This is a temp to hire opportunity
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.
