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We are currently seeking a committed and experienced Senior Manager RAQA for a global leader within medical devices. The ideal candidate should possess a keen interest in quality assurance and regulatory affairs, with the ability to manage and lead the team effectively.
We are seeking a detail-oriented Labelling Specialist / Project Coordinator to assist with all aspects of labelling coordination within the labelling department. The ideal candidate will have a passion for detail, a high level of organisational skills, and high levels of administration experience.
We are seeking a meticulous and dedicated Senior Regulatory Affairs Associate with a strong background in Regulatory Affairs (Medical Devices). The successful candidate will be responsible for ensuring compliance with regulatory standards (MDD-MDR experience is essential).
Providing support within the regulatory function maintaining and expanding the specified product registrations within UK and EU.
An ideal role for someone experienced within QA/QC roles working to ISO17025
You will be responsible for the development, validation & verification and other scientific processes for all their labs to meet the needs of the business, complying with all relevant quality standards. You will be working closely with the Laboratory Operations Managers and Heads of Departments, to ensure the efficient development, implementation, operation and quality of their service delivery.
Our client are seeking a detail-oriented Operations Coordinator to join their supply chain department. The candidate will play a crucial role in streamlining operations and ensuring efficiency within the pharmaceutical industry.
This role as a Project Planning Specialist is perfect for a highly organised professional who thrives in a technology-driven environment. Looking for someone who does this as a specialist rather than a Project or Programme Manager who does it as part of their job.
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