Who we are

REGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities.

The Opportunity

REGENXBIO is currently searching for a Gene Therapy Manufacturing Supervisor (Downstream) to help us build our team! As Gene Therapy Manufacturing Supervisor, you will play a critical role in helping to establish REGENXBIO’s first internal GMP BDS and FDP clinical and commercial AAV gene therapy manufacturing capability. As a member of the highly engaged and collaborative Manufacturing Operations team, you will have the unique opportunity to start-up an agile, multi-product, single-use facility. You will play an important role in leading the establishment of new processes, procedures and ways of working, as well as performing manufacturing process related tasks and unit operations within Downstream.

What You'll Be Doing:

• Opportunity to work in an “ALL” stream environment that allows for cross-functional development between the differing manufacturing areas, i.e. media/buffer prep, upstream (US), downstream (DS)
• Embody our core values by working collaboratively, building strong relationships and using clear communication to meet shared objectives.
• Support and maintain a safety-first culture emphasizing individual accountability, safe systems of work, and management commitment.
• Partner with Quality to maintain a robust quality and compliance culture and performance that meets applicable GMP regulatory standards and supports regulatory inspections.
• Execute and support operational readiness activities for the NEW internal manufacturing facility, including the establishment of manufacturing procedures and standard practices, facility start-up, commissioning, and qualification of equipment and automation.
• Serve a lead role in process tech transfers and batch record establishment.
• Coordinate daily operations and lead on the floor manufacturing employees to complete production activities safely and compliantly in accordance with OSHA and cGMP guidelines.
• Proactively work to achieve training competency in an expanding manufacturing facility.
• Perform as a subject matter expert (SME) and qualified trainer for most GMP manufacturing operations, processes and equipment for DS areas.
• Lead root cause analysis for manufacturing events of varying complexity.
• Lead projects of minor to moderate scope with the support of cross-functional stakeholders.

• Bachelor’s degree OR Associate’s degree/High School Diploma or equivalent with relevant cGMP experience.
• 6 years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation.
• Excellent oral and written communication skills with strong technical writing ability required.
• Excellent teaching and facilitation skills for on-the-job training delivery.
• Expert in authoring, revising and/or reviewing GMP documentation (i.e. SOPs, Batch Records, etc.).
• Strong organizational and leadership skills.
• Strong experience in GMP quality systems, including deviation root cause analysis tools.
• Ability to apply continuous improvement and operational excellence strategies within a manufacturing organization.
• Ability to think critically in regard to problem solving and troubleshooting.
• Ability to work collaboratively with colleagues in a results-driven, team-oriented environment.
• Strong subject matter expertise of Downstream GMP Manufacturing operations for processes and equipment
• Ability to adapt to changing priorities and tight production schedules.
• Experience in aseptic fill finish and AAV manufacturing/viral transfection.
• Experience in supporting facility start-up, commissioning and qualification activities.
• Proficiency in relevant Downstream single-use technologies and systems.
• Experience using DeltaV PCS system.
• Excellent communication skills for effective collaboration with cross-functional teams
• Strong analytical and problem-solving skills to optimize production efficiency
• Experience with technical writing as it relates to Manufacturing deviations