Quality Assurance Associate
Successful candidate will author quality assurance documents including method transfer, master batch record, stability study and system suitability protocol in support of contract custom organic synthesis of potential new drug candidates intended to treat a variety of illnesses. These materials are either radiochemicals, stable labeled compounds or small scale (milligram to gram) non-labeled compounds. The compounds that are will be supported by this Quality Assurance Associate include nucleic acids, amino acids, peptides and heterocycles.
Moravek, Inc. is a CMO and once our custom synthesis work has been completed, the compounds are sent to various CROs for testing on behalf of leading universities and pharmaceutical companies.
Experience with drafting master batch records, method transfers, stability studies under GMP and system suitability parameters is required.
Familiarity with analytical information derived from qualified HPLC, NMR and MS instrumentation is required.
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