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Process Engineer - Indiana, United States - Eli Lilly
Description
Process Engineer - Indy Device Manufacturing Asset Delivery page is loadedProcess Engineer - Indy Device Manufacturing Asset Delivery
Apply
locations
US, Indianapolis IN
time type
Full time
posted on
Posted 2 Days Ago
job requisition id
R-64778
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.Indianapolis Device Manufacturing (IDM) - Asset Deliver Process Engineering provide the technical leadership in developing, designing, constructing, and delivering/upgrading automated device assembly and packaging lines for IDM globally to both Lilly sites and Contract Manufacturers (CMO).
Responsibilities:
IDM Asset Delivery Process engineers coordinate the technical aspects of developing, designing, constructing, and delivering automated device assembly and packaging lines for IDM globally to both Lilly sites and Contract Manufacturers in support of new product launches, capacity expansions, and line extensions.
In addition, when primary support teams for the global installed base (CMO and Lilly sites) require assistance, these engineers provide assistance or leadership in returning lines to service or optimizing lines.
These engineers also develop and implement best practices for design and startup of device assembly lines and deploy systems to collect and use process data.
Lead the technical assessment of OEM technical proposals and make recommendations as to OEM suitabilityLead the generation rationalization of user requirements for each project
Lead the definition and mitigation of technical and patient risks, including use of FMEA
Assure each design includes maximum appropriate re-use of technology from prior projects
Lead the OEM's design process, assuring questions are resolved and barriers to progress are removed
Lead detailed design reviews to assure the design meets requirements and local/corporate standards
Lead characterization of unit operations and setting operating conditions by defining an Engineering Studies Plan, developing detailed studies and completing them
Assure testing is appropriately developed and is in accordance with the risk level of the item being tested
Document research and investigations as technical reports
Find and document opportunities to optimize line performance, using the capital to generate more value
Basic Qualifications:
Bachelors Degree preferred (Engineering, Mechanical, Chemical, or Biomedical Eng preferred)
Experience dealing with design, startup, and/or operation of high-speed mechanical assembly lines
Minimum 2 years engineering experience, preferably in manufacturing
Experience in capital project delivery
Additional Skills:
Demonstrated high degree of ownership / accountability
Strong communication, teamwork, and networking skills
Mechanical proficiency
Solid technical writing skills
Ability to coordinate and prioritize multiple tasks
Strong attention to detail
Proven problem solving skills
Ability to work independently as well as in a team environment
Experience with Medical Device assembly
Experience with engineering in a regulated pharmaceutical
environment/cGMPs/Commissioning
and Qualification
Experience programming control systems for high-speed assembly lines
Ability to lead and influence across organizational and company boundaries; ability to form relationships with others not in your organization
Experience with DOE, GR&R, Statistical methods as applied to engineering studies and reports
Experience in large capital project delivery and management of sub-projects within a larger project
Expertise in automation networks, vision systems for part inspection, debugging of assembly lines
Expertise in process data historian configuration and/or use
Additional Information:
Ability to travel 25% on average, with peaks over 50% for a few months at a time.
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.
) 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.
Our current groups include:
Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities.
Learn more about all of our groups.#WeAreLilly
About Us
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#J-18808-Ljbffr
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