Process Engineer

3 weeks ago

Indiana, United States CareerBuilder Full time

Process Engineer - Indy Device Manufacturing Asset Delivery page is loaded

Process Engineer - Indy Device Manufacturing Asset Delivery

Apply

locations

France, Fegersheim

time type

Full time

posted on

Posted Yesterday

job requisition id

R-43614

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. Were looking for people who are determined to make life better for people around the world.
Organization Overview:
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 oversee 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 doing this, they function as the Technical Lead for the project. 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 capture and utilize process data.
Lead the technical assessment of OEM technical proposals and make recommendations as to OEM suitability
Lead 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
Oversee the OEM's design process, assuring questions are resolved and barriers to progress are removed
Lead thorough 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 rigorous studies and executing 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, leveraging the capital to generate more value
Basic Requirements:
BS in an Engineering (Mechanical, Chemical, or Biomedical Eng preferred)
Experience dealing with design, startup, and/or operation of high-speed mechanical assembly lines
Minimum 4 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 Aptitude
Solid technical writing skills
Proven ability to organize 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. 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.
#WeAreLilly
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