Master Data Associate

hace 2 semanas

Guadalajara, México AstraZeneca A tiempo completo

**Master Data Associate**

Positions are open to Mexican Citizens and official residents of Mexico.
Location: Guadalajara (hybrid)
Strong English interpersonal skills required

**About the AstraZeneca**

AstraZeneca is a global, science-led, patient-focused pharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. At Astra Zeneca, we’re dedicated to being a Great Place to work

The Data Associate is part of the Data management Team whose role is to team provides expertise on supply chain designs, setting standards and principles to ensure the system reflects the most efficient flow. The team set up and maintain master data for end-to-end Supply chain processes covering Plan, Source, Make, deliver and Manage finance as well as coordinate any of these setups with teams outside ESM for our Supply chains.

**Accountabilities**

Manage and maintain 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 ESM and EQ teams. Training ESM/ EQ 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. Oversight of approval of user access changes for their processes, including the agreed list of Approvers via LPCs / Super Users

**Requirements**:

- Graduate status or equivalent
- Knowledge of SAP ERP systems
- Business Acumen especially experience in BPM, LEAN and Quality Assurance Processes
- Analytical, detail oriented, highly organized
- Good interpersonal and coordination skills.
- 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.

**Expectation of working in the office 3 days a week statement**

When we put unexpected teams in the same room, we ignite ambitious thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility.

Join us in our outstanding and bold world

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