Job Description:

JOB RESPONSBILITIES:· Obtain and maintain qualifications necessary for the performance of aseptic activities.· Responsible for the production, formulation, and banking of cellular products (including GMP, GDP, and aseptic processing).· Write, under supervision, GMP required documents including standard operating procedures, product specifications, equipment specifications and batch production records.· Provide support in validation efforts related to the manufacturing process.· Participate in all aspects of manufacturing activities including raw material support, cell culture, and continuous improvement.· Consistently practice appropriate clean room behaviors, upkeep of clean room areas.· Must be able to work night, weekends, and holidays, as necessary.· Must be able to meet physical requirements established in this job description.· Drafting, with support deviations and other necessary documentation.· Perform other duties as assigned. QUALIFICATIONS:-AS or BS in a scientific field strongly preferred-Must be able to work in a clean room environment that potentially includes hazardous materials, and Medical equipment (including blood, tissues, and needles)-Must have ability to perform algebraic math-Must be detail oriented and have excellent organizational skills-Must possess effective written and oral communication skills-Must display a high degree of professionalism and confidentiality * this position is temp to hire.