Eli Lilly and Company
Technician - Visual Inspection Operations
Eli Lilly and Company, Durham, North Carolina, United States, 27703
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, and we are building a new state-of-the-art Parenteral, Device Assembly, and Packaging Facility in Raleigh‑Durham, North Carolina. This is an exciting opportunity to help build the facility of the future from the ground up.
Key Benefits
Medical, Dental, Vision, Prescription benefits are effective on your first day of employment
Paid vacation—starting annually at 120 hours (prorated based on start date)
Responsibilities
During the project phase, support commissioning/qualification activities required to bring inspection lines, utilizing semi-automated and automated technology, into service as well as supporting site operational readiness activities.
After project phase completion, be responsible for the safe operation of highly automated equipment used to inspect syringes. Model current Good Manufacturing Practices and ensure compliance with all safety standards. Support the Line Lead in development of operators and identification of opportunities for operational improvement.
Perform inspections on product to identify defects.
Support leadership on the manufacturing floor by ensuring a high level of safety, quality, and productivity to maintain reliable supply of products to patients.
Proactively monitor documentation and product quality; properly document all activities and report issues to supervision.
Provide key support for leadership during troubleshooting, functioning as a reliable point of contact for issue escalation on the shop floor.
Drive departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
Key Objectives
Provide commissioning, qualification, and operational readiness support during project phase.
Adhere to RTP Plant safety policies and procedures, contributing to a safe work environment.
Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
Support leadership on the manufacturing floor by ensuring a high level of safety, quality, and productivity to maintain reliable supply of products to patients.
Proactively monitor documentation and product quality; properly document all activities and report issues to supervision.
Key support for leadership during troubleshooting, functioning as a reliable point of contact for issue escalation on the shop floor.
Drive departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
Perform inspections on product to identify defects.
Basic Requirements
High School Diploma or equivalent
Minimum 1 year relevant experience (education may be substituted for experience with manager discretion)
Additional Skills/Preferences
Ability to effectively communicate (written and verbal)
Flexibility and problem‑solving skills
2+ years relevant experience in pharmaceutical, or equivalent regulated industry
Scientific/technical degrees or certifications
Knowledge of current Good Manufacturing Practices (CGMPs)
Previous experience utilizing semi‑automated and automated visual inspection equipment
Previous experience with pre‑filled syringe (PFS) technology
Previous experience with Manufacturing Execution Systems and electronic batch records
Knowledge of lean manufacturing principles
Additional Information
The position is for the Lilly Research Triangle Park site
Ability to wear safety equipment (safety glasses, safety shoes, protective gloves, etc.)
Ability to work 12‑hour shifts on days (2‑2‑3 schedule)
Ability to work overtime as required
Ability to travel during Project Phase and
Ability to pass an annual job fitness exam
This role requires passing a yearly vision exam for acuity and color, with or without corrective lenses.
Compensation Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $17.30 – $38.08.
Full‑time equivalent employees will also 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; life insurance and death benefits; certain time off and leave of absence benefits; and well‑being benefits.
Legal and Other Requirements As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID‑19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).
To request a workplace accommodation, email Lilly Human Resources at Lilly_Recruiting_Compliance@lists.lilly.com. 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 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.
#J-18808-Ljbffr
Key Benefits
Medical, Dental, Vision, Prescription benefits are effective on your first day of employment
Paid vacation—starting annually at 120 hours (prorated based on start date)
Responsibilities
During the project phase, support commissioning/qualification activities required to bring inspection lines, utilizing semi-automated and automated technology, into service as well as supporting site operational readiness activities.
After project phase completion, be responsible for the safe operation of highly automated equipment used to inspect syringes. Model current Good Manufacturing Practices and ensure compliance with all safety standards. Support the Line Lead in development of operators and identification of opportunities for operational improvement.
Perform inspections on product to identify defects.
Support leadership on the manufacturing floor by ensuring a high level of safety, quality, and productivity to maintain reliable supply of products to patients.
Proactively monitor documentation and product quality; properly document all activities and report issues to supervision.
Provide key support for leadership during troubleshooting, functioning as a reliable point of contact for issue escalation on the shop floor.
Drive departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
Key Objectives
Provide commissioning, qualification, and operational readiness support during project phase.
Adhere to RTP Plant safety policies and procedures, contributing to a safe work environment.
Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
Support leadership on the manufacturing floor by ensuring a high level of safety, quality, and productivity to maintain reliable supply of products to patients.
Proactively monitor documentation and product quality; properly document all activities and report issues to supervision.
Key support for leadership during troubleshooting, functioning as a reliable point of contact for issue escalation on the shop floor.
Drive departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
Perform inspections on product to identify defects.
Basic Requirements
High School Diploma or equivalent
Minimum 1 year relevant experience (education may be substituted for experience with manager discretion)
Additional Skills/Preferences
Ability to effectively communicate (written and verbal)
Flexibility and problem‑solving skills
2+ years relevant experience in pharmaceutical, or equivalent regulated industry
Scientific/technical degrees or certifications
Knowledge of current Good Manufacturing Practices (CGMPs)
Previous experience utilizing semi‑automated and automated visual inspection equipment
Previous experience with pre‑filled syringe (PFS) technology
Previous experience with Manufacturing Execution Systems and electronic batch records
Knowledge of lean manufacturing principles
Additional Information
The position is for the Lilly Research Triangle Park site
Ability to wear safety equipment (safety glasses, safety shoes, protective gloves, etc.)
Ability to work 12‑hour shifts on days (2‑2‑3 schedule)
Ability to work overtime as required
Ability to travel during Project Phase and
Ability to pass an annual job fitness exam
This role requires passing a yearly vision exam for acuity and color, with or without corrective lenses.
Compensation Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $17.30 – $38.08.
Full‑time equivalent employees will also 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; life insurance and death benefits; certain time off and leave of absence benefits; and well‑being benefits.
Legal and Other Requirements As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID‑19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).
To request a workplace accommodation, email Lilly Human Resources at Lilly_Recruiting_Compliance@lists.lilly.com. 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 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.
#J-18808-Ljbffr