Senior MSAT Advisor — Bioconjugate Manufacturing

100 Eli Lilly and Company

Richmond (VA)

On-site

USD 129,000 - 209,000

Full time

7 days ago
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Benefits offered by this job

401(k)
Pension
Vacation benefits
Medical benefits

Job summary

Lilly is building an advanced manufacturing facility in Goochland County, VA. We seek an Advisor/Sr. Advisor TS/MS (MSAT) to provide technical stewardship across the start-up bioconjugate manufacturing facility.

The role requires deep expertise in conjugation chemistry, purification, and process controls, with data-driven decision-making and cross-functional leadership. You will mentor scientists and engineers, drive continuous improvements, ensure cGMP compliance, and support regulatory

Qualifications

  • MSc in Biochemistry, Cell Biology, Biotechnology, Biochemical Engineering or related field.
  • 5+ years in ADC/mAb development.
  • Experience in commercial ADC/mAb mfg support.
  • Experience in inspection support.
  • PhD and 10+ years in biopharmaceutical industry preferred.

Responsibilities

  • Provide mentorship and scientific expertise to TS/MS bioprocess and laboratory scientists.
  • Support management of daily manufacturing operations.
  • Drive solutions to complex situations with cross-site impact.
  • Ensure compliance with safety and regulatory expectations under cGMP.
  • Lead investigations and document technical studies.

Skills

Technical leadership
Data-driven decisions
Strong communication
Mentoring
Problem solving

Education

MSc in Biochemistry, Cell Biology, Biotechnology, Biochemical Engineering or related discipline
PhD in Biochemistry, Cell Biology, Biotechnology, Biochemical Engineering or related discipline

Job description

Lilly is building an advanced manufacturing facility in Goochland County, VA. We seek an Advisor/Sr. Advisor TS/MS (MSAT) to provide technical stewardship across the start-up bioconjugate manufacturing facility.

The role requires deep expertise in conjugation chemistry, purification, and process controls, with data-driven decision-making and cross-functional leadership. You will mentor scientists and engineers, drive continuous improvements, ensure cGMP compliance, and support regulatory

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