Trabajos medical devices regulatory affairs en Liverpool

Senior/Principal EU Regulatory Consultant - Remote NAMSA pioneered the industry and was the first independent company in the world to focus solely on Medical Device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such pro...

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...

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. ...

My client who is a leading M&E contractor within the commercial & retail sector has a Key Requirement for a Mechanical Project Manager based in Leeds. Previous experience as a M&E Project Manager. Capable of managing and leading operatives to successful completion of projects. ...

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...

Candidates must have experience in a Quality Control environment. The QC Manager is responsible for managing and leading the QC department at Deeside. This includes personnel, equipment and facilities in the cGMP quality control function/laboratory to support the contract manufacture of parentera...

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...

You'll be responsible for the day-to-day monitoring of production processes ensuring the quality of parts produced is compliant with the relevant standards and to ensure that all Quality, H&S and Environmental standards are adhered to. Due to rapid expansion and having recently moved to a new pre...

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...

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. ...

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. Seeking a detail-oriented Regulatory Affairs Manager with experience in Parallel Impor...

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 ...

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...

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 ...

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 ...

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 ...

Delivery Project Manager required for an International Developer and Consultancy for Renewable Energy Generation. Candidates must have 3+ years of project management experience within BESS (Battery Energy Storage Systems), Solar experience is beneficial but not essential. Suitable candidates will...

Series Eight is seeking a full-time Digital Project Manager to join our remote team of designers, developers, project managers, marketers, copywriters and founders. Working independently on your own projects, whilst keeping in sync and collaborating with other project managers and directors. You’...

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...

NEW EXCITING OPPOURTUNITY - MECHANICAL PROJECT MANAGER***. Develop comprehensive project plans for each project, including scope, timeline,budget, and resource allocation. Estimate project costs at pre-contract stage using Senate's project forecast system. Continued monitoring of project costs du...

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:. ...

Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remote Company Description: We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies. Our commitment to quality and compliance drives us to seek talented profession...

... the medical devices. You will play a crucial role in maintaining the highest standards of product quality and compliance with regulatory requirements. Role Responsibilities * To carry out ...