Remote CMC Regulatory Consultant, Biotech (50%+ Time)

A biotech firm is seeking a Freelance Regulatory CMC Consultant to manage regulatory submissions and oversee CDMO operations. The candidate should possess over 7 years of experience in biotech or pharma environments, specifically with regulatory documentation like IMPDs and INDs. This remote role requires occasional travel to Torino and the UK. The firm is focused on developing inhaled peptide therapeutics. The ideal candidate will excel in strategic planning and technical review processes.
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