💼 About This Role

You'll support manufacturing operations in a GMP facility, performing aseptic processing and cleanroom maintenance. Your work ensures sterility and compliance with FDA regulations for cell therapy products. This contractor role offers hands-on experience in a regulated biotech environment.

🎯 What You'll Do

• Perform routine aseptic processing of in-house solutions per cGMPs
• Prepare cleaning solutions and sanitize cleanrooms
• Complete cleaning logs and batch records with accuracy
• Track inventory of cleaning materials and supplies

📋 Requirements

• High school diploma or equivalent required
• 0-2 years in biotechnology manufacturing or GMP facilities
• Strong documentation practices including batch records