Manufacturing Technician

Responsibilities

• Obtain and maintain qualifications necessary for the performance of aseptic activities.
• Consistently practice appropriate clean room behaviors and upkeep of clean room areas.
• Responsible for the production, formulation, and banking of cellular products (including GMP, GDP, and aseptic processing).
• Participate in all aspects of manufacturing activities including raw material support, cell culture, and continuous improvement.
• Promotes safety and conducts themselves in accordance with all safety guidelines at all times.
• Perform proper disinfection methods, such as emptying trash, wiping equipment, and mopping ceilings, walls, and floors.
• Responsible for the operation and maintenance of all cleaning equipment.
• Responsible for the preparation of cleaning/sanitation solutions and cleaning materials.
• Identifies and communicates any material or procedural discrepancies.
• Provide support in validation efforts related to the manufacturing process.
• Write, under supervision, GMP required documents including standard operating procedures, product specifications, equipment specifications and batch production records.
• Adheres to all regulatory and compliance requirements defined in current Good Manufacturing Practices (cGMPs).
• Follows and executes Charles River Laboratories’ Standard Operating Procedures (SOPs).
• Accurately documents cleaning activities in logbooks according to Good Documentation Practices (GDPs).
• Perform all other related duties as assigned.