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Technician - Visual Inspection

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: BioSpace
Full Time position
Listed on 2026-01-14
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Manufacturing Production
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below

Join to apply for the Technician - Visual Inspection role at Bio Space
.

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 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.

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 supporting 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 based on business 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, contributing to a safe work environment.
  • Adhere to standard operating procedures and current Good Manufacturing Practices to ensure product quality.
  • Support leadership on the manufacturing floor by ensuring high level of safety, quality, and productivity to maintain a 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, serving as reliable point of contact for issue escalation on the shop floor.
  • Assist Supervisor in the development and training of shift operators.
  • Drive 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.
  • 2+ years relevant experience in pharmaceutical or equivalent regulated industry.
Additional Skills and Preferences
  • Demonstrated ability to train and coach others.
  • Effective communication (written and verbal).
  • Flexibility and problem‑solving skills.
  • Scientific/technical degrees or certifications.
  • Knowledge of current Good Manufacturing Practices (CGMPs).
  • Experience utilizing semi‑automated and automated visual inspection equipment.
  • Experience with pre‑filled syringe (PFS) technology.
  • Experience with Manufacturing Execution Systems and electronic batch records.
  • Knowledge of lean manufacturing principles.
Additional Information
  • Ability to conduct and qualify machine operation trainings, including defect detection for syringes.
  • Must be able to stand for several hours and bend as needed for tasks such as equipment cleanings and line clearances.
  • 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 < 5% after startup.
  • Ability to pass an annual job fitness exam.
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).
  • $3,000 sign‑on bonus.

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 at 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 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.

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