Director of Quality
The company is a leading International cGMP Contract Development and Manufacturing Organisation (CDMO) supporting the global life sciences industry in the development and manufacture of DNA, viral vectors, microbiota, proteins and pharmaceuticals for clinical trials and commercial supply.
They provide a comprehensive biologics and pharmaceuticals service offering, with multi-functional and experienced Advanced Therapies project teams nurturing customers’ plasmid DNA, viral vector and microbiota products from pre-clinical through to clinical and commercial manufacture within GMP approved facilities.
The Associate Director of Process Development will work closely with site management and the wider Group community to reduce development and platform process timelines, improve process efficiencies and platform productivities and enhance the Site’s scientific profile externally. Focus on enhancing internal technology transfer and facilitating continuous scientific & technical improvement.
Ideally, you will have a thorough understanding of the biologics manufacturing services market and the process required to develop a biologic product’ along with a track record in contract development and/or contract manufacturing for the Life Sciences sector.
As part of a larger Group, with 100 sites globally, biologics is a key focus and they are investing heavily in the company to facilitate growth. Future prospects across the Group are exceptional. They have two GMP approved facilities, located in the UK and Europe and are planning to develop a further site shortly in the UK. These sites offer a comprehensive service to nurture projects from conception to fill and finish.
To apply, please forward your CV to firstname.lastname@example.org