Seeking gene therapy industry experience to oversee activities related to the Process Development and in-house production of recombinant Adeno-associated Viral Vectors using cell culture systems, and cGMP vector production at contract manufacturing organizations.
*** Oversee large-scale cGMP production of rAAVs, including upstream cell culture, downstream processing, scale-up, and fill finish operations for both the in-house team and contract manufacturing organizations.
*** Coordinate the transfer, qualification, and implementation of process improvements and scale-up.
*** Coordinate production activities with research, non-clinical development, Quality Assurance, Quality Control, and clinical development.
*** Lead the reporting, investigation and resolution of deviations encountered during GMP production activities.
*** Master of Science or Ph.D. in bioprocessing, chemicalengineering, vector biology, or biological sciences.
***10+ years experience in upstream cell culture process development and manufacturing operations for biologics.
High growth visible position with top company. Generous salary plus bonus plan; company paid full family coverage medical, dental, prescription and vision; matched 401(k); stock; tuition reimbursement and more.
Education Requirements: Master Degree
Minimum Experience Requirements: 5-10 years
Job City Location: Cambridge
Job State Location: MA
Job Country Location: USA
Salary Range: $160,000 to $200,000