Post project delivery, this role will support GMP manufacturing operations in small molecule or oligonucleotides. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.
Key Deliverables:
Champion a strong safety culture, mentor and coach others, and utilize engineering and automation fundamental principles in design and problem solving.
Collaborate with Lilly engineering, A&E firms, and system integrators to develop requirements and specifications that will be the foundation for software development and system architecture.
Manage one or more system integrators for fully deliver and test DeltaV software.
Collaborate with Tech@Lilly to deliver a fully integrated Automation/MES solution that is scaled for the needs of business.
Participate in basic and detailed design that also includes staffing, statements of work, supplier management, and delivery strategies for automation systems.
Participate in developing computer system validation strategies.
Develop and build capabilities within the Houston site automation team.
Develop site procedures for automation platforms and associated administration activites.
Provide engineering support for Process Safety Management (PSM) and Process Hazard Reviews (PHRs).
Provide technical oversight during development of equipment and process system User Requirements and related Design Review/Qualification documentation to ensure equipment and systems are appropriate for intended purpose.
Requirements
Bachelor's degree in engineering or related applicable discipline required.
5+ years of experience Process Automation with experience on the Emerson DeltaV Platform preferred. Other platform experience will be considered.
5+ years of experience in API/Drug Substance manufacturing preferred. Related manufacturing experience will be considered.
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor wor
Benefits
Health insurance
Additional Information
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.
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 40,000 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.
Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Houston, TX. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the site technical team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the Processes, the facility and the culture to enable a successful startup into GMP manufacturing operations.
Eli Lilly · Houston TX