Introduction to role Join our dynamic team as an Associate Director, Pharmacovigilance Processes, where you will work closely with the PV Processes Manager, Associate Director, and Director. You will be responsible for handling assigned AstraZeneca projects and processes, including implementation, communication, compliance, performance, and inspection readiness. You will develop relationships across Patient Safety and other relevant areas of AstraZeneca to complete the delivery of the processes strategy and priorities, alongside governance and management of current procedural documents. Accountabilities Find opportunities for and drive the enhancement of existing processes through knowledge of internal and external environments. Work with Process Managers, Associate Directors, Patient Safety, and Regulatory authorities to develop, establish, monitor, report, and assess global KPIs related to safety and regulatory data reporting. Lead the management of process updates in Patient Safety; initiate updates, project manage the delivery of new documents, work with the BPO for content updates, address comments, and release the document. Be an expert in the ECMS tool and associated processes. Support PS Process owners with guidance, advice, and support on PD processes. Use safety and regulatory knowledge to maintain and support the global inspection readiness strategy. Provide process or compliance support to regulatory teams and submissions using a deep understanding of pharmacovigilance processes and regulations. Establish a culture of continuous improvement, high performance, flexibility, and quality emphasizing a can do attitude and innovative approaches. Contribute to the overall management and oversight of the Pharmacovigilance Quality System. Develop and maintain a vision and strategy for nominated pharmacovigilance or regulatory processes. Coordinate and own the lifecycle management of nominated processes, enabling business continuity and compliance. Find opportunities to improve and simplify methodologies in processes and guidance, provide practical solutions, and drive implementation. Promote innovation and new ways of working to drive efficiency and improved deliverables in all processes and partnerships. Lead the development or enhancement of standards or techniques to improve the quality, compliance, and efficiency of deliverables for the overall group. Develop and improve reporting tools and analysis processes and technology. Perform monitoring, analysis, and trending of data. Identify issues and risks and propose options to mitigate them. Monitor, interpret, and validate current, new, and changing legislation, handling the impact of changes. Ensure appropriate, up-to-date records are maintained for compliance. Participate in or support activities for GVP, GCP, GRP, and GMP audits/inspections. Deliver on project assignments supporting the business, e.g., representation or leadership on global cross-functional task forces. Provide process training to relevant functional groups. Seek personal and professional development opportunities and share knowledge gained in open forums. Represent AstraZeneca on industry bodies when appropriate. Serve as the delegate for Process Directors where appropriate. Contribute to communication and change management activities associated with process initiatives. Build relationships with stakeholders and customers to support pharmacovigilance and regulatory activities and responsibilities including successful partnerships. Work collaboratively to provide expertise and share best practices across all regions and partnerships. Essential Skills/Experience A science/pharmacy/nursing degree with at least 5 years relevant experience (pharmaceutical, regulatory, safety, and partnership) Experience in working cross-functionally Leadership skills, including proven leadership of project teams experience Thorough scientific knowledge sufficient to understand all aspects of regulatory/pharmacovigilance and partnership issues Thorough knowledge of the drug development process Good attention to detail Excellent written and verbal communication skills Proven track record to work across cultures Knowledge of AZ Business and processes Able to influence whilst maintaining an independent and objective view Strong collaboration skills Strong negotiation, conflict management, and interpersonal skills Relationship builder Able to work effectively as a member of a cross-functional or global team Understanding of change management process Desirable Skills/Experience MSC/PhD in scientific field Knowledge of new and developing regulatory and pharmacovigilance expectations Knowledge of existing AstraZeneca external alliances and collaborative projects Knowledge of CoE and CMO operating model Experience working with third-party suppliers Experience working in a global organization, preferably within the pharmaceuticals industry, with knowledge of the drug development life cycle and commercial aspects of the industry

Job Title: Manager, Global Clinical Solutions Introduction to role Global Clinical Solutions (GCS) drives the delivery of services and technology for AstraZeneca for its internal and external partners. The Manager, GCS supports teams to improve process effectiveness and performance in operational processes/procedures within the department, as well as providing support and guidance in the development of processes owned by Global Clinical Solutions. Individuals with this job will coordinate/lead and deliver GCS services across projects and/or other activities that enable delivery of Clinical Development programs to time, cost, and quality across all delivery models. They may be assigned one or more roles relating to the development and maintenance of processes, systems, and services. All Managers, GCS will lead and project run improvement projects as needed. Accountabilities As a member of a specific activity team, the Manager, GCS: Coordinates and delivers GCS services and coordinates life