Lead Technician - Engineering (night Shift)

Eli Lilly Eli Lilly · Pharma · Concord, NC

Lead Technician for Engineering (Night Shift) at Eli Lilly, responsible for device assembly and packaging equipment performance, providing technical support, and implementing process improvements in a GMP-regulated healthcare manufacturing environment.

What you'd actually do

  1. Assure that operational, automation and maintenance activities, procedures and practices reflect safety culture and operational excellence.
  2. Provide technical support to maintenance and automation technicians by investigating and resolving issues during production and operation of the equipment
  3. Perform activities in accordance with cGMPs, site procedures, and applicable regulatory requirements.
  4. Identify opportunities to improve quality and reliability using equipment performance data to make technically sound decisions.
  5. Effectively communicate with all levels to ensure work activities, escalations, and issues are communicated and coordinated with minimal disruption to operations.

Skills

Required

  • High school diploma or GED
  • Minimum of 2 years of experience supporting manufacturing, packaging, or device assembly equipment
  • Demonstrated ability to work safely in a participative manufacturing environment
  • Strong mechanical and/or automation troubleshooting skills
  • Demonstrated proficiency in PLC troubleshooting, logical problem solving, and technical right-first-time execution
  • Demonstrated proficiency with Microsoft Word and Excel, including technical documentation
  • Ability to work independently with strong organizational skills and attention to detail
  • Strong interpersonal and communication skills with a customer-service mindset
  • Responsible for maintaining a safe work environment and supporting all HSE corporate and site goals

Nice to have

  • Associate degree in engineering, a technical discipline, or equivalent technical experience preferred
  • Experience in a GMP-regulated manufacturing environment
  • Knowledge of parenteral, device assembly, or packaging manufacturing operations preferred
  • Experience with computerized maintenance management systems (e.g., Maximo) preferred
  • Experience supporting highly automated device assembly or packaging equipment preferred

What the JD emphasized

  • cGMPs
  • GMP-regulated manufacturing environment