Latest Medical Affairs Partner - Nephrology & R Jobs

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will manage health economics and outcomes research, collaborate with cross-functional teams, and ensure a consistent evidence generation strategy across markets.

Pfizer United States

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will lead the generation of health economics and outcomes research, manage global value dossiers, and coordinate with cross-functional teams to ensure a consistent and robust evidence strategy.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Clinical Sciences Project Manager

This role involves developing and refining processes, risk management strategies, and other activities essential to the success of the Global Collaborative Studies Group (CSG) at ViiV Healthcare. You will lead the Request for Proposal study process, manage study-related activities, and work cross-functionally with various teams to ensure timely and compliant delivery of supported studies.

GSK

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to protocol development, and providing medical oversight and support. You will work closely with internal and external stakeholders to ensure the successful execution and interpretation of clinical studies, with a focus on advancing HIV treatments and prevention.

GSK United Kingdom

On-site Permanent

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Vulnerability Analyst

This role involves assessing known software vulnerabilities in Windows-based applications used in regulated medical devices. Responsibilities include performing exploitability and risk analysis, evaluating third-party component risks, and producing clear security documentation. The position requires 2+ years of commercial experience in application security and a strong understanding of CVEs and secure software concepts.

Real Limerick, Limerick County, Ireland £47 ph

Hybrid Contract

Head of Product Development & Engineering

This role involves leading the product development and engineering lifecycle for complex medical technology products, from concept to launch and ongoing support. Responsibilities include managing R&D projects, mentoring a specialist team, and collaborating with quality, operations, and commercial teams to ensure regulatory compliance and commercial success.

Concept Technical Worthing, West Sussex, United Kingdom £70,000 – £80,000 pa

On-site Permanent

Embedded Systems Engineer

Embedded Systems EngineerA long-established global manufacturer of high-voltage power solutions used in medical devices, semiconductor equipment, scientific instruments and industrial systems. The organisation operates design and manufacturing facilities across North America, Europe and Asia and partners with leading OEMs developing...

Terry Parris Associates Codmore Hill, West Sussex, RH20 1DQ, United Kingdom

Regulatory Manager

As a Regulatory Manager, you will lead regulatory strategy for drug-device combination products, working closely with global regulatory bodies and clients. You will manage a small team, review key documentation, and contribute to regulatory intelligence, with opportunities for career growth in a forward-thinking, innovative company.

Hays Life Sciences Cheshire, United Kingdom

On-site Permanent

Process Project Engineer – Moulding / Manufacturing

Process Project Engineer – Moulding / ManufacturingRoleExciting new role with our client a multinational Medical Device and Healthcare products provider. NIRAS is actively recruiting for an energetic and hands-on Manufacturing/Project Engineer to lead a key project within our Client’s Advanced...

NIRAS Ireland Castlebar, Mayo County, Ireland

Quality Manager

This role involves leading and improving the ISO 13485 Quality Management System within a medical device manufacturer producing Class IIa and IIb products. The Quality Manager will manage non-conformances, CAPAs, and returned product investigations while supporting supplier quality and leading internal and external audits. The position operates in a hands-on manufacturing environment with a focus on regulatory compliance and continuous quality improvement.

ProTech Recruitment Ltd Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £60,000 – £70,000 pa

On-site Permanent

Assembly Technician

Client;We are proud to be working alongside a truly ground-breaking medical device business, who are looking to appoint a process/assembly technician.POSITION; Process/Assembly TechnicianSHIFT; Monday - Friday 8 - 4:30Hourly Rate - £14.00 - £14.25 an hour.The key responsibilities for this...

Planet Recruitment Oxford, Oxfordshire, United Kingdom £14 – £14 ph

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Quality and Test Technician

This role involves hands-on quality and testing activities in a medical device manufacturing environment, including inspections, non-conformance investigations, CAPA support, and audit readiness. You'll work across the full quality lifecycle, conducting pressure vessel testing and driving continuous improvement while collaborating with engineering and production teams. The position offers mentorship and career development within a regulated, quality-driven setting.

ReeVR Talent Granborough, Buckinghamshire, MK18 3LR, United Kingdom £32,000 – £40,000 pa

On-site Permanent

Technical Documentation and Development Engineer

This role involves creating, managing, and improving technical documentation and CAD models for medical devices, ensuring compliance with MDR regulations. The engineer will own technical files, support product development and legacy improvements, and collaborate with R&D, regulatory, and manufacturing teams. Emphasis is placed on accuracy, regulatory adherence, and structured design control processes.

Michael Page Sheffield, South Yorkshire, United Kingdom £42,000 pa

On-site Permanent