Immediate need for a talented Validation/CSV Engineer. This is a 12+months contract opportunity with long-term potential and is located in Round Lake, IL(Onsite). Please review the job description below and contact me ASAP if you are interested.

Job ID:25-69753

Pay Range: $40 - $45/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Under direction of supervisor or the sterility assurance focal point, contributes to the design, development or enhancement of new products and processes.
• Effectively contribute solid technical knowledge to a variety of projects within the sterility assurance discipline with minimal assistance.
• Display basic technical understanding of related sterility assurance disciplines, specifically sterilization modalities.
• Utilize engineering tools to solve straightforward problems.
• With minimal assistance, perform standard engineering assignments and provide sound technical recommendations regarding projects/matters that are more routine than not.
• Independently execute routine assignments within negotiated deadlines.
• In-depth knowledge and understanding of GxP and related regulations and guidance.
• Provide support to the Sterility Assurance Focal Point for product development or on change controls.
• Write, execute and review validation and qualification protocols and reports.
• Evaluate and interpret technical data and test results.
• Display a solid technical understanding of engineering principles and procedures.
• Demonstrate application of engineering principles on individual/small projects .

Key Requirements and Technology Experience:

• Key Skills:Microbiology, Sterilization, bioburden and bacterial endotoxin .
• Basic technical understanding of sterilization (Moist Heat, Aseptic, Irradiation).
• Basic technical understanding of microbiological method validations (sterility, bioburden and bacterial endotoxin) (specific for the Research Associate II).
• Ability to write, execute and review validation and qualification protocols and reports.
• Ability to Evaluate and interpret technical data and test results.
• B.S. in Engineering and 3 - 5 years related experience.
• Understanding of aseptic technique (RAII) .
• Ability to conduct experiments with minimal assistance.
• Knowledge and understanding of GxP and related regulations and guidance.

Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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