Principal Engineer - Manufacturing Science and Technology (Upstream Lab)

Overview

Ready to join a team committed to developing and commercializing gene therapies for patients and families devastated by rare neurological genetic diseases? AveXis is advancing cutting-edge science, starting with our proprietary gene therapy for the treatment of spinal muscular atrophy (SMA). We are in the midst of an incredible journey and are looking for passionate individuals to join us on this important mission.

AveXis, a Novartis company, is dedicated to developing and commercializing novel treatments for patients suffering from rare and life-threatening neurological genetic diseases. Our initial product is a proprietary gene therapy approved by the US Food and Drug Administration for the treatment of pediatric patients with SMA. In addition to developing a treatment for SMA, AveXis also plans to develop other novel treatments for rare neurological diseases, including Rett syndrome and a genetic form of amyotrophic lateral sclerosis caused by mutations in the superoxide dismutase 1 (SOD1) gene.

The Principal Engineer/Scientist is responsible for defining and leading development and improvement activities for the manufacturing processes used to manufacture AveXis gene therapy products at a site. This individual will be responsible for the collection and interpretation of continued process verification data and collaboration with other departments on manufacturing related issues to drive resolution and process improvements. In addition, this individual will lead a cross functional team for process tech transfers to the site while serving as the technical lead.

Responsibilities

• Utilizing small-scale production processes and scaled-down lab processes to enable process troubleshooting, with the potential to oversee these experiments at external partners.
• Evaluating and summarizing data using analytical methodologies, interpreting results, drawing conclusions and recommending options for future experiments to achieve project goals.
• Serving as a scientific and technical lead for process-related issues and investigations when necessitating laboratory experiments.
• Utilizing design of experiments for range finding and characterization studies.
• Performing trending and monitoring of critical quality attributes/critical process parameters to maintain product quality and to control process drift.
• Defining potential process improvements in conjunction with the Global process owners and operations and leading implementation of process changes.
• Participating in start-up efforts of new equipment, software or processes.
• Provide leadership for tech transfer of new products and processes to ensure smooth transition from process development into GMP manufacturing.
• Identify opportunities to implement operational excellence and continuous improvement.
• Partner with Quality to ensure a compliant development environment.
• Completion of requisite training, as well as applicable policies and procedures, related to the job function is an expectation to support ongoing manufacturing support.

Qualifications

• PhD in biochemistry, chemical engineering, bioengineering, or related technical field and at least 8 years of experience in support of biopharmaceutical manufacturing or
  M.S. degree in biochemistry, chemical engineering, bioengineering, or related technical field and at least 10 years of experience in support of biopharmaceutical manufacturing or
  B.S. degree in biochemistry, chemical engineering, bioengineering, or related technical field and at least 12 years of experience in support of biopharmaceutical manufacturing.
• Excellent oral and written communication skills.
• Ability to effectively and efficiently analyze and interpret data to further progress development strategies.
• Experience in biopharmaceutical based GMP manufacturing operations including direct experience in cell culture, recovery, purification, and/or aseptic fill/finish preferred.
• Working knowledge in Design Of Experiments is preferred.
• Familiar with global regulations on cGMP manufacturing of drug substance, drug products devices, validation/qualification requirements.
• Proven ability to effectively lead and participate on teams.
• Leadership of technical staff either directly or in a matrix organization.

The level of this position will be based on the final candidate's qualifications.

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.

AveXis is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, national origin, genetics, disability, age, sexual orientation or veteran status. #LI-JB1