Master Data Specialist I

AbbVie•Waco, TX

4h•$65,500 - $125,500

About The Position

The Master Data Specialist I is responsible for ensuring the end-to-end lifecycle of the process orders including opening records, closing records and managing iDocs from SAP/POMS. The objective is to manage a feasible production plan for the operations and quality site functions. To achieve this, the Master Data Specialist I builds strong relationships with all the key stakeholders including planning, BTS, operations and quality. The Supply Chain Planner knows the business and anticipates future opportunities and risks, and continuously raises the bar to ensure success for Abbvie and the patients.

Requirements

Bachelor or Master level, preferably in operations, supply chain or business management.
2+ years of work experience.
Ability to be a team player with focus on improvement and strong drive for results.
Must possess high-level analytical skills.
Excellent written and oral communication skills are required.
Excellent organizational skills are required.
Persistent, resilient and resourceful when confronted with obstacles, and resolved issues in a timely manner.
Must be experienced with advanced planning systems and ERP systems (SAP).
Ability to be a team player with focus on improvement and strong drive for results
Must possess excellent overall view and analytical skills
Excellent written and oral communication skills are required
Proven ability to possess strong problem solving, negotiation and conflict resolution skills

Responsibilities

Daily contact with one or more stakeholders (internal and external) to support coordination of the supply of finished product, bulk, active pharmaceutical ingredients or supporting materials.
Create, monitor and maintain all process orders from end-to-end to ensure that the supply chain plan outlined at the site is executed.
Manage all iDocs related issues to ensure that process orders are completed on time
Responsible for trouble shooting issues related to iDocs.
Participate in or initiate the periodic S&OP process.
Participate in the discussions and execution around Life Cycle Management.
Daily contact with one or multiple (internal/external) supplying plants to coordinate the supply of pharmaceutical finished product, bulk, active pharmaceutical ingredient or supporting materials.
Drive continuous improvements and participate in continuous improvement initiatives led by colleagues.
Develop and maintain effective relationships with internal and external stakeholders, within the organization, AbbVie manufacturing plants, Third party suppliers and cross functional personnel.
Participate in cross functional projects as Subject Matter Expert for supply chain planning.