Healthcare jobs in Life Sciences

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.

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.

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.

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

An exciting opportunity has arisen for a Regulatory Affairs Compliance Specialist, who will be responsible for ensuring compliance with regulatory requirements and standards.

• The QC Technician is responsible for ensuring that medical devices meet regulatory, quality, and safety standards.
• Inspecting raw materials, in-process components, and finished products, performing tests, and maintaining compliance with industry regulations.

Great opportunity to join a global Animal health business as a National Contact Pharmacovigilance Manager.

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.

• Develop and implement cost-effective solutions to improve machinery efficiency, reliability and performance to minimise downtime
• Following planned schedules and troubleshooting reactive repairs, your work will include installation, commissioning, maintenance and modification of electrical and mechanical equipment and site service systems across the pharmaceutical production cycle, in-line with business needs

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.

We are seeking a Senior RAQA Consultant with significant experience in Regulatory Affairs/Quality within SaMD/AIaMD. This role will work with a portfolio of medical device manufacturers so the successful candidate will be working with a varied portfolio of devices and stages.

The Head of RAQA will be a pivotal figure, steering the Regulatory Affairs and Quality Assurance department within a IVD medical device manufacturer start up. This individual will be responsible for ensuring the company meets industry standards and regulations.

As a Scientist - Assay Development you will be supporting a number of allocated clinical trials utilising your virology expertise to develop, optimise and validate a range of assays and related techniques.

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.