Analytical Development Advisor for Genetic Medicines

Initial Therapeutics, Inc.; Indianapolis (IN); On-site; USD 126,000 - 244,200; Full time

Benefits offered by this job

Comprehensive benefits program

Company bonus eligibility

401(k) participation

Job summary

Lilly in Indianapolis is seeking an Advisor for the BRD Analytical Development team to support analytical development for genetic medicines. The role involves developing and qualifying analytical methods and executing PCR-based methods. The ideal candidate should have a Ph.D. or relevant work experience in the pharmaceutical industry.

Responsibilities include supporting assay qualification and maintaining GMP compliance. Candidates must have practical experience with molecular biology and analytical techniques.

Qualifications

• 0-5+ years of relevant pharmaceutical or biotech industry experience.
• 6+ years of experience with M.S. or 12+ years with B.S.
• Practical proficiency with techniques for quantitative nucleic acid analysis.

Responsibilities

• Develop, qualify, and execute PCR-based methods for viral vector genome.
• Apply molecular biology techniques for product characterization.
• Support assays qualification, verification, and validation activities.

Skills

Practical proficiency with qPCR

Experience with immunoassay platforms

Hands-on experience with molecular biology techniques

Independently design experiments

Familiarity with GMP/GLP requirements

Education

Ph.D. in Molecular Biology, Biochemistry, Biology, or Analytical Chemistry

M.S. in Molecular Biology, Biochemistry, Biology, or Analytical Chemistry

B.S. in Molecular Biology, Biochemistry, Biology, or Analytical Chemistry

Tools

qPCR

ddPCR

ELISA

NGS workflows

Electronic lab notebooks

Job description

Lilly in Indianapolis is seeking an Advisor for the BRD Analytical Development team to support analytical development for genetic medicines. The role involves developing and qualifying analytical methods and executing PCR-based methods. The ideal candidate should have a Ph.D. or relevant work experience in the pharmaceutical industry.

Responsibilities include supporting assay qualification and maintaining GMP compliance. Candidates must have practical experience with molecular biology and analytical techniques.