Engineer - Warehouse

BioSpace; Indianapolis (IN); On-site; USD 64,000 - 143,000; Full time

Job summary

A leading healthcare company seeks an Engineer for its Warehouse operations in Indianapolis. The role involves maintaining equipment systems and ensuring compliance with safety standards while engaging in cross-functional projects to improve operational efficiency. Ideal candidates will have a background in engineering and a strong command of automation technologies.

Benefits

Comprehensive benefit program

Company bonus eligibility

401(k) and pension options

Flexible benefits options

Employee assistance program

Qualifications

• 1-2 years of experience in engineering roles preferred.
• Knowledge in pharmaceutical manufacturing processes.
• Ability to work cross-functionally in teams.

Responsibilities

• Ensure a safe working environment and safe equipment operation.
• Lead troubleshooting efforts for complex equipment issues.
• Support the development and deployment of automation solutions.

Skills

Interpersonal skills

Control system programming

Project management

Problem-solving techniques

Education

Bachelor’s degree in science or engineering

Tools

PLC

HMI

MES systems

Job description

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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.

Organization Overview

The Engineer – Warehouse is responsible for establishing and maintaining the reliable operation and qualified state of the equipment/robotics systems in the area they support. The engineer engages with the project and cross-functional support teams as an equipment/automation subject matter expert to ensure the business meets defined safety, quality, and productivity goals. The engineer also ensures that systems and platforms are in-control, compliant, and capable of meeting customer needs, while delivering on projects associated with regulatory compliance, commercialization, capacity, and process improvement efforts.

This specific role will be responsible for engineering delivery activities for multiple equipment/systems within the K116 project in Indianapolis Parenteral Manufacturing, delivering capability for fully automated material movements within IPM. Following project delivery, this role will become a member of the warehouse process team, providing engineering support to the warehouse areas during production operations.

Responsibilities

• Ensure a safe working environment by following safety rules and helping improve safety culture.
• Responsible for the safe design and safe operation of the equipment within the area.
• Ensure that process automation solutions/systems are in-control, capable, and compliant throughout K116 Warehouse systems.
• Lead or assist in C&Q and Verification activities (including commissioning activities of new equipment or areas).
• Support the development, deployment, and operation of material movement solutions within K115 and K116 projects.
• Partner with the Global Robotics Program team to support design and implementation of systems.
• Communicate effectively with others, especially project team members, process team members, operations, maintenance, and crafts personnel.
• Perform impact assessments for varying levels of changes to responsible equipment/systems.
• Understand equipment reliability issues with the objective of process improvement.
• Identify and drive improvements associated with equipment within the area.
• Lead troubleshooting efforts to resolve more difficult equipment and operational problems.
• Apply formal problem-solving techniques, including Root Cause Analysis, to resolve equipment issues.
• Engage with original equipment manufacturers and other service vendors to build knowledge base and deliver on projects and troubleshooting efforts.
  
  
  

Basic Requirements

• Bachelor’s degree in a science or engineering field; preferably with 1-2 years of experience.
  
  
  

Additional Skills/Preferences

• Ability to work cross-functionally with other areas of Indianapolis Parenteral Manufacturing (Operations, Quality, etc.).
• Good interpersonal and communications skills to be able to work effectively in a team-based environment.
• Knowledge in control system programming and integration with Robotics platforms, PLC, HMI, and MES systems.
• Experience in pharmaceutical manufacturing, parenteral, and/or packaging processes.
• Experience in Commissioning & Qualification, asset delivery, validation activities, and cGMP regulations.
• Demonstrated ability to communicate effectively to customers, business partners, and staff including good oral, written, and visual presentations.
• Experience utilizing and implementing various tools, systems, and processes resulting in improved operational excellence.
• Proficiency in working cross-functionally to deliver on highly complex tasks that may have aggressive timelines.
  
  
  

Additional Information

• 8-hour dayshift work schedule.
• Must be willing to work extended hours during peak periods.
• Must be willing to respond to off-hour support needs, as necessary.
• Occasional travel may be required for project delivery activities, training, conferences, capital projects, etc.
  
  
  

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 proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, 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 are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$64,500 - $143,000

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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