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At Avidity Biosciences, we are passionate about the impact of every employee in bringing potentially life-changing therapeutics to patients in need. Avidity is pioneering a new class of oligonucleotide-based therapies called AOCs designed to overcome the current limitations of oligonucleotide therapies to treat a wide range of serious diseases. We utilize our proprietary AOC platform to design, engineer and develop transformative therapeutics that combine the tissue selectivity of monoclonal antibodies (mAbs) and the precision of oligonucleotide-based therapies to access previously undruggable tissue and cell types and more effectively target underlying genetic drivers of diseases. If you are a committed, solution-oriented thinker, come make a difference with us. The Manager, Quality Control Stability will lead QC activities associated with the day-to-day coordination and execution of the stability program at Avidity. This position will oversee stability data generated at CMOs/CROs relating to the GMP testing of Avidity’s products including drug substance intermediates, drug substance and drug product. This individual will provide input to cross-functional teams and ensure effective communication with colleagues and external partners. Excellent verbal and written communication skills are essential for success in this position including extensive experience successfully managing multiple CTOs and CMOs. This position will report to the Sr. Manager, QC Stability and be a part of Avidity’s CMC / Technical Operations team.