GMP / Process Development / Clinical Trials / Quality and R&D Roles
Our Belgium based client are currently recruiting for a Principal Scientist to join their Infectious Diseases Biomarkers team.
This is a pivotal role, working within a dedicated team of experts developing and defining strategies to identify novel biomarkers and ultimately gain a deeper understanding of disease and treatment response.
Experience Business Development Manager with clinical trial operational experience.
We are currently looking for additional temporary GMP operators to work with Cobra at our site in Keele, North Staffordshire. The temporary vacancies have arisen as a result of Cobra’s involvement in the COVID-19 vaccine production.
We are looking to recruit a home based, full or part-time Communications Executive to support the comms side of the business both internally and for our clients. Full or part-time, £Neg
We are currently looking to recruit a GMP Production Leader reporting to the Head of Product Delivery at the Keele facility. The GMP Production Leader will be responsible for the operational management and delivery of all assigned Viral Vector manufacturing and technical transfer contracts. The successful candidate will manage GMP production streams, be responsible for scheduling of production activities, ensuring operational, quality and health & safety targets are met as required by the Company and providing technical expertise and guidance as required.
Bruntwood SciTech are now seeking to recruit a new Head of Science and Innovation to shape and drive the delivery of science services, innovation support and community engagement for our life sciences customers through the local ecosystem of partnerships
We are currently looking to recruit a Senior Scientist within the Product Delivery Department at Keele, Staffordshire, UK. The successful candidate will be working within the GMP facility, leading processes and responsible for a team of GMP scientists.
The role as Senior Technician is to be responsible for performing a range of routine analyses ensuring that projects are completed effectively and meet the customer’s contractual agreements. Perform microbiological analysis and report work in accordance with the quality standards. This role focuses on the analysis of products using techniques such as those found in the pharmacopoeias.
We are looking for an exceptional Quality Systems Manager - IVD to join our innovative in-vitro diagnostic client based in central Scotland.