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.