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

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Will participate in process and equipment improvement teams charged with enhancing the compliance ... Knowledge and understanding of cGMPs, industry guidance, and aseptic techniques * Understanding of ...

New

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Will participate in process and equipment improvement teams charged with enhancing the compliance ... Knowledge and understanding of cGMPs, industry guidance, and aseptic techniques * Understanding of ...

Validation Engineer

Melrose Park, IL · On-site

$65K - $80K/yr

Will participate in process and equipment improvement teams charged with enhancing the compliance ... Knowledge and understanding of cGMPs, industry guidance, and aseptic techniques * Understanding of ...

New

This position mentors engineers and leads process improvement initiatives. Responsibilities: * Lead ... Experience conducting evaluations to meet aseptic presentation requirements per Section 7 of ISO ...

This position mentors engineers and leads process improvement initiatives. Responsibilities: * Lead ... Experience conducting evaluations to meet aseptic presentation requirements per Section 7 of ISO ...

This position mentors engineers and leads process improvement initiatives. Responsibilities: Lead ... Experience conducting evaluations to meet aseptic presentation requirements per Section 7 of ISO ...

This position mentors engineers and leads process improvement initiatives. Responsibilities: * Lead ... Experience conducting evaluations to meet aseptic presentation requirements per Section 7 of ISO ...

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CNC Lathe Machinist

Chicago, IL · On-site

$32 - $40/hr

Weiler Engineering, Inc.'s focus is to provide the most advanced aseptic liquid processing technology through ASEP-TECH ® Blow/Fill/Seal machinery and integrated services.

Urgent

Bachelor's degree in engineering preferred. * Minimum 3 years of experience with engineering and/or ... Ideally knowledge of dairy, beverage, powder, and/or Aseptic processing and packaging. Pay Equity ...

New

Minimum 3 years of experience with engineering and/or managing projects. * Experience with food ... Ideally knowledge of dairy, beverage, powder, and/or Aseptic processing and packaging. Pay Equity ...

New

Automation Engineer

Des Plaines, IL · On-site

$45.73 - $57.17/hr

Strong expertise in Building Automation, Process Control Systems, Utilities, and HVAC ... Preferred: Water For Injection (WFI) experience and Cleanroom / Aseptic Pharma experience.

Showing results 41-60

Aseptic Process Engineer information

See Chicago, IL salary details

$51K

$94.8K

$146.8K

How much do aseptic process engineer jobs pay per year?

As of Sep 4, 2026, the average yearly pay for aseptic process engineer in Chicago, IL is $94,792.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,700.00 and $106,100.00 per year, depending on experience, location, and employer.

What is an aseptic process engineer?

Aseptic process engineers are professionals who design, develop, and maintain sterile manufacturing systems, primarily in the pharmaceutical, biotechnology, and food industries. Their main responsibility is to ensure that products are produced in a contamination-free environment, using processes that prevent the introduction of microorganisms. This involves overseeing the design of cleanrooms, validating equipment, developing standard operating procedures, and ensuring regulatory compliance. Aseptic process engineers work closely with quality assurance teams to maintain high standards of product safety and efficacy. Their expertise is crucial for industries where product sterility is critical to consumer safety.

What are the key skills and qualifications needed to thrive as an aseptic process engineer, and why are they important?

Aseptic Process Engineers need a strong background in chemical, mechanical, or biomedical engineering, along with experience in aseptic manufacturing environments and a solid understanding of GMP regulations. Familiarity with process automation systems, sterilization equipment, and industry certifications such as Six Sigma or Lean Manufacturing are often required. Attention to detail, strong problem-solving abilities, and effective communication are vital soft skills for ensuring product quality and process efficiency. These skills are crucial for maintaining sterile conditions, regulatory compliance, and the safe production of pharmaceuticals or biotechnology products.

What are some common challenges faced by aseptic process engineers, and how can they be addressed?

