Trabajos medical devices regulatory affairs en Leeds

Senior Regulatory Affairs Specialist - Medical Device Main Purpose of Job and Objectives: 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 exi...

About us For over 30 years, Surgical Innovations have proudly designed, developed and manufactured high quality, precision engineered instruments for minimally invasive surgery and are a leading UK manufacturer of medical devices in its respective field. Our success is our people and we curre...

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. ...

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...

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...

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 ...

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...

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. ...

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 regulatory requirements and standards governing the manufacturing, labelling, and marketing of OTC p...

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...

Senior Director of Regulatory Affairs – UK remote. We are looking for a Senior Director of Regulatory Affairs, who will report into the senior leadership team and play a key role for the company strategy & direction by acting as their primary liaison to the EMEA, and wider EEA. Extensive experien...

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...

Project Management of Mobilisation and Implementation projects covering systems, continuous improvement, and strategic projects. Support with PMO tools & templates to enable project managers to better deliver projects. Act as Project Manager by planning, supporting, facilitating and monitoring pr...

This is a full-time on-site role for an Architect/Project Manager at Push Design Ltd in central London. We bring diverse experience and knowledge to every project, ensuring high-quality results with value for money solutions from concept to completion. The right candidate will be responsible for ...

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...

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...

This is a great opportunity for an experienced Digital Project Manager looking for a step up or an established Senior Project Manager looking to take an active role in further shaping their delivery proposition. As Digital Project Manager, you will be working across a range of projects for a wide...

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...

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 ...

The role of Senior Regulatory Affairs Associate is focused on the regulatory requirements of the business in line with timelines set by relevant authorised bodies. Provide regulatory input on project teams for projects including but not limited to new product development, continuous improvement, ...

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. ...

... UK manufacturer of medical devices in its respective field. Our success is our people and we ... About the Position The role of Senior Regulatory Affairs Associate is focused on the regulatory ...

Produce and maintain up to date technical files for medical devices to the required standards ... When required, compile and submit reportable events to relevant regulatory authorities in timely ...