Job Information
Lilly QC Technician in Concord, North Carolina
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.
Company Overview:
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 39,000 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. #WeAreLilly
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.
Position Brand Description:
The Incoming QC Lab Technician performs accurate and timely testing of routine lab samples in accordance with appropriate GMP and safety guidelines. The Incoming QC Lab Technician will also participate in second person verification (SPV) of analytical data, laboratory investigations, and maintenance by executing well-defined protocols and procedures. The Incoming QC Lab Technician identifies and communicates opportunities for improvement within the lab.
Key Objectives/Deliverables:
Accurately and safely performs analytical test methods or related support activities as per procedures or protocols and reviews that results conform to standards.
Performs data entry and reviews own work for accuracy in accordance with laboratory procedures, standards, and GMP requirements.
Recognizes when a deviation from procedures, etc. has occurred and initiates an investigation, notifies supervision.
Verifies (SPV) analytical data of other analysts within the lab as required.
Identifies and communicates opportunities for improvement initiatives in daily work activities.
Troubleshoots equipment and methods as required.
Participates in laboratory investigations.
Maintains a safe work environment, works safely, and is accountable for supporting all HSE Corporate and Site goals.
Basic Experience Requirements:
Teamwork and interpersonal skills
Strong verbal and written communication skills
Ability to focus on continuous improvement.
Education Requirements:
- High school diploma and at least one year of demonstrated relevant experience in a GMP (analytical chemistry or microbiology) lab.
Additional Skills/Preferences:
Proficiency with computer systems including Microsoft Office products, LIMS (list other lab systems), etc.
Ability to work in a lab environment including wearing appropriate PPE and other safety required equipment and considerations.
Ability to work in a highly regulated environment.
Demonstrated documentation skills.
Ability to repetitively lift up to 20 pounds.
Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
Other Information:
8 hour days – Monday through Friday
Travel may be required during project phase.
Ability to work in various areas within the site. Some allergens are present in the parenteral plant.
Tasks may require repetitive motion (e.g., keyboarding).
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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.
#WeAreLilly