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Bioinformatics Engineering Jobs in Algonquin, IL

Tempus

Manager, Regulatory Submissions (Remote)

Chicago, IL · Remote

$110K - $150K/yr

Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Ability to work well with quality, clinical, medical, bioinformatics, and laboratory teams across a ...

Tempus

Manager, Regulatory Submissions (Remote)

Chicago, IL · On-site +1

$110K - $150K/yr

Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Ability to work well with quality, clinical, medical, bioinformatics, and laboratory teams across a ...

Tempus

Data Scientist II, Outcomes Research

Chicago, IL · On-site +1

$100K - $150K/yr

Partner with interdisciplinary groups of scientists, engineers, and product developers to translate ... Advanced degree (Master's with 2+ years experience or equivalent) in data science, bioinformatics ...

Tempus

Data Scientist II, Outcomes Research

Chicago, IL · On-site

$100K - $150K/yr

Partner with interdisciplinary groups of scientists, engineers, and product developers to translate ... Advanced degree (Master's with 2+ years experience or equivalent) in data science, bioinformatics ...

Tempus

Scientist II, Translational Research

Chicago, IL · On-site +1

$100K - $150K/yr

Work with Product and Engineering teams to streamline workflow of computational analyze Contribute ... Biostatistics/Statistical Genetics, Cancer Genetics,Bioinformatics, Computational Biology ...

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Showing results 21-40

All JobsBioinformatics Engineering JobsBioinformatics Engineering Jobs in Algonquin, IL

Bioinformatics Engineering information

See Algonquin, IL salary details

$42.1K

$128.2K

$233.3K

How much do bioinformatics engineering jobs pay per year?

As of Aug 23, 2026, the average yearly pay for bioinformatics engineering in Algonquin, IL is $128,211.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,900.00 and $153,600.00 per year, depending on experience, location, and employer.

What is a bioinformatics engineer?

A bioinformatics engineer is a professional who develops and applies computational tools and techniques to analyze and interpret biological data, such as DNA sequences or protein structures. They combine expertise in computer science, biology, and mathematics to create software, manage databases, and solve complex biological problems. Bioinformatics engineers often work in research, pharmaceuticals, healthcare, and biotechnology industries to help advance scientific discoveries and medical innovations.

What are the key skills and qualifications needed to thrive as a bioinformatics engineer?

To thrive as a Bioinformatics Engineer, you need a solid background in biology, computer science, and statistics, often supported by a degree in bioinformatics or a related field. Familiarity with programming languages like Python or R, experience with bioinformatics tools (e.g., BLAST, GATK), and proficiency with databases and cloud computing platforms are typically required. Strong problem-solving, analytical thinking, and collaboration skills set standout professionals apart in this interdisciplinary field. These competencies are crucial for effectively analyzing complex biological data and driving innovation in life sciences research.

How do bioinformatics engineers typically collaborate with biologists and data scientists in a research setting?

Bioinformatics engineers frequently work in cross-disciplinary teams, partnering closely with biologists to understand experimental goals and with data scientists to analyze complex datasets. Effective communication is key, as engineers must translate biological questions into computational workflows and interpret results in a way that is meaningful to non-technical team members. This collaborative approach not only accelerates research but also helps engineers gain a deeper understanding of biological processes, which can lead to more innovative solutions and professional growth.

What is the difference between Bioinformatics Engineering vs Bioinformatics Analyst?

AspectBioinformatics EngineeringBioinformatics Analyst
Required CredentialsBachelor's or Master's in Bioinformatics, Computer Science, or related fields; programming skillsBachelor's or Master's in Bioinformatics, Biology, or related fields; data analysis skills
Work EnvironmentResearch labs, biotech companies, healthcare institutionsResearch institutions, healthcare, pharmaceutical companies
Employer & Industry UsageDevelops tools, pipelines, and software for data analysisInterprets data, generates reports, supports research projects

Bioinformatics Engineering focuses on developing software and pipelines for data processing, requiring programming expertise. In contrast, Bioinformatics Analysts primarily interpret data and generate insights, often with a stronger emphasis on biological knowledge. Both roles are vital in biotech and healthcare industries, but they differ in technical scope and daily tasks.

What do bioinformatics engineers do?

Bioinformatics engineers develop and implement computational tools and algorithms to analyze biological data, such as genetic sequences and molecular structures. They often work with programming languages like Python or R, utilize databases, and collaborate with biologists to interpret data for research and medical applications.

What cities near Algonquin, IL are hiring for Bioinformatics Engineering jobs?

Cities near Algonquin, IL with the most Bioinformatics Engineering job openings:

Bioinformatics Engineering jobs near you
Infographic showing various Bioinformatics Engineering job openings in Algonquin, IL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $128,211 per year, or $61.6 per hour.

Manager, Regulatory Submissions (Remote)

Tempus

Chicago, IL • Remote

$110K - $150K/yr

Full-time

Re-posted 11 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

At Tempus, we are building a regulatory team that will adopt creative approaches as we develop regulated medical devices and seek marketing authorization from FDA. Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians, quality professionals, and legal team to support our efforts to advance personalized medicine.

Responsibilities

  • Developing and leading global regulatory strategies to support business objectives

  • Leading and assisting with submissions and correspondence with global regulatory authorities, including 510(k), PMA, De Novo authorizations, IDE, MDR CE marking, UKCA marking, etc.

  • Establishing processes for efficiently addressing the requirements of multiple regulatory frameworks at scale

  • Developing and executing premarket and postmarket regulatory project plans and strategies, including assessments of change controls

  • Working closely with cross-departmental subject matter experts to guide the creation of documentation needed for regulatory applications and internal records

  • Work closely with business leadership to ensure regulatory strategy aligns with commercial goals

  • Making regular reports to our executive team, operationalizing leadership direction quickly and efficiently

What your background might look like:

  • Oncology IVD, IUO, and CDx experience required

  • Experience with complex medical devices, such as some combination of:

    • Genomics

    • NGS

    • Software and artificial intelligence based devices

    • Clinical decision support software

    • Oncology

  • Experience with:

    • Premarket Approval (PMA) applications, de novo Requests for Reclassification, 510(k)s, Investigational Device Exemption (IDE) requirements

    • Ex-US, CE Marking, UKCA registration, performance studies as required under IVDR and MDR

    • Software validation and risk management

    • Cybersecurity in medical devices

    • Machine learning validation requirements

    • Lifecycle management of medical devices/IVDs

    • Changes to medical devices or IVDs, including those that trigger reporting or regulatory submissions

    • Relevant sections of 21 CFR 820/ISO 13485, 21 CFR 812, CAP/CLIA

    • Strong communication, presentation. and interpersonal skills

    • Guiding cross-functional teams of subject matter experts

    • Working in a startup-like environment

    • Interacting with regulators

    • Ability to work well with quality, clinical, medical, bioinformatics, and laboratory teams across a variety of therapeutic areas

    • Responsive to feedback, willing to change direction, and able to identify creative solutions to meet business and regulatory needs

    • Excellent attention to detail

    • Strong project management skills and the ability to execute on project plans in a fast-paced environment

  • Scientific background

    • PhD preferred.

    • Minimum of 5+ years of experience in Regulatory Affairs experience related to medical devices

    • Knowledge of engineering concepts and biology with ability to evaluate device performance data and develop testing plans

#LI-remote

$110,000-$150,000

The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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