Associate Director - Tsms Dry External Manufacturing

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN +1

Associate Director responsible for managing TS/MS and ENG personnel supporting external manufacture of dry products. Requires knowledge of cGMPs, regulatory manufacturing guidance, and validation/engineering practices. Role involves cross-functional collaboration, technical oversight, process optimization, and staff management within a pharmaceutical manufacturing environment.

What you'd actually do

  1. Ensure technical review and approval for documents, including investigations, change controls, regulatory submissions, expert opinions, validations, annual product reviews, manufacturing tickets, procedures, process flow documents, personnel qualification strategies, control strategies, technical studies, etc.
  2. Performance management and development of staff.
  3. Partner within TS/MS , ENG and across functional disciplines to influence and implement the technical agenda, site business plan objectives, functional objectives, and GMP Quality Plan objectives
  4. Ensure appropriate technical and Engineering oversight and stewardship of oral solid dose form manufacturing and packaging including drug product intermediates (e.g. spray dried dispersions/amorphous solid dispersions).
  5. Interact with regulators, customers, or other outside stakeholders on business issues or in support of internal and external agency audits

Skills

Required

  • Bachelor's Degree in scientific disciplines of Chemistry, Biology, Biotechnology, Pharmacy, Engineering or another related field.
  • 8+ years’ experience in Dry Products/Oral Solid Dose pharmaceutical manufacturing environment in any of the following associated disciplines: TSMS, Production, Engineering at a manufacturing site .
  • Previous leadership/people management experience.

Nice to have

  • Ability to represent Eli Lilly's mission, policies and practices in a positive, professional and ethical manner to influence CMs.
  • Responsible for maintaining a safe work environment
  • Ability to influence and inclusively lead diverse groups
  • Influences complex regulatory/quality, business, or technical issues within the site and function
  • Experience in statistics

What the JD emphasized

  • cGMP
  • regulatory manufacturing guidance
  • validation
  • engineering practices