TECHNICAL EXPERT

About Atos Group

Atos Group is a global leader in digital transformation with c. 67,000 employees and annual revenue of c. €10 billion, operating in 61 countries under two brands — Atos for services and Eviden for products. European number one in cybersecurity, cloud and high performance computing, Atos Group is committed to a secure and decarbonized future and provides tailored AI-powered, end-to-end solutions for all industries. Atos Group is the brand under which Atos SE (Societas Europaea) operates. Atos SE is listed on Euronext Paris.

The purpose of Atos Group is to help design the future of the information space. Its expertise and services support the development of knowledge, education and research in a multicultural approach and contribute to the development of scientific and technological excellence. Across the world, the Group enables its customers and employees, and members of societies at large to live, work and develop sustainably, in a safe and secure information space.

Lead Consultant – Pharma GxP MDM Support (Data Profiling)

Position Overview

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.

Key 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.

Required Qualifications

• 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.

Here at Atos, diversity and inclusion are embedded in our DNA. Read more about our commitment to a fair work environment for all.

Atos is a recognized leader in its industry across Environment, Social and Governance (ESG) criteria. Find out more on our CSR commitment. 

Choose your future. Choose Atos.