cycle management and business continuity for projects, services, and technology. Provides authority support to user communities including: I. Conducting relevant process/system/tool trainings II. Facilitating knowledge sharing III. Establishing standard methodologies IV. Ensuring communication with relevant partners across GCS and AZ Conducts critical analyses of processes and tools to define business usage and finds opportunities to improve efficiency/effectiveness of systems/services/processes whilst reducing business continuity risks. Chips in to and/or develops cases for continuous improvement projects. Leads or handles business improvement projects according to lean principles, including planning, prioritizing, implementing, and tracking delivery. Acts as a source of knowledge in one or more areas of GCS. Supports the implementation of changes to improve the way various functions and teams perform. Evaluates and monitors the performance and efficiency of programs to ensure that program implementation is on target. Responsible for training colleagues to use continuous improvement in the new ways of working and embed change culture. Grows capabilities, applies new approaches to improve work; and has a positive impact on team performance creating learning opportunities for others. Responsible for knowledge management of continuous improvement activities and ensuring that the knowledge is used in the selection and execution of future activities. Essential Skills/Experience University degree in related subject area, preferably in biological science or healthcare-related fields, such as medicine, nursing, or equivalent experience Ability to work collaboratively; shown organizational and analytical skills, and shown skills to deliver to time, cost, and quality Good project management skills Excellent knowledge of spoken and written English Strong business communication, partner management, and presentation skills Well-developed organizational and social skills Ensures risks and issues management to ensure effective delivery. Authoritatively applies issue routes and governance to gain traction and deliver rapid solutions Shares lessons learned and standard methodology recommendations with relevant partners to drive continuous improvement Builds relationships and achieves results without line management input Curious and self-motivated Desirable Skills/Experience Expert in their relevant service Experience of utilizing standard process improvement methodologies (e.g., Lean Six Sigma) to identify root causes of process issues and identify areas of process improvement Some experience of Quality Systems and Quality Management, including process definition and process improvement, ideally within an Information Systems environment Experience in multiple fields of clinical development At least 2 years experience in Drug Development within a pharmaceutical or clinical background Understanding ICH GCP guidelines in relation to study delivery Experience of working in a global organization with complex/geographical context When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. Thats why we work, on average, a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Date Posted 12-Mar-2025 Closing Date 29-Apr-2025

About us At AstraZeneca we are guided in our work by a strong set of values, and we re resetting expectations of what a biopharmaceutical company can be. By truly following the science, we pioneer new methods, new thinking and bring unexpected teams together. From scientists to sales, lab techs to legal, we re on a mission to turn ideas into life changing medicines that transform lives. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. If you re swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. Typical Accountabilities : Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. Leads Local Study Team consisting of Study Start-up Manager(s), Contract Manager(s), CRA(s), CSA(s), for assigned study/studies. Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with AZ Procedural Documents, ICH-GCP and local regulations. Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality. Leads the site selection process by identifying potential sites/investigators with Feasibility Lead (and (acting) Site Engagement Lead- where applicable) , performing initial Site Quality Risk Assessment in collaboration with CRA, and conducting or overseeing Site Qualification Visits to evaluate suitability and quality risks. Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in AZ clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head). Ensures timely preparation of local Master CSA (including site budget) and amendments as needed. Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant AZ SOPs and local regulations. Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with AZ SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction). Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations. Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans in collaboration with Clinical Research Associate Director as appropriate. Reviews or oversees the review of monitoring visit reports (as required and following AZ SOPs) and pro-actively advices the monitor(s) on study related matters. Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs. Proactively identifies risks and facilitates resolution of complex study problems and issues. Organizes regular Local Study Team meetings on an agenda driven basis. - Is responsible to coordinate LST and specific meetings with the local medical affairs team through ECPLIPSE2.0 Actively works towards achieving good personal relationships with all Local Study Team members, sites staff, local (eg medical affairs) and global stakeholders. AstraZeneca Job Profile. Is responsible to pro-actively share Reports study progress/update, risks and mitigation plan to the Global Study Associate Director/ Global Study Team, including SMM Lead. Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary and set-up of recruitment vendor solutions. Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meetings, in line with local codes, as required. Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies. Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are set-up, updated and access is organized at country level. Ensures accurate payments related to the study are performed according to local regulations and agreements. Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and AZ Procedural Documents. Ensures completeness of the eTMF and ensures essential documents are uploaded in a timeline manner to maintain the eTMF Inspection Ready . Ensures that all study documents are ready for final archiving and completion of local part of the eTMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA. Provides input to process development and improvement. Provides regular information to Line Managers at country level on studies and planned study milestones/key issues. Updates Line Managers about the performance of the CRAs/CSAs. Ensures that study activities at country level comply with local policies and code of ethics. Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. Ensures compliance with AstraZeneca s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). Collaborates with local Medical Affairs team on the study execution and delivery. Supports SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management. May act as Site Management & Monitoring Lead for the study Education, Qualifications, Skills and Experience Bachelor s degree in relevant discipline. Significant experience in Study Management within a pharmaceutical or clinical background. Thorough knowledge of Patient Safety processes and local regulations Advanced degree within field Professional certification Clinical study delivery operational experience Project management experience Why AstraZeneca? At AstraZeneca we re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We re on an exciting journey to pioneer the future of healthcare. Date Posted 18-Mar-2025 Closing Date 30-Mar-2025

About us At AstraZeneca we are guided in our work by a strong set of values, and we re resetting expectations of what a biopharmaceutical company can be. By truly following the science, we pioneer new methods, new thinking and bring unexpected teams together. From scientists to sales, lab techs to legal, we re on a mission to turn ideas into life changing medicines that transform lives. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. If you re swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. Roles & Responsibilities: Ensure Zero breach in the SOTC Process Agility in purchase order execution with mitigation of Risks Detailed reading of Tender, Rate Contract and Purchase Orders terms and conditions and mitigate the risks with right external & internal consents. Validate the Purchase Orders with internal references and Regularization of the Purchase Orders Coordinate with CFTs (Tender / Sales / Finance / Distribution / and Quality) for the execution of Purchase Orders Timely communications to the internal and external stakeholders on the purchase order related issues/Status Ensuring to keep sufficient stock inventories at the sales depots by coordinating with the Sales Team. Prepare and submit the documents as per terms of tender, rate contract and purchase orders with all the supplies for the payment realization against the purchase order. Preparation of m onthly dashboards on the purchase order executions and pending order details with the internal stakeholders. Coordinate with Tender Support for the Security Deposits for the Rate Contract finalization and Purchase Order Execution. Filing all the purchase order related documents and support the internal and external audit process. Skills Required: Assertive ness : follow the process and execute the job within the SOP Attention to details & Problem Solving : should be able to understand the challenge in hand and support with the solutions as an option to the CFT. Communication : effective in verbal and written communication. Collaboration : Person should have the good collaboration mindset and a great team payer. Proactiveness & Time Management : Should be able to pre-empt the next bottle necks and work proactively to resolve the issue in timely manner with race against the time mindset. Essential Education al Qualification: B Pharmacy/ bachelor s degree with relevant experience in the SOTC Advance d Microsoft O ffice Desirable : Experience in Pharma SOTC process will be an advantage. Experience in tender operations/Pharma Operations (Supply chain/procurement) will be an advantage. Why AstraZeneca? At AstraZeneca we re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We re on an exciting journey to pioneer the future of healthcare. Date Posted 18-Mar-2025 Closing Date 17-Apr-2025

Accountabilities Review and develop working practices to ensure that data science work is delivered to robust quality standards Interpret and analyze complex datasets using statistical and machine learning techniques. Collaborate with various teams to understand data needs and contribute to data-driven strategies. Coordinate the implementation of novel modelling solutions designed to drive the interrogation of datasets for insights in scientific and business application areas within defined project scope. This includes integrating complex data from multiple different sources and modalities includes the application of specialized approaches in classification, regression, clustering, NLP, image analysis, graph theory and/or other techniques. Using domain-specific understanding, translates unstructured, complex business problems into the appropriate data problem, model and analytical solutions Researches and develops advanced predictive models and computational methods to guide and shape decision-making within the project scope. Provide training and advice to collaborators on optimal use of key data, analysis platforms and the appropriate use of