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Manufacturing Process Engineer
1 month ago
Location: Round Lake, IL
Hire Type: Onsite, Long-Term Contract (with full employee benefits)
Target Pay Range: $50.00 - $60.00/hour (W2)
Job Summary:
We are seeking a skilled Process Engineer to support the Engineering & Maintenance department of a global medical device manufacturing company. The successful candidate will be responsible for optimizing and improving operational processes related to the facility's aseptic systems and maintenance activities.
Key Responsibilities:
- Analyze and assess existing aseptic manufacturing processes to identify areas for improvement in sterility, efficiency, and reliability.
- Implement and oversee process changes to enhance the performance of aseptic systems, including cleanrooms, utilities, and sterile production environments.
- Lead and support engineering projects focused on maintaining and improving sterile manufacturing standards, ensuring timely project completion, budget adherence, and alignment with company operational goals.
- Collaborate with the maintenance team to optimize preventive maintenance plans for aseptic equipment, troubleshoot equipment failures, and minimize downtime in sterile environments.
- Collect and analyze data on aseptic operations and engineering performance, supporting decision-making and long-term process improvements while ensuring strict adherence to cGMP (current Good Manufacturing Practices).
- Ensure all process engineering activities comply with aseptic manufacturing regulations, safety standards, and best practices, including ISO standards, FDA guidelines, and OSHA requirements.
- Collaborate with cross-functional teams in engineering, production, and quality to drive continuous improvements in aseptic operations and facility systems.
- Support sustainability and energy efficiency initiatives within sterile environments to reduce resource consumption without compromising product safety or quality.
Requirements:
- Bachelor's Degree in Engineering (Mechanical, Chemical, or Industrial preferred) or related field.
- 3-5 years of process engineering experience, with a focus on aseptic manufacturing or sterile environments.
- Expertise in optimizing and managing aseptic systems, such as cleanrooms, HVAC, and utilities within pharmaceutical or sterile production facilities.
- Experience leading projects related to aseptic manufacturing, from concept to execution, including coordination with cross-functional teams.
- Experience in the medical device industry is preferred.
- Experience with downstream manufacturing processes.