Scientist to join our Corporate Audit and Worldwide Compliance &amp; Business Ethics teams in Hyderabad, India. This role is ideal for a strategic thinker and technical leader who thrives on driving innovation, leading analytics initiatives, and mentoring others. The Senior Data Scientist will leverage advanced analytics, machine learning, and emerging AI technologies &mdash; including generative and agentic AI &mdash; to enhance compliance monitoring, audit capabilities, and risk management processes.<br>
<br>
This position combines technical expertise, project leadership, and cross-functional collaboration to strengthen Amgen&rsquo;s global compliance and audit operations.</p><p>
Key Responsibilities</p><ul><li><p>
Lead the design, development, and deployment of advanced analytics, statistical models, and machine learning solutions to generate actionable insights that enhance compliance monitoring, auditing, and risk assessment.</p></li><li><p>
Manage and oversee data science projects end-to-end, including project scoping, planning, execution, and delivery; ensure quality control (QC) and validation of work produced by junior data scientists.</p></li><li><p>
Develop scalable, automated data pipelines and AI-driven analytics products to improve efficiency and accuracy in audit and compliance processes.</p></li><li><p>
Partner with cross-functional stakeholders across Compliance, Internal Audit, Commercial, R&amp;D, and Information Systems to design and implement analytics solutions aligned with business priorities.</p></li><li><p>
Access, integrate, and analyze data from multiple enterprise systems (e.g., SAP, Concur, Salesforce.com) to identify trends, anomalies, and compliance risks.</p></li><li><p>
Serve as a technical and analytical mentor to data scientists and analysts, promoting best practices in data science methodology, documentation, and reproducibility.</p></li><li><p>
Stay current with emerging technologies and techniques, including generative AI, agentic AI, and automation frameworks, to continuously advance analytical capabilities.</p></li><li><p>
Effectively communicate complex analytical concepts and findings to both technical and non-technical audiences, including senior leaders.</p></li><li><p>
Contribute to strategic planning and roadmap development for analytics initiatives within Compliance and Internal Audit.</p></li></ul><p>
Basic Qualifications</p><ul><li><p>
Bachelor&rsquo;s degree in Data Science, Statistics, Computer Science, Business Analytics, or a related field, with 8&ndash;14 years of relevant experience</p></li></ul><p><b>
What you can expect of us</b></p><p>
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&rsquo;ll support your journey every step of the way.</p><p>
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p><p></p><p><b>
Apply now for a career that defies imagination</b></p><p>
Objects in your future are closer than they appear. Join us.</p><p>
careers.amgen.com</p><p></p><p>
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.</p><p>
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.</p><p>
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.</p></div>

