Sr. Manager/Assoc Director, Manufacturing Sciences & Technology (MSAT)

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY The MSAT group plays a critical role in the successful tech transfers and manufacturing of clinical and commercial products. The Associate Director, MSAT provides strategic and operational leadership for Genezen’s Lexington, MA manufacturing processes, ensuring alignment with business objectives and compliance with GMP guidelines. This role is responsible for driving process excellence, scalability, and continuous improvement across new products and existing clinical and commercial programs while fostering cross-functional collaboration and organizational growth. JOB RESPONSIBILITIES Provide strategic leadership for MSAT to support new and commercial manufacturing operations. Lead all aspects of process technology transfer from process development for clinical and commercial manufacturing. Manage, mentor and provide leadership to team of direct reports. Collaborate with Process Development, Manufacturing, QC, QA, Engineering, SC, Validation, CMC and Regulatory affairs and ensure that cross functional teams are functioning smoothly to deliver and maintain processes and controls that are timely, phase-appropriately ready for manufacturing to meet clinical and commercial supply needs. Ability to represent technical process related topics in client meetings. Lead all aspects of process validation including PPQ strategy, execution, data analysis and campaign summary reports. Responsible for process monitoring and CPV to ensure process robustness and to identify process capabilities/improvements. Identifies personnel needs, trains, develops, and motivates subordinates in support of manufacturing, tech transfers, process change controls, CAPAs, and deviation resolution. Author/review relevant CMC sections of clinical and commercial product regulatory filings and provide technical SME support during site regulatory inspections. Author technical reports, risk assessment documents, and prepare scientific presentations as needed. SPECIAL WORK REQUIREMENTS Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned EDUCATION/CERTIFCATIONS/LICENSES Bachelor’s 1 0 + , Master’s or PhD 7 + in a scientific discipline such as Biotechnology, Biochemistry, Chemical Engineering, or related field. Essential ON-THE-JOB EXPERIENCE 7 + years of operating in a sterile GMP fill finish/ Cell and Gene therapy site . Essential 3+ years of experience in CDMO industry <span class="NormalTextRun SCXW198590422 BCX8"