In this role you will be writing regulatory and clinical documents such as clinical study reports and DSURs. You will be providing expertise in Medical Writing, leading the in house Medical Writing function.

In this role you would be leading the writing and editing team. You would also be dealing with clients and other stakeholders.

This role requires the candidate to be able to travel into the office when needed, based in London. Alongside the writing, you would be required to mentor less experienced members of the team to build the team's strengths.

An exciting opportunity to join growing Oncology Medical team, looking at candidates with Medical Advisor experience looking to improve their career.

An exciting opportunity to a join growing Medical team, looking at candidates with Medical Advisor experience looking to further develop their career.

The proposal developer is responsible for all steps and interactions required to write and prepare Sponsored Editorial proposals for submission in a defined time scale, to the highest quality, and with minimal supervision.

In the role of Events Manager you will be responsible for planning and implementing internal and external events within the Medical Sector, you will be expected to manage and support the day-to-day event co-ordination and delivery.

Responsible for overseeing processes for Design Examination; Technical Documentation reviews and Vigilance for medical devices, with particular emphasis on Pre-Clinical and Clinical issues. Ensure the effective interaction between Product Assessors, In house Clinicians and Medical Device Technical team to provide an efficient and compliant service to the approved body and global delivering affiliates.

Work with external DPO and Information Security partners to ensure the technology environment is as secure as possible for our client and practice data.Requires expert knowledge and experience as a Data Practitioner and showing familiarity in a number of technology infrastructures including MS365, SharePoint, OneDrive and Azure

You will be working in an established team on global projects, developing and implementing Marketing campaigns.

The RA Associate will provide regulatory expertise in the research, development and marketing of products. The role holder will prepare regulatory submissions and ensure regulatory approvals are obtained and maintained within project registration plans and the needs of the business.

An exciting opportunity to a join growing Medical team, looking at candidates with MSL management and leadership experience looking to further develop their career.

This role of a medical writer is to author relevant, specific materials including PSURs, RMPs, RFIs etc. You would also be leading product safety review meetings and deliver training presentations to varying levels of experience.

The Principle Regulatory Affairs Specialist will develop Regulatory strategies related to regulatory documents, submissions, investigations, product development planning and regulatory agency interaction

• Set up procurement alongside a Head of Procurement
• This will involve setting procurement strategies, and supporting and guiding the business to understand

Healthcare Research Project requires an experienced Receptionist/Admin for their site based in Southall. This is not an NHS or Hospital based role but is based within a community centre. Background in healthcare/medical is preferred.

The Sourcing Manager will focus on sourcing a variety of products from suppliers around the world to aid in the further expansion of our global presence, and will play a key role in procurement, sourcing, analysing suppliers and products, and carrying out efficient procurement processes to provide our customers with the highest possible levels of service

Reporting to the Head of QA you will be responsible for ensuring that regulatory and customer requirements are met, monitoring and identifying trends to provide early warning of potential quality issues.

The Production Manager is responsible for supervising three Production Technicians and overseeing the expansion of the laboratories on their UK site.

The bio-compatibility Engineer vacancy is a newly created role, sitting within the research and development arm of the business. The appointee will be responsible for scaling up the current product range by commissioning tests to determine the toxicity of the medical devices.

• Assist customers in establishing an accessible life. And offer advice when choosing ancillary products.
• Consistent communication with customers on the phone and via video to support them in their care plan.

Under the supervision of the Clinical Trials Manager we are looking for an energetic, focused individual to set up, monitor and close-out clinical trials involving the Swift medical device. This position is a key role and is ideal for a candidate who has experience in clinical research trials.

Due to company expansion this medical device manufacturer are aiming to add several Production technicians to Manufacturing team.

The Regulatory Affairs Specialist will be responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for the company products globally

The role is to develop software to transform metadata to healthcare standards, performing detailed image analysis & refinement, capturing distributed faults/usage/metric for analytics processing in the cloud.

You will be programming in C# and lead the design and development of performant, scalable middleware components.

This role is an exciting opportunity for an experienced Account Director to take control of a team. You need a number of skills including people management, client management, financial management and business development.

The Senior Editor is a remote role for a large Med Comms agency. They are looking for you to act as a role model to junior team members and lead the team.

This role is a hybrid role with the business based in Cambridge. You would be responsible for operations, projects and external events alongside pushing engagement activity in collaboration with other teams within the organisation.

You would be joining a growing team as a Senior Regulatory Writer in an expanding Med Comms business. You would have experience in CTD Modules, ISS, ISE, Scientific advice/briefing documents.