data science. Apply expert AI research techniques, including establishment of hypotheses that can be approached using computational methods and tools. Present or publish findings for conferences and in peer reviewed journals. Build and manage effective relationships with stakeholders to ensure utilization and value of information resources and services. Clearly and objectively communicate results, as well as their associated uncertainties and limitations to shape solutions Provide advanced data science expertise to cross-functional projects and shape delivery of data science solutions that drive value to AstraZeneca Apply a range of data science methodologies, developing novel data science solutions where off-the-shelf methodologies do not fit Develop, implement and maintain required tools and algorithms in a manner which meets regulatory and evidential requirements within project scope Leads data science projects of defined scope and provide coaching for team members Developing, maintaining and applying ongoing knowledge and awareness in trends, standard methodology and new developments in analytics and data science Develop, test, and deploy machine learning models to solve business problems. Present data insights and models to stakeholders with clarity and effectiveness. Continuously evaluate data models and tools to enhance data accuracy and performance. Mentor and provide guidance to other team members on analytical techniques. Flexibility to support diverse data tasks and projects as they arise. Essential Skills/Experience Bachelor s or Master s degree in Computer Science, Engineering, or related field. Demonstrable experience in data analysis and machine learning projects. Proficiency in programming languages such as Python and experience with ML libraries like TensorFlow or Scikit-learn. Strong knowledge of data visualization tools, e.g., Tableau, PowerBI Experience with big data technologies, such as Hadoop or Spark.. Excellent problem-solving skills and attention to detail. Good communication skills and ability to interpret data analytics into actionable insights. Desirable Skills/Experience Experience in enterprise-level integrations and data engineering projects. Familiarity with data visualization tools such as Tableau or Power BI Join a team with the backing and investment to win! Youll be working with ground breaking technology. This marriage between our purposeful work and the use of high-tech platforms is what sets us apart. Lead the way in digital healthcare. From exploring data and AI to working in the cloud on new technologies. Join a team at the forefront. Help shape and define the technologies of the future, with the backing you need from across the business. Ready to make an impactApply now! Date Posted 11-Mar-2025 Closing Date 14-Apr-2025

About us At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. In assigned therapeutic area and geographical territory, engages in clinical and scientific exchange with medical and scientific experts, including Healthcare Professionals, and where appropriate non-traditional stakeholders (e.g. policy and decision makers, PAGs, government, innovative solution providers) consistent with medical objectives. Scientific Expertise: Maintain clinical/scientific expertise in disease state management, AstraZeneca products, emerging therapies, and the competitive landscape. Contribute to the development and provide project leadership/ management of the therapeutic area Field MedicalStrategic Plan (FMSP). Act as a subject matter expert/resource for internal and external stakeholders. Work with internal stakeholders in the development and delivery of appropriate training and mentoring needs within therapeutic area. Scientific Exchange: Engage in peer-to-peer level dialogue with key customers and deliver appropriate clinical/scientific content through utilizing the correct channel mix, which will differentiate AstraZeneca products from those of other companies. Respond to unsolicited customer inquiries and provide focused and balanced clinical / scientific information that supports the safe and appropriate use of AstraZeneca s products and services. Provide scientific/clinical support and deliver presentations to internal and external stakeholders. Identify and establish relationships with key customers and other scientific thought leaders for engaging them in ongoing scientific dialogue on AstraZeneca products and unsolicited discussions about compounds in development. Organize and facilitate scientific events such as MSL events, Symposiums, Scientific Exchanges, Advisory Boards/Expert Panels, non-promotional standalone events, Meet the Professor sessions, etc., with KEEs and HCPs. Prioritize these events based on their relevance in the patient journey for the related disease. Deliver informative lectures at scientific events tailored to healthcare professionals, aligning with the field medical Communication strategy. Collaborate with KEEs on study proposals (ESR or Local Study) and/or publications of interest to AstraZeneca. Customer Insight: Effectively identify, gather, analyze, synthesize, report and forward relevant new knowledge about the external scientific/medical environments to internal stakeholders Provide internal stakeholders with actionable items related to medical / product strategy or clinical development based on customer perspectives. Partner with traditional and non-traditional stakeholders to identify gaps in the patient experience journey as insights to be included in the medical / product strategies. Strategic Relationship: Develop peer-level relationships with medical and scientific experts, including Healthcare Professionals and collaborate with other internal teams for other key external stakeholders (e.g. policy and decision makers, PAGs, government, innovative solution providers) consistent with Medical objectives. Identify pre-clinical, clinical, and post-marketing study investigators in alignment with Medical Plans. Support data