Sr. Data Scientist

<div><p>Increasing demand for observational research (now commonly referred to as real-world evidence [RWE]) from regulatory and reimbursement authorities makes observational research a key component of drug development and commercialization. Amgen's Center for Observational Research (CfOR) is a global organization with an industry-leading analytical capability that generates RWE to support business needs across a product&rsquo;s lifecycle. CfOR scientists partner with internal stakeholders and industry experts to design, conduct, interpret and publish observational research that informs decision-making from the early development of a molecule to the design of clinical trials and the safety and efficacy of Amgen medicines.</p><p></p><p>
We are seeking a <b>Senior Associate, Strategic Planning &amp; Operations</b>, to join the Center for Observational Research (CfOR). This role will work with other Amgen teams to oversee and drive execution of CfOR&rsquo;s operational projects and non-interventional studies ensuring timely completion within budget and at the highest quality. This role requires strong project management capabilities combined with a growth mindset and openness to leveraging emerging AI tools to improve productivity and drive CfOR-wide initiatives.</p><p></p><p><b>
Key Responsibilities:</b></p><ul><li>
Provide specialized support to a team of Observational Research Scientists specializing in real-world evidence projects in multiple regions</li><li>
Provide comprehensive document requirement support, mainly to a team of Observational Research Scientists specializing in real-world evidence studies across the globe</li><li>
Support adoption and integration of platforms such as Smartsheet, AI, Microsoft Teams, and Miro to enhance team collaboration and project tracking</li><li>
Support strategic initiatives, including operational pilots, change management efforts that elevate CfOR&rsquo;s organizational capabilities</li><li>
Contribute to department/unit by ensuring quality of tasks/services provided
</li><li>Communicate status and issues effectively to appropriate parties, both within CfOR and across Amgen</li><li>
Assist leaders with study start-up and study close-out processes
</li><li>Identify and implement process improvements through automated technology to increase efficiency, reduce cycle time and replace manual operations</li><li>
Create, analyze, and maintain process flow diagrams to ensure efficient and effective operational workflows</li><li>
Track and reconcile study milestones and deliverables, ensuring accurate data population in internal systems</li><li>
Conduct regular meetings with study leads to discuss operational activities</li><li>
Identify potential department/cross functional process improvement activities</li><li>
Execute financial transactions, including purchase order processing, invoice verification, payment processing, and engaging with other functions to help plan and manage resource expenses, using Anaplan, Ariba or SAP software</li></ul><p></p><p><b>
Basic Qualifications:</b></p><ul><li>
Bachelor&rsquo;s degree and 6+ years of Scientific or Operations experience OR</li><li>
Master&rsquo;s degree and 4+ years of Scientific or Operations experience</li></ul><p></p><p><b>
Preferred Qualifications/Skills:</b></p><ul><li>
Minimum of 3 years of project management experience, with 2+ years in pharma/biotech within regulated, cross-functional environments</li><li>
Hands-on experience with budgeting, vendor management, and regulated document management systems</li><li>
Demonstrates autonomy and reliability in managing tasks and contributing to team goals</li><li>
Highly organized, with the ability to prioritize and deliver on projects independently or collaboratively</li><li>
Quick learner with strong analytical skills and adaptability to new tools and concepts</li><li>
Effective communicator with strong written, verbal, and presentation abilities</li><li>
Builds positive relationships and fosters collaboration with a proactive, &ldquo;can-do&rdquo; attitude</li><li>
Demonstrated proficiency &amp; adaptability with related software tools (ChatGPT, Copilot, Smartsheet, Miro, SharePoint, MS Teams, Office 365, etc.)</li><li>
Familiarity with drug commercialization &amp; business practices</li><li>
Comprehensive understanding of Good Clinical Practices (GCP), FDA regulations, and applicable regulatory/compliance frameworks critical to clinical and commercial operations</li></ul></div>

