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DescripciónDescription
Perform Quality Control analyses according to Specifications, Test Methods, SOPs, Pharmacopeia (USP, EP, JP) following all Safety rules applicable. Prepare accurate analysis reports, prepare and standardize solutions. Conduct analytical testing and release of raw materials and packaging components. Analyze complaint and Stability samples in a timely and accurate manner, report any quality issue to the Lab Manager. Assure analytical results are neat and accurate.
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Requisitos Requirements
Bachelor’s Degree in Chemistry, 0-1 years of experience in laboratory testing, preferably in regulated manufacturing of pharmaceutical or medical devices. No experience required, but ample knowledge and learning capabilities needed. Ability to operate laboratory test equipment, computer literate, able to interpret and convert units of measure such as temperature, pressure, flow, area, mass, distance, volume, among other. Mathematical skills and ability to use calculator. Ability to follow written procedures and/or verbal instructions. Basic GMP knowledge. Fully Bilingual. Must be available for third shift. Temporary contract
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