Lilly Visual Inspection Steward in Indianapolis, Indiana
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 35,000 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.
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 39,000 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. #WeAreLilly
The mission of Technical Services/Manufacturing Sciences (TS/MS) is to provide scientific leadership and technical support for manufacturing to make medicine today and tomorrow. The Visual Inspection Steward is a key member in a cross-functional team who provides technical leadership for inspection operations and projects involving existing and new inspection processes.
The Indianapolis Parenteral Manufacturing TS/MS Visual Inspection Steward will assume broad responsibility across the manufacturing site in terms of ownership and harmonization of local control strategy that are implemented and executed at the site. The role will regularly interact with peers within the network and in Global TS/MS to share learning and ensure strategies are in line with technical, quality, and regulatory guidance, while supporting business expectations. The Visual Inspection Steward will also own technical capability building at the sites to ensure capabilities are in place to meet business objectives.
Serve as technical subject matter expertand program ownerfor all topics related to visual inspection supportingthe Indianapolis Parenteral Manufacturing site.
Be responsible and influential with respect toimplementation of regulatory guidance, technology advancements, broaderexternal trends and understanding of how changes could impact Eli Lilly
Providetechnical consultationregarding defect classification and visual inspection technique
Author, review, or approvetechnicaldocuments, includingpersonnel qualification strategies, control strategies,investigations, change controls, expert opinions,qualifications, procedures, defect classifications, personnel qualification strategies, control strategies, technical studies, etc.
Interact with regulators, customers, or other outside stakeholders on business issues or in support of internal and external agency audits
Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability
Leadthe development and implementation of process improvements to improve process control, yield, and/or productivity
Technical writing and communication skills are used daily and the ability to effectively communicate and transfer knowledge to all levels ofthe organizationis essential.
Although not a supervisory role, technicalleadership,and the ability totrain/coach others andcross functionallyinfluence are important in this role.
- Minimum of bachelor's degree in scienceor engineeringfield
Preferred10yearsexperiencedirectly supportingpharmaceutical manufacturing or quality, with experience invisual inspection ofpharmaceuticalproducts.
Ability to influenceand communicate todiverse groupsoncomplex regulatory, business, or technical issues within the site and function
Responsible for maintaining a safe work environment
Experience in statistics and stackable tolerance analysis
Builds relationships with internal and external customers and partners
Proficiency in delivering highly complex tasks and/or tasks that are highly cross-functional
Demonstrated Project Management skills and ability to coordinate complex projects
Strong analytical and quantitative problem solving skills
Strategic thinking and ability to balance short term needs with long term business evolution
This position is tech ladder approved (P4-R+).
This position willbe inIndianapolis, but could requiresometravel, less than10%;including international
This position is day shift, Monday-Friday, with off hours support needed,by request.
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 ( LillyRecruitingCompliance@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 is an EEO/Affirmative Action Employer and 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.
At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!