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MDM Analyst
Ref No.: 18-11505
Location: Waltham, Massachusetts
Start Date / End Date: 08/27/2018 to 08/16/2019
The Master Data Management (MDM) Analyst will be responsible for consistency, quality, accessibility, and security of strategic shared data and information to Client's Supply Chain and Technical Operations organizations.
Responsible for gathering information requirements and working with the business to define standards and rules to ensure master data is compliant with defined information, policies, and quality requirements as defined by the data owner.


Contribute to the creation and maintenance MDM processes and procedures.
Execute a data management strategy and assist with continuous improvement of data management in ERP and QMS systems.
Understand the requirements of master data and the relationship with IT systems, Quality requirements, and broader business processes.
Monitor and facilitate the workflow processes for new data requests, changes, and deletions.
Identify, analyze, and report/resolve data issues, related to uniqueness, integrity, accuracy, consistency, and completeness.
Actively participate in IT implementation projects and various other projects as deemed necessary to ensure data management standards are recognized.
Work with cross-functional teams to identify and acquire new strategic data.
Provide analytical support on business metadata and ensure that it is accessible and meaningful to data users.
Ensure data documentation policies and procedures are properly developed and maintained.
Actively advocate for data management.
Take on other responsibilities and special projects as directed by management.
Serve as subject matter expert regarding product change control impacting the Supply Chain
Represent the Supply Chain functional area as a subject matter expert on product change control during regulatory and third-party inspections
Develop, implement and track an End to End Change control process. QUALIFICATIONS
3+ of pharmaceutical industry experience
Experience in master data management and change control process in regulated pharmaceutical industry
Experience with ERP (Oracle, SAP, etc.) systems and Quality Management Systems (QMS)
Ability to communicate effectively both orally and in writing, both internally and with external vendors and partners
Ability to multi-task and work in a fast paced and dynamic environment
Strong working knowledge of standard business software, including MS Excel, Word, PowerPoint and Project
Strong analytical and organizational skills

Bachelor's degree in Engineering or Life Sciences

Required / Desired Skills
Skill Required / Desired Amount of Experience
Bachelor's degree in Engineering or Life Sciences Required 4 Years
Pharmaceutical industry experience Required 3 Years
Experience with ERP (Oracle, SAP, etc.) systems and Quality Management Systems (QMS) Required 3 Years