Senior Tech Lead, Parenteral Drug Product Manufacturing

Lilly

Indianapolis (IN)

On-site

USD 131,000 - 211,000

Full time

44 hours ago
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Benefits offered by this job

401(k) plan
Pension
Vacation benefits
Medical benefits
Dental benefits
Vision benefits
Prescription drug benefits
Flexible benefits
Life insurance
Employee clubs

Job summary

Lilly in Indianapolis is seeking a senior scientist to lead the development of parenteral drug products from clinical to commercialization. You will define manufacturing processes, drive tech transfer, and collaborate with cross-functional teams across manufacturing, quality, and regulatory.

The role emphasizes advancing biologics and small molecules, implementing new technologies, and ensuring compliance with cGMP.

Qualifications

  • PhD/MS/BS in Engineering or related field with industry experience as specified.
  • Experience in pharmaceutical development or manufacturing.
  • Knowledge of biologics parenteral product development and regulatory guidelines.

Responsibilities

  • Define and develop clinical manufacturing processes for parenteral drug products.
  • Drive collaboration with cross functional stakeholders to develop process control strategies.
  • Lead manufacturing related process design, scale up, and mentor junior scientists.
  • Technology transfer: internal and external capacity evaluation, risk assessment, and docs.
  • Collaborate to define process qualification and control strategy; address gaps.

Skills

Process development
Tech transfer
Regulatory documentation
Cross-functional collaboration

Education

PhD in Engineering
MS in Engineering
BS in Engineering or Pharma/ Chemistry

Tools

Lab automation
AI/ ML in pharma

Job description

Lilly in Indianapolis is seeking a senior scientist to lead the development of parenteral drug products from clinical to commercialization. You will define manufacturing processes, drive tech transfer, and collaborate with cross-functional teams across manufacturing, quality, and regulatory.

The role emphasizes advancing biologics and small molecules, implementing new technologies, and ensuring compliance with cGMP.

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