Senior Advisor, Solid Dose Manufacturing

BioSpace

Indianapolis (IN)

On-site

USD 117,000 - 209,000

Full time

14 days+

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Benefits offered by this job

Bonus program
Comprehensive benefits

Job summary

Lilly, headquartered in Indianapolis, Indiana, seeks a Sr. Principal Scientist to integrate commercialization work plans across Product Development, CMC, and Manufacturing to bring solid oral dosage forms to market. The role requires deep expertise in development, commercialization, and manufacturing science.

Candidate should drive process robustness, data-driven decisions, and cross-functional collaboration, influencing global strategies and technical standards for solid dosage platforms.

Qualifications

  • BS, MS, and/or PhD in Chemistry, Engineering, Pharmaceutical Science, or related science.
  • Minimum 7-10 years of direct experience in Oral Solid Dose Form Manufacturing and Development/Commercialization.
  • A minimum of 3 years of commercial manufacturing support (post process validation) of solid oral dosage forms.

Responsibilities

  • Serve as Manufacturing TS/MS representative to integrate commercialization work plans across Product Development, CMC teams, Manufacturing sites, and applicable functional areas.
  • Leverage commercial manufacturing and development experience to anticipate manufacturing challenges for new oral products.
  • Provide technical leadership for manufacturing process transfers between Lilly and external sites and support external manufacturing as needed.

Skills

Manufacturing TS/MS liaison
Solid oral dosage knowledge
Data analysis
Cross-functional leadership

Education

BS/MS/PhD in Chemistry/Engineering/Pharmaceutical Science

Job description

Lilly, headquartered in Indianapolis, Indiana, seeks a Sr. Principal Scientist to integrate commercialization work plans across Product Development, CMC, and Manufacturing to bring solid oral dosage forms to market. The role requires deep expertise in development, commercialization, and manufacturing science.

Candidate should drive process robustness, data-driven decisions, and cross-functional collaboration, influencing global strategies and technical standards for solid dosage platforms.

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