Medical devices regulatory affairs jobs in Cambridge

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. ...

Due to recent success within one our Innovative Biotech Clients I am recruiting for a Regulatory Affairs manager at ICON - Working in a client-dedicated yet fully embedded role ICON’s Regulatory Strategy group, you will lead or contribute to the development and execution of the drug development s...

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...

Senior Manager Regulatory Affairs Writing. A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. You will lead a team responsible for developing the content for submissions to both US and EU regulatory agencies. ...

Job title: Senior Regulatory Affairs Manager CMC. A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. CMC Regulatory Affairs within the pharmaceutical or biotechnology industry. The role will be responsible for the development, executio...

We are seeking a highly motivated and experienced OTC Pharmaceuticals Specialist to join our team. The successful candidate will play a key role in product development, regulatory compliance, marketing strategies, and customer support within the OTC pharmaceutical sector. Ensure compliance with r...

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...

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 ...

Regulatory Affairs Manager (Parallel Import). Regulatory Affairs Manager opportunity working for a family-run pharmaceutical company that specialise in generic, OTC, medical devices, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-orient...

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 ...

The Project Manager will report into the Property / Business Director and be responsible for the 360 oversight of nursery new build, reconfiguration and fit-out projects valued up to circa £2/3 million each from initial feasibility and DD at acquisitions stage through appointing and managing exte...

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...

Control Now (CN) is looking for a Regulatory Affairs Manager to support the business with monitoring and interpreting regulatory change and notifications. The Regulatory Affairs Manager will play a vital role in supporting the product, marketing and management teams to stay informed with changes ...

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 ...

I have a new opportunity for an experienced project manager to join a reputable housing business with ambitions to deliver circa 250 quality homes and communities per year across Cornwall. They will also effectively monitor and present project updates to relevant stakeholders, clients, or project...

Based in the UK, the Regulatory Affairs Associate is expected to;. Keeping up to date with regulatory and legal changes in EU. Preparing pre- and post-authorisation regulatory documentation and applications. Providing general regulatory advice to company's staff. ...

Interim Dynamics Business Central Project Manager. Project Management: Lead the end-to-end implementation of Microsoft Dynamics 365 Business Central, ensuring adherence to project timelines, budget, and quality standards. Strong project management skills, with the ability to effectively plan, org...

We are seeking a talented and experienced Creative Project Manager to spearhead creative marketing campaigns for our clients in the video game industry. Oversee client marketing projects from concept through execution, ensuring alignment with client goals and industry standards. Strong project ma...

We are looking for a Project Manager to join our Central Banking projects team, providing project management support across one of our esteemed Banking & Finance accounts for ISS UK&I. You will be an experienced and driven Project Manager with a passion for delivering successful projects. As a Pr...

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 ...

RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. Working knowledge and experience within an IVD Regulatory Affairs function. Experience wi...

Medical Devices Consultant - Senior Mechanical Engineer - Cambridge Due to the growth of a leading ... Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors.

Senior Manager Regulatory Affairs Writing A growing Biotech in Cambridge with multiple Phase 3 ... Responsibilities: * scientific contribution to the development of medical, regulatory and clinical ...