Bioinformatics Engineer-San Diego, CA, US

OMG Technology; San Diego (CA); Hybrid; USD 110,000 - 160,000; Full time

Job summary

OMG Technology is seeking a Bioinformatics Engineer in San Diego for a hybrid, 6+ month contract. You will design analyses, collect requirements, develop software modules, and help integrate pipelines. Collaboration across cross-functional teams and strong communication are essential.

You will contribute to scientific outputs and ensure compliance with Quality policies while traveling up to 15% as needed.

Qualifications

• Bachelor’s degree required in software or related field.
• 4+ years of experience or equivalent combination.
• Experience with JIRA and Smartsheet for ticketing and progress tracking.
• Knowledge of coding and documentation best practices.
• Knowledge of molecular biology/biochemistry/NGS/genomics.

Responsibilities

• Design and implement bioinformatics analyses to support assay development and testing.
• Collect and document product and software requirements from analyses.
• Design software modules based on data analysis requirements.
• Assist with integration of modules into pipelines.
• Automate data analyses with software modules.
• Prepare information for abstracts, conferences and meetings.
• Identify trends in study data and report findings.
• Collaborate with cross-functional teams.
• Communicate clearly in written and verbal form.
• Adhere to Quality Management System policies and procedures.
• Ability to travel up to 15% as needed.

Skills

Bioinformatics

Statistics

Genomics

R

JMP

Education

Bachelor’s degree in Software Engineering, Computer Engineering, Computer Science, or field as outlined in the essential duties

PhD or Masters in a relevant field

Tools

JIRA

Smartsheet

Job description

Hello,

We are seeking a Bioinformatics Engineer for our client based out of San Diego,CA. This is a hybrid role. Job description is below.

Position Overview:

Role-Bioinformatics Engineer

Location- San diego,CA[Hybrid]

Contract

Duration:6+ months with a high possibility of extension

Job Overview:

• Design and implement bioinformatics analyses to support the development of novel assays, improvement of assays under development, and hypothesis testing requested Product Development and Computational Biology team.
• Collect and document product and software requirements and findings from analyses executed by themself and others.
• Design and implement software modules implementing the requirements collected from data analyses.
• Assist with the integration of software modules into pipelines.
• Design and implement software modules to automate data analyses.
• Prepare and provide information and data for scientific abstracts/conferences/project meetings/publications.
• Identify and address trends in study data.
• Ability to work collaboratively in cross-functional teams.
• Strong written and verbal communication skills.
• Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
• Support and comply with the company’s Quality Management System policies and procedures.
• Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 50% of a typical working day.
• Ability and means to travel 10% between local Exact Sciences locations.
• Ability to travel 5% of working time away from work location, may include overnight/weekend travel.

Minimum Qualifications

• Bachelor’s degree in Software Engineering, Computer Engineering, Computer Science, or field as outlined in the essential duties.
• 4+ years of experience, or equivalent combination of experience and education as outlined in the essential duties.
• Experience with software ticketing, progress tracking, and timeline tracking systems: JIRA, Smartsheet.
• Knowledge and adherence to good coding and documentation practices.
• Knowledge of molecular biology and/or biochemistry and/or next-generation sequencing (NGS) and genomics.
• Working knowledge of statistical and mathematical methods in biology/genetics/genomics, including experience with statistical software, such as JMP or R.
• Basic computer skills to include Internet navigation, Email usage, and word processing.
• Proficient in Microsoft Office to include Excel, Word, and PowerPoint.
• Demonstrated ability to perform the essential duties of the position with or without accommodation.
• Authorization to work in the United States without sponsorship.

Preferred Qualifications

• Advanced degree (PhD or Masters).
• 6+ years of relevant experience.
• Experience in an FDA-regulated environment, ideally in medical device development.
• Experience with computer vision, image analysis, or machine-learning workflows in a biomedical or scientific setting.
• Experience in a biotech manufacturing environment, preferably in a GMP and/or ISO environment.
• Familiarity with Laboratory Information Management Systems (LIMS), Next-Generation Sequencing (NGS), and clinical and diagnostic test development.
• Experience with PDP (Product Development Process) and/or Cancer Genomics.

Other Job Details

• Work Schedule: PST Hours
• Interviews: Video interviews.
• Docs required: ID proof will be required.
• Availability: Candidates able to join immediately are preferred