Latest In-House Legal & Ip Director - Remote Jobs

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents within a global medical writing team, with a focus on cross-functional collaboration and scientific strategy. The individual will guide teams, ensure compliance with regulatory standards such as ICH, and mentor junior staff. Based in a hybrid work model, the position supports multiple therapeutic areas and drives process improvements in medical writing operations.

Johnson & Johnson MedTech €78,300 – €135,700 pa

Hybrid Permanent

Manager, Trial Delivery Management

Manages the execution of clinical trial activities, including development of trial-specific documentation, vendor oversight, budget management, and regional coordination. Provides leadership in operational strategy, risk mitigation, and compliance across global studies. Supports compound training and mentors team members within a matrixed, global environment.

Johnson & Johnson MedTech Belgium €79,800 – €137,770 pa

On-site Permanent

Senior Training and Development Specialist EMEA and APAC

Designs and delivers hands-on, field-based training programmes for clinical and sales teams across EMEA and APAC, translating complex clinical data into practical sales and procedural knowledge. Develops simulation tools and scenario-based learning to improve product understanding and customer engagement. Works cross-functionally with Medical Affairs, Marketing, and HCPs to support product launches and commercial effectiveness in the endoscopy space.

Medtronic

Senior Training and Development Specialist EMEA and APAC

Designs and delivers hands-on, field-based training programmes for Medtronic’s Endoscopy unit across EMEA and APAC, translating clinical data into practical sales and clinical tools. Develops simulations and scenario-based learning to improve field performance and customer engagement. Works cross-functionally with marketing, medical affairs, and HCPs to align training with business goals and product launches.

Medtronic £53,600 – £80,400 pa

Product Design Mechanical Engineer - Medical Device - Warwick

This role involves designing and developing medical devices as part of a multidisciplinary engineering team. The engineer will work on life-saving and life-improving products, contributing to full product development cycles within a regulated environment. The company emphasizes innovation, staff growth, and career progression.

Newton Colmore Warwick, United Kingdom

On-site Permanent

Regulatory Affairs and Quality Assurance Assistant - Cambridge

This role involves supporting quality assurance and regulatory affairs activities within a medical devices R&D environment, ensuring compliance with ISO 13485, FDA 510(k), and 21 CFR Part 820 standards. The assistant will collaborate closely with R&D teams, providing guidance on regulatory requirements during product development and improvement. The position plays a key part in maintaining quality management systems and enabling the delivery of innovative, life-improving medical technologies.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

Senior Regulatory Affairs Specialist

This role involves managing regulatory compliance for advanced wound care medical devices throughout their lifecycle, including preparing global regulatory submissions, guiding product development teams, and liaising with regulatory authorities. The specialist ensures adherence to standards such as ISO 13485, FDA 21 CFR Part 820, cGMP, and cGDP, while reviewing product documentation and supporting continuous improvement. Based in Hull, the position operates within a collaborative, global team environment focused on bringing innovative healthcare products to market.

Smith & Nephew United Kingdom

Hybrid Permanent

Surgical Training Specialist

Deliver high-quality surgical training to healthcare professionals by supporting hands-on courses, managing lab equipment and specimens, and ensuring regulatory compliance. Collaborate with cross-functional teams to maintain training standards and advance surgical techniques. The role emphasizes technical support, safety, and continuous improvement in a state-of-the-art training environment.

Smith & Nephew Watford, United Kingdom

Hybrid Permanent

Clinical Advisor

The RoleTPP are expanding their clinical team and are seeking a clinical advisor to support the ongoing development of SystmOne.TPP’s world-class technology supports professionals across all areas of the NHS health and social care system, as well as providers in...

TPP (The Phoenix Partnership) Horsforth, United Kingdom

Permanent

Radiographer - MRI - Bexhill

Perform routine MRI scans and administer contrast under established protocols, ensuring high image quality and patient comfort. Work across multiple centres in Sussex within a supportive team environment, contributing to quality improvement and clinical development. Gain exposure to advanced 1.5T and 3T MRI technology with opportunities for cross-training in CT and general imaging.

Medical Imaging Partnership Bexhill-on-Sea, TN39 3JX, United Kingdom £22,200 – £25,800 pa

Systems Engineer

Design and develop advanced automotive health and wellbeing systems, integrating medical and holistic wellbeing technologies with electronic hardware and software. Work across the full product lifecycle from concept to production, focusing on occupant state sensing, in-car measures, and connected services within a systems engineering framework.

Envisage Recruitment Limited Manchester, United Kingdom £35 pa

Production Scientist

This role involves hands-on development and optimisation of human stem cell-derived 3D culture models for drug discovery. The Production Scientist will design and run complex in vitro experiments, establish robust protocols, and contribute to platform validation and scalability. Working in a startup environment, the individual will play a key role in shaping scientific workflows and processes while ensuring high reproducibility and quality in experimental outputs.

Vero Hr Harehills, West Yorkshire, LS8 5JF, United Kingdom £35,000 – £45,000 pa

On-site Contract

Defect, Risk & Configuration Manager

The role involves managing the full defect lifecycle, leading technical risk assessments, and maintaining configuration baselines in SAP across engineering projects within the medical devices sector. Responsibilities include developing defect tracking systems in RETINA, defining KPIs and dashboards, writing management plans and reports, and applying structured risk processes. The position requires close collaboration with test and product teams to ensure compliance and resolution.

Talentmark Motherwell, Lanarkshire, ML1 1RB, United Kingdom £22 – £25 pa

Principal Electronics Engineer

Lead electronics design and development for advanced medical devices, managing a small team and guiding products from concept to launch. Responsible for technical leadership, circuit and system innovation, and acting as the key link between engineering and senior stakeholders. Involves hands-on bench work, embedded software development, and direct customer liaison.

Vector Recruitment Milton, Cambridgeshire, Cambridgeshire, United Kingdom £80,000 – £100,000 pa

Production Process Engineer

The role involves leading continuous improvement initiatives in a medical equipment manufacturing environment, applying Lean Manufacturing principles to enhance safety, quality, productivity, and cost efficiency. The engineer will develop production processes, resolve issues through root cause analysis, and collaborate with cross-functional teams to ensure efficient manufacturing and product improvements.

Medstrom Diseworth, Leicestershire, DE74 2QD, United Kingdom £48,000 pa

On-site Permanent