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Biotech Software Engineer Jobs in Chicago, IL (NOW HIRING)

... Software Engineering, Informatics, Biomedical, or relevant engineering disciplines. * 5+ years experience in FDA regulated domain (e.g. medical device, pharma, biotech) * 3+ years experience in ...

... Software Engineering, Informatics, Biomedical, or relevant engineering disciplines. * 5+ years experience in FDA regulated domain (e.g. medical device, pharma, biotech) * 3+ years experience in ...

Sr. CQV Lead

Waukegan, IL · On-site

$65 - $75/hr

Waukegan, IL 60064 - onsite daily pay rate $65.00 - $75.00 per hour on a W2 I'm looking for a hands-on CQV Lead / Senior Validation Engineer that has 5+ years of experience in pharma, biotech, API or ...

... careers in the pharmaceutical, biotechnology, and medical device industries. We offer an ... Plant 3D or similar process design software * Scan-to-BIM workflows * Strong ability to collaborate ...

Service Controls Engineer

Elgin, IL · On-site

$83K - $107K/yr

Troubleshoot hardware and software for automated equipment as well as program development while ... Technical understanding of pharmaceutical / biotechnology unit operations a plus. * Fundamental ...

Service Controls Engineer

Elgin, IL · On-site

$83K - $107K/yr

Troubleshoot hardware and software for automated equipment as well as program development while ... Technical understanding of pharmaceutical / biotechnology unit operations a plus. * Fundamental ...

Integrate AI platforms with AWS services and enterprise data, software, security, identity, and ... Experience working in a regulated environment, preferably pharmaceutical, biotechnology, healt ...

Showing results 41-60

Biotech Software Engineer information

See Chicago, IL salary details

$65.4K

$151.9K

$211.7K

How much do biotech software engineer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for biotech software engineer in Chicago, IL is $151,943.00, according to ZipRecruiter salary data. Most workers in this role earn between $123,600.00 and $178,200.00 per year, depending on experience, location, and employer.

What is a biotech software engineer?

A Biotech Software Engineer develops software solutions for the biotechnology industry, enabling research, data analysis, and automation in fields like genomics, bioinformatics, and drug discovery. They work with scientists to design algorithms, manage biological data, and create applications that support experiments and workflows. This role requires expertise in programming, cloud computing, and biological sciences to bridge the gap between technology and life sciences.

What does a biotech software engineer do?

As a Biotech Software Engineer, you'll often develop and maintain software tools for analyzing biological data, automate laboratory workflows, or create user-friendly interfaces for scientific researchers. Your daily tasks might include writing code, troubleshooting algorithms, reviewing scientific data, and collaborating closely with biologists, data scientists, and laboratory technicians. Depending on the company, you may be involved in developing cloud-based platforms, integrating new laboratory hardware, or ensuring software compliance with industry regulations. This dynamic and collaborative environment means your work directly impacts ongoing research and helps accelerate scientific discoveries in the biotech sector.

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

To thrive as a Biotech Software Engineer, you need a solid background in computer science or software engineering, coupled with an understanding of biology, genetics, or related life sciences. Familiarity with programming languages such as Python or Java, experience using bioinformatics tools (like BLAST or Bioconductor), and, in some settings, knowledge of regulatory standards are highly valuable. Strong problem-solving abilities, effective communication, and the ability to work well in interdisciplinary teams distinguish top performers in this field. These skills are crucial for building reliable software solutions that support scientific discovery and innovation in biotechnology organizations.

What are the most commonly searched types of Biotech Software Engineer jobs in Chicago, IL?

The most popular types of Biotech Software Engineer jobs in Chicago, IL are:

Infographic showing various Biotech Software Engineer job openings in Chicago, IL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 79% In-person, and 21% Remote job distribution, with an average salary of $151,943 per year, or $73 per hour.

Capital Project Site Engineer

Sterling Engineering Inc.

North Chicago, IL • On-site

$65 - $80/hr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 15 days ago


Job description

Job Description
Job Description
Job Title: Capital Project Site Engineer
Location: North Chicago, IL
Hire Type: Long-term Contract (1+ Year), Onsite
Target Pay Rate: $65.00 - $80.00/hour (W2)
Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), & ESOP

Job Summary:
Our client is seeking an experienced Site Engineer to lead capital construction and facility improvement projects supporting GMP manufacturing, laboratory, warehouse, and office facilities. This individual will serve as the owner's representative, managing projects from planning and design through construction, commissioning, and project turnover while ensuring projects are completed safely, on schedule, within budget, and in compliance with quality and regulatory requirements.
The ideal candidate has experience managing capital construction projects within pharmaceutical, biotechnology, medical device, or other highly regulated manufacturing environments and is comfortable coordinating multiple contractors, engineering firms, and internal stakeholders.
Must-Have Skills:
  • 5+ years of facility capital project management experience
  • Experience managing capital construction and facility improvement projects
  • Experience serving as an owner's representative on light construction projects
  • Experience working in GMP-regulated manufacturing environments
  • Knowledge of construction management principles, scheduling, budgeting, and contractor management
  • Experience coordinating architects, engineering firms, and general contractors
  • Strong understanding of commissioning and project turnover processes
  • Excellent communication and leadership skills
  • Ability to manage multiple projects simultaneously
  • Willingness to work overtime, evenings, and weekends as project schedules require
Job Duties:
  • Lead capital construction and facility improvement projects from planning through completion
  • Serve as the owner's representative throughout all phases of project execution
  • Manage project scope, schedule, budget, quality, and overall project performance
  • Coordinate architects, engineering firms, general contractors, consultants, validation teams, and internal stakeholders
  • Oversee construction activities to ensure compliance with safety, quality, GMP, and regulatory requirements
  • Monitor project schedules and proactively resolve issues impacting timelines or budgets
  • Support commissioning, qualification, startup, and project turnover activities
  • Ensure construction documentation is complete and accurate
  • Participate in contractor meetings, design reviews, and project status updates
  • Support regulatory inspections and facility audits as required
  • Promote safe work practices and ensure contractor compliance with site safety requirements
  • Drive continuous improvement and sustainability initiatives throughout project execution
  • Perform additional project management responsibilities as assigned
Qualifications:
  • Bachelor's degree in Engineering, Construction Management, Architecture, or a related technical field preferred
  • 5+ years of construction project management experience
  • Experience managing capital projects within pharmaceutical, biotechnology, medical device, food manufacturing, or other regulated industries
  • Strong knowledge of construction management, project scheduling, budgeting, and contractor oversight
  • Experience supporting GMP manufacturing facilities and regulated environments
  • Familiarity with commissioning, qualification, and validation processes
  • Strong understanding of applicable building codes, safety regulations, and construction best practices
  • Excellent leadership, organizational, and problem-solving skills
  • Strong verbal and written communication skills
  • Proficiency with Microsoft Office and project management software
  • Ability to manage multiple priorities in a fast-paced environment
  • Flexibility to support projects during evenings, weekends, and extended work hours as needed


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.