Sr Associate Is Analyst

Career Category Information Systems 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 IS Analyst - docuBridge What you will do Sr Associate IS Analyst - DocuBridge in this role will play a key role in implementation and lifecycle management of structured regulatory submission solutions with a main focus on Lorenz DocuBridge This role demands strong technical expertise hands-on experience with Lorenz DocuBridge and the ability to assist in managing multi-functional partner relationships across business IT and vendor teams The candidate will collaborate with internal Regulatory Affairs team members and vendor partners to ensure accurate interpretation of requirements delivery of compliant submissions and successful deployment of the solution The role includes assisting in validation testing user grievance resolution and overall user experience optimization Timely submission is critical and the candidate must support the project to closure within set timelines and quality standards Assist in the implementation and system ownership of Lorenz DocuBridge Suite ensuring the solution meets both global and regional regulatory requirements e g eCTD NeeS Collaborate with multi-functional partners including Regulatory Affairs Quality Assurance IT Security and vendor teams to gather detailed business requirements and translate them into scalable compliant technical solutions Support the team in defining and managing project plans timelines resource allocation and key landmarks to ensure end-to-end project execution - from system assessment procurement configuration validation launch to post-production support Assist in driving validation and compliance readiness by overseeing the development of validation plans IQ OQ PQ protocols and related documentation as per GXP 21 CFR Part 11guidelines Ensure regulatory submission readiness by enabling structured document authoring workflows lifecycle management and integration with content sources such as Regulatory Veeva RIM Oversee user access controls role-based privileges and audit trail configurations to ensure system integrity and security are maintained Support the change control process for the submission system by aligning with ITIL standards and ensuring traceability for all updates patches and configuration changes Support team to Develop training materials and conduct hands-on user training to onboard regulatory users and business owners ensuring effective adoption of the system Monitor production performance and work with business team and vender partner to solve issues ensuring timely resolution of incidents with minimal impact on business continuity Lead continuous improvement initiatives to enhance system usability performance and regulatory compliance alignment Track KPIs and provide regular status updates to leadership on system performance user adoption and project level challenges and risks Contribute to technology roadmap planning by finding opportunities for tool upgrades integration with newer modules e g Lorenz eValidator and regulatory intelligence platforms Act as the SME for structured submissions and represent the function during audits inspections and regulatory reviews Demonstrate adaptability to agile methodology ensuring flexibility and responsiveness to changing project requirements Manage and lead teams effectively fostering collaboration and productivity Use Jira and ServiceNow for project tracking issue resolution and service management What we expect of you We are all different yet we all use our unique contributions to serve patients The professional we seek is someone with these qualifications Basic Qualifications Master s degree Bachelor s degree and 5 to 9 years of relevant experience Must-Have Skills Demonstrate a deep understanding of pharma industry regulations and compliance requirements for including FDA and EUCTR Have good knowledge of submission publishing systems like Lorenz s docuBridge application and Regulatory Veeva RIM Demonstrated experience in managing technology initiatives and teams with a track record of successful innovation and fostering the development of talent Must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment Experience in applying technology standard process methodologies such as Scaled Agile SAFe and ITIL Exceptional collaboration communication must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment Possess strong knowledge of information systems and network technologies 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 Mandatory SAFe for Teams Preferred Soft Skills Excellent analytical and troubleshooting 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 Shift Information 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 based on business requirements 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