NCBiotech
Process Technician - Visual Inspection (Night Shift)
NCBiotech, 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. 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.
At Lilly, we believe in the talent of our workforce. One of the best ways to utilize and develop that talent is to use our existing workforce to fill new and/or open positions. If you are looking for a new position within Lilly, you can view and apply to open roles posted in the internal job posting system. You must meet the minimum qualifications outlined in the job description and have/obtain work authorization in the country the position is located in order to be considered. When applying internally for a position, your current supervisor will receive notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying.
Path/Level B1
The annual base salary for this position in country = United States of America ranges from: $35,000.00 - $80,000.00 USD
Organization Overview At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Lilly is designing and 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.
Quick Benefit Overview
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, the Visual Inspection Technician will support commissioning/qualification activities required to bring inspection lines, utilizing semi‑automated and automated technology, into service as well as support site operational readiness activities. This role includes the opportunity to become a subject matter expert for the inspection equipment/process with the potential for development into a Line Lead or other leadership role. This position may require domestic travel with the opportunity for international travel based on program need.
After project phase completion, this role will be responsible for the safe operation of highly automated equipment used to inspect syringes. The Inspection Technician is expected to model current Good Manufacturing Practices and ensure compliance with all safety standards. They will support the Line Lead in development of operators and identification of opportunities for operational improvement.
Key Objectives
Provide commissioning, qualification, and operational readiness support during project phase.
Adhere to RTP Plant safety policies and procedures, contribute 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 high level of safety, quality, and productivity to maintain reliable supply of products to patients.
Proactively monitor documentation and product quality; properly documenting all activities and reporting issues to supervision.
Key support for leadership during troubleshooting, functions as reliable point of contact for issue escalation on the shop floor.
Drives key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
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 and during the project phase will allow for a flexible working environment with the ability to periodically work remotely based on the project phase and site activities.
Position may require a short duration assignment of 1-2 months in Indianapolis to establish specific device knowledge, establish global contacts, and provide production support. Additionally, this position may require short (less than 1 month) international travel to support Factory Acceptance Testing of equipment.
Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.).
Ability to work 12‑hour shifts on nights (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.
Compensation $17.30 - $38.08
COVID‑19 Vaccination Requirement 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).
EEO Statement Lilly is a proud 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. 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 P1‑P4.
#J-18808-Ljbffr
At Lilly, we believe in the talent of our workforce. One of the best ways to utilize and develop that talent is to use our existing workforce to fill new and/or open positions. If you are looking for a new position within Lilly, you can view and apply to open roles posted in the internal job posting system. You must meet the minimum qualifications outlined in the job description and have/obtain work authorization in the country the position is located in order to be considered. When applying internally for a position, your current supervisor will receive notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying.
Path/Level B1
The annual base salary for this position in country = United States of America ranges from: $35,000.00 - $80,000.00 USD
Organization Overview At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Lilly is designing and 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.
Quick Benefit Overview
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, the Visual Inspection Technician will support commissioning/qualification activities required to bring inspection lines, utilizing semi‑automated and automated technology, into service as well as support site operational readiness activities. This role includes the opportunity to become a subject matter expert for the inspection equipment/process with the potential for development into a Line Lead or other leadership role. This position may require domestic travel with the opportunity for international travel based on program need.
After project phase completion, this role will be responsible for the safe operation of highly automated equipment used to inspect syringes. The Inspection Technician is expected to model current Good Manufacturing Practices and ensure compliance with all safety standards. They will support the Line Lead in development of operators and identification of opportunities for operational improvement.
Key Objectives
Provide commissioning, qualification, and operational readiness support during project phase.
Adhere to RTP Plant safety policies and procedures, contribute 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 high level of safety, quality, and productivity to maintain reliable supply of products to patients.
Proactively monitor documentation and product quality; properly documenting all activities and reporting issues to supervision.
Key support for leadership during troubleshooting, functions as reliable point of contact for issue escalation on the shop floor.
Drives key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
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 and during the project phase will allow for a flexible working environment with the ability to periodically work remotely based on the project phase and site activities.
Position may require a short duration assignment of 1-2 months in Indianapolis to establish specific device knowledge, establish global contacts, and provide production support. Additionally, this position may require short (less than 1 month) international travel to support Factory Acceptance Testing of equipment.
Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.).
Ability to work 12‑hour shifts on nights (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.
Compensation $17.30 - $38.08
COVID‑19 Vaccination Requirement 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).
EEO Statement Lilly is a proud 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. 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 P1‑P4.
#J-18808-Ljbffr