Process Engineer

North Chicago, IL 60064

Employment Type: Contract Job Category: Project Management Job Number: Jr530631418 Compensation: $40-80 / hour

Job Description

Title: Process Engineer

Location: North Chicago, Illinois
Hire Type: Contract
Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S.
As a contract employee of Sterling, you are eligible to receive a Full Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental & vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan.
Job Summary: 
We are seeking a highly motivated and experienced Process Engineer to join our team. In this role, you will be responsible for supplementing the group's current capacity and supporting the upgrade of our Fermentation equipment. Your experience with downstream purification coming from fermentation will be crucial to the success of this project.
Job Duties:
  • Collaborate with the team to upgrade our Fermentation equipment to improve product quality, yield, and efficiency.
  • Work closely with other engineers and cross-functional teams to ensure project timelines and deliverables are met.
  • Provide technical support and troubleshooting for manufacturing processes, equipment, and systems.
  • Design and execute experiments to optimize process parameters and identify process improvements.
  • Perform data analysis and present findings to key stakeholders.
  • Ensure compliance with cGMP and other regulatory requirements.
  • Maintain accurate and up-to-date documentation.
  1. Bachelor's or Master's degree in science or engineering.
  2. At least 3 years of experience in a pharmaceutical or biotech manufacturing environment.
  3. Experience with fermentation process is required.
  4. Knowledge and experience with downstream purification coming from fermentation is a must-have.
  5. Knowledge of cGMP regulations and FDA guidance for pharmaceutical manufacturing.
  6. Strong problem-solving skills and attention to detail.
  7. Excellent communication and interpersonal skills.
  8. Ability to work effectively in a team environment.

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

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