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Under general supervision, reviews processing equipment specification used in the development of Solid Oral, semi solid, liquid and Injectable dosage form products. Provides support in the areas of project coordination and follow through, assists with problem solving, efficiency studies and identification of process improvement opportunities. Involves developing manufacturing processes for pharmaceutical products, creating and updating procedures and specifications, writing reports on documentation studies performed and results obtained. Involvement in new product formulation, scale-up process optimization, process validation and technology transfers. Participates in the timely manufacture of supplies in support of clinical and stability programs.
JOB DUTIES & RESPONSIBILITIESMinimum Education & Experience:
Required Knowledge & Skills:
Full Time
$89k-109k (estimate)
04/28/2024
05/11/2024