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Providing support within the regulatory function maintaining and expanding the specified product registrations within UK and EU.
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).
The head of Quality and Regulatory must lead the quality and regulatory agenda ensuring customer and regulatory requirements are met.Also the succesful applicant will need to develop Quality culture, and ensure that all staff within the business are operating to the highest level of compliance.
The IT Infrastructure Manager is responsible for maintaining and maturing all elements of IT Infrastructure to deliver IT Infrastructure services to the business.You will be responsible for the management and mentoring a team of technical staff that provides a service that truly supports the business.
Working in the Project Management team as project owner, assisting with technical and commercial aspects. Running projects in a controlled and timely manner, utilising project management methodologies and planning in accordance with multi-site processes.
This is an exciting opportunity to join as an Operations Manager, where you would be orchestrating internal operations, during a period of growth and innovation for the business. The successful candidate will be working alongside the founders, being at the heart of their administrative effectiveness, taking charge of key operations.
This is a prestigious opportunity for a VP/SVP of Partnerships to play a pivotal role in a leading Life Science company. The successful candidate will spearhead collaborations, develop strategic partnerships, and champion growth initiatives across the US with flexible working out of the HQ in San Francisco.
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