AI Success™

Job Description

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.

Lilly’s Purpose

Lilly is entering an exciting period of growth, and we are committed to delivering innovative medicines to patients around the world. Lilly is investing around the world to build new state-of-the-art manufacturing site’s and continue growing our existing facilities to created capacity required to continue with our mission. Seishin site started journey to apply the newest technology, advanced highly integrated and automated manufacturing systems, and have a focus on minimizing the impact to our environment.

What You’ll Be Mainly Doing:

We are on a daring journey to transform our manufacturing operations, and the Manufacturing Execution System (MES) is pivotal to achieving this transformation. Multiple projects are currently underway to expand the footprint of MES, enabling Seishin site to operate paperless and modernizing MES in established operations worldwide.

This position will ensure the successful implementation of the MES solutions and other production systems by bridging business needs and technology. This role will develop expertise in PharmaSuite , supporting, developing and validating global electronic batch records to fulfil business needs. Working closely with global and site teams, they will ensure compliance with validation requirements, and proactively address technical, operational, and business challenges.

Key Responsibilities:

Develop and integrate MES common and site-specific components.
Develops and/or assists in the creation and maintenance of the MES interfaces with other Lilly systems.
Support MES solutions start up activities.
Evaluate and translate functional requirements into technical solutions not limited to MES.
Work with site resources towards replication & standardization to drive value and implement the appropriate technical solutions.
Ensure project and/or validation documentation is maintained during lifecycle & release management.
Evaluate new technologies and implications to existing Lilly footprint.
Benchmark on innovative solutions (external and internal to Lilly)
Maintain open communication with MES vendor(s) to address needs in standard solution or via functional packs.
Dynamically adapt roadmap to site evolution/strategic directions, and new trends/issues.
Establish a strong site culture based in Lilly values, expectations, and operational excellence standards.

What You Should Bring (preferred skills):

Effective people and team leadership skills
Ability to manage and contribute to multiple concurrent activities and adapt to changes in priorities.
Ability to cross functionally collaborate.
Business level written and oral English communication skills.
Demonstrate creativity, analytical thinking, and the ability to troubleshoot and tackle problems.
History of promoting safety and maintaining a safe work environment
Demonstrated adhere adherence to compliance for internal and external quality guidance.
Demonstrated and promote Operational Excellence
Effectively encourage knowledge sharing and education
Ability to problem solving and work through manufacturing situations. Have experience serving as an escalation contact with vendor(s)

Basic Requirements:

Bachelor’s degree in engineering, Computer Science, Information Technology, or a related technical field or Minimum 2 years of experience working with Manufacturing Execution Systems (MES).

Experience with any MES platforms such as PMX, PharmaSuite (Rockwell), Syncade-DeltaV MES (Emerson), Werum PAS-X, or similar is strongly preferred.
From the perspective of employee well-being and productivity, Lilly has established a commuting distance and time limit policy. Specifically, the maximum allowable commuting distance iswithin 90 km and commuting time should not exceed 90 min from candidates nearest station to the workplace using the cheapest public transportation. If candidates live further away than the above range, they will generally be required to relocate to a location within commuting distance (rented company housing may be provided). The above applies even if commuting by car is permitted.
Excellent written and oral Japanese communication skills.

Additional Preferences

Understanding of GMP regulations and Computer System Validation (CSV) principles (e.g., GAMP 5, 21 CFR Part 11, Annex 11).
Experience authoring and validating Master Batch Records (MBRs) in a regulated environment.

Strong documentation skills and attention to detail, with experience in generating validation deliverables and training materials.
Ability to work cross-functionally and communicate effectively with technical and non-technical stakeholders.

Additional Information:

Position locations: Seishin, Kobe, Japan
Occasional off-hours and weekend work expected.
In principle, work at the site
Some international travel may require.

Business Title : Manufacturing IT, Production Function Business Integrator ・MES Engineer 

Lilly’s Purpose
Lillyは現在、成長の著しい時期を迎えており、世界中の患者に革新的な医薬品を届けることに尽力しています。Lillyは世界各地で最先端の製é æ ç¹ãæ°è¨ããæ¢åæ½è¨ã®æ¡å¼µã«ãæè³ãè¡ããããã·ã§ã³ã®ç¶ç¶ã«å¿è¦ãªçç£è½åãç¢ºä¿ãã¦ãã¾ããè¥¿ç¥å·¥å ´ã§ã¯ãææ°æè¡ãé«åº¦ã«çµ±åãããèªååè£½é ã·ã¹ãã ã®å°å¥ãé²ãã¦ãããç°å¢ã¸ã®å½±é¿ãæå°éã«æãããã¨ã«ãæ³¨åãã¦ãã¾ãã

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https://now.lilly.com/landingoverview/JP-change-in-career-system/JP-changes-in-my-career-faqs

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 ( https://careers.lilly.com/us/en/workplace-accommodation) 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.

#WeAreLilly

About Eli Lilly and Company

We're a medicine company turning science into healing to make life better for people around the world. It all started nearly 150 years ago with a clear vision from founder Colonel Eli Lilly: "Take what you find here and make it better and better." Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing science to solve some of the world's most significant health challenges.

General Information and Guidelines:

When you engage with us on LinkedIn, you're agreeing to these Community Guidelines: https://e.lilly/guidelines.

If you have questions about a Lilly medicine, contact The Lilly Answers Center at 1-800-Lilly-Rx (1-800-545-5979) Monday through Friday, excluding company holidays.

Industry

Chemicals & Materials

Company Size

10,000+ employees

Headquarters

Indianapolis, Indiana

Year Founded

Unknown

Website

lilly.com

Social Media

＜製造情報技術部＞Manufacturing IT, Production Function Business Integrator・MES Engineer / Associate・Manager・Senior Manager /Seishin Manufacturing Site）

Job Description

About Eli Lilly and Company