Our client is seeking a highly qualified candidate to support analytical assay outsourcing associated with execution of external development and clinical supply.
The position will be a key enabling role in a high performing cross functional organization. The associate will be responsible for supporting analytical demand for assay execution related to stability and development.
Additional responsibilities :
Overseeing stability studies, method placement, standards, and release testing at external sites.
Coordination of shipments between sites.
Management of external projects, maintenance of clear email communications, meeting coordination. Requirements / Qualifications :
Bachelor degree OR Associate degree and 4 years of experience
Must hold a minimum of a B.S. in Biology / Chemistry or related field.
Analytical background in drug substance / product testing. Experience in small molecule (synthetics). knowledge of stability testing for those products.
5+ years of synthetic / small molecule analytical experience
Familiar with ICH guidelines and GMP / GLP testing.
Industry experience is preferred
Experience with Pharmaceutical Stability Studies
This person will be interacting with outsourced partners and must have excellent communication skills. Ability to multitask.
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