Director of Development

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.

A Director of Development is sought to provide management and leadership to the process and analytical development teams focusing on Viral Vector, DNA and Analytical Development, whilst delivering contract development revenue generating activities and driving innovation for the site.

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.

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.

To apply, please forward your CV to lifescience@chestertongray.com

Reference 880247