What are the responsibilities and job description for the GMP Cell Therapy Expert position at AmplifyBio?
About Our Company
AmplifyBio is a leading contract research organization with a comprehensive range of services that span from being an outsourcing partner for discovery stage R&D work to preclinical CRO performing safety efficacy and toxicology studies for small molecules and advanced therapies alike. We have recently expanded into manufacturing services for cell, gene, and mRNA-based therapeutics.
Job Description
We are seeking a highly skilled Process Engineer/Senior Process Engineer to join our Manufacturing Science and Technology (MSAT) team. This role will be a unique opportunity to see your ideas rapidly translate into the clinic and impact patient lives.
Responsibilities
Hands-on experience with cGMP cell and/or gene therapy manufacturing and implementation of new processes into GMP facilities.
Support the completion of all goals and objectives of manufacturing.
Work closely with other internal functional departments as well as external clientele to ensure deliverables are met.
Requirements
BS, MS, or PhD degree in engineering or scientific field plus at least 6 years of experience.
Minimum of 6 years of experience in Manufacturing or Development roles with more than 2 years in a drug product development and manufacturing function at a biotechnology or pharmaceutical company.
Knowledge and experience in transferring a process into a new facility.
Experience with aseptic processing, cell and/or gene therapy manufacturing.
Experience in leading meetings, teams, and projects.
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