Aseptic Process Engineers often encounter challenges such as maintaining strict sterility standards, troubleshooting equipment issues, and ensuring compliance with changing regulatory requirements. Addressing these challenges requires strong attention to detail, proactive communication with cross-functional teams, and staying current with industry best practices and regulations. Collaborating closely with quality assurance, production, and maintenance teams helps to identify and resolve issues quickly, ensuring that processes remain efficient and compliant.

What is the difference between Aseptic Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectAseptic Process EngineerPharmaceutical Manufacturing Technician
CredentialsBachelor's degree in engineering, life sciences, or related field; GMP trainingHigh school diploma or associate degree; GMP training often required
Work EnvironmentCleanroom, sterile environments, manufacturing facilitiesManufacturing floors, production areas, sometimes cleanrooms
Industry UsageDesign, optimize, and validate aseptic processes in pharmaOperate equipment, assemble products, support manufacturing

The Aseptic Process Engineer focuses on designing and validating sterile manufacturing processes, requiring specialized engineering knowledge. In contrast, the Pharmaceutical Manufacturing Technician handles day-to-day production tasks, often with less formal education but essential for maintaining manufacturing flow. Both roles are vital in pharmaceutical production but differ in responsibilities and qualifications.

What job categories do people searching Aseptic Process Engineer jobs in Chicago, IL look for?

The top searched job categories for Aseptic Process Engineer jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Aseptic Process Engineer jobs?

Cities near Chicago, IL with the most Aseptic Process Engineer job openings:

Infographic showing various Aseptic Process Engineer job openings in Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $94,792 per year, or $45.6 per hour.

Validation Engineer

Freseniusglobal

Melrose Park, IL • On-site

$65K - $80K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Job SummarySalary Range: $65,000 to $80,000
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.Responsibilities

THIS POSITION IS NOT A REMOTE CONTRACT POSITION. THIS IS AN ONSITE, FULL-TIME SALARIED ROLE.

THIS POSITION IS NOT ELIGIBLE FOR VISA SPONSORSHIP NOW OR IN THE FUTURE.

Responsible for providing technical support to operations in terms of equipment/system/process initial validation and equipment/system/process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. The individual must become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required.

Job Responsibilities:

  • Schedules and executes equipment requalifications per Standard Operating Procedures (SOPs). Coordinates and communicates all testing with affected functional groups and evaluates test results. Assembles and composes the final report and circulates for approval.
  • Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to include protocol preparation, scheduling, protocol execution, and final report preparation. Presents results to Regulatory Agency when necessary.
  • Programs and operates department analytical instruments (such as temperature/humidity dataloggers) to perform controlled temperature/humidity chamber qualifications (examples lyophilizers, warehouses, sterilizers, incubators, etc.).
  • Develops/improves validation programs as needed to remain current with cGMPs and industry standards.
  • Schedules and executes HEPA Filter and Critical Area (Class 100) testing per SOP. Programs and operates test equipment such as smoke generators, photometers, velocity meters, etc., and accurately records and evaluates results.
  • Represents Technical Services in teams assembled to specify, install, validate, troubleshoot and maintain systems, equipment and processes.
  • All employees are responsible for ensuring the compliance to company documents, programs and activities related to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities.

Job Requirements:

  • Bachelor's degree in a Science or Engineering field of study required
  • Minimum of one year relevant work experience in a cGMP regulated industry.
  • Experience generating reports, deviations or other technical documents.
  • Experience with Installation, Operational and Performance Qualification protocol generation and execution strongly preferred.
  • Analytical datalogger programming, operating, troubleshooting, data-collecting preferred.
  • PC literate with standard office application (Word, Excel, PowerPoint, Project, Access) competency
  • Knowledge and understanding of cGMPs, industry guidance, and aseptic techniques
  • Understanding of statistical analysis tools and methods.
  • Knowledge of cGMP room classifications, HEPA filter testing and Airflow Pattern testing tools and techniques.
  • Knowledge of cGMP Cleaning Validation requirements and techniques
  • Knowledge of cGMP Process and Product Validation requirements and techniques.
  • Knowledge and experience in cGMP CA/PA, root-cause analysis, risk assessment and investigation tools & techniques

The Company's primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.

Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company contribution, andwellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is atwill, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.