Medical devices regulatory affairs jobs in Epsom

Implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements and manage the development of the regional product label by collaborating with the Labeling Working Group. CK Group are recruitin...

Make a real difference to people’s lives byjoining as a Care Assistant with TrinityHomecare. Experiencedor not - we can offer you one of the most rewarding experiences bybecoming a Care Assistant. As a Carer, you will be care matched withyour clients where you will be supporting them in and aroun...

As a Senior Regulatory Affairs Associate, you will play a crucial role in ensuring regulatory compliance for our medical devices. Regulatory Affairs Specialist - Medical Device. You will collaborate closely with the Regulatory Affairs Manager and cross-functional teams to prepare and review regul...

Senior Regulatory Affairs Specialist - Medical Device. Perform Regulatory tasks to ensure compliance with regulations. Prepare regulatory documentation and submissions for product approvals. Develop regulatory plans/strategies for new products and changes to existing products. ...

Senior Regulatory Affairs Officer (Maternity Cover). Senior Regulatory Affairs Officer opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-orient...

Regulatory Affairs Specialist - Lifecycle Maintenance. We are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle ...

Provide high level strategic and operational regulatory direction and mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approvals in international markets, regulatory strategic development plans and risk ...

Join a dynamic team in the heart of London as a Data Quality Specialist! My insurance understands the paramount importance of data-driven decisions in the industry. That's why we're seeking a talented individual to spearhead the efforts in ensuring consistently high-quality, actionable data acros...

You will be the specialist in supporting the quality team with the technical requirements of the business, ensuring that the brand constantly delivers safe, high-quality food for pets. At least five years of quality management experience and a track record of supporting businesses on their qualit...

The Project Manager will be effectively managing construction projects within the Midlands and North regions and the delivery of Mechanical, Electrical and Civil project activities, and coordinate with the Engineers, Designers, Planners and QS/Legal teams. Experience of delivering multi-million p...

Senior Regulatory Affairs & PV Manager. Senior Regulatory Affairs & PV Manager opportunity working for a growing pharmaceutical company specialising in medicinal, non-medicinal, medical devices, and OTC products. Ensuring that regulatory processes are completed and products are launched in line w...

Associate Director (Regulatory Affairs). As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory Affairs. Title: Associate Director (Regulatory Affairs). Lead an...

Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulatory experience!. Manage the operational and technical as...

We are now looking for a detail-oriented Project Manager to lead and coordinate our numerous physical projects. The Project Manager will be an integral part of our dynamic team, responsible for the scope, schedule, finances, risk, quality, and resources of a project. Has a background as a project...

As a Senior Regulatory Affairs Officer, you will be responsible for managing regulatory submissions in the UK and European markets including supporting over 150 product licenses. Senior Regulatory Affairs Officer. Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical ...

The Clinical Trial Project Manager will be responsible for managing, planning, and executing clinical trials. Achieves study objectives by working with team members to set project priorities and milestones and resolve project conflicts. Lead regular meetings/calls with sponsor to ensure they are ...

Associate Director (Regulatory Affairs). As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory Affairs. Title: Associate Director (Regulatory Affairs). Lead an...

Job title: Senior Regulatory Affairs Associate. A food and nutrition business in London are seeking a Senior Regulatory Affairs Associate to join their team. Proven experience in regulatory affairs. ...

Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...

Join our dynamic team as a Regulatory Affairs Manager, where you'll support regional regulatory activities for innovative products. Regulatory Affairs Manager (Inside IR35). As a key member of the Global Regulatory Team (GRT), you'll develop and execute regulatory strategies and ensure compliance...

Well known and respected Wellness brand are looking for a Senior Regulatory Affairs Manager who has experience in Herbal Medicines (ideally) Medical Devices and CosmeticsAs a Senior Regulatory ...

Up to £50,000 Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical company that specialising in medicinal, non-medicinal, medical devices, and OTC products. The ...

... Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an ... trials and medical products. * Contributing regulatory guidance in order to enhance product ...

UK CW Regulatory Affairs Manager (Inside IR35) This role will support one or more products from a ... medical device companies. Proclinical Staffing is an equal opportunity employer.