Technician - Process - Visual Inspection (night Shift)

Eli Lilly Eli Lilly · Pharma · US: Research Triangle Park, NC

This role is for a Process Visual Inspection Technician in a new pharmaceutical manufacturing facility. Responsibilities include supporting commissioning and qualification of automated inspection lines, operating automated and manual inspection equipment, ensuring compliance with Good Manufacturing Practices (CGMPs) and safety standards, and supporting leadership in troubleshooting and operator development. The role requires experience in a regulated industry and familiarity with automated inspection equipment.

What you'd actually do

  1. Provide commissioning, qualification, and operational readiness support during project phase.
  2. Adhere to RTP Plant safety policies and procedures, contribute to a safe work environment.
  3. Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
  4. Support leadership on the manufacturing floor by ensuring high level of safety, quality, and productivity to maintain reliable supply of products to patients.
  5. Proactively monitor documentation and product quality; properly documenting all activities and reporting issues to supervision.

Skills

Required

  • High School Diploma or equivalent
  • 2+ years relevant experience in pharmaceutical, or equivalent regulated industry
  • Ability to work 12-hour shifts on nights (2-2-3 schedule)
  • Ability to work overtime as required
  • Ability to pass an annual job fitness exam

Nice to have

  • Demonstrated ability to train and coach others
  • Ability to effectively communicate (written and verbal)
  • Flexibility and problem-solving skills
  • 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

What the JD emphasized

  • 2+ years relevant experience in pharmaceutical, or equivalent regulated industry
  • Qualified applicants must be authorized to work in the United States on a full-time basis.