Visual Inspection Engineering Sme, Parenteral

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN +3

This role is an Engineering Subject Matter Expert (SME) for visual inspection of semi-finished products in parenteral manufacturing. It focuses on the evaluation, delivery, implementation, and support of automated, semi-automated, and manual inspection equipment. The position involves technical leadership, ensuring safety and compliance, global consultation, knowledge sharing, supporting major capital projects and external manufacturing, owning equipment platforms, and investigating emerging technologies. The core responsibilities are related to engineering support and optimization of inspection processes within a regulated healthcare manufacturing environment.

What you'd actually do

  1. Technical and Discipline leadership –Partners with other technical staff to direct discipline activities, oversight of the community, new technology development and technology assessments, creation and maintenance of Engineering Standards, Master specifications and Best Practices for the discipline, and coaching and mentorship of junior engineering staff.
  2. Safety and Compliance – Ensure personal and team compliance with all applicable regulatory and corporate policy requirements; ensure appropriate safety practices and procedures are in place and are followed to prevent injuries; ensures the ETC meets current Quality expectations and is a part of actively monitoring evolving Quality and other regulatory expectations related to engineering
  3. Consultation - Assists sites globally with technical evaluations, master planning, technology assessments, and specific problem resolution including troubleshooting and root cause analysis
  4. Knowledge sharing - Provides ongoing technical support to site engineering groups, domestic and global. Serves as a mentor to Lilly engineers with a focus on technical development and functional capability building. Interfaces with and develops site technical experts in Parenteral Engineering. Reviews and prepares protocols and technical reports.
  5. External Influence - Monitors and, when appropriate, influences change in external codes and standards on Lilly’s behalf. Ensures external learnings are effectively communicated within Lilly and works to ensure ongoing compliance with these learnings.

Skills

Required

  • Bachelor's degree
  • 4+ years of experience in cGMP manufacturing or manufacturing support role
  • Extensive knowledge of parenteral visual inspection equipment and operations including automated, semi-automated and/or manual inspection equipment

Nice to have

  • Familiarity with technology advances in vial, cartridge, and syringe container closure systems
  • Strong interpersonal and communication skills
  • Ability to work across boundaries
  • Demonstrated learning agility
  • Ability to work effectively with outside suppliers
  • Demonstrated ability to solve technical problems and implement

What the JD emphasized

  • Extensive knowledge of parenteral visual inspection equipment