Scientist II, Bioanalytical

The Position (LCMS Bioanalytical Scientist II)

• Design, develop, and execute novel quantitative LCMS assays supporting in‑vivo and in‑vitro pharmacology studies.
• Work across diverse modalities (proteins, peptides, small molecules, oligonucleotides, conjugates).
• Contribute to PK/PD and biomarker understanding for efficacy/toxicity; advance experimental design and execution to improve methods and therapeutic area efforts.
• Ensure data integrity/reproducibility; summarize and communicate results to project teams.
• Perform predominantly hands‑on laboratory work: build analytical methods, interpret experimental results, and maintain instrumentation/reagents.
• Provide LCMS bioanalytical expertise (qualitative/quantitative analysis, PK assays, Met , biomarker exploration); serve as a representative to project teams.
• Collaborate with external CROs via statements of work and data oversight.
• Maintain and troubleshoot lab instruments; manage consumables, reagents, sample inventories, and shared resources.

• BS/BA with 8+ years, or MS with 6+ years, or PhD/Doctoral with 2+ years relevant experience.
• Expertise in LCMS assay concepts/tech platforms; sample prep/analyte extraction (e.g., protein precipitation, SPE, LLE, IP-MS).
• Experience with diverse modalities; solid PK/PD modeling understanding.
• Practical LCMS/software experience (e.g., Thermo, Sciex, Waters/Acquity; triple quad/HRMS; Xcalibur, Chromeleon, etc.).
• Experience in a bioanalytical laboratory.
• Preferred: lab automation/liquid handling, Win Nonlin, CRO experience, GLP bioanalytical principles.
• Excellent verbal/written communication; strong organizational/project management.

Base compensation range: $99,600–$184,200; eligible for company bonus.

Benefits may include medical/dental/vision, life/disability, 401(k), flexible spending, EAP, tuition reimbursement, voluntary benefits, sick time/flexible vacation, parental leave.

For application assistance/accommodations: call (accommodation requests only).