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 35,000 employees worldwide work to discover and bring life-changing medicines to those in need, improve disease understanding and management, and give back through philanthropy and volunteerism. We are committed to putting people first and making a difference.
Due to the growth of our Monoclonal pipeline, Eli Lilly & Company has invested in a new facility in Ireland, Lilly Limerick. To support this exciting expansion and ensure a successful start-up, we seek talented individuals to join our team and help establish Lilly Limerick as a reliable supplier of our innovative medicines.
If you seek a challenging and rewarding career and meet the requirements below, we invite you to consider a role at Lilly, Limerick.
Downstream Scientist - Technical Services/Manufacturing Sciences Laboratory
The TS/MS downstream scientist will provide technical support for the design, startup, and operation of the TS/MS laboratory. This includes expertise in laboratory startup activities such as facility design, equipment procurement and qualification, supporting downstream operations. The ideal candidate will have experience with laboratory scale models for downstream processes, strong data-driven decision-making skills, and a focus on process improvement using data analytics and process analytical technology.
Key Responsibilities
1. Deep knowledge of biotech manufacturing science, laboratory models, and analytical testing for downstream processing.
2. Operate and troubleshoot laboratory equipment effectively.
3. Understand molecule-specific control strategies, specifications, and critical quality attributes.
4. Collaborate with network and development teams to develop and transfer robust laboratory models, especially for next-generation bioprocessing.
5. Experience with chromatographic separations, tangential flow filtration, and high-concentration processing.
6. Lead laboratory investigations supporting production operations.
7. Support laboratory startup, including equipment setup, data management, and protocol development.
8. Ensure safety and environmental compliance during startup and operation.
9. Develop and review SOPs, specifications, protocols, and work instructions.
10. Partner with quality control and other Lilly sites to meet startup objectives.
11. Apply basic statistical methods and experimental design.
12. Identify and implement process improvements and Lean initiatives.
13. Contribute to regulatory submissions and responses.
Attributes for the Role
* High technical capability and productivity.
* Curiosity and eagerness to learn.
* Self-starting with initiative and data-driven problem-solving skills.
* Strong interpersonal, verbal, and written communication skills.
* Flexibility and adaptability in various environments and teams.
* Ability to facilitate decision-making.
* Proficiency in English.
Educational Requirements
* Bachelor’s degree in biology, chemistry, biochemistry, or related field (Advanced degrees like MSc or PhD preferred).
* Over 3 years of experience in pharmaceutical laboratories and GMP manufacturing environments.
Work Environment
* Roles are primarily 8-hour days, with occasional evening or weekend support as needed.
* Travel to other Lilly sites in Ireland or abroad may be required occasionally.
Lilly is committed to equal opportunity employment and supports individuals with disabilities. If you need accommodations to apply, please complete the workplace accommodation request form. We do not discriminate based on age, race, religion, gender, sexual orientation, gender identity, or other protected statuses.
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