Idap Ts/ms Steward

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN

This role is for a Technical Services Manufacturing Scientist (TS/MS) Product Steward at Eli Lilly, supporting and developing technical agendas for manufacturing processes and products. Responsibilities include maintaining validated states, establishing metrics, improving processes, and leading technical aspects of commercialization. The role requires technical leadership, support for investigations, document review, process monitoring, and mentorship within a regulated pharmaceutical manufacturing environment.

What you'd actually do

  1. Own Tech Transfer and Validation strategy for the manufacturing site
  2. Participate in equipment/product/format commissioning, qualification, and validation activities
  3. Represent TS/MS team to the IDAP Site Lead team
  4. Provide technical support to non-routine (e.g., deviation, complaint) investigations
  5. Prepare, review, and approve, as required, relevant technical documents such as: annual product reviews, change controls, regulatory submissions, deviations, validations, procedures, PFDs, PFMEAs, etc.

Skills

Required

  • Bachelors degree or higher in engineering, science, or related field
  • Good written and oral communications
  • Clear understanding of cGMPs
  • Good teamwork and interpersonal skills
  • Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals
  • Qualified applicants must be authorized to work in the United States on a full-time basis

Nice to have

  • 5 years of experience in a manufacturing organization
  • Experience in multiple functions within a manufacturing site (operations, engineering, quality, etc.)
  • Previous experience in TS/MS or technical function within manufacturing organization
  • Pharmaceutical manufacturing experience
  • Root Cause Investigation Experience
  • Demonstrated successful leadership/mentorship of cross-functional teams
  • Demonstrated technical writing skills

What the JD emphasized

  • clear understanding of cGMPs
  • Qualified applicants must be authorized to work in the United States on a full-time basis