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Our client is a leading GMP pharmaceutical business, and we are looking to hire a Senior Regulatory Associate for a 12 Month Fixed Term contract.
Join a well respected business, with excellent Validation department, as a Senior Validation officer. You will be tasked with a varied range of validation activities in accordance with the SVMP.
Join a Pharmaceutical business in Leeds, as a QA Supervisor focusing on Vendor and Supplier Quality.
As a Biomedical Engineer you will be supporting the development of novel electrochemical biosensor technologies for use in Biosafety and Diagnostic applications.
As a Production Operative you will be responsible for hands-on manufacturing activities of a class III medical device, alongside providing technical and project support to the business. You will work in a GMP Cleanroom facility.
You will oversee daily operations ensuring compliance with ISO13485 & GMP regulations at all times. You will work closely with internal and external stakeholders / partners to deliver high quality production whilst driving improvements to operational efficiency and cost.
Working in R&D as a Scientist you will be supporting the team with advancing the portfolio from ideation to commercialisation. This is a lab-based role where you will be developing, optimising and executing a range of electrochemical immunoassays.
You will utilise your experience to analyse complex data sets,develop computational models, and build machine learning algorithms to support with the development of novel diagnostic platforms.
This role will join a small team of validation and QA professionals, meaning it will be varied and allow good exposure to various aspects of validation.
As a Technical Advisor you will be supporting customers by identifying and advising on novel solutions to challenges in the plant nutrition space. You will work to understand and identify gaps in the market, advising R&D functions on new areas of development.
As the Organics Lab Manager you will oversee the organics function, leading a team of circa 20 scientist to deliver analytical data against agreed time-frames in a high-throughput lab, adhering to ISO standards at all times.
As the Inorganics Lab Manager you will oversee the inorganics function, leading a team of circa 20 scientist to deliver analytical data against agreed time-frames in a high-throughput lab, adhering to ISO standards at all times.
An exciting opportunity has arisen for a Regulatory Affairs Compliance Specialist, who will be responsible for ensuring compliance with regulatory requirements and standards.
Exciting opportunity to join a market leading global animal health business.
The Senior Director, Regulatory Affairs provides support to the Regulatory Affairs team across a range of projects as needed to support the group's activities, and works with the Vice President, Regulatory Affairs, for oversight of the team.
The Client Project and Resource Manager key roles and responsibilities encompass client project initiation through to close including delegating tasks, monitoring progress, budgeting, ensuring coordination among team members and collaboration.
This is a fantastic opportunity to lead the R&D and PD teams in development of novel biosensing technology. You will provide technical leadership as an SME and guide strategy to successfully deliver new products.
You will supervise the successful transfer of manufacturing processes from R&D to Manufacturing.You will be responsible for optimising the performance of manufacturing systems.
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