Anand P.
Master Data Steward @ Merck
- Role
- Master Data Steward at Merck
- Location
- Hillsborough, NC, US
- LinkedIn followers
- 500 followers
About Anand P.
At Merck, my role as ISO Steward in the Master Data CoE centers on ensuring data integrity and governing its lifecycle. With an unwavering commitment to data quality, my expertise in logistics management and problem solving has been instrumental in leading continuous improvement initiatives. My proficiency with SAP and Six Sigma methodologies propels the organization forward by fostering a culture of excellence in data governance. Collaborating across departments, our team has successfully enhanced master data processes, contributing to the efficiency and effectiveness of supply chain operations.
Experience
Master Data Steward
Jan 2020 — Present · Durham, NC, US
Create master data for materials for various departments. Responsible for enforcing data governance and establishing and improving the data creation and change process. Establishing plans and objectives for maintaining Master Data integrity and a gatekeeper for Data Governance best practices. Actively engaged in data and process related projects and continuous improvement initiatives to ensure that the team operates at a level of efficiency. Promotes Data Governance and helps build a collective, shared vision for focused, consistent, and ongoing data quality initiatives.
Education
Sandhills Community College, Southern
Associates of Science
1997 — 2000
University of North Carolina Wilmington
Bachelor's of Biology, Biology/Biological Sciences, General
North Carolina State University
Bachelor of Science, Biotechnology
2008 — 2009
University of North Carolina Wilmington
B.S. in Biology, Science
2000 — 2006
Skills
- Sap R/3
- Osisoft Pi
- Delta V
- Microsoft Office
- Sentry
- Maximo
- Lims
- Sharepoint
- Sop Development
- Mpr
- Gmp
- Microbiology
- Aseptic Processing
- Manufacturing Operations
- Quality Control
- Quality Assurance
- Formulation
- Sap
- Downstream Processing
- Trackwise
- Cgmp Manufacturing
- Gxp
- Vaccines
- Validation
- Technology Transfer
- Aseptic Technique
- Biotechnology
- Deviations
- Manufacturing
- Change Control
- Pharmaceutical Industry
- Capa
- Cgmp Practices
- 21 Cfr Part 11
- Fda
- Quality System
- Midas
- Biopharmaceuticals
- Cell
- Cleaning Validation
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