The role involves leading and managing new parenteral product and process technology transfer and commercialization projects, including development studies and regulatory support
Job Summary
The role involves leading and managing new parenteral product and process technology transfer and commercialization projects, including development studies and regulatory support.
Applicants will work in various areas within the parenteral plant and must be able to work Monday through Friday with overtime and off-shift availability as required.
Lilly is dedicated to diversity and inclusion, providing accommodations for individuals with disabilities and ensuring equal opportunities for all applicants.
Matching Summary
The role involves leading and managing new parenteral product and process technology transfer and commercialization projects, including development studies and regulatory support.
Skills & Requirements
Must-have
parenteral manufacturing site experience
GMP environment expertise
technology transfer management
process optimization and improvements
regulatory registration support
deviation investigation
project management skills
Nice-to-have
cross-department collaboration
strong English communication
computer proficiency
leadership and influence ability
analytical thinking
multi-tasking capabilities
decision-making skills
Key Requirements
minimum three years parenteral GMP experience
strong English communication skills
experience in sterile product manufacturing
ability to work overtime and travel
knowledge of GMP documentation and electronic systems