zenith lifescience

Zenith LifeScience LLC. is seeking a Research Associate II to support and execute nonclinical bioanalytical activities in GLP and non-GLP environments. You will handle sample processing, assay execution, data analysis, documentation, and training of other analysts.Responsibilities include extracting nucleic acids from tissue, running ddPCR/qPCR/ELISA/MSD,...

Zenith LifeScience in Santa Monica, CA seeks a Research Associate, Analytical Sciences to execute routine molecular and cell-based testing and to help characterize T cell therapy products. The role focuses on DNA/RNA extraction, dPCR, live cell imaging, and plate-based assays within a fast-paced analytical sciences team.The candidate will contribute to lab...

Zenith LifeScience LLC. is seeking a Research Associate in Analytical Sciences in Santa Monica, CA. You will execute routine molecular and cell-based assays, process DNA/RNA workflows, and support daily lab operations within a fast-paced team environment.The role emphasizes accurate documentation, data analysis, and collaboration across development,...

Zenith LifeScience is seeking a Scientist II QC Microbiology to act as a senior technical subject matter expert, overseeing microbiological testing programs within GMP operations. The role provides technical leadership across QC Microbiology and Manufacturing, mentoring staff and delivering aseptic technique training to ensure contamination control and...

Zenith LifeScience LLC is seeking a highly motivated scientist to join the Chemical Biology and Proteomics group within Discovery Sciences. You will apply proteomics to advance drug discovery and interrogate mechanisms of action in CVRM contexts. You will design mass-spectrometry–based discovery assays, perform proximity biotinylation, and validate protein...

Zenith LifeScience LLC. in Cambridge, MA is seeking an Associate Proteomics Scientist for a 12-month contract to apply proteomics in drug discovery.You will work in the Chemical Biology and Proteomics group within Discovery Sciences, collaborating with cross-functional teams to advance therapeutic development. The role focuses on cellular profiling, mass...

Job Description: - Support data validation activities in our digital tool for oncology regulatory approval information. - Help with presentation of regulatory intelligence data analyses using AI tools. - Undertake background literature research for regulatory intelligence queries using publicly available and commercial tools. - Research and analyze...

This position will support rare disease–focused cell therapy programs, distinct from traditional oncology CAR‑T development. The scientific focus is on non‑malignant, genetically defined, or ultra‑rare indications, where therapeutic goals, experimental design, and success criteria differ from oncology applications.Key characteristics of this rare...

The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company’s core therapeutic areas in all phases of clinical...

Job Description: Support data validation activities in our digital tool for oncology regulatory approval information. Help with presentation of regulatory intelligence data analyses using AI tools. Undertake background literature research for regulatory intelligence queries using publicly available and commercial tools. Research and analyze regulatory...

This position will support rare disease–focused cell therapy programs, distinct from traditional oncology CAR-T development. The scientific focus is on non-malignant, genetically defined, or ultra-rare indications, where therapeutic goals, experimental design, and success criteria differ from oncology applications. Key characteristics of this rare...

Job Description:Support data validation activities in our digital tool for oncology regulatory approval information.Help with presentation of regulatory intelligence data analyses using AI tools.Undertake background literature research for regulatory intelligence queries using publicly available and commercial tools.Research and analyze regulatory guidance,...

The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company’s core therapeutic areas in all phases of clinical...

This position will support rare disease–focused cell therapy programs, distinct from traditional oncology CAR‑T development. The scientific focus is on non‑malignant, genetically defined, or ultra‑rare indications, where therapeutic goals, experimental design, and success criteria differ from oncology applications.Key characteristics of this rare...

DNA extraction (manual or automated), safe handling of human cells, and performing genomic assaysExperience using DPCR technology is preferredJob DescriptionThe Research Associate, Analytical Sciences will be responsible for the execution of routine testing, including but not limited to molecular biology assays and cell-based assays and to characterize T...

The Research Associate II supports and executes nonclinical bioanalytical activities to generate high-quality, reliable data in GLP and non-GLP environments. This role encompasses sample processing, assay execution, data analysis, documentation, and training of other analysts in support of nonclinical research and development programs.Responsibilities and...

The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company’s core therapeutic areas in all phases of clinical...

This position will support rare disease–focused cell therapy programs, distinct from traditional oncology CAR‑T development. The scientific focus is on non‑malignant, genetically defined, or ultra‑rare indications, where therapeutic goals, experimental design, and success criteria differ from oncology applications. Key characteristics of this rare...

The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company’s core therapeutic areas in all phases of clinical...

This position will support rare disease–focused cell therapy programs, distinct from traditional oncology CAR‑T development. The scientific focus is on non‑malignant, genetically defined, or ultra‑rare indications, where therapeutic goals, experimental design, and success criteria differ from oncology applications. Key characteristics of this rare...