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

Danaher

Software Engineer Internships

Aurora, IL

Producing documentation to support medical device regulatory processes Who This Is For * Students ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Danaher

Software Engineer Internships

Gary, IN · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Danaher

Software Engineer Internships

Aurora, IL · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Danaher

Software Engineer Internships

Hammond, IN · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Danaher

Software Engineer Internships

Chicago, IL · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Flex

Quality Engineer

Buffalo Grove, IL · On-site

$77K - $106K/yr

Approves product, process and equipment qualifications. * Provides liaison to various regulatory ... medical device, Pharma or Biotechnology industry experince * ISO13485 * CAPAS, SCARS, NCMRs ...

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Showing results 21-40

All JobsBiotech Process Engineer JobsBiotech Process Engineer Jobs in Chicago, IL

Biotech Process Engineer information

See Chicago, IL salary details

$51K

$94.9K

$146.9K

How much do biotech process engineer jobs pay per year?

As of Aug 11, 2026, the average yearly pay for biotech process engineer in Chicago, IL is $94,866.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,800.00 and $106,200.00 per year, depending on experience, location, and employer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

What are the key skills and qualifications needed to thrive as a Biotech Process Engineer, and why are they important?

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.
What are popular job titles related to Biotech Process Engineer jobs in Chicago, IL? For Biotech Process Engineer jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Biotech Process Engineer jobs in Chicago, IL look for? The top searched job categories for Biotech Process Engineer jobs in Chicago, IL are:
Biotech Process Engineer jobs near you
Infographic showing various Biotech Process Engineer job openings in Chicago, IL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution, with an average salary of $94,866 per year, or $45.6 per hour.

Capital Project Site Engineer

Sterling Engineering Inc.

North Chicago, IL

$65 - $80/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago

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.