Monte Rosa Therapeutics. looking for a CMC Scientist with ADQC expertise to support the supply of drug substance and drug product for molecular glue degrader (MGD) programs. The successful candidate will be involved in Chemistry Manufacturing and Control activities from preclinical to clinical and commercial stage. This person will interface with a variety of CRO and CDMO activities not limited to monitoring and guiding analytical methods development and phase appropriate validations, QC oversight, managing outsourcing activities of both drug substance (including synthesis design, trouble shooting, process development) and drug product, contributing to the quality section of regulatory submissions. Superior experience in analytical development field of small molecule API in fast paced environments and in (early) phase development are considered an asset. Quality control experience is considered a plus. The candidate should also have excellent skills for working in a collaborative and cross-functional, dynamic environment.
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