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.

For 140 years, Lilly has manufactured medicines that improve people’s lives around the world. We produce our medicines using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards, procedures and behaviors to develop medicines with safety first and quality always.

The Associate- Fill/Finish Ops for PFS3 Filling will report to the Associate Director of PFS3 Operations. The Associate will be responsible for implementation and monitoring of C4I projects in the manufacturing process. This includes: providing a leadership role for the area process team, managing improvement projects and process improvements for the area, acting as a liaison between operations and multiple support groups in execution of improvements, change controls, and projects, and assisting in providing supervisory coverage in the absence of the Associate Director. PFS3 Filling is part of the global syringe platform. Potential business travel opportunities to PFS2 (Sesto, Italy), Concord (North Carolina), or RTP (North Carolina) may be required to increase knowledge of the global platform.

Key Objectives/Deliverables

• Development and monitoring of metrics
• Provide education on concepts
• Drive projects for improvement
• Provide a leadership role in the area of C4I and process improvements for the process team.
• Projects as generated by Process Team and CAPA
• Investigate problems, conduct root cause analysis and implement countermeasures
• Potential to back up Process Team Leader
• Lead specific functions of the process team
• Lead by example in using data to influence change and improvement
• Ensure that all safety practices, policies, and rules are followed and enforced
• Complete safety audits Be an active participant in safety improvements and reduction of incidents

Minimum Requirements

• Bachelors Degree (technical or science degree preferred).
• Experience: Parenteral Operations experience or support preferred.

Additional Information / Preferences

• Previous leadership/supervisory experience helpful
• Career interests in operations leadership
• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

Other Information

• Other Information: The position is for 1st shift, start/stop times somewhat flexible.
• Must be flexible to attend meetings or support off-shifts as necessary.
• Some allergens are present in the parenteral plant. Mobility requirements and exposure to allergens should be considered when applying for this position.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and 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.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

Advisor, Delivery Device Systems

Responsibilities

DDCS is seeking an Engineer or Scientist to support the design, development, and maturity of delivery systems to enable Eli Lilly and Company’s growing therapeutic portfolio. In this role you will be an integrated member of project teams and will be responsible for ensuring robustness of the design for existing and new delivery devices/technologies. Key responsibilities for this role include:

• Lead and deliver complex projects through effective cross-functional collaboration in support of the organization and business strategy
• Provide technical expertise and ensure that design concepts are based on sound engineering principles utilizing the latest tools/technologies
• Develop new ideas and/or apply innovative solutions to accelerate timelines and/or improve quality of work product
• Understand, inform and support the delivery and device platform strategies
• Establish and leverage strategic relationships with external partners (including academia and startups) to accelerate and access emerging innovation
• Contribute to multiple projects simultaneously and exercise good triage and judgement skills
• Understand IP, freedom to operate and competitive landscape in targeted areas of research
• Mentor peers and/or interns on research, engineering, and product development best practices
• Assess and evaluate design concepts for technical risk and DFx (manufacturability, reliability, assembly)
• Author technical reports, work instructions, change control documentation and development plans
• Demonstrate engagement and employ a quality mindset in all endeavors by proactively identifying quality issues and communicating appropriately

Basic Requirements

• BS degree in engineering (mechanical engineering, chemical engineering, biomedical engineering, or a related field) or technical science
• 10+ years of experience working in industry demonstrating successful application of fundamentals

Additional Skills/Preferences

• 5+ years of industry experience developing drug delivery systems
• Advanced degree in applicable area of course work
• Ability to take ownership of project work and complete work according to project timelines
• Technical understanding of common commercial manufacturing and commercialization processes
• Outstanding interpersonal skills and the ability to work efficiently in an interdisciplinary environment
• Strong written communication skills, including technical report writing
• Effective problem solving and decision-making skills
• Fundamental knowledge of cGMP/laboratory compliance requirements.

