TECHNICAL EXPERT

AtosTroy, IA
17hRemote

About The Position

We are seeking a highly skilled Lead Consultant to provide Pharma GxP Master Data Management (MDM) support with a strong focus on data profiling and compliance. This role is fully remote within the USA and requires expertise in pharmaceutical regulatory standards, data governance, and MDM solutions to ensure high-quality, compliant master data across critical business processes.

Requirements

  • Bachelor’s or Master’s degree in Computer Science, Information Systems, Life Sciences, or related field.
  • 8+ years of experience in Master Data Management (MDM), with at least 4 years in Pharma GxP environments.
  • Strong knowledge of FDA 21 CFR Part 11, EMA guidelines, and other GxP compliance frameworks.
  • Hands-on experience with data profiling, cleansing, and governance tools.
  • Expertise in one or more MDM platforms (SAP MDG, Informatica MDM, Reltio, etc.).
  • Excellent communication and stakeholder management skills.
  • Ability to work independently in a remote, cross-functional environment.

Responsibilities

  • Lead MDM support initiatives for Pharma GxP environments, ensuring compliance with FDA, EMA, and other global regulatory requirements.
  • Perform data profiling, cleansing, and validation to maintain accuracy, consistency, and integrity of master data.
  • Collaborate with cross-functional teams (Quality, Regulatory, IT, and Business Units) to align master data processes with GxP compliance standards.
  • Develop and implement data governance frameworks and best practices for pharmaceutical master data.
  • Provide technical and functional expertise in MDM tools and platforms (Informatica, SAP MDG, Reltio, or similar).
  • Conduct root cause analysis of data quality issues and recommend corrective/preventive actions.
  • Support audits and inspections by ensuring master data processes meet GxP documentation and traceability requirements.
  • Mentor junior consultants and act as a subject matter expert (SME) for Pharma GxP MDM.
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