generation activities including participating in reviews of Investigator sponsored studies. Looks to broaden the My MA contact list where appropriate to include non-traditional KEEs from government, payer groups, researchers and clinical advisors who may support practice change initiatives. Establish win-win partnerships with traditional and non-traditional stakeholders to deliver on strategic, scalable and sustainable solutions addressing patient healthcare access gaps within the ecosystem. Other: Responsible for leveraging digital and innovation / technology as enablers for scientific exchange and creating patient centric solutions. Possesses a solid grasp of pharmacovigilance and GxP principles, showcasing a clear understanding of their significance. This includes practical knowledge of Good Clinical Practice (GCP), various types of clinical studies, and requirements for reporting adverse events (AEs). Possesses a solid grasp of pharmacovigilance and GxP principles, showcasing a clear understanding of their significance. This includes practical knowledge of Good Clinical Practice (GCP), various types of clinical studies, and requirements for reporting adverse events (AEs). Exhibits a robust understanding of the Ethical Interactions Policy, along with relevant standards, local laws, and regulations. Moreover, possesses the ability to provide training to others in this domain. Adherence to internal processes and AstraZeneca Global Field Medical Standards and the external regulations including but not limited to clinical trials, promotional activity (e.g. Local Code of Conduct) and pharmacovigilance activities to meet internal SOP and local regulations. Education, Qualifications, Skills and Experience Doctoral degree in a scientific discipline (e.g. M.D., Ph.D., Pharm.D.) Experience in pharmaceutical industry, regulatory environment, clinical or preclinical research, and knowledge of a therapeutic area disease state and treatment. Experience with basic research, drug discovery, drug development and KEE interactions. Why AstraZeneca? At AstraZeneca we re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We re on an exciting journey to pioneer the future of healthcare. Date Posted 28-Feb-2025 Closing Date 27-Mar-2025

Job Title: Senior Consultant - SAP Security Career Level - D2 YOE - 7 to 9 Years Introduction to role As a Senior Security Consultant, you will be a key contributor to a technical team for a large SAP implementation project spanning across countries and continents. You should possess strong knowledge in security, authorization, and compliance, with proven expertise in implementing, configuring, and supporting SAP landscapes. Accountabilities Design and deploy solutions for maintaining the compliance and security of SAP applications and underlying HANA databases. Collaborate closely with the statutory Risk and Compliance Team, engaging with SAP teams and key members across business units to develop creative, scalable, and sustainable security solutions while ensuring SOx and Audit compliance. Deliver clear, well-structured, and meaningful information to a target audience using suitable communication mediums and language tailored to the audience. Provide architectural guidance and design technical solutions that meet functional requirements. Develop innovative ideas for automating repetitive processes and tasks. Interact with Business Users, Application Engineering Leads, EPO, EPF for requirement gathering, analyzing issues, and providing timely updates on progress made. Essential Skills/Experience In-depth SAP Security understanding shown implementation experience in S/4 HANA Fiori, ECC, BI/BW, GRC Access Controls Well versed with foundational Security concepts across various business processes In-depth understanding of SAP role design considering segregation of duties (SoD) In-depth understanding of Fiori authorization concepts, UI/UX aspects with SAP Security Space (Pages Spaces, App Support, unified launchpad) Experience in requirement gathering, designing roles for hub embedded deployment of S/4 HANA Hands-on experience in configuration of GRC Access Control modules (ARA, ARM, ARA BRM) Hands-on experience in managing SAP SoD ruleset (Create, operate maintain) Hands-on experience on Security activities for SAP system upgrade/transformation Very good understanding of integration of SAP modules in end-to-end business processes Ability to understand business requirements from business users and prepare functional specifications, prepare test scenarios inclusive of security design, support during various test phases, perform cutover activities post go-live support. Accountable/Responsible to provide audit support, monitor report manual/automated SOx controls, coordinate and communicate with various stakeholders on effective execution of SOx controls Evaluate drive enhancements to existing SOx Controls to improve efficiency and effectiveness, evaluate scope for simplification automation. Proactive approach to problem solving. Ability to work in large and diverse teams. Good communication in English (spoken written) and interpersonal skills. Open to Hybrid model: 3 days/week from office Desirable Skills/Experience SAP S/4HANA related certification or willingness to complete such certification. Exposure to SAP Solution Manager, JIRA, UI/UX tools At AstraZeneca, we lead transformation by fusing our digital and data capabilities with business backing. We accelerate the business forward by leveraging leading technologies and exploring data to make improved decisions. Our constantly evolving environment challenges us to innovate and find bold new ways of approaching everyday tasks. Empowerment and collaboration are key as we work together as one diverse team of specialists. We continuously expand our knowledge and develop through a two-way feedback loop. Our work positively impacts patients across the world. Join us now to shape the future of digital healthcare! Date Posted 19-Mar-2025 Closing Date 01-Apr-2025