Additional Information

• Estimated travel of up to 15% both domestic and international

Operator, Device Assembly & Packaging – Fulltime – $3,000 Sign-on Bonus – Starting at $22/hour + Benefits – Night Shift

Key Objectives/Deliverables

• Lilly is dedicated to the safety of our employees. We require our employees to maintain a safe work environment, work safely, and adhere to site safety policies and procedures.
• Setup and operations of automated, semi-automated or manual equipment in assembly, labeling, and packaging areas in accordance with operating procedures
• Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product
• Follow a manufacturing batch record and ensure good documentation practices during all entries in batch records, logbooks, and forms
• Attain and maintain qualification for operation of assigned process equipment and duties in the area
• Learn and apply knowledge and skills to complete standard tasks in their area of responsibility

Responsibilities

• Upholding our commitment to employee safety by maintaining a secure work environment and adhering to safety protocols.
• Operating automated, semi-automated, or manual equipment for assembly, labeling, and packaging, following operational guidelines.
• Ensuring product quality by strictly adhering to standard operating procedures and Good Manufacturing Practices.
• Maintaining accurate documentation practices in batch records, logbooks, and forms throughout the manufacturing process.
• Attaining and sustaining qualifications for equipment operation and related duties.

Basic Requirements

• High School diploma/GED
• Completion of the required exams or simulations
• Authorization to work in the United States without employment visa sponsorship.

Additional Skills/Preferences

• Direct manufacturing experience with automatic, manual, or semi-automated equipment, following operational procedures.
• Problem-solving abilities, technical skills, and a curious mindset.
• Strong multitasking capabilities and effective teamwork skills.
• Proficiency in verbal and written communication, along with excellent documentation skills.
• Familiarity with Good Manufacturing Practices, attention to detail, basic math, and computer skills.

Additional Information

• Manufacturing operates on 12-hour shifts following a 3-2-2-3 schedule.
• This role specifically caters to the night shift initially, with potential training on different schedules before transitioning to the permanent shift.
• Some overtime might be required, and certain products handled could be allergens, necessitating an allergy test post-offer.
• Safety equipment (safety glasses, shoes, gloves, etc.) is mandatory, and training will be provided for material handling equipment.
• This position offers an opportunity to contribute to a meaningful cause while being part of a dynamic, safety-focused team.

GenAI – NLP Data Scientist

Generative AI – Proactive, Predictive, Powerful!

Are you passionate about using data and technology to answer business and scientific questions? If so, bring YOUR skills and talents to Lilly where you’ll have the chance to create an impact on the lives of patients.

What You’ll Be Doing

As a GenAI Data Scientist, you will implement generative AI models, and identifying insights that can be used to drive business decisions. You will work closely with multi-functional teams to understand business problems, develop hypotheses, and test those hypotheses with data.

How You’ll Succeed

• Develop and implement enterprise-level GenAI models and tools to solve business problems.
• Collaborate with customers to identify business problems and provide data-driven solutions.
• Communicate insights and recommendations to technical and non-technical customers.
• Conduct research to identify emerging trends and technologies in Gen AI and other areas of data science.
• Run and prioritize multiple projects simultaneously.
• Ensure data quality and accuracy.

Your Basic Qualifications

• PhD in computer science, information science, mathematics, statistics, engineering, or related field
• OR Master’s in stem field with 2+ years of industry experience Post – Master’s education in a NLP/GenAI role.
• Experience with machine learning and GenAI algorithms such as large language models
• Prior experience working with Python or other programming languages

What You Should Bring

• Experience working with cloud based platforms (example: AWS, Azure or related)
• Strong problem-solving and analytical skills
• Proficiency in handling various data formats and sources
• Prior statistical modeling experience
• Demonstrable experience with deep learning algorithms and neural networks
• Experience with data engineering and data pipeline development
• Proven leadership and project management skills.
• Superb communication and presentation skills
• Ability to work in a fast-paced, collaborative environment

Additional Information

• Position located in Indianapolis, Indiana working in a hybrid model.
• Relocation to Indianapolis is required
• Up to 10% travel may be required depending on project