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.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
Organization Overview:
Lilly is entering an exciting period of growth and we are committed to delivering innovative medicines to patients around the world. Lilly is investing over $1 billion to create a new state-of-the-art manufacturing site, in Concord, North Carolina. The brand-new facility will utilize the latest technology to increase the company's manufacturing capacity in parenteral (injectable) medications, device assembly and packaging operations. This is an exciting once-in-a-lifetime opportunity to help build and operate a new site. The Lilly Concord site will be built using the latest high-tech equipment, advanced highly integrated and automated manufacturing systems, and have a focus on minimizing the impact to our environment. This is an opportunity you don’t want to miss!
Responsibilities:
- Bachelor’s degree in a science, engineering, computer, or pharmaceutical related field of study
- Experience working in the pharmaceutical or medical device industry in QA roles
- Previous batch disposition experience
- Ability to make technical decisions, provide guidance to the site
- Proficiency with applicable computer systems
- Demonstrated strong oral and written communication skills
- Demonstrated interpersonal skills and the ability to work as a team
- Root causeanalysis/troubleshootingskills
- Demonstrated attention to detail and ability to maintain quality systems
- Previous regulatory inspection readiness and inspection execution experience
- Ability to travel up to 10% for meetings and coordination with global or existing manufacturing sites
- Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals
- Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for employment positions on the B or S paths or at levels M1-M2 or R1-R4.
Bachelor’s degree in a science, engineering, computer, or pharmaceutical related field of study
Experience working in the pharmaceutical or medical device industry in QA roles
Previous batch disposition experience
Ability to make technical decisions, provide guidance to the site
Proficiency with applicable computer systems
Demonstrated strong oral and written communication skills
Demonstrated interpersonal skills and the ability to work as a team
analysis/troubleshooting
Demonstrated attention to detail and ability to maintain quality systems
Previous regulatory inspection readiness and inspection execution experience
Ability to travel up to 10% for meetings and coordination with global or existing manufacturing sites
Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for employment positions on the B or S paths or at levels M1-M2 or R1-R4.
- Ability to work 8-hour days – Monday through Friday Day Shift (not eligible for remote work)
- Proven ability to work independently or as part of a Team to resolve an issue
- Previous experience with Event and Change Management process
- Proficiency with SAP, MES, and Trackwise
- Previous experience with device and parenteral product materials
Ability to work 8-hour days – Monday through Friday Day Shift (not eligible for remote work)
Proven ability to work independently or as part of a Team to resolve an issue
Previous experience with Event and Change Management process
Proficiency with SAP, MES, and Trackwise
Previous experience with device and parenteral product materials
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.
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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