If working in cutting edge and market leading science is attractive to you, then this could be the perfect next move!
I’m partnered with a groundbreaking CDMO who operate within the advanced bioprocessing space and am supporting the hire of a QA Manager to oversee the day to day operations of a growing facility.
Working in a small team, this position won’t take direct people management responsibility but will instead take on specialist level expertise, managing the QA process from a hands on perspective. Working directly with clients and taking a direct accountability with the regulatory bodies, external collaboration will be a big part of the position.
The opportunity for further development is most certainly realistic given how the business has expanded over recent years, as well as significant incoming projects over the next two years.
Quality management experience in a Quality capacity, in a pharmaceutical GMP manufacturing environment
Any experience of bioprocessing or fermentation technology would be a significant advantage but is not essential – experience can come within a small or large molecule setting
Any client facing experience is beneficial but not essential
Knowledge or experience of regulatory affairs could be of interest but again is not essential
Being an aspiring QP, or even better, an eligible QP would be of interest
Please apply or contact Mark Bux-Ryan to discuss further.
Quality, QA, compliance, strategy, global, capa, deviation, sop, change, control, system, manufacturing, operations, bioprocessing, fermentation, cdmo, customer, client, usp, bioreactor, gmp, manager, supervisor, team, leader, specialist