We value a positive attitude. We make working a more pleasant experience for everyone.
We value communication, for it creates better intercultural relationships.
We focus on things that matter most and help each other drive success.
We see the good. We work hard. We keep things in balance.
We empower each other to produce better results by providing professional advancement and personal growth.
We are driven by the challenge of creating something new and discovering better opportunities.
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healthier, more productive place to work.
Are you a seasoned professional looking
for your next challenge? Be one of us!
The post holder will join a multi-discipline team tasked with the development and manufacture of novel cell and gene therapy products. The Quality Lead will initially focus in early procedural and protocol development in preparation and implementation for a newly build GMP manufacturing facility for Cell and Gene Therapy and other ATMPs. The Quality Lead will form part of a new expanding team that will implement Esco Aster’s manufacturing and product pipeline agenda for its new facility and will play a key role in the start-up of the new facility and it’s processes and will subsequently drive manufacturing development. The candidate will be reporting to the Chief Executive Officer and will work closely with both the R&D department as well build out the Quality Department to ensure translational development of product candidates is conducted to regulatory compliance in the rapidly evolving field of cell and gene therapy for clinical applications. This is a unique opportunity. The Quality Lead will also be expected to, assist quality investigation and process deviations, and support internal and external inspections. In addition, the Quality Lead is expected to actively contributing to maintain Good Manufacturing Practice (GMP) compliance and to a Healthy and Safe Working Environment.