We're looking for Data Associates!
AstraZeneca AB / Datajobb / Södertälje
Observera att sista ansökningsdag har passerat.
Visa alla datajobb i Södertälje,
Salem,
Ekerö,
Nykvarn,
Botkyrka eller i
hela Sverige Visa alla jobb hos AstraZeneca AB i Södertälje,
Stockholm,
Solna,
Göteborg,
Mölndal eller i
hela Sverige Do you have expertise in, and passion for, data management? Would you like to apply your expertise to impact the supply of products to patients in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!
Join the team where everyone feels a personal connection to the people that we impact. From our science labs to manufacturing at scale, we are committed to delivering at the highest quality. It's inspiring and rewarding work, influencing every part of the product lifecycle to deliver life-changing medicines. To ultimately make people's lives better - from patients and their families to all of us in society!
Our function, Global External Sourcing (GES) supports the Operations strategy by establishing and managing suppliers across the world that meet our global standards. Through external suppliers, the team manages approximately one third of AstraZeneca's value of production. GES plays a key role in ensuring the external supply chains are robust and deliver value to AstraZeneca through driving continuous improvement. The team also supports New Product Introduction through external supply, plays a pivotal role in integrating companies and products that AstraZeneca acquires and bringing innovation through supply chain programmes e.g. Market Access.
The role of the Data Associate (DA) enables GES to deliver our Master Data Management vision which supports the successful delivery of the Ops 2025 strategy. The DA will manage Master Data across different enterprise systems including SAP MDM, SAP ERPs and Azure covering value chain processes (Plan, Source, Make, Deliver and Manage Finance) to ensure timely and quality supply of products to patients. The DA is accountable for providing complete oversight of the highlighted Master data and the processes governing it in compliance with GMP requirements to ensure that there are no interruptions to product manufacture and supply.
What you'll do:
* Manage and maintain (create, change and delete) master data across different SAP/Non-SAP systems for different processes across Product data lifecycle.
* Develop processes and define standards for Data Management activities for the rest of GES and GSQ teams
* Initiate, sustain and successfully accomplish process improvement activities within the defined scope of work.
* Training GES / GSQ users on processes and standards to raise capability in the organization around Data Management
* Participate, as needed in data contributor meetings for New Product Introductions (NPI) to proactively identify improvements to the master data entry processes and implement changes to improve efficiency.
* Lead master data collection from various functional areas via SAP Workflow. Ensure completion of material master data and the release of materials into SAP to our customers as needed.
* Have a continuous improvement mindset and implement master data process improvements
* Oversight of approval of user access changes for their processes, including the agreed list of Approvers via LPCs / Super Users
* Support Master data project change management activities such as UAT / URT and user training
* Drive standardisation, cross-process alignment of decisions and develop the processes
* Represents GES in relevant Global data fora to ensure GES align with global standards
Essential skills and experience:
* Degree or equivalent
* Knowledge of SAP ERP systems
* Eye For Business especially experience in BPM, LEAN and Quality Assurance Processes
* Analytical, detail oriented, highly organized
* Ability to work with complexity and manage ambiguity
Desirable:
* Experience in pharmaceutical and logistics environment
* Safety Health and Environmental and GxP management knowledge
* Project Management, Change Management.
* Knowledge of GMP and FDA regulations involving data management and validation requirements.
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. Always committed to lifelong learning, growth and development.
You'll be able to build a long-term career by unlocking opportunities for lifelong learning. Build unrivalled capabilities in a place that promotes learning agility and offers development opportunities. We never stand still so you'll have the chance to constantly grow your abilities, skills and knowledge. Here we are a fusion of challenging and interesting work, in an energising and inspiring environment.
So, what's next?
Are you ready to bring new ideas and fresh thinking to the table? Great! We have one seat available, and we hope it's yours.
We welcome your application, no later than the 13th of March.
Please note that this position is a fixed term contract of 12 months.
Varaktighet, arbetstid
Heltid Temporary
Publiceringsdatum2022-02-18ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2022-03-11
Klicka på denna länk för att göra din ansökanFöretagAstrazeneca AB
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "R-131166".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Astrazeneca AB (org.nr 556011-7482)
Arbetsplats AstraZeneca
Jobbnummer 6360018
Observera att sista ansökningsdag har passerat.