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.
Organization Overview:
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
For more than 145 years Lilly has been committed to bringing life-changing medicines to those who need them, advancing the understanding and management of disease, and supporting communities where we live and work. We’re proud of our heritage, we value integrity, excellence, and respect for people. The role will be within the Regulatory Affairs Department. Regulatory Affairs is core to delivering our product pipeline via management of global submissions for both New Chemical Entities (NCE’s) & New Molecular Entities (NME’s) and global post approval change management for commercial products, thus ensuring reliable supply and continuous improvement.
Purpose:
The purpose of the Principal Scientist- Global Regulatory Affairs-CMC role is to provide strategic, tactical and operational direction to expedite CMC development of Lilly’s portfolio and technical agenda by supporting global clinical trial, market registration submissions, and post-approval submissions. These activities are accomplished with a strong working knowledge of global regulations, guidelines and regulatory precedence coupled with a strong technical knowledge of CMC development and manufacturing processes. To accomplish this purpose, it is necessary for the Regulatory Scientist to develop collegial and mutually productive relationships and by a demonstrated ability to establish and/or to promote / refine key regulatory CMC positions and to effectively influence development, manufacturing, and GRA leadership on these positions.
Responsibilities:
The Principal Scientist- Global Regulatory Affairs-CMC:
Minimum Qualification Requirements:
Additional Skills/Preferences:
The applicant should have :
The role is most suited towards a conscientious individual who has excellent verbal and written communication skills and, is fully proficient in using common Microsoft applications to create and present work. The successful applicant must have good organizational skills, with the ability to prioritize and work on their own initiative, both collaboratively as a team member and also on individual projects.
Additional Information:
The role holder:
Position location: The position is located at the Eli Lilly site in Limerick, Ireland.
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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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