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.
Owing to the continuous growth of our Monoclonal pipeline of products, Eli Lilly & Company has invested in a new facility in Ireland, Lilly Limerick. To support this exciting new investment and meet the requirements of a safe and successful start-up, we are eager for talented individuals to join our team(s) and contribute to establishing Lilly Limerick as a reliable supplier of our innovative medicines and our goal of making a difference to people's lives.
If you are looking for a challenging, rewarding career and feel you meet the requirements listed below, we would love to consider you for a role at Lilly, Limerick.
Principal/Senior Principal Scientist - Technical Services/Manufacturing Sciences Laboratory The TS/MS Principle/Senior Principal Scientist will provide direct technical support for the design, startup and execution of the TS/MS laboratory. This role will provide technical expertise for the laboratory startup activities including facility design, instrument procurement and qualification in support of up- and downstream operations as well as analytical instrumentation. This role will be that of a technical leader and mentor of other laboratory scientists and integral in defining the laboratory technical agenda. The successful applicant will have deep technical expertise in their areas of responsibility and demonstrate strong data-driven decision-making and problem-solving capabilities. They will work to continuously improve process efficiency by implementing new technologies and process improvements in addition to investigation support. This role will be heavily involved in incorporating the use of data analytics and process analytical technology to support the next generation bioprocessing facility in laboratory scale models to drive process development.
Key Responsibilities Have an in-depth knowledge of the science of biotech manufacturing and associated laboratory models and analytical tests, supporting both up- and downstream processing.Understand molecule-specific control strategy and basis of specifications and critical quality attributes.Work with the network and development organizations to ensure a well-understood, robust and fit-for-purpose laboratory models are developed and transferred. This will include those specific to the NGB processing including implementation of process analytical technologies in support of multivariate analyses and process modelling.Expertise in laboratory scale equipment operation and troubleshooting.Supporting the development and mentorship of other laboratory scientists in alignment with area management.Leading laboratory investigations in support of production operations.Support the design and start-up of the laboratory including equipment configuration and purchase, development of the laboratory data management strategy, establishment of laboratory protocols.Support a laboratory startup plan in alignment with the health, safety and environmental team to ensure safe startup and operation.Create and review documents including laboratory SOPs, material specifications, protocols, and work instructions.Establish partnerships to enable cross-functional work with the quality control laboratory and other Lilly sites to ensure facility startup objectives are met.Understand basic statistical methodologies and statistically based experimental design.Identify process improvements and participate in implementation of Lean manufacturing initiatives.Contribute to the authorship and review of regulatory submissions and responses to regulatory agencies.Attributes for the Role Ability to provide technical leadership in a laboratory setting with experience in up- and downstream processing.Demonstrated technical capability with high productivity.Proven track record of curiosity with learning agility.Self-starter with high initiative and data-driven approach to problem-solving.Demonstrated strong interpersonal skills.Demonstrated strong verbal and written communication skills.Demonstrated adaptability and flexibility to working in different environments, teams etc.Demonstrated ability to participate in and facilitate decision-making.Proficient in English.Educational Requirements: PhD or MSc degree based in biology, chemistry, biochemistry or similar discipline.7-10 years' experience working in pharmaceutical laboratory and GMP manufacturing environments.Work Environment: These are 8-hour day roles. As a manufacturing support function, the need for occasional evening or weekend support can arise.Although expected to be minimal, occasional travel is possible including to other Lilly sites both in- and outside of Ireland.
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