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Project Manager Biotech Jobs in Chicago, IL (NOW HIRING)

Minimum of 6 years of industry experience related to the pharmaceutical, biotechnology, and/or medical device industries in project management, purchasing, supply chain, or similar roles * Minimum of ...

Minimum of 6 years of industry experience related to the pharmaceutical, biotechnology, and/or medical device industries in project management, purchasing, supply chain, or similar roles * Minimum of ...

Minimum of 6 years of industry experience related to the pharmaceutical, biotechnology, and/or medical device industries in project management, purchasing, supply chain, or similar roles. * Minimum ...

Project Engineer II

Munster, IN · On-site

$67K - $86K/yr

Bachelor's Degree in Construction Engineering, Management or a related field is required * Minimum ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

Project Engineer II

Munster, IN · On-site

$67K - $86K/yr

Bachelor's Degree in Construction Engineering, Management or a related field is required * Minimum ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

Coordinate and oversee capital improvement projects, working with engineering teams, contractors ... pharmaceutical, biotech, or similarly regulated environments * Demonstrated expertise in GMP ...

Showing results 41-60

Project Manager Biotech information

See Chicago, IL salary details

$22

$47

$78

How much do project manager biotech jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for project manager biotech in Chicago, IL is $47.63, according to ZipRecruiter salary data. Most workers in this role earn between $41.35 and $52.26 per hour, depending on experience, location, and employer.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What job categories do people searching Project Manager Biotech jobs in Chicago, IL look for?

The top searched job categories for Project Manager Biotech jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Project Manager Biotech jobs?

Cities near Chicago, IL with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Chicago, IL as of August 2026, with employment types broken down into 83% Full Time, 15% Part Time, 1% Contract, and 1% Nights. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $99,084 per year, or $47.6 per hour.

Capital Project Site Engineer

Sterling Engineering Inc.

North Chicago, IL • On-site

$65 - $80/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 16 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.