Key Responsibilities
- Lead development and establishment of high-throughput bioanalytical methods to support preclinical PK studies of large molecules and ADCs.
- Independently design, develop, optimize and run bioanalytical assays using ligand binding and mass analytical techniques, leveraging robotic automation.
- Independently analyze, interpret, and report bioanalytical and pharmacokinetic data using industry standard analytical tools.
- Operate and maintain analytical instruments such as LC-MS systems and ligand binding assay platforms.
- Prepare and deliver internal scientific reports, presentations, and documentation.
- Identify opportunities to improve current approaches and propose innovative solutions to expand bioanalytical capabilities.
Basic Qualifications
- 6+ Years with BS
- OR 4+ Years with MS
- OR 0+ Years with PhD/PharmD
Preferred Qualifications
- BS (6+ years), MS (4+ years), or PhD (0+ years) in Pharmaceutical Sciences, Chemistry, Biochemistry, Biology, or related discipline.
- 2β5 years hands-on industry experience in bioanalysis and PK.
- Expert knowledge of ligand binding bioanalysis; hands-on immunoprecipitation, enzymatic digestion, LC-MS/MS, MSD platforms, ligand binding assays.
- Ability to process, extract, and quantify biologics, small molecules, ADCs, and payloads incl. biotransformation analysis.
- Proficiency with Phoenix NonWinLin (non-compartmental PK analysis).
- Experience standardizing/implementing bioanalytical methods; proficiency with lab automation; HTS (96/384/1536-well) experience.
Application Instructions
- For current Gilead employees and contractors: apply via the Internal Career Opportunities portal in Workday.