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Process Support Engineer

  • Process Support Engineer job type Posted on: Oct 28, 2026
  • Process Support Engineer experience level Sterling Engineering Inc.
  • Process Support Engineer employment type Waukegan, Illinois
  • Process Support Engineer salary Salary: $35 per hour
  • Process Support Engineer employment type Onsite
  • Process Support Engineer salary Full-time
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Job Title :

Process Support Engineer

Job Type :

Full-Time

Job Location :

Waukegan Illinois United States

Remote :

No

Jobcon Logo Job Description :

View Full Description

Job Description

Job Description
 Job Title: Chemical Engineer (Process Support)
 Location: Waukegan, IL
 Hire Type: 12++ month contract
 Schedule: Full-Time, Monday–Friday
 Target Pay Rate: $35-$45/hr
 Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), & ESOP

Overview:
Seeking a Process Support Engineer to join a pharmaceutical manufacturing environment and provide hands-on engineering support for manufacturing operations. This position will support new product introduction, process development, and improvements to established commercial manufacturing processes. The ideal candidate will be comfortable working directly with manufacturing and technical teams, analyzing processes, developing technical documentation, and identifying opportunities to improve efficiency, quality, and safety. This role requires strong attention to detail and an understanding of GMP-regulated operations and documentation practices.

Responsibilities:
  • Provide engineering support for manufacturing activities, process improvement initiatives, and new product introduction projects.
  • Partner with manufacturing, technical operations, quality, and other cross-functional groups to execute project activities.
  • Support the evaluation, development, and optimization of manufacturing processes.
  • Work hands-on with manufacturing personnel to troubleshoot process-related issues and identify opportunities for improvement.
  • Assist with process documentation, technical specifications, reports, and other engineering deliverables.
  • Ensure engineering and manufacturing activities are performed in accordance with applicable GMP and Good Documentation Practices (GDP).
  • Collect and evaluate process information to support troubleshooting, optimization, and continuous improvement efforts.
  • Participate in projects designed to improve manufacturing efficiency, product quality, process reliability, and operational safety.
  • Provide technical input during manufacturing activities and help translate process requirements into practical manufacturing solutions.
  • Maintain accurate and thorough documentation of engineering activities and project work.
  • Continuously develop technical knowledge related to process engineering, pharmaceutical manufacturing, and regulated operations.
Required:
  • Bachelor’s degree in Engineering, Science, or a closely related technical discipline. Chemical Engineering background preferred.
  • Experience supporting manufacturing or process engineering activities.
  • Strong analytical, troubleshooting, and problem-solving abilities.
  • Ability to work effectively in a fast-paced manufacturing environment.
  • Strong written and verbal communication skills.
  • Ability to collaborate effectively with cross-functional teams while also working independently.
  • Strong attention to detail and commitment to accurate technical documentation.
  • Ability to adapt to changing priorities and learn new processes and technologies.
Preferred:
  • Experience within a pharmaceutical, biotechnology, medical device, or other GMP-regulated manufacturing environment.
  • Previous exposure to New Product Introduction (NPI) activities.
  • Experience with process optimization or continuous improvement initiatives.
  • Familiarity with GMP and Good Documentation Practices (GDP).
  • Experience developing technical reports, specifications, or manufacturing documentation.
Technical Skills:
  • Process Engineering
  • Manufacturing Process Support
  • New Product Introduction (NPI)
  • Process Optimization
  • Troubleshooting & Root-Cause Analysis
  • GMP / GDP Documentation
  • Technical Reporting
  • Process Documentation
  • Continuous Improvement
  • Cross-Functional Project Support

Ideal Candidate:
The ideal candidate is a hands-on Process or Manufacturing Engineer who enjoys working closely with operations and technical teams in a regulated manufacturing environment. They should be analytical, adaptable, and comfortable moving between the production floor, project work, and technical documentation. A strong candidate will bring a continuous-improvement mindset and the ability to identify practical opportunities to improve manufacturing processes while maintaining quality and compliance.

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.

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Jobcon Logo Position Details

Posted:

Oct 28, 2026

Reference Number:

fd325820

Employment:

Full-time

Salary:

$35 per hour

City:

Waukegan

Job Origin:

ziprecruiter

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Job Description

Job Description
 Job Title: Chemical Engineer (Process Support)
 Location: Waukegan, IL
 Hire Type: 12++ month contract
 Schedule: Full-Time, Monday–Friday
 Target Pay Rate: $35-$45/hr
 Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), & ESOP

Overview:
Seeking a Process Support Engineer to join a pharmaceutical manufacturing environment and provide hands-on engineering support for manufacturing operations. This position will support new product introduction, process development, and improvements to established commercial manufacturing processes. The ideal candidate will be comfortable working directly with manufacturing and technical teams, analyzing processes, developing technical documentation, and identifying opportunities to improve efficiency, quality, and safety. This role requires strong attention to detail and an understanding of GMP-regulated operations and documentation practices.

Responsibilities:
  • Provide engineering support for manufacturing activities, process improvement initiatives, and new product introduction projects.
  • Partner with manufacturing, technical operations, quality, and other cross-functional groups to execute project activities.
  • Support the evaluation, development, and optimization of manufacturing processes.
  • Work hands-on with manufacturing personnel to troubleshoot process-related issues and identify opportunities for improvement.
  • Assist with process documentation, technical specifications, reports, and other engineering deliverables.
  • Ensure engineering and manufacturing activities are performed in accordance with applicable GMP and Good Documentation Practices (GDP).
  • Collect and evaluate process information to support troubleshooting, optimization, and continuous improvement efforts.
  • Participate in projects designed to improve manufacturing efficiency, product quality, process reliability, and operational safety.
  • Provide technical input during manufacturing activities and help translate process requirements into practical manufacturing solutions.
  • Maintain accurate and thorough documentation of engineering activities and project work.
  • Continuously develop technical knowledge related to process engineering, pharmaceutical manufacturing, and regulated operations.
Required:
  • Bachelor’s degree in Engineering, Science, or a closely related technical discipline. Chemical Engineering background preferred.
  • Experience supporting manufacturing or process engineering activities.
  • Strong analytical, troubleshooting, and problem-solving abilities.
  • Ability to work effectively in a fast-paced manufacturing environment.
  • Strong written and verbal communication skills.
  • Ability to collaborate effectively with cross-functional teams while also working independently.
  • Strong attention to detail and commitment to accurate technical documentation.
  • Ability to adapt to changing priorities and learn new processes and technologies.
Preferred:
  • Experience within a pharmaceutical, biotechnology, medical device, or other GMP-regulated manufacturing environment.
  • Previous exposure to New Product Introduction (NPI) activities.
  • Experience with process optimization or continuous improvement initiatives.
  • Familiarity with GMP and Good Documentation Practices (GDP).
  • Experience developing technical reports, specifications, or manufacturing documentation.
Technical Skills:
  • Process Engineering
  • Manufacturing Process Support
  • New Product Introduction (NPI)
  • Process Optimization
  • Troubleshooting & Root-Cause Analysis
  • GMP / GDP Documentation
  • Technical Reporting
  • Process Documentation
  • Continuous Improvement
  • Cross-Functional Project Support

Ideal Candidate:
The ideal candidate is a hands-on Process or Manufacturing Engineer who enjoys working closely with operations and technical teams in a regulated manufacturing environment. They should be analytical, adaptable, and comfortable moving between the production floor, project work, and technical documentation. A strong candidate will bring a continuous-improvement mindset and the ability to identify practical opportunities to improve manufacturing processes while maintaining quality and compliance.

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.

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