Senior Oligonucleotide Process Advisor

100 Eli Lilly and Company

Houston (TX)

On-site

USD 131,000 - 211,000

Full time

14 days+

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Benefits offered by this job

401(k) savings plan
Pension plan
Vacation benefits
Medical, dental, vision benefits
Well-being programs
Employee assistance program

Job summary

Lilly is building a greenfield API manufacturing site in Houston, TX, to produce oligonucleotides and other molecules. This role supports technical transfer, process validation, and manufacturing excellence in a GMP environment.

Ideal candidates have a strong chemistry/biochemistry background, 10+ years of cGMP manufacturing experience, and proven leadership and communication skills to drive cross-functional collaboration and continuous improvement.

Qualifications

  • Bachelor's degree in chemistry, microbiology, biochemistry, biochemical engineering, or related science.
  • 10+ years of experience in cGMP oligonucleotide, peptide, or small molecule API commercial-scale manufacturing.

Responsibilities

  • Provides technical oversight and stewardship for one or more molecules manufactured at the Lilly Houston facility.
  • Leads the technical transfer of processes between facilities and addresses scale-up issues.
  • Mentors Process Team members, monitors, trends, and analyzes production data.
  • Supports management of daily manufacturing operations and prepares technical reports.
  • Reviews manufacturing batch records and related documentation; supports change controls and investigations.

Skills

Leadership skills
Communication skills
cGMP knowledge
Process knowledge

Education

Bachelor's degree in Chemistry, Microbiology, Biochemistry, Biochemical engineering or related science field

Job description

Lilly is building a greenfield API manufacturing site in Houston, TX, to produce oligonucleotides and other molecules. This role supports technical transfer, process validation, and manufacturing excellence in a GMP environment.

Ideal candidates have a strong chemistry/biochemistry background, 10+ years of cGMP manufacturing experience, and proven leadership and communication skills to drive cross-functional collaboration and continuous improvement.

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