At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Primary responsibility for data management activities within the site.

Main Responsibilities

• Own site actions associated with the enterprise data management and integrity initiatives.
• Facilitate the Site Data Lead Team.
• Maintain site data management metrics and track status of the data integrity action plans; Report the status to the Site Data Lead Team.
• Provide direction on the operationalization of the data management action plan.
• Partner with site leadership to ensure data integrity initiatives are given appropriate priority and resources.
• Implement defined data standards (e.g., data structure, metadata) and usage guidelines as information passes through multiple systems/functions and ensure processes are in place to manage the data throughout its lifecycle.
• Implement data strategy actions (e.g., digitization, contextualization, visualization) to enable appropriate use of data at the appropriate time to enable robust decision making, drive productivity, and facilitate continuous improvement.

The minimum requirements for the performance of the job:

• Minimum of 3 years of experience in GMP or QMS operations.
• Understanding and working knowledge of domestic and international data integrity regulations and other policies/regulations as applicable.
• Understanding of IT system design, controls, and usage.
• English: Speaking and Listening Skills (GSE: 42 or higher).
• Japanese: Native level.

Skills/Preferences:

• Demonstrated proficiency in planning and the ability to carry out tasks with a high degree of independence as well as being able to work in a team environment.
• Strong project management and organizational skills are a must.
• Strong knowledge and technical expertise in areas of cGMPs/QMS, production practices, and quality systems.
• Strong collaboration with colleagues at all levels.

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Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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