Latest regulatory affairs Jobs

Assistant Production Manager

This role involves overseeing the servicing, repair, and testing of medical and veterinary devices, managing workflow and technician teams, and ensuring compliance with quality standards including ISO 13485 and ISO 14971. The Assistant Production Manager will also lead training, conduct audits, and support quality management systems. Key responsibilities include technical problem-solving, customer liaison, and maintaining accurate service documentation.

Rotherwood Keighley, West Yorkshire, United Kingdom £35,000 – £40,000 pa

On-site Temporary

8a Advanced Practitioner BMS - Blood Transfusion

This role involves providing expert technical and operational leadership in blood transfusion services across two NHS hospital laboratories. The Advanced Practitioner ensures regulatory compliance, leads quality and governance initiatives, oversees specialist training, and drives continuous improvement in transfusion science. The position requires deep expertise in haematology and blood sciences, with a focus on patient safety and high-quality diagnostic delivery.

Synlab Taunton, Somerset, TA1 1HP, United Kingdom £57,528 – £64,750 pa

On-site Permanent

Senior Compliance Engineer (Medical Equipment)

Oversee legislative compliance and product safety for medical equipment through testing, certification, and documentation. Lead teams in ensuring adherence to global standards and contribute to product design for compliance. Maintain certification databases and drive continuous improvement across quality and safety frameworks.

Ernest Gordon Recruitment Cheltenham, Gloucestershire, United Kingdom £55,000 pa

On-site Permanent

Senior Supplier Quality Engineer

This role involves ensuring compliance of logistics, warehousing, and distribution activities with medical device regulations and quality standards across the supply chain. The engineer will lead supplier audits, manage CAPA and risk assessments, and provide quality oversight for sterile medical device handling and transport validation. It focuses on maintaining traceability, distribution controls, and continuous improvement within a regulated QMS environment.

Aurora Life Sciences Leeds, West Yorkshire, United Kingdom £52,500 – £60,000 pa

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer United States

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and site selection criteria. The role also involves training and supporting site-facing colleagues, participating in safety review meetings, and contributing to continuous improvement initiatives.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including external committees and site-facing colleagues, to ensure the successful execution of clinical studies.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including investigators, regulatory bodies, and safety review teams.

Pfizer

On-site Permanent

Embedded Engineer

This role involves developing and maintaining embedded software for STM32 and ESP32-based medical devices, including control firmware and real-time systems using FreeRTOS. The engineer will perform system integration, electronics fault-finding, PCB updates, and collaborate with cross-functional teams to build prototype medical devices. Emphasis is placed on hands-on hardware-software interaction and adherence to software lifecycle processes in a regulated medtech environment.

KO2 Embedded Recruitment Solutions Manchester, United Kingdom £40,000 – £50,000 pa

On-site Permanent

Cluster HTA Hub Senior Manager

In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans to enhance the value of Pfizer's medicines. You will collaborate with sales teams and utilize health economic models to maximize sales and improve customer interactions.

Pfizer Poland

On-site Permanent

Cluster HTA Hub Senior Manager

In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans. You will also collaborate with sales teams to maximize sales and enhance customer interactions using health economic models.

Pfizer London, N1 5EA, United Kingdom

Hybrid Permanent