Sr. Associate - Strategic Planning & Operations

<div><p>As a Senior Associate Software Engineer at Amgen, you will be responsible for developing and maintaining software applications to meet business needs. You will collaborate with a team of software engineers, participate in the full software development life cycle, and ensure the delivery of high-quality code and solutions. Your strong programming skills, problem-solving abilities, and attention to detail will contribute to the development of robust and scalable software solutions.</p><p></p><p><b>
Responsibilities</b></p><ul><li><b>
Design, develop, and maintain</b> secure, scalable applications and integrations across QC and commercial platforms (AWS, Databricks, Salesforce Marketing Cloud, Mulesoft, LIMS, ELN, and CDS).</li><li><b>
Serve as a system owner</b> by managing lifecycle activities (configuration, validation, upgrades, change control, documentation, and audit readiness) in compliance with GxP and 21 CFR Part 11 requirements.</li><li><b>
Collaborate with business analysts, developers, and stakeholders</b> to gather requirements, deliver validated solutions, and support Agile/DevOps practices.</li><li><b>
Champion continuous improvement</b> by troubleshooting issues, optimizing workflows, and evaluating new platform capabilities to enhance business value and user experience.</li></ul><p></p><p><b>
Win</b></p><p><b>
What we expect of you</b></p><p>
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a person with these qualifications.</p><p>
Would you like to take your software engineering skills and help deliver the world's most advanced and life-changing biotech medicines? If you are excited to work on latest and greatest technology stack, we are looking for you. The Associate will work with some of the brightest minds in the industry and get opportunities to solve some of the most challenging business problems. At Amgen, your work will improve the lives of millions of patients around the world.</p><p></p><p><b>
Responsibilities</b></p><ul><li>
Serve as the System Owner for Quality Control Laboratory Platforms (Sample Manager LIMS, Biovia OneLab ELN) ensuring the platform is compliant, validated, secure, and aligned with regulatory requirements (e.g., GxP, 21 CFR Part 11, data integrity standards).</li><li>
Own the system lifecycle &mdash; oversee implementation, upgrades, validation, and retirement activities, following Amgen&rsquo;s system development life cycle (SDLC) and change management processes.</li><li>
Act as the primary liaison between product team, support team and client facing technology leads.</li><li>
Collaborate closely with developers and technical teams to design, configure, integrate, and validate enhancements, extensions, and interfaces (e.g., to LIMS, data lakes, or other lab systems).</li><li>
Lead and coordinate validation activities, including authoring/reviewing test scripts, managing traceability matrices, and supporting audit readiness.</li><li>
Manage integrations and data workflows between OneLab ELN and supporting systems, ensuring seamless interoperability and secure data exchange.</li><li>
Maintain system documentation including requirements, design, SOPs, training materials, validation documents, and user guides.</li><li>
Monitor vendor product roadmaps for Biovia OneLab ELN and evaluate applicability to Amgen&rsquo;s business needs; drive adoption of new features when beneficial.</li><li>
Ensure audit readiness by maintaining compliant system records, addressing deviations/incidents, and supporting regulatory inspections.</li><li>
Champion best practices and innovation in digital lab solutions, helping to modernize workflows while maintaining compliance and quality standards.</li><li>
Contribute to Agile ceremonies (standups, sprint planning, retrospectives) and support DevOps/CI/CD activities as applicable.</li></ul><p>
Basic Qualifications</p><p>
Master's degree</p><p>
OR</p><p>
Bachelor's degree and 2 - 6 years of Information Science experience</p><p></p><p><b>
Preferred Qualifications</b></p><ul><li>
2 + years of direct experience with Biovia OneLab ELN, THermo Fisher Sample Manager LIMS or comparable ELN solutions (e.g., Biovia Workbook, LabWare, Labguru).</li><li>
Strong understanding of system ownership responsibilities including:</li></ul><p>
GxP compliance, 21 CFR Part 11 requirements, and validation</p><p>
System lifecycle management, change control, and audit readiness</p><p>
Ensuring data integrity and security of scientific records</p><ul><li>
Proven experience integrating and validating systems within a regulated environment (GxP, FDA, EMA).</li><li>
Experience with integrating OneLab ELN, LIMS into broader Operations, R&amp;D and IT ecosystems (e.g., LIMS, inventory systems, data warehouses).</li><li>
Familiarity with scientific workflows (biologics, chemistry, lab processes) and ability to translate them into digital solutions.</li><li>
Hands-on technical skills with SQL, Python, AWS, and APIs for data workflows, automation, and system integration.</li><li>
Knowledge of DevOps/Agile practices, release management, and vendor management for SaaS/enterprise platforms.</li><li>
Strong communication skills with the ability to define, document, and understand customer requirements, ensuring alignment between business needs and technical delivery.</li></ul><p><b>
Thrive</b></p><p><b>
Some of the vast rewards of working here</b></p><p>
As we work to develop treatments that take care of others, we also work to care for our teammates&rsquo; professional and personal growth and well-being.</p><ul><li>
Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey</li><li>
A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>
Generous Total Rewards Plan&mdash;comprising health, finance and wealth, work/life balance, and career benefits&mdash;with compensation and benefits rated above 4 stars (out of 5) on Glassdoor</li></ul><p><b>
Apply now</b></p><p><b>
for a career that defies imagination</b></p><p>
Objects in your future are closer than they appear. Join us.</p><p><b>
careers.amgen.com</b></p></div><p></p>

