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The Director of Technology Transfer will oversee cross-functional teams ensuring the transition of gene and cell therapy products from clinical development to commercial manufacturing, providing technical leadership, mentoring staff, and ensuring regulatory compliance.

The Upstream Process Development Scientist will develop and optimize processes for producing various viral vectors. Responsibilities include designing experiments, analyzing data, collaborating with teams, and ensuring compliance with regulatory standards. The role emphasizes process scale-up and optimization to improve yield and quality while maintaining communication with clients and internal teams.

The Downstream Process Development Scientist will focus on developing and optimizing purification processes for gene therapy viral vectors. Responsibilities include scaling processes, conducting experiments, analyzing data, collaborating with cross-functional teams, and ensuring compliance with client and regulatory standards.

The role involves directing the development of processes in Downstream Process Development within a gene therapy context. Responsibilities include process optimization, monitoring performance, maintaining safety compliance, and serving as a subject matter expert during audits. Strong collaboration with stakeholders and technical expertise in bioprocessing, GMP, and regulatory aspects are essential to ensure product safety and quality.

The Analytical Development Scientist I will develop and standardize analytical methods for various viral vectors, ensuring compliance with cGMP standards. Responsibilities include method transfer to Quality Control, interacting with clients, collaborating with teams, and training associates, while maintaining high quality and timely deliverables.