Healthcare jobs in Life Sciences

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.

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.

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 a Development Engineer you will play a key role in advancing the organisations technology. You will be responsible for developing instrumentation and test strips to support a range of activities, driving transition of the product from prototypes to pilot-scale, and ultimately full commercial launch.

This is a standalone Quality Manager role within a Business Operations team, working on business processes and ensuring compliance with ISO9001, and managing the internal audits.

Taking ownership of the site QC function, leading the team and providing strategic input.

Joining an established and growing business, leading the Quality function from a GCP perspective.

This role will join an established Quality team, providing technical support on Quality and Compliance, in adherence to 13485 and MDR.

The Managing Director will lead a Midlands-based medical device company, responsible for driving strategic growth, overseeing financial and operational management, and ensuring regulatory compliance. This is a hands-on leadership role, offering the opportunity to shape the future of a growing business with a global presence in the healthcare sector.

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 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.

• 
  
  The Quality Engineer will be responsible for ensuring the quality of products and processes.
• 
  
  Develop and implement quality control processes, procedures, and policies to ensure compliance with industry 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.

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.