Ready to join a team committed to moving gene therapies into the clinical and commercial settings for patients and families devastated by rare neurological genetic diseases? AveXis is advancing cutting-edge science to treat rare and life-threatening genetic diseases starting with our clinical-stage, proprietary gene therapy candidate, AVXS-101. We are in the midst of an incredible journey and are looking for passionate individuals to join us on this important mission.
AveXis, Inc., a Novartis Company, is a clinical-stage gene therapy company, dedicated to developing and commercializing novel treatments for patients suffering from rare and life-threatening neurological genetic diseases. Our initial product candidate, AVXS-101, is our proprietary gene therapy product candidate currently in development for the treatment of spinal muscular atrophy, or SMA, Type 1, the leading genetic cause of infant mortality, and for the treatment of SMA Type 2. The U.S. Food and Drug Administration, or FDA, has granted AVXS-101 Orphan Drug Designation for the treatment of all types of SMA and Breakthrough Therapy Designation, as well as Fast Track Designation for the treatment of SMA Type 1. In addition to developing AVXS-101 to treat SMA Type 1 and Type 2, we also plan to develop other novel treatments for rare neurological diseases, including Rett syndrome (RTT) and a genetic form of amyotrophic lateral sclerosis (ALS) caused by mutations in the superoxide dismutase 1 (SOD1) gene.
The Summer Intern will work at an AveXis site on various activities included, but not limited to, produce product, troubleshoot and/or validate equipment, help drive process improvements, help investigate deviations, provide market and other strategic analysis, and/or work with supply chain vendors.
Responsibilities of primary importance are to ensure the successful time-sensitive GMP manufacture and release of gene therapy products with minimal to zero deviations, promote a culture of quality and compliance while driving a sense of continuous improvement and operational excellence. Complete requisite training as well as all applicable policies and procedures related to the specific job function. The successful candidate will take accountability to ensure all documentation is complete and accurate, so issues can be addressed real time.
Project based scope could include manufacturing operations, documentation support, continuous improvement, and/or technology implementation.
Support the product requirements to ensure that all products are produced according to plan.
Ensure cGMP documentation is being filled out correctly, training is current and all Quality requirements are being followed.
Responsible for maintaining quality standards to meet cGMP requirements, CFR’s, and internal company policies directly related to the manufacturing process.
Support tech transfer of new products and processes to ensure smooth transition from process development into GMP manufacturing.
Look for opportunities to implement operational excellence and continuous improvement.
Partner with Quality to ensure a quality and compliant manufacturing environment.
Enrolled in a 4 year program, or recently completed a bachelor’s degree in biochemistry, chemical engineering, bioengineering or life sciences.
Excellent oral and written communication skills.
Experience in leading projects.
Must be able to routinely lift over 35 lbs.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.