Generation Sequencing Scientist

Job Description

We support preclinical and clinical research teams by applying genomic profiling technologies with the goal of improving the success rates for drug discovery and development.

We apply genomic profiling technologies to identify and validate targets and biomarkers, improve understanding of preclinical models and candidate drug molecules, select/stratify patients and understand patient responses in clinical trials.

We are seeking to hire a scientist proficient in Next-Generation-Sequencing (NGS) to support single cell and Visium spatial transcriptomic profiling capabilities.

The successful candidate will work closely with NGS technical leads and be responsible for carrying out end-to-end NGS experiments and communicating results to stakeholders and collaborators.

This role is expected to be on-site and in the lab full time unless otherwise approved by the supervisor.

• Hands-on single cell sequencing experience
• Hands-on spatial transcriptomics experience
• NGS data QC experience
• Hands-on NGS experience
• Molecular biology/NGS technical knowledge

• Reporting to the Single Cell Lead, work closely with other NGS Technical Leads and staff to fulfill single cell/spatial transcriptomic profiling needs for active studies from Genomic Research Center (GRC) stakeholders and therapeutic area (TA) scientists
• Support single cell and spatial transcriptomic workflows. Perform sample and library prep, and sequencing, initial data QC and first pass analysis of results.
• Closely work with NGS technical leads and partner with bioinformatics specialists and disease area scientists to interpret results and troubleshoot.
• Operate and maintain NGS and its supportive platforms within centralized technology group. Prepare written summaries of experimental results and verbally present at team meetings.
• Maintain accurate documentation of experiments, protocols, and results.
• Support inventory and maintenance.
• Effectively communicate with stakeholders, especially around experimental design, troubleshooting, and responding to changes in priorities and adjusting timelines.

• Bachelor’s Degree or equivalent education and typically 7 years of experience,
• Master’s Degree or equivalent education and typically 5 years of experience in molecular biology, genetics, genomics or a related field
• Demonstrated record of high-proficiency, hands‑on molecular biology experience with PCR‑based assays and technical knowledge of high‑throughput genomic profiling technologies with emphasis on Illumina sequencing platforms and complex library preparation workflows for bulkRNA-seq, 10X Genomics scRNA‑seq, and 10X Genomics Visium spatial transcriptomics
• Knowledge of QC metrics, interpretation, and demonstrated use of approaches for assessing the quality of samples and libraries for bulkRNA, scRNA, and spatial profiling, such as capillary electrophoresis, qPCR, fluorometry, spectrophotometry, cell counting and viability
• Proficiency with basic bioinformatics tools and sequencing data analysis concepts, such as Illumina SAV, bcl2fastq/BCLConvert, fastQC, and working in a UNIX HPC environment.
• Experience with 10X Genomics Cell ranger and/or Space ranger software is highly preferred.
• Experience being part of a centralized high‑throughput genomic lab is highly desirable.
• Industry experience is preferred but willing to consider individuals with equivalent years of experience in academic or non‑industry research core lab settings.
• High attention to detail, self‑motivated, critical thinking, strong written and verbal communication skills
• Ability to work in fast‑paced, dynamic environment both collaboratively and independently
• Proven direct end‑to‑end hands‑on experience with 10X Genomics technologies such as single‑cell RNAseq or Visium is highly preferred.