Upvote
Downvote
Associate Director, Analytical Development / Quality Control
Share Job
- Suggest Revision
Full-time
- With its proprietary FORCE platform, Dyne is developing modern oligonucleotide therapeutics that are designed to?
- The position is responsible for analytical development, analytical technology transfer and validation, and overall management of CMC activities related to external QC testing/release and stability of antibody drug conjugates and intermediates.
- Depending on the product phase, the Associate Director provides both guidance and active management of analytical development and QC activities in Phase 1 thru BLA and commercial production.
- This role works closely with key stakeholders including CMC, Supply Chain, Development, R&D, Clinical, Regulatory Affairs and Project Management to define the QC capabilities required to effectively manage Dyne's complex clinical supply chain and support eventual launch and commercialization efforts.
- Aspects of analytical development and QC of intermediates, drug substance, and drug product including analytical development, validation, characterization, tech transfer, analytical method qualification, specifications, release, and stability testing
Expired 30 days agoInactive Job
Similar Job
Relevance
Active