Sr. Manager/AD CMC
Kennedy Bond, Boston, MA, United States
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 ~8–10 years of CMC or technical operations experience Strong experience managing CDMO manufacturing programs Background in GMP manufacturing and tech transfer Oligonucleotide experience preferred
Please reach out to s.viall@kennedybond.com for more information.
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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 ~8–10 years of CMC or technical operations experience Strong experience managing CDMO manufacturing programs Background in GMP manufacturing and tech transfer Oligonucleotide experience preferred
Please reach out to s.viall@kennedybond.com for more information.
#J-18808-Ljbffr