Sr. Associate Master Data Management
Juncos, PR, US
Professional (Other)
Bachelors Degree
Full Time, Temporary
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Juncos, PR, US
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Professional (Other)
Bachelors Degree
First Shift (Day)
Job details
Job Title: Sr. Associate Master Data Management
Location: Juncos, PR
Job Type: Full-Time
Salary: $28.17 per hour
Summary:
The Sr. Associate Master Data Management is responsible for the accurate creation, maintenance, and integrity of both basic and complex Master Data, including Material Master, Bills of Materials, Recipes, Resources, and Production Versions. This role ensures the quality of data in SAP and supports process improvement initiatives, contributing to the overall efficiency of the supply chain.
Key Responsibilities:
- Ensure the quality of personal work and the work of others that impacts SAP.
- Verify the accurate setup of information in the system and maintain precise information in the material master files.
- Monitor Master Data error metrics and work towards their resolution.
- Provide input for the update of policies and procedures related to Master Data Management.
- Support or manage process improvement initiatives as necessary.
- Test SAP functionality and support ERP releases as needed.
- Perform data entry for all required data fields according to Standard Operating Procedures (SOPs), guidelines, and work instructions.
- Extract, compile, and interpret data relevant for periodic metrics and reporting needs, leading master data business processes.
- Uphold the global master data governance process, partnering with Business Process Owners (BPOs) as necessary.
- Provide business process mentorship and training to internal clients, acting as a technical resource within the niche area.
- Apply analytical skills to evaluate and interpret complex situations or problems using multiple sources of information.
- Participate in BPO’s global forums and contribute to discussions regarding best practices.
- Monitor functional area data quality reports, identifying revisions to prevent, identify, and manage master data errors proactively.
Education/Qualifications:
- Master’s Degree or Bachelor’s Degree with 2 years of directly related experience, or
- Associate’s Degree with 6 years of directly related experience, or
- High school diploma/GED with 8 years of directly related experience.
Competencies/Skills:
- Experience in supply chain data management.
- Familiarity with SAP systems.
- Proficient in English, both oral and written communication.
- Strong knowledge of Microsoft Word and Excel, with the ability to adapt to new software quickly.
- Working knowledge of regulatory and pharmaceutical processes.
- Proven project management, cross-functional facilitation, communication, and presentation skills.
- Team player, self-starter, persistent, considerate, persuasive, organized, and capable of driving tasks/projects to completion independently.
- Ability to adapt to and manage change effectively.
- Capacity to balance multiple responsibilities and priorities simultaneously under tight timelines.
- Strong analytical skills in data management, interpretation, and reporting.
- Ability to establish relationships with key stakeholders across multiple disciplines, both onsite and virtually.
- Experience in a pharmaceutical/GMP environment.
- Experience in a Supply Chain environment.
- Ability to meet strict timelines and work in a dynamic, evolving environment.
- Strong follow-through on tasks and ability to meet deadlines consistently.
Why Join Us?
This is an excellent opportunity to be part of a dynamic team that values innovation and efficiency in Master Data Management. If you are passionate about data integrity and thrive in a fast-paced environment, we encourage you to apply!
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