Latest Business Insights Manager Jobs

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. Key responsibilities include architecting and operating scalable cloud platforms using AWS services, defining reusable infrastructure patterns, and mentoring engineers to improve operational maturity across multiple teams.

Pfizer

On-site Permanent

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. Key responsibilities include architecting and operating scalable cloud platforms using AWS services, defining reusable infrastructure patterns, and mentoring engineers to improve deployment reliability and operational maturity.

Pfizer

On-site Permanent

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and deployment systems that power enterprise-scale generative AI applications. Responsibilities include defining infrastructure architecture, building scalable cloud platforms using AWS services, and improving CI/CD, observability, and security practices.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, data review, and safety assessments. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer United States

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

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)

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 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 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 investigators.

Pfizer

On-site Permanent

QA/RA Manager

This role involves leading the design and implementation of regulatory and quality management systems for a portfolio of Class I medical devices, ensuring compliance with ISO 13485 and 21 CFR 820. The candidate will oversee digital EQMS deployment, lead audits, manage post-market surveillance, and build a distributed team while embedding a proactive compliance culture across R&D, supply chain, and commercial functions.

SRG London, United Kingdom

Hybrid Permanent

Pharmaceutical Manufacturing Process Operator

The role involves setting up and operating manufacturing equipment in a highly regulated pharmaceutical environment, ensuring products meet quality standards and compliance with cGMP, health and safety, and company procedures. Responsibilities include accurate documentation, equipment maintenance, and supporting continuous improvement initiatives.

ARx Recruitment Services Watford, Hertfordshire, United Kingdom £28,000 pa

On-site Permanent

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, internal and external audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Walkden, Manchester, M28 3DR, United Kingdom £40,000 – £45,000 pa

On-site Permanent