Scientist II, Process Development - Downstream

Location
Durham, NC, US
Posted
Oct 28, 2020
Ref
5746
Hotbed
Bio NC
Required Education
Bachelors Degree
Position Type
Full time
Overview

Ready to join a team committed to developing and commercializing gene therapies for patients and families devastated by rare neurological genetic diseases? Since 2013, Novartis Gene Therapies (formerly AveXis) has had one focus: bringing change to those devastated by genetic diseases.

The Novartis Gene Therapies culture embraces this mission. As a compassionate and dedicated team, we are enthusiastic about the science behind our work and finding answers to difficult questions. We are dedicated to communities affected by rare diseases, and these patients and families are the motivation for everything we do.

We have built a team with exceptional depth of experience, unified by a common vision; to develop gene therapies with the potential to positively impact the lives of the patients and families devastated by rare and life-threatening neurological genetic diseases. Though we are proud of what we have achieved to date, we remain relentlessly focused on making that vision a reality.

The Scientist II, Process Development - Downstream, supports laboratory operations in process design, experimental design and execution, scale model development and management, investigational testing for manufacturing operations support, platform development project planning, execution, and therapeutic product program development support. Laboratory operations support process development activities for drug substance (upstream, intermediate and downstream), drug product (formulation, filling, packaging and labeling) and critical raw materials, as well as media and buffer manufacturing.

Responsibilities
  • Independently plans, executes and documents experimental procedures for complex studies in support of process development activities supporting investigational, clinical and commercial gene therapy programs.
  • Collaborates in multiple technical development areas.
  • Advances complex downstream process development efforts, occasionally as a technical lead, within a cross-functional team across sites.
  • Executes and sometimes leads projects within the downstream unit to enhance manufacturing AAV purification technologies, capabilities, and processes.
  • Plans, designs, executes and interprets, sometimes independently and as a lead, complex development studies (with multiple experiment sets) related to process development and scale-up, ensuring studies balance time and resources.
  • Drives results and generates innovative solutions; able to take independent action to solve scientific problems and drive their resolution.
  • Supports active pre-clinical, clinical and commercial manufacturing through laboratory studies designed to illuminate fundamental process performance (e.g. NOR and PAR setting, CPP edge of failure, impurity clearance performance).
  • With the support of senior colleagues, authors technical reports of studies in support of process development activities such as Tech Transfer, unit operation design through characterization and Quality attribute impact assessments.
  • Ensures all documentation and reports are accurate, complete, and suitable for use in support of platform development summary reporting, manufacturing records development as well as Quality investigations and regulatory dossiers.
  • Analyzes and interprets experimental data from process studies aimed at building fundamental process understanding.
  • Troubleshoots scientific and technical challenges, and contributes to their resolution.
  • Mentors junior colleagues while fostering a team environment committed to the principles of scientific excellence.
  • Completes requisite training, as well as applicable policies and procedures, related to the job function.
  • Other related job duties as assigned.

Qualifications
  • Bachelor's with 6 years' experience or Master's with 4 years' experience or PHD with 2 years' experience.
  • Demonstrated experience with experimental design, execution, and interpretation (Design of Experiment a plus) that drives downstream project progress and with laboratory biosafety practices. Lean laboratory implementation (e.g. 6S) a plus.
  • Experienced with a variety of biopharmaceutical purification processes such as chromatography, depth filtration, precipitation and flocculation, tangential flow filtration, adventitious viral clearance, ultracentrifugation, and impurity clearance.
  • Experienced in the laboratory setting with single use and automated systems (e.g. Mobius, AKTA)
  • Knowledge and understanding of viral particle purification in clinical and commercial manufacturing settings, direct experience in those environments highly preferred.
  • Direct experience and knowledge of AAV development including empty/full capsid separation development, scale-up, and increasing step yield performance preferred.
  • Demonstrated experience and understanding of developing and optimizing downstream manufacturing process steps and performing scale-up and scale-down, including leveraging scale models of biopharmaceutical processes.
  • Understanding of and experience with global regulations pertaining to cGMP manufacturing of Drug Substance and/or Drug Product and the translation of those regulations into process development work products, specifically within the downstream context.
  • Experience with, and participation on, complex, multi-disciplinary technical teams of scientists and engineers tasked with rapid and comprehensive development of new biopharmaceutical manufacturing platforms.
  • Up to 25% travel.


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.

Novartis Gene Therapies 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.

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