Senior Director, AAV Upstream Development
Alexion

This is what you will do:

The Senior Director's is responsible for leading and directing the cell culture activities for Alexion's AAV production platform. The Senior Director will work collaboratively with key functional experts in our Research, Product Development, and Analytics teams, among others to advance our growing portfolio. The incumbent will be part of the Viral Vector Product Development Leadership Team in defining overall strategy, team growth, budgeting, and providing expertise to project team on all aspects of upstream process development.

You will be responsible for:

• Accountable for all upstream development activities, including life-cycle management, externalization, due-diligence, academic partnerships and in-licensing, across the entire product life-cycle, from pre-clinical to commercialization.
  
• Provide product development leadership and strategy on project teams (or mentoring junior Project Leaders) and collaborating across all areas of CMC and clinical development functions from early discovery into development
  
• Collaborate on the development and characterization of plasmid vectors and high-productivity cell lines to establish systems with appropriate quality and expression levels.
  
• Identifying, negotiating, and delivering partnerships with academic institutions or industry to evaluate, development and implement new technologies and improved workflows.
  
• Establish positive relationships across AstraZeneca teams to share innovative technologies
  
• Provide subject matter expertise for regulatory interactions including inspections, audits, and is accountable for the technical content of process development sections of regulatory submissions.
  
• Lead and develop an innovative team of process development scientists.
  
• Devote significant time and effort in developing colleagues and the requisite bench strength to deliver on Alexion's growing R&D pipeline.
  

You will need to have:

• The successful candidate will have 10+ years of process development experience with direct experience in AAV and late-stage molecular biologics development, including participation in projects involving cross-functional teams
  
• Must be proficient in upstream state-of-the art technologies to establish viral vector systems in compliance with global regulatory standards and guidance.
  
• Knowledge of current regulatory guidelines and cGMP requirements is essential. Knowledge of preclinical and clinical drug development is a prerequisite
  
• Direct experience in preparing and supporting regulatory submissions including INDs/CTAs, BLA/MAAs and engaging with regulatory agencies is required. Be a key subject matter expert in for CLD activities when working with CMOs, Quality, Commercial, and other key stakeholders, both internal and external.
  
• The candidate will have people-leadership, management, and development expertise, with a proven track record of leading, prioritizing, and managing multiple successful projects and support strategy thinking and actions.
  
• Well-developed leadership, communication, team building and influencing skills; unquestioned integrity; and the experience to help establish a global function that is critical to our organization's success
  
• Ability to travel up to 20%
  

• The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.
  

We would prefer for you to have:

• Bachelor's, Master's, or Doctorate degree or equivalent in Pharmaceutical Sciences, Bio/Chemical Engineering, Biochemistry, Molecular Biology, or related discipline.
  
• At least 8+ years of experience (from Doctorate) in managing a process development group with direct deep expertise in developing processes from pre-clinical through licensure of viral vectors, gene therapies, and/or molecular biologics
  

Date Posted
29-Mar-2024

Closing Date
31-May-2024Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact accommodations@Alexion.com. Alexion participates in E-Verify.

AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.

This job has expired.