Medical devices regulatory affairs jobs in Wolverhampton

My Large Public Sector client is looking to recruit a number of Interim HR Project Managers to join the established PMO team with the remit of delivering the organisations Equal Pay Agenda. ...

... Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

... Regulations Authority and/or CILEX professional conduct rules and standards / ISO / firm ... affairs · Self-motivated and able to use initiative · Sound grasp of your own discipline · ...

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...

This will be a highly diverse role; typical duties include answering complex customer regulatory enquiries, researching/impact assessing emerging regulatory issues, regulatory support to NPD, product notifications, REACH registrations, managing external expert consultants and, sharing your regula...

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 ...

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 ...

As such, they are looking for a Project Manager to join them on a contract basis to lead the migration process. Working closely with People, Finance, and IT colleagues, responsible for project vision, objectives, and scope, solution design, delivery, and embedding. ...

Bioconjugation projects are carried out in Germany, Enzyme projects are based in Austria and biological IVD reagents in Ireland. To manage and deliver Complex Chemicals projects globally and with external partners, within budget, to agreed quality standards and other stipulated criteria. To manag...

Provide project management support for Development Projects. Leading and co-ordinating role in project managing all new product launch programs within NPD, participate in and manage supply chain planning, sourcing decisions and quality assessment to ensure all party readiness for product launch t...

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

Panoramic Associates are working with a construction company that are seeking a highly organised and experienced Project Manager to oversee operations on the proposed new Care Home development. The Project Manager will be responsible for managing and supervising all aspects of the site, ensuring ...

Front of House Coordinator/Receptionist- Leamington Spa. ...

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...

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...

Client Relations & Project Manager | Fast Growth Music Distribution Business. Harmonic are delighted to be working on a retained basis with one of the UK music industry’s fastest growing management and distribution businesses, in the search for a Client Relations & Project Manager, in an exciting...

Receptionist – Private Members Club. One of the most exclusive private members club in London, the place to be for politicians, royals and A-list alike is looking for a talented and passionate Receptionist to join their team. The successful Receptionist will be rewarded with:. ...

A luxury Resort group is seeking and experienced Project manager to lead a large team in the development of 2 resorts in the Caribbean for a listed global hotel group. The ideal candidate for this position will provide project management for planning, and organising all aspects of two luxury 5 st...

To co-ordinate and project manage all activity related to specified event and travel projects from inception through to project delivery and post-project actions. To act as trip leader, project manager or designated 2 i/c (or other support function) and to understand and carry out full responsibi...

My client is looking to appoint a Senior Project Manager to lead an education projects in West London. Senior Project Manager taking full responsibility for project delivery. Candidates will need to have relevant experience as a Project Manager with a main contractor ideally gained on projects of...

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 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. ...