Sr. Manager/AD CMC

A clinical-stage biotech in the RNAi space is seeking an Associate Director or Senior Manager of CMC to lead external manufacturing activities for a key therapeutic program. Key Responsibilities Manage drug product manufacturing with global CDMOs Lead tech transfer, scale-up, and GMP manufacturing campaigns Manage batch records, deviations, and quality documentation Coordinate analytical testing and stability activities Contribute to CMC sections of regulatory submissions Qualifications ~810 years of CMC or technical operations experience Strong experience managing CDMO manufacturing programs Background in GMP manufacturing and tech transfer Experience supporting clinical-stage development Oligonucleotide experience preferred Please reach out to s.viall@kennedybond.com for more information.