Biotechnology Jobs

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

The Clinical Development Medical Director (Associate Director) oversees medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and clinical support for studies, with potential mentorship and strategic input.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.

Pfizer

On-site Permanent

Biomedical Field Service Engineer

This role involves daily repair, preventative maintenance, and asset management of medical devices across multiple hospital locations. Key responsibilities include performing scheduled maintenance, completing repairs, supporting the site manager, and maintaining safe working practices and service documentation. The role requires travel to various sites and maintaining strong customer relationships.

Focus Resourcing Berkshire, United Kingdom

On-site Permanent

Biomedical Field Service Engineer

This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will work closely with the site manager, maintain service documentation, and interact with customers and OEM staff. The position requires strong communication skills and familiarity with regulatory standards.

Focus Resourcing United Kingdom

On-site Permanent

Junior Biomedical Field Engineer

This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, supporting the site manager and team leader in achieving contractual KPIs, and maintaining safe working practices. The job requires strong customer relationship skills, familiarity with regulatory standards, and experience in a clinical environment.

Focus Resourcing United Kingdom

On-site Permanent

Software Engineer (HPC Platform), London

As a Software Engineer focused on GPU infrastructure, you will play a key role in designing, optimizing, and managing the large-scale AI/ML infrastructure that powers Isomorphic Labs' groundbreaking research. You will collaborate with machine learning experts, biotech researchers, and various teams to ensure the reliability and efficiency of the company's AI-driven drug discovery efforts.

Isomorphic Labs London, United Kingdom

On-site Permanent

Member of Technical Staff, Applied AI

Member of Technical Staff, Applied AIThe opportunityWe are looking for a Member of Technical Staff with deep expertise in generative modelling to work at the interface between our frontier models and the customers who depend on them. You will join...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Forward Deployed AI Engineer

Forward Deployed AI EngineerThe opportunityWe are looking for a Forward Deployed AI Engineer to serve as the critical bridge between Latent Labs’ frontier generative models and the customers who rely on them. You will work directly with pharmaceutical and biotech...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Member of Technical Staff

We are looking for a highly skilled machine learning researcher with significant experience in generative modeling. You will join an interdisciplinary team of machine learners, protein engineers and biologists, jointly working to change the way that we control biology and...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Computational Protein Designer

Computational Protein DesignerThe opportunityWe are seeking a Computational Protein Design Scientist to join our team working at the interface of generative AI and synthetic biology. Working closely with our Lead Computational Protein Designer, you will play a key role amongst...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Quality Lead

This role involves leading quality and regulatory compliance for a multinational manufacturer across Europe and Africa, with a focus on medical devices and consumer products. The candidate will oversee the Quality Management System, drive product launches, conduct audits, and ensure adherence to standards like MDD/MDR, ISO 13485, and MHRA. It requires a technically strong quality professional who can lead cross-functionally and balance strategic oversight with hands-on problem-solving.

New Appointments Group Folkestone, Kent, United Kingdom

On-site Permanent