Sr. Associate Software Engineer

<div><div><div><p>ABOUT AMGEN</p></div><div><p>
Amgen harnesses the best of biology and technology to fight the world&rsquo;s toughest diseases, and make people&rsquo;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&rsquo;s known today.</p></div><p></p><div><p><br>
ABOUT THE ROLE</p></div><div><p>
Role Description:</p></div><div><p>
Amgen is seeking a <b>Sr Associate Software Engineer</b><b> </b>to contribute to designing, building, maintaining, analyzing, and interpreting data to provide actionable insights that drive business decisions. This role involves working with large datasets, developing data pipelines, supporting and executing data governance initiatives and visualizing data to ensure data is accessible, reliable, and efficiently managed. The ideal candidate has strong technical skills and experience with MuleSoft, Databricks, Airflow and AWS.</p></div><div><p>
Roles &amp; Responsibilities:</p></div><div><ul><li><p>
Design, develop, and maintain data solutions for data generation, collection, and processing using Databricks and Airflow</p></li></ul></div><div><ul><li><p>
Design, build and maintain APIs and MuleSoft jobs leveraging best practices to build robust integrations between CRM and cross-functional systems</p></li></ul></div><div><ul><li><p>
Be a key team member that assists in design and development of the data pipeline</p></li></ul></div><div><ul><li><p>
Create data pipelines and ensure data quality by implementing ETL processes to migrate and deploy data across systems</p></li></ul></div><div><ul><li><p>
Contribute to the design, development, and implementation of data pipelines, ETL/ELT processes, and data integration solutions</p></li></ul></div><div><ul><li><p>
Take ownership of data pipeline projects from inception to deployment, manage scope, timelines, and risks</p></li></ul></div><div><ul><li><p>
Collaborate with cross-functional teams to understand data requirements and design solutions that meet business needs</p></li></ul></div><div><ul><li><p>
Develop and maintain data models, data dictionaries, and other documentation to ensure data accuracy and consistency</p></li></ul></div></div><div><div><ul><li><p>
Implement data security and privacy measures to protect sensitive data</p></li></ul></div><div><ul><li><p>
Leverage cloud platforms (AWS preferred) to build scalable and efficient data solutions</p></li></ul></div><div><ul><li><p>
Collaborate and communicate effectively with product teams</p></li></ul></div><div><ul><li><p>
Collaborate with Data Architects, Business SMEs, and Data Scientists to design and develop end-to-end data pipelines to meet fast-paced business needs across geographic regions</p></li></ul></div><div><ul><li><p>
Identify and resolve complex data-related challenges</p></li></ul></div><div><ul><li><p>
Adhere to best practices for coding, testing, and designing reusable code/component</p></li></ul></div><div><ul><li><p>
Explore new tools and technologies that will help to improve ETL platform performance</p></li></ul></div><div><ul><li><p>
Participate in sprint planning meetings and provide estimations on technical implementation</p></li></ul></div><div><p>
Basic Qualifications and Experience:</p></div><div><ul><li><p>
Master&rsquo;s degree and 3 to 7 years of Computer Science, IT or related field experience OR</p></li></ul></div><div><ul><li><p>
Bachelor&rsquo;s degree and 5 to 9 years of Computer Science, IT or related field experience OR</p></li></ul></div><div><ul><li><p>
Diploma and 7 to 11 years of Computer Science, IT or related field experience</p></li></ul></div><div><p>
Functional Skills:</p></div><div><p><b>
Must-Have Skills</b></p></div><div><ul><li><p>
Hands-on experience with big data technologies and platforms, such as Databricks, Apache Spark (PySpark, SparkSQL), workflow orchestration, performance tuning on big data processing</p></li></ul></div><p></p><div><ul><li><p><br>
Proficiency in data analysis tools (eg. SQL) and experience with data visualization tools</p></li></ul></div><div><ul><li><p>
Skilled in MuleSoft API and Mulesoft integration job design and development</p></li></ul></div><div><ul><li><p>
Excellent problem-solving skills and the ability to work with large, complex datasets</p></li></ul></div><div><ul><li><p>
Strong understanding of data governance frameworks, tools, and best practices.</p></li></ul></div></div><div><div><ul><li><p>
Knowledge of data protection regulations and compliance requirements (e.g., GDPR, CCPA)</p></li></ul></div><div><p><b>
Good-to-Have Skills:</b></p></div><div><ul><li><p>
Experience with ETL tools such as Apache Spark, and various Python packages related to data processing, machine learning model development</p></li></ul></div><div><ul><li><p>
Strong understanding of data modeling, data warehousing, and data integration concepts</p></li></ul></div><div><ul><li><p>
Knowledge of AnyPoint Platform, Python/R, Databricks, SageMaker, Airflow, AWS cloud data platforms</p></li></ul></div><div><ul><li><p>
Proficiency in using Databricks Assistant, and other AI tools</p></li></ul></div><div><p>
Professional Certifications</p></div><div><ul><li><p>
Certified in MuleSoft Certified Developer 1 or higher (preferred)</p></li></ul></div><div><ul><li><p>
Certified Associate or Professional Data Engineer / Data Analyst (preferred on Databrick)</p></li></ul></div><div><ul><li><p>
Certified AWS Professional or Associate certification (preferred)</p></li></ul></div><div><p>
Soft Skills:</p></div><div><ul><li><p>
Excellent critical-thinking and problem-solving skills</p></li></ul></div><div><ul><li><p>
Strong communication and collaboration skills</p></li></ul></div><div><ul><li><p>
Demonstrated awareness of how to function in a team setting</p></li></ul></div><div><ul><li><p>
Demonstrated presentation skills</p></li></ul></div><p></p><div><p><br>
EQUAL OPPORTUNITY STATEMENT</p></div><div><p>
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.</p></div><div><p>
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.</p></div></div></div>

Sr. Associate Integration Software Engineer

Join Amgen and explore 53   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.