Site QC Analytical Steward - Startup Lab & Method Transfer

100 Eli Lilly and Company; Houston (TX); On-site; USD 65,000 - 169,000; Full time

Benefits offered by this job

401(k) matching program

Vacation benefits

Medical, dental, vision benefits

Job summary

Lilly Houston is seeking a Site Analytical Steward to provide day-to-day analytical support as the site stands up small molecule and oligonucleotide DS testing. You will work under the Analytical Molecule Steward, performing hands-on problem solving and supporting investigations, with mentorship and growing independence.

As you gain capability, you will take ownership of routine batch review, method support, deviations, and training of QC analysts, contributing to site readiness and compliance

Qualifications

• Bachelor's degree in a science field; 3–5 years GMP lab experience preferred.
• Proficiency in laboratory analysis including chromatographic, spectroscopic, or microbiological assays.
• Ability to work safely in a laboratory and follow regulatory expectations.
• Proven problem-solving and analytical thinking with mentorship.
• Willingness to develop depth and independence over time.

Responsibilities

• Provide day-to-day analytical support as the site stands up testing capabilities.
• Assist investigations into out-of-spec results and aberrant data under mentorship.
• Support equipment qualification, method transfer, and batch review activities.
• Mentor QC analysts as capability develops and contribute to training materials.

Skills

GMP laboratory experience

Laboratory data analysis

Problem solving

Interpersonal communication

Education

Bachelor's degree in a science field

Job description

Lilly Houston is seeking a Site Analytical Steward to provide day-to-day analytical support as the site stands up small molecule and oligonucleotide DS testing. You will work under the Analytical Molecule Steward, performing hands-on problem solving and supporting investigations, with mentorship and growing independence.

As you gain capability, you will take ownership of routine batch review, method support, deviations, and training of QC analysts, contributing to site readiness and compliance