Sr. Bioinformatics Scientist, MRD

Abbott (abbottcareers2 board)

San Diego (CA)

On-site

USD 180,000 - 240,000

Full time

3 days ago
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Job summary

Abbott is seeking a Senior Bioinformatics Scientist to serve as a technical lead in the MRD program, collaborating with senior scientists and leaders on complex R&D projects. You will independently determine methods, plan analyses, and drive end-to-end data science workflows across data collection, curation, modeling, and validation.

You will develop novel methods to identify and integrate genomic and epigenetic biomarkers to improve MRD assay sensitivity and specificity, contributing to

Qualifications

  • Ph.D. in bioinformatics, computational biology, computer science, mathematics, or related field; or Master’s with 4+ years of experience; or Bachelor’s with 6+ years of experience.
  • 5+ years of industry or academia experience in bioinformatics.
  • 3+ years of experience in medical device/IVD, biotech, life science or pharmaceutical industry.
  • Extensive experience in Linux-based HPC or cloud computing environments and related tools.
  • Ability to write code in at least three programming or scripting languages.
  • Expert in molecular biology/biochemistry and/or next-generation sequencing and genomics.
  • Knowledge of product/assay research, design, or development.
  • Working knowledge of statistics and mathematical methods in biology/genetics.

Responsibilities

  • Lead or participate in project and analysis planning across R&D programs.
  • Independently analyze experimental data, interpret results, and recommend next steps.
  • Develop methods, procedures, and development plans for new studies.
  • Manage bench-generated data and bioinformatics outputs in HPC or cloud environments.
  • Present findings at meetings and communicate with stakeholders and management.
  • Mentor research associates and junior scientists, managing multiple projects.

Skills

Linux HPC/cloud computing
Programming languages
Bioinformatics leadership
Statistics in biology
NGS/genomics
Data interpretation

Education

PhD in bioinformatics/computational biology/related
MS in bioinformatics/computational biology/related +4 years experience
BS in bioinformatics/computational biology/related +6 years experience

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Job Description
Position Overview

The Senior Bioinformatics Scientist will serve as a technical lead and subject matter expert within the Minimal Residual Disease (MRD) program, working collaboratively with senior scientists and leaders on complex Research and Development projects. In this role, you will participate in or lead the planning of projects and analyses, and often act as the bioinformatics lead responsible for successful project execution. You will independently determine methods and procedures for new assignments, make detailed observations, analyze data, interpret results, and provide insights that shape the next steps and direction of the project. Your work will center on developing novel methods to identify and integrate genomic and epigenetic biomarkers that improve the sensitivity and specificity of MRD assays, contributing end-to-end across the data science workflow: collecting public datasets, curating internal data, forming hypotheses, building and validating models, and exploring machine learning and AI-based approaches. You will also research new technologies, contribute ideas and concepts to improve or develop processes, and help establish methods and workflows that advance product development toward diagnostic assay products.

Essential Duties
  • Technical leadership: Serve as bioinformatics lead and subject matter expert on one or more complex R&D projects, including those supporting diagnostic assay product development, and lead or participate in project and analysis planning.
  • Analysis and interpretation: Independently analyze experimental data across several product or technology areas, interpret results, identify trends, problems, and discrepancies, and recommend next steps and project direction.
  • Complex problem solving: Tackle problems of extremely complex scope where intangible variables must be evaluated, applying independent judgment to define methods, techniques, and evaluation criteria.
  • Method and study design: Independently develop methods, procedures, and development plans for new studies, and give technical input on project planning and experimental design.
  • Data and computational management: Manage bench-generated data and bioinformatics outputs in HPC or cloud computing environments, selecting and applying the right methods and technologies.
  • Data quality: Evaluate the impact of nonconforming data on products or processes and address trends in study data.
  • Innovation and IP: Track industry and technology developments, propose new techniques, lead process improvements, and contribute to the intellectual property portfolio.
  • Communication and presentation: Present and defend scientific findings at data, group, project, and departmental meetings, and communicate clearly with stakeholders at all levels, including functional managers and the clinical lab.
  • Documentation and compliance: Prepare and approve technical procedures, protocols, and reports, support abstracts, conferences, and publications, and follow legal, ISO, QSR, and Quality Management System requirements.
  • Mentorship and collaboration: Train and mentor research associates and junior scientists, foster a trusting, collaborative team environment, and manage multiple projects with shifting priorities.
  • Maintain regular and reliable attendance.
  • Ability to act with an inclusion mindset and model these behaviors for the organization.
  • Ability to travel 5% of working time away from work location, may include overnight/weekend travel.
Minimum Qualifications
  • Ph.D. in bioinformatics, computational biology, computer science, mathematics, or related field; or Master's degree in bioinformatics, computational biology, computer science, mathematics, or related field plus 4 years of experience in lieu of a Ph.D.; or Bachelor's degree in bioinformatics, computational biology, computer science, mathematics, or related field plus 6 years of experience in lieu of Ph.D.
  • 5+ years of industry or academia experience in bioinformatics.
  • 3+ years of experience in medical device/IVD, biotech, life science or pharmaceutical industry.
  • Extensive experience in Linux-based HPC or cloud computing environments and associated tools.
  • Ability to write custom code in at least three programming or scripting languages.
  • Technical expert in the area of molecular biology and/or biochemistry and/or next-generation sequencing (NGS) and genomics.
  • Knowledge of product/assay research, design, or development.
  • Working knowledge of statistical and mathematical methods in biology/genetics
  • Demonstrated ability to perform the essential duties of the position